Journal Description
Nanomaterials
Nanomaterials
is an international, peer-reviewed, interdisciplinary scholarly open access journal, published semimonthly online by MDPI. It publishes reviews, regular research papers, communications, and short notes that are relevant to any field of study that involves nanomaterials, with respect to their science and application. The Spanish Carbon Group (GEC) is affiliated with Nanomaterials and their members receive discounts on the article processing charges.
- Open Access— free for readers, with article processing charges (APC) paid by authors or their institutions.
- High Visibility: indexed within Scopus, SCIE (Web of Science), PubMed, PMC, CAPlus / SciFinder, Inspec, and other databases.
- Journal Rank: JCR - Q1 (Physics, Applied) / CiteScore - Q1 (General Chemical Engineering)
- Rapid Publication: manuscripts are peer-reviewed and a first decision is provided to authors approximately 13.6 days after submission; acceptance to publication is undertaken in 2.5 days (median values for papers published in this journal in the second half of 2023).
- Recognition of Reviewers: reviewers who provide timely, thorough peer-review reports receive vouchers entitling them to a discount on the APC of their next publication in any MDPI journal, in appreciation of the work done.
- Companion journals for Nanomaterials include: Nanomanufacturing and Applied Nano.
Impact Factor:
5.3 (2022);
5-Year Impact Factor:
5.4 (2022)
Latest Articles
The Role of Oxygen Vacancies in Phase Transition and the Optical Absorption Properties within Nanocrystalline ZrO2
Nanomaterials 2024, 14(11), 967; https://doi.org/10.3390/nano14110967 (registering DOI) - 2 Jun 2024
Abstract
Zirconia (ZrO2) nanoparticles were synthesized using a solvothermal method under varying synthesis conditions, namely acidic, neutral, and alkaline. X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) were leveraged to investigate the phase evolution and topographical features in detail. The
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Zirconia (ZrO2) nanoparticles were synthesized using a solvothermal method under varying synthesis conditions, namely acidic, neutral, and alkaline. X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) were leveraged to investigate the phase evolution and topographical features in detail. The resulting crystal phase structures and grain sizes exhibited substantial variation based on these conditions. Notably, the acidic condition fostered a monoclinic phase in ZrO2, while the alkaline condition yielded a combination of tetragonal and monoclinic phases. In contrast, ZrO2 obtained under neutral conditions demonstrated a refinement in grain sizes, constrained within a 1 nm scale upon an 800 °C thermal treatment. This was accompanied by an important transformation from a monoclinic phase to tetragonal phase in the ZrO2. Furthermore, a rigorous examination of XPS data and a UV-visible spectrometer (UV-vis) analysis revealed the significant role of oxygen vacancies in phase stabilization. The notable emergence of new energy bands in ZrO2, in stark contrast to the intrinsic bands observed in a pure monoclinic sample, are attributed to these oxygen vacancies. This research offers valuable insights into the novel energy bands, phase stability, and optical absorption properties influenced by oxygen vacancies in ZrO2. Moreover, it proposes an innovative energy level model for zirconia, underpinning its applicability in diverse technological areas.
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(This article belongs to the Special Issue Synthesis and Application of Optical Nanomaterials)
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Encapsulation and Evolution of Polyynes Inside Single-Walled Carbon Nanotubes
by
Kunpeng Tang, Yinong Li, Yingzhi Chen, Weili Cui, Zhiwei Lin, Yifan Zhang and Lei Shi
Nanomaterials 2024, 14(11), 966; https://doi.org/10.3390/nano14110966 (registering DOI) - 2 Jun 2024
Abstract
Polyyne is an sp-hybridized linear carbon chain (LCC) with alternating single and triple carbon–carbon bonds. Polyyne is very reactive; thus, its structure can be easily damaged through a cross-linking reaction between the molecules. The longer the polyyne is, the more unstable it becomes.
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Polyyne is an sp-hybridized linear carbon chain (LCC) with alternating single and triple carbon–carbon bonds. Polyyne is very reactive; thus, its structure can be easily damaged through a cross-linking reaction between the molecules. The longer the polyyne is, the more unstable it becomes. Therefore, it is difficult to directly synthesize long polyynes in a solvent. The encapsulation of polyynes inside carbon nanotubes not only stabilizes the molecules to avoid cross-linking reactions, but also allows a restriction reaction to occur solely at the ends of the polyynes, resulting in long LCCs. Here, by controlling the diameter of single-walled carbon nanotubes (SWCNTs), polyynes were filled with high yield below room temperature. Subsequent annealing of the filled samples promoted the reaction between the polyynes, leading to the formation of long LCCs. More importantly, single chiral (6,5) SWCNTs with high purity were used for the successful encapsulation of polyynes for the first time, and LCCs were synthesized by coalescing the polyynes in the (6,5) SWCNTs. This method holds promise for further exploration of the synthesis of property-tailored LCCs through encapsulation inside different chiral SWCNTs.
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(This article belongs to the Special Issue Preparation, Properties, and Applications of One-Dimensional Carbon Nanomaterials)
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Open AccessArticle
Structural, Electrical, and Optical Properties of Single-Walled Carbon Nanotubes Synthesized through Floating Catalyst Chemical Vapor Deposition
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Melorina Dolafi Rezaee, Biplav Dahal, John Watt, Mahir Abrar, Deidra R. Hodges and Wenzhi Li
Nanomaterials 2024, 14(11), 965; https://doi.org/10.3390/nano14110965 (registering DOI) - 2 Jun 2024
Abstract
Single-walled carbon nanotube (SWCNT) thin films were synthesized by using a floating catalyst chemical vapor deposition (FCCVD) method with a low flow rate (200 sccm) of mixed gases (Ar and H2). SWCNT thin films with different thicknesses can be prepared by
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Single-walled carbon nanotube (SWCNT) thin films were synthesized by using a floating catalyst chemical vapor deposition (FCCVD) method with a low flow rate (200 sccm) of mixed gases (Ar and H2). SWCNT thin films with different thicknesses can be prepared by controlling the collection time of the SWCNTs on membrane filters. Transmission electron microscopy (TEM) showed that the SWCNTs formed bundles and that they had an average diameter of 1.46 nm. The Raman spectra of the SWCNT films suggested that the synthesized SWCNTs were very well crystallized. Although the electrical properties of SWCNTs have been widely studied so far, the Hall effect of SWCNTs has not been fully studied to explore the electrical characteristics of SWCNT thin films. In this research, Hall effect measurements have been performed to investigate the important electrical characteristics of SWCNTs, such as their carrier mobility, carrier density, Hall coefficient, conductivity, and sheet resistance. The samples with transmittance between 95 and 43% showed a high carrier density of 1021–1023 cm−3. The SWCNTs were also treated using Brønsted acids (HCl, HNO3, H2SO4) to enhance their electrical properties. After the acid treatments, the samples maintained their p-type nature. The carrier mobility and conductivity increased, and the sheet resistance decreased for all treated samples. The highest mobility of 1.5 cm2/Vs was obtained with the sulfuric acid treatment at 80 °C, while the highest conductivity (30,720 S/m) and lowest sheet resistance (43 ohm/square) were achieved with the nitric acid treatment at room temperature. Different functional groups were identified in our synthesized SWCNTs before and after the acid treatments using Fourier-Transform Infrared Spectroscopy (FTIR).
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(This article belongs to the Special Issue Advances in Carbon Nanotubes: Synthesis, Properties, and Cutting-Edge Applications)
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Open AccessArticle
Photonic Nanochains for Continuous Glucose Monitoring in Physiological Environment
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Gongpu Shi, Luying Si, Jinyang Cai, Hao Jiang, Yun Liu, Wei Luo, Huiru Ma and Jianguo Guan
Nanomaterials 2024, 14(11), 964; https://doi.org/10.3390/nano14110964 (registering DOI) - 1 Jun 2024
Abstract
Diabetes is a common disease that seriously endangers human health. Continuous glucose monitoring (CGM) is important for the prevention and treatment of diabetes. Glucose-sensing photonic nanochains (PNCs) have the advantages of naked-eye colorimetric readouts, short response time and noninvasive detection of diabetes, showing
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Diabetes is a common disease that seriously endangers human health. Continuous glucose monitoring (CGM) is important for the prevention and treatment of diabetes. Glucose-sensing photonic nanochains (PNCs) have the advantages of naked-eye colorimetric readouts, short response time and noninvasive detection of diabetes, showing immense potential in CGM systems. However, the developed PNCs cannot disperse in physiological environment at the pH of 7.4 because of their poor hydrophilicity. In this study, we report a new kind of PNCs that can continuously and reversibly detect the concentration of glucose (Cg) in physiological environment at the pH of 7.4. Polyacrylic acid (PAA) added to the preparation of PNCs forms hydrogen bonds with polyvinylpyrrolidone (PVP) in Fe3O4@PVP colloidal nanoparticles and the hydrophilic monomer N-2-hydroxyethyl acrylamide (HEAAm), which increases the content of PHEAAm in the polymer shell of prepared PNCs. Moreover, 4-(2-acrylamidoethylcarbamoyl)-3-fluorophenylboronic acid (AFPBA), with a relatively low pKa value, is used as the glucose-sensing monomer to further improve the hydrophilicity and glucose-sensing performances of PNCs. The obtained Fe3O4@(PVP-PAA)@poly(AFPBA-co-HEAAm) PNCs disperse in artificial serum and change color from yellow-green to red when Cg increases from 3.9 mM to 11.4 mM, showing application potential for straightforward CGM.
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(This article belongs to the Section Nanofabrication and Nanomanufacturing)
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Influence of Hole Transport Layers on Buried Interface in Wide-Bandgap Perovskite Phase Segregation
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Fangfang Cao, Liming Du, Yongjie Jiang, Yangyang Gou, Xirui Liu, Haodong Wu, Junchuan Zhang, Zhiheng Qiu, Can Li, Jichun Ye, Zhen Li and Chuanxiao Xiao
Nanomaterials 2024, 14(11), 963; https://doi.org/10.3390/nano14110963 (registering DOI) - 1 Jun 2024
Abstract
Light-induced phase segregation, particularly when incorporating bromine to widen the bandgap, presents significant challenges to the stability and commercialization of perovskite solar cells. This study explores the influence of hole transport layers, specifically poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine (PTAA) and [4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz), on the dynamics of
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Light-induced phase segregation, particularly when incorporating bromine to widen the bandgap, presents significant challenges to the stability and commercialization of perovskite solar cells. This study explores the influence of hole transport layers, specifically poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine (PTAA) and [4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz), on the dynamics of phase segregation. Through detailed characterization of the buried interface, we demonstrate that Me-4PACz enhances perovskite photostability, surpassing the performance of PTAA. Nanoscale analyses using in situ Kelvin probe force microscopy and quantitative nanomechanical mapping techniques elucidate defect distribution at the buried interface during phase segregation, highlighting the critical role of substrate wettability in perovskite growth and interface integrity. The integration of these characterization techniques provides a thorough understanding of the impact of the buried bottom interface on perovskite growth and phase segregation.
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(This article belongs to the Special Issue Advancing the Sustainable Application of Nanostructured Materials in Solar Cells)
Open AccessArticle
Performance Projection of Vacuum Gate Dielectric Doping-Free Carbon Nanoribbon/Nanotube Field-Effect Transistors for Radiation-Immune Nanoelectronics
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Khalil Tamersit, Abdellah Kouzou, José Rodriguez and Mohamed Abdelrahem
Nanomaterials 2024, 14(11), 962; https://doi.org/10.3390/nano14110962 (registering DOI) - 1 Jun 2024
Abstract
This paper investigates the performance of vacuum gate dielectric doping-free carbon nanotube/nanoribbon field-effect transistors (VGD-DL CNT/GNRFETs) via computational analysis employing a quantum simulation approach. The methodology integrates the self-consistent solution of the Poisson solver with the mode space non-equilibrium Green’s function (NEGF) in
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This paper investigates the performance of vacuum gate dielectric doping-free carbon nanotube/nanoribbon field-effect transistors (VGD-DL CNT/GNRFETs) via computational analysis employing a quantum simulation approach. The methodology integrates the self-consistent solution of the Poisson solver with the mode space non-equilibrium Green’s function (NEGF) in the ballistic limit. Adopting the vacuum gate dielectric (VGD) paradigm ensures radiation-hardened functionality while avoiding radiation-induced trapped charge mechanisms, while the doping-free paradigm facilitates fabrication flexibility by avoiding the realization of a sharp doping gradient in the nanoscale regime. Electrostatic doping of the nanodevices is achieved via source and drain doping gates. The simulations encompass MOSFET and tunnel FET (TFET) modes. The numerical investigation comprehensively examines potential distribution, transfer characteristics, subthreshold swing, leakage current, on-state current, current ratio, and scaling capability. Results demonstrate the robustness of vacuum nanodevices for high-performance, radiation-hardened switching applications. Furthermore, a proposal for extrinsic enhancement via doping gate voltage adjustment to optimize band diagrams and improve switching performance at ultra-scaled regimes is successfully presented. These findings underscore the potential of vacuum gate dielectric carbon-based nanotransistors for ultrascaled, high-performance, energy-efficient, and radiation-immune nanoelectronics.
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(This article belongs to the Section Nanoelectronics, Nanosensors and Devices)
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Effects of Composition and Polymerization Conditions on the Electro-Optic Performance of Liquid Crystal–Polymer Composites Doped with Ferroelectric Nanoparticles
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Gaby Nordendorf, Gisela Jünnemann-Held, Alexander Lorenz and Heinz-Siegfried Kitzerow
Nanomaterials 2024, 14(11), 961; https://doi.org/10.3390/nano14110961 (registering DOI) - 31 May 2024
Abstract
The presence of a polymer network and/or the addition of ferroelectric nanoparticles to a nematic liquid crystal are found to lower transition temperatures and birefringence, which indicates reduced orientational order. In addition, the electro-optic switching voltage is considerably increased when a polymer network
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The presence of a polymer network and/or the addition of ferroelectric nanoparticles to a nematic liquid crystal are found to lower transition temperatures and birefringence, which indicates reduced orientational order. In addition, the electro-optic switching voltage is considerably increased when a polymer network is formed by in situ polymerization in the nematic state. However, the resulting polymer network liquid crystal switches at similar voltages as the neat liquid crystal when polymerization is performed at an elevated temperature in the isotropic state. When nanoparticle dispersions are polymerized at an applied DC voltage, the transition temperatures and switching voltages are reduced, yet they are larger than those observed for polymer network liquid crystals without nanoparticles polymerized in the isotropic phase.
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(This article belongs to the Special Issue Nanoelectronics: Materials, Devices and Applications)
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Synthesis, Structural Characterization, and Infrared Analysis of Double Perovskites Pr2NiMnO6, Gd2NiMnO6, and Er2NiMnO6 Functional Nano-Ceramics
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Mebark Elhamel, Zoulikha Hebboul, Djamal Benbertal, Pablo Botella and Daniel Errandonea
Nanomaterials 2024, 14(11), 960; https://doi.org/10.3390/nano14110960 (registering DOI) - 30 May 2024
Abstract
We synthesized Pr2NiMnO6, Gd2NiMnO6, and Er2NiMnO6 double perovskites in a nano-ceramic form by a sol–gel method. By means of room-temperature X-ray powder diffraction measurements, we determined the crystal structure of the three
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We synthesized Pr2NiMnO6, Gd2NiMnO6, and Er2NiMnO6 double perovskites in a nano-ceramic form by a sol–gel method. By means of room-temperature X-ray powder diffraction measurements, we determined the crystal structure of the three compounds, which is monoclinic, corresponding to a double perovskite structure, described by space group P21/n structure. From the determined structures, the bulk moduli were estimated to be 173–179 GPa. The average size particle of nanoparticles was determined from X-ray diffraction by the Langford method plot and by the Scherrer formula. The morphology and homogeneity of nanoparticles were analyzed by scanning electron microscopy. We found that they form compact agglomerations of approximately 200 nm in diameter. Fourier transform infrared spectroscopy measurements were performed, determining the absorption spectrum. The assignment of the measured infrared absorption bands is discussed.
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(This article belongs to the Section Nanocomposite Materials)
Open AccessArticle
Effect of MnO2 Nanoparticles Stabilized with Cocamidopropyl Betaine on Germination and Development of Pea (Pisum sativum L.) Seedlings
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Andrey Nagdalian, Andrey Blinov, Alexey Gvozdenko, Alexey Golik, Zafar Rekhman, Igor Rzhepakovsky, Roman Kolesnikov, Svetlana Avanesyan, Anastasiya Blinova, Maxim Pirogov, Pavel Leontev, Alina Askerova, Evgeniy Tsykin and Mohammad Ali Shariati
Nanomaterials 2024, 14(11), 959; https://doi.org/10.3390/nano14110959 (registering DOI) - 30 May 2024
Abstract
This study aimed to synthesize, characterize, and evaluate the effect of cocamidopropyl betaine-stabilized MnO2 nanoparticles (NPs) on the germination and development of pea seedlings. The synthesized NPs manifested as aggregates ranging from 50–600 nm, comprising spherical particles sized between 19 to 50
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This study aimed to synthesize, characterize, and evaluate the effect of cocamidopropyl betaine-stabilized MnO2 nanoparticles (NPs) on the germination and development of pea seedlings. The synthesized NPs manifested as aggregates ranging from 50–600 nm, comprising spherical particles sized between 19 to 50 nm. These particles exhibited partial crystallization, indicated by peaks at 2θ = 25.37, 37.62, 41.18, 49.41, 61.45, and 65.79°, characteristic of MnO2 with a tetragonal crystal lattice with a I4/m spatial group. Quantum chemical modelling showed that the stabilization process of MnO2 NPs with cocamidopropyl betaine is energetically advantageous (∆E > 1299.000 kcal/mol) and chemically stable, as confirmed by the positive chemical hardness values (0.023 ≤ η ≤ 0.053 eV). It was revealed that the interaction between the MnO2 molecule and cocamidopropyl betaine, facilitated by a secondary amino group (NH), is the most probable scenario. This ascertain is supported by the values of the difference in total energy (∆E = 1299.519 kcal/mol) and chemical hardness (η = 0.053 eV). These findings were further confirmed using FTIR spectroscopy. The effect of MnO2 NPs at various concentrations on the germination of pea seeds was found to be nonlinear and ambiguous. The investigation revealed that MnO2 NPs at a concentration of 0.1 mg/L resulted in the highest germination energy (91.25%), germinability (95.60%), and lengths of roots and seedlings among all experimental samples. However, an increase in the concentration of preparation led to a slight growth suppression (1–10 mg/L) and the pronounced inhibition of seedling and root development (100 mg/L). The analysis of antioxidant indicators and phytochemicals in pea seedlings indicated that only 100 mg/L MnO2 NPs have a negative effect on the content of soluble sugars, chlorophyll a/b, carotenoids, and phenols. Conversely, lower concentrations showed a stimulating effect on photosynthesis indicators. Nevertheless, MnO2 NPs at all concentrations generally decreased the antioxidant potential of pea seedlings, except for the ABTS parameter. Pea seedlings showed a notable capacity to absorb Mn, reaching levels of 586.5 μg/L at 10 mg/L and 892.6 μg/L at 100 mg/L MnO2 NPs, surpassing the toxic level for peas according to scientific literature. However, the most important result was the observed growth-stimulating activity at 0.1 mg/L MnO2 NPs stabilized with cocamidopropyl betaine, suggesting a promising avenue for further research.
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(This article belongs to the Section Biology and Medicines)
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Electrochemical Determination of Uric Acid Using a Nanocomposite Electrode with Molybdenum Disulfide/Multiwalled Carbon Nanotubes (MoS2@MWCNT)
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Johisner Penagos-Llanos, Rodrigo Segura, Amaya Paz de la Vega, Bryan Pichun, Fabiana Liendo, Fernando Riesco and Edgar Nagles
Nanomaterials 2024, 14(11), 958; https://doi.org/10.3390/nano14110958 (registering DOI) - 30 May 2024
Abstract
This paper presents an application for a molybdenum disulfide nanomaterial with multiwalled carbon nanotubes (MoS2@MWCNT/E) in a modified electrode substrate for the detection of uric acid (UA). The modified electrode generates a substantial three-fold increase in the anodic peak current for
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This paper presents an application for a molybdenum disulfide nanomaterial with multiwalled carbon nanotubes (MoS2@MWCNT/E) in a modified electrode substrate for the detection of uric acid (UA). The modified electrode generates a substantial three-fold increase in the anodic peak current for UA compared to the unmodified MWCNT electrode (MWCNT/E). The MoS2@MWCNT/E surface was characterized by cyclic voltammetry (CV), scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS) and electrochemical impedance spectroscopy (EIS). The achieved detection limit stood at 0.04 µmol/L, with a relative standard deviation (RSD) of 2.0% (n = 10). The method’s accuracy, assessed through relative error and percent recovery, was validated using a urine standard solution spiked with known quantities of UA.
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(This article belongs to the Special Issue Carbon Nanomaterials for Electrochemical Applications)
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Solvent-Induced Lignin Conformation Changes Affect Synthesis and Antibacterial Performance of Silver Nanoparticle
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Dan Li and Liheng Chen
Nanomaterials 2024, 14(11), 957; https://doi.org/10.3390/nano14110957 (registering DOI) - 30 May 2024
Abstract
The emergence of antibiotic-resistant bacteria necessitates the development of novel, sustainable, and biocompatible antibacterial agents. This study addresses cytotoxicity and environmental concerns associated with traditional silver nanoparticles (AgNPs) by exploring lignin, a readily available and renewable biopolymer, as a platform for AgNPs. We
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The emergence of antibiotic-resistant bacteria necessitates the development of novel, sustainable, and biocompatible antibacterial agents. This study addresses cytotoxicity and environmental concerns associated with traditional silver nanoparticles (AgNPs) by exploring lignin, a readily available and renewable biopolymer, as a platform for AgNPs. We present a novel one-pot synthesis method for lignin-based AgNPs (AgNPs@AL) nanocomposites, achieving rapid synthesis within 5 min. This method utilizes various organic solvents, demonstrating remarkable adaptability to a wide range of lignin-dissolving systems. Characterization reveals uniform AgNP size distribution and morphology influenced by the chosen solvent. This adaptability suggests the potential for incorporating lignin-loaded antibacterial drugs alongside AgNPs, enabling combined therapy in a single nanocomposite. Antibacterial assays demonstrate exceptional efficacy against both Gram-negative and Gram-positive bacteria, with gamma-valerolactone (GVL)-assisted synthesized AgNPs exhibiting the most potent effect. Mechanistic studies suggest a combination of factors contributes to the antibacterial activity, including direct membrane damage caused by AgNPs and sustained silver ion release, ultimately leading to bacterial cell death. This work presents a straightforward, adaptable, and rapid approach for synthesizing biocompatible AgNPs@AL nanocomposites with outstanding antibacterial activity. These findings offer a promising and sustainable alternative to traditional antibiotics, contributing to the fight against antibiotic resistance while minimizing environmental impact.
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(This article belongs to the Special Issue Biomass-Based Functional Nanomaterials: Synthesis and Application)
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SnS Quantum Dots Enhancing Carbon-Based Hole Transport Layer-Free Visible Photodetectors
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Rui Zhang, Jing Li, Sainan Liao, Shuxin Huang, Chenguang Shen, Mengwei Chen and Yingping Yang
Nanomaterials 2024, 14(11), 956; https://doi.org/10.3390/nano14110956 (registering DOI) - 29 May 2024
Abstract
The recombination of charges and thermal excitation of carriers at the interface between methylammonium lead iodide perovskite (PVK) and the carbon electrode are crucial factors that affect the optoelectronic performance of carbon-based hole transport layer (HTL)-free perovskite photodetectors. In this work, a method
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The recombination of charges and thermal excitation of carriers at the interface between methylammonium lead iodide perovskite (PVK) and the carbon electrode are crucial factors that affect the optoelectronic performance of carbon-based hole transport layer (HTL)-free perovskite photodetectors. In this work, a method was employed to introduce SnS quantum dots (QDs) on the back surface of perovskite, which passivated the defect states on the back surface of perovskite and addressed the energy-level mismatch issue between perovskite and carbon electrode. Performance testing of the QDs and the photodetector revealed that SnS QDs possess energy-level structures that are well matched with perovskite and have high absorption coefficients. The incorporation of these QDs into the interface layer effectively suppresses the dark current of the photodetector and greatly enhances the utilization of incident light. The experimental results demonstrate that the introduction of SnS QDs reduces the dark current by an order of magnitude compared to the pristine device at 0 V bias and increases the responsivity by 10%. The optimized photodetector exhibits a wide spectral response range (350 nm to 750 nm), high responsivity (0.32 A/W at 500 nm), and high specific detectivity (>1 × 1012 Jones).
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(This article belongs to the Section Synthesis, Interfaces and Nanostructures)
Open AccessArticle
Effects of Gold Nanoparticles on Mentha spicata L., Soil Microbiota, and Human Health Risks: Impact of Exposure Routes
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Alexandra Peshkova, Inga Zinicovscaia, Liliana Cepoi, Ludmila Rudi, Tatiana Chiriac, Nikita Yushin, Tran Tuan Anh, Ho Manh Dung and Serghei Corcimaru
Nanomaterials 2024, 14(11), 955; https://doi.org/10.3390/nano14110955 (registering DOI) - 29 May 2024
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Nanoparticles, due to their extensive production and application, can have significant consequences for the environment, including soil and plant pollution. Therefore, it is very important to assess how nanoparticles will affect plants depending on the exposure pathways. The effect of gold nanoparticles in
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Nanoparticles, due to their extensive production and application, can have significant consequences for the environment, including soil and plant pollution. Therefore, it is very important to assess how nanoparticles will affect plants depending on the exposure pathways. The effect of gold nanoparticles in a concentration range of 1–100 mg/L on Mentha spicata L. during a 28-day experiment was investigated. Two routes of nanoparticles exposure were applied: root and foliar. Transmission electron microscopy was used to characterize nanoparticles and their effect on plant leaves’ ultrastructure. Gold content in soil and plant segments was determined using k0-neutron activation analysis. For root exposure, gold was mainly accumulated in soil (15.2–1769 mg/kg) followed by root systems (2.99–454 mg/kg). The maximum accumulation of gold in leaves (5.49 mg/kg) was attained at a nanoparticle concentration of 100 mg/L. Foliar exposure resulted in the maximum uptake of gold in leaves (552 mg/kg) and stems (18.4 mg/kg) at the highest applied nanoparticle concentration. The effect of nanoparticles on the Mentha spicata L. leaves’ biochemical composition was assessed. Nanoparticles affected the content of chlorophyll and carotenoids and led to an increase in antioxidant activity. Root exposure to gold nanoparticles resulted in an increase in the number of starch grains in chloroplasts and also suppressed the activity of the soil microbiota. Gold extraction from mint leaves into herbal infusion varied from 2 to 90% depending on the concentration of nanoparticles in the solution and the exposure route. The health risk as a result of gold exposure via herbal tea intake was assessed through estimated daily intake. The hazard quotient values were found to be less than the cutoff, indicating that a cup of tea infusion should not cause a serious impact to human health.
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Open AccessArticle
Er-Doped BiVO4/BiFeO3 Nanocomposites Synthesized via Sonochemical Process and Their Piezo-Photocatalytic Application
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Thanaphon Kansaard, Maneerat Songpanit, Russameeruk Noonuruk, Chakkaphan Wattanawikkam, Wanichaya Mekprasart, Kanokthip Boonyarattanakalin, Chalicheemalapalli Kulala Jayasankar and Wisanu Pecharapa
Nanomaterials 2024, 14(11), 954; https://doi.org/10.3390/nano14110954 (registering DOI) - 29 May 2024
Abstract
In this work, Er-doped BiVO4/BiFeO3 composites are prepared using the sonochemical process with a difference of rare earth loading compositions. The crystallinity and chemical and morphological structure of as-synthesized samples were investigated via X-ray diffraction, Raman scattering, and electron microscopy,
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In this work, Er-doped BiVO4/BiFeO3 composites are prepared using the sonochemical process with a difference of rare earth loading compositions. The crystallinity and chemical and morphological structure of as-synthesized samples were investigated via X-ray diffraction, Raman scattering, and electron microscopy, respectively. The diffuse reflectance technique was used to extract the optical property and calculate the optical band gap of the composite sample. The piezo-photocatalytic performance was evaluated according to the decomposition of a Rhodamine B organic compound. The decomposition of the organic compound was achieved under ultrasonic bath irradiation combined with light exposure. The Er-doped BiVO4/BiFeO3 composite heterojunction material exhibited significant enhancement of the piezo-photocatalytic activity under both ultrasonic and light irradiation due to the improvement in charge generation and separation. The result indicates that Er dopant strongly affects the phase transformation, change in morphology, and alternation in optical band gap of the BiVO4 matrix. The incorporation of BiFeO3 in the composite form with BiVO4 doped with 1%Er can improve the photocatalytic performance of BiVO4 via piezo-induced charge separation and charge recombination retardment.
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(This article belongs to the Section Nanocomposite Materials)
Open AccessArticle
Controllable Synthesis of Titanium Silicon Molecular Zeolite Nanosheet with Short b-Axis Thickness and Application in Oxidative Desulfurization
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Tieqiang Ren, Yujia Wang, Lulu Wang, Lisheng Liang, Xianming Kong and Haiyan Wang
Nanomaterials 2024, 14(11), 953; https://doi.org/10.3390/nano14110953 (registering DOI) - 29 May 2024
Abstract
Titanium silicon molecular zeolite (TS-1) plays an important role in catalytic reactions due to its unique nanostructure. The straight channel on TS-1 was parallel to the orientation of the short b-axis and directly exposed to the aperture of the 10-member ring with a
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Titanium silicon molecular zeolite (TS-1) plays an important role in catalytic reactions due to its unique nanostructure. The straight channel on TS-1 was parallel to the orientation of the short b-axis and directly exposed to the aperture of the 10-member ring with a diameter of 0.54 nm×0.56 nm. This structure could effectively reduce the diffuse restriction of bulk organic compounds during the oxidative desulfurization process. As a kind of cationic polymer electrolyte, polydimethyldiallyl ammonium chloride (PDDA) contains continuous [C8H16N+Cl−] chain segments, in which the Cl− could function as an effective structure-directing agent in the synthesis of nanomaterials. The chain of PDDA could adequately interact with the [0 1 0] plane in the preparation process of zeolite, and then the TS-1 nanosheet with short b-axis thickness (6 nm) could be obtained. The pore structure of the TS-1 nanosheet is controlled by regulating the content of PDDA. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), N2 physical adsorption analysis, infrared absorption spectrum and ultraviolet–visible spectrum were used to determine the TS-1. The thinner nanosheets exhibit excellent catalytic performance in oxidative desulfurization of dibenzothiophene (DBT), in which the removal rate could remain at 100% after three recycles. Here, the TS-1 nanosheet with short b-axis thickness has a promising future in catalytic reactions.
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(This article belongs to the Topic Porous Materials for Energy and Environment Applications)
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Preparation and Characterization of Chitosan Nanofiber: Kinetic Studies and Enhancement of Insulin Delivery System
by
Sarah A. Fouad, Amel M. Ismail, M. Abdel Rafea, M. A. Abu Saied and Ali El-Dissouky
Nanomaterials 2024, 14(11), 952; https://doi.org/10.3390/nano14110952 (registering DOI) - 29 May 2024
Abstract
Insulin-loaded nanofibers were prepared using chitosan as a natural polymer. The loaded insulin with polyethylene oxide was used for preparing monolayer batch S1. Nanofiber S1 was coated by seven layers of film on both sides to form batch S2 as a sandwich containing
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Insulin-loaded nanofibers were prepared using chitosan as a natural polymer. The loaded insulin with polyethylene oxide was used for preparing monolayer batch S1. Nanofiber S1 was coated by seven layers of film on both sides to form batch S2 as a sandwich containing Layer A (CS, PEG and PEO) and Layer B (PEG and PEO) using electrospinning apparatus. SEM, TEM and FT-IR techniques were used to confirm the drug loading within the composite nanofibers. The in vitro activity that provided a sustained and controlled release of the drug from the nanofiber batch was studied at different pH values spectrophotometrically using a dialysis method. In batches S1 and S2, the release of insulin from nanofiber proceeds via burst release necessary to produce the desired therapeutic activity, followed by slow step. The rate and the percentage release of insulin in batch S2 are found to be higher at all pH values.
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(This article belongs to the Special Issue Advanced Nano Polymer Processing)
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Ag/MXene as Saturable Absorber for Tm:Ho Co-Doped Q-Switched Fiber Laser
by
Xiaoli Zhao, Jingxuan Sun, Yachen Wang, Xiaogang Wang and Bo Fu
Nanomaterials 2024, 14(11), 951; https://doi.org/10.3390/nano14110951 (registering DOI) - 29 May 2024
Abstract
Q-switched fiber lasers have become reliable light sources for generating high-energy pulses, which can be passively modulated by saturable absorbers with excellent nonlinear optical properties. The composite combining Ag and MXene exhibits a broadband nonlinear response and high modulation depth, making it a
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Q-switched fiber lasers have become reliable light sources for generating high-energy pulses, which can be passively modulated by saturable absorbers with excellent nonlinear optical properties. The composite combining Ag and MXene exhibits a broadband nonlinear response and high modulation depth, making it a promising candidate for saturable absorbers in pulsed lasers. Herein, we demonstrate a Q-switched Tm:Ho co-doped fiber laser centered at 2 µm, where the Ag/MXene composite serves as a saturable absorber to generate pulses. The typical spectrum, pulse train, and radio frequency spectrum of Q-switched pulses were observed, in which the 60 dB signal-to-noise ratio was higher than that of 2 µm Q-switched fiber lasers based on other materials, demonstrating the stability of the output pulses. Additionally, the long-term stability of the laser was evaluated over 2 h, where the well-maintained central wavelength and output power also indicated the robustness of the Q-switched laser. Furthermore, the influence of the pump power on the parameters of Q-switched pulses was also investigated, which is conducive to control the output characteristics of lasers. Specifically, the pulse width of the Q-switched pulse decreased, while the repetition rate, output power, and single pulse energy all increased with the increase in pump power. These experimental results demonstrate the ability of Ag/MXene as a saturable absorber and show its potential for generating high-performance pulses in ultrafast lasers.
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(This article belongs to the Special Issue Metal-Based Nanomaterials: Fabrications, Optical Properties, and Ultrafast Photonics)
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Greatly Enhanced Thermoelectric Performance of Flexible Cu2−xS Composite Film on Nylon by Se Doping
by
Xinru Zuo, Xiaowen Han, Zixing Wang, Ying Liu, Jiajia Li, Mingcheng Zhang, Changjun Huang and Kefeng Cai
Nanomaterials 2024, 14(11), 950; https://doi.org/10.3390/nano14110950 - 28 May 2024
Abstract
In this work, flexible Cu2−xS films on nylon membranes are prepared by combining a simple hydrothermal synthesis and vacuum filtration followed by hot pressing. The films consist of Cu2S and Cu1.96S two phases with grain sizes from
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In this work, flexible Cu2−xS films on nylon membranes are prepared by combining a simple hydrothermal synthesis and vacuum filtration followed by hot pressing. The films consist of Cu2S and Cu1.96S two phases with grain sizes from nano to submicron. Doping Se on the S site not only increases the Cu1.96S content in the Cu2−xS to increase carrier concentration but also modifies electronic structure, thereby greatly improves the electrical properties of the Cu2−xS. Specifically, an optimal composite film with a nominal composition of Cu2−xS0.98Se0.02 exhibits a high power factor of ~150.1 μW m−1 K−2 at 300 K, which increases by ~138% compared to that of the pristine Cu2-xS film. Meanwhile, the composite film shows outstanding flexibility (~97.2% of the original electrical conductivity is maintained after 1500 bending cycles with a bending radius of 4 mm). A four-leg flexible thermoelectric (TE) generator assembled with the optimal film generates a maximum power of 329.6 nW (corresponding power density of 1.70 W m−2) at a temperature difference of 31.1 K. This work provides a simple route to the preparation of high TE performance Cu2-xS-based films.
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(This article belongs to the Special Issue Study on the Thermoelectric Properties of Nanostructured Materials)
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The Incorporated Drug Affects the Properties of Hydrophilic Nanofibers
by
Črt Dragar, Robert Roškar and Petra Kocbek
Nanomaterials 2024, 14(11), 949; https://doi.org/10.3390/nano14110949 - 28 May 2024
Abstract
Hydrophilic nanofibers offer promising potential for the delivery of drugs with diverse characteristics. Yet, the effects of different drugs incorporated into these nanofibers on their properties remain poorly understood. In this study, we systematically explored how model drugs, namely ibuprofen, carvedilol, paracetamol, and
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Hydrophilic nanofibers offer promising potential for the delivery of drugs with diverse characteristics. Yet, the effects of different drugs incorporated into these nanofibers on their properties remain poorly understood. In this study, we systematically explored how model drugs, namely ibuprofen, carvedilol, paracetamol, and metformin (hydrochloride), affect hydrophilic nanofibers composed of polyethylene oxide and poloxamer 188 in a 1:1 weight ratio. Our findings reveal that the drug affects the conductivity and viscosity of the polymer solution for electrospinning, leading to distinct changes in the morphology of electrospun products. Specifically, drugs with low solubility in ethanol, the chosen solvent for polymer solution preparation, led to the formation of continuous nanofibers with uniform diameters. Additionally, the lower solubility of metformin in ethanol resulted in particle appearance on the nanofiber surface. Furthermore, the incorporation of more hydrophilic drugs increased the surface hydrophilicity of nanofiber mats. However, variations in the physicochemical properties of the drugs did not affect the drug loading and drug entrapment efficiency. Our research also shows that drug properties do not notably affect the immediate release of drugs from nanofibers, highlighting the dominant role of the hydrophilic polymers used. This study emphasizes the importance of considering specific drug properties, such as solubility, hydrophilicity, and compatibility with the solvent used for electrospinning, when designing hydrophilic nanofibers for drug delivery. Such considerations are crucial for optimizing the properties of the drug delivery system, which is essential for achieving therapeutic efficacy and safety.
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(This article belongs to the Special Issue Nanomaterials and Textiles)
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Electrochemical Detection of Glyphosate in Surface Water Samples Based on Modified Screen-Printed Electrodes
by
Elisabeta-Irina Geana, Corina Teodora Ciucure, Amalia Soare, Stanica Enache, Roxana Elena Ionete and Livia Alexandra Dinu
Nanomaterials 2024, 14(11), 948; https://doi.org/10.3390/nano14110948 - 28 May 2024
Abstract
This study addresses the necessity to monitor the presence of glyphosate (Gly) in waters, highlighting the need for on-site detection of Gly by using electrochemical sensors in environmental and agricultural monitoring programs. Two approaches were employed: (1) modification with graphene decorated with gold
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This study addresses the necessity to monitor the presence of glyphosate (Gly) in waters, highlighting the need for on-site detection of Gly by using electrochemical sensors in environmental and agricultural monitoring programs. Two approaches were employed: (1) modification with graphene decorated with gold nanoparticles (AuNPs-Gr) and dispersed in either dimethylformamide (DMF) or a solution containing Nafion and isopropanol (NAF), and (2) molecularly imprinted polymers (MIPs) based on polypyrrole (PPy) deposited on gold SPEs (AuSPE). Electrochemical characterization revealed that sensors made of AuNPs-Gr/SPCE exhibited enhanced conductivity, larger active area, and improved charge transfer kinetics compared to unmodified SPEs and SPEs modified with graphene alone. However, the indirect detection mechanism of Gly via complex formation with metallic cations in AuNPs-Gr-based sensors introduces complexities and compromises sensitivity and selectivity. In contrast, MIPPy/AuSPE sensors demonstrated superior performance, offering enhanced reliability and sensitivity for Gly analysis. The MIPPy/AuSPE sensor allowed the detection of Gly concentrations as low as 5 ng/L, with excellent selectivity and reproducibility. Moreover, testing in real surface water samples from the Olt River in Romania showed recovery rates ranging from 90% to 99%, highlighting the effectiveness of the detection method. Future perspectives include expanding the investigation to monitor Gly decomposition in aquatic environments over time, providing insights into the decomposition’s long-term effects on water quality and ecosystem health, and modifying regulatory measures and agricultural practices for mitigating its impact. This research contributes to the development of robust and reliable electrochemical sensors for on-site monitoring of Glyphosate in environmental and agricultural settings.
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(This article belongs to the Special Issue Nanostructured Materials for the Assay of Organic/Inorganic Water Pollutants)
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