Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

Article Types

Countries / Regions

Search Results (78)

Search Parameters:
Keywords = nanoneedle

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
14 pages, 4216 KiB  
Article
Redox-Active Anthraquinone-1-Sulfonic Acid Sodium Salt-Loaded Polyaniline for Dual-Functional Electrochromic Supercapacitors
by Yi Wang, Enkai Lin, Ze Wang, Tong Feng and An Xie
Gels 2025, 11(8), 568; https://doi.org/10.3390/gels11080568 - 23 Jul 2025
Viewed by 236
Abstract
Electrochromic (EC) devices are gaining increasing attention for next-generation smart windows and low-power displays due to their reversible color modulation, low operating voltage, and flexible form factors. Recently, electrochromic energy storage devices (EESDs) have emerged as a promising class of multifunctional systems, enabling [...] Read more.
Electrochromic (EC) devices are gaining increasing attention for next-generation smart windows and low-power displays due to their reversible color modulation, low operating voltage, and flexible form factors. Recently, electrochromic energy storage devices (EESDs) have emerged as a promising class of multifunctional systems, enabling simultaneous energy storage and real-time visual monitoring. In this study, we report a flexible dual-functional EESD constructed using polyaniline (PANI) films doped with anthraquinone-1-sulfonic acid sodium salt (AQS), coupled with a redox-active PVA-based gel electrolyte also incorporating AQS. The incorporation of AQS into both the polymer matrix and the gel electrolyte introduces synergistic redox activity, facilitating bidirectional Faradaic reactions at the film–electrolyte interface and within the bulk gel phase. The resulting vertically aligned PANI-AQS nanoneedle films provide high surface area and efficient ion pathways, while the AQS-doped gel electrolyte contributes to enhanced ionic conductivity and electrochemical stability. The device exhibits rapid and reversible color switching from light green to deep black (within 2 s), along with a high areal capacitance of 194.2 mF·cm−2 at 1 mA·cm−2 and 72.1% capacitance retention over 5000 cycles—representing a 31.5% improvement over undoped systems. These results highlight the critical role of redox-functionalized gel electrolytes in enhancing both the energy storage and optical performance of EESDs, offering a scalable strategy for multifunctional, gel-based electrochemical systems in wearable and smart electronics. Full article
(This article belongs to the Special Issue Smart Gels for Sensing Devices and Flexible Electronics)
Show Figures

Graphical abstract

25 pages, 1263 KiB  
Review
Nanoneedle-Based Transdermal Gene Delivery: A Minimally Invasive Strategy for Gene Therapy
by Fatma Julide Akbuğa, Muhammet Davut Arpa and Emine Şalva
Int. J. Mol. Sci. 2025, 26(13), 6235; https://doi.org/10.3390/ijms26136235 - 27 Jun 2025
Cited by 1 | Viewed by 493
Abstract
Transdermal drug delivery systems have recently been explored as an alternative to oral systems, which have many challenges. Due to the limitations of first-generation transdermal systems, second- and third-generation systems have been developed, among which microneedles have been the most remarkable products. Building [...] Read more.
Transdermal drug delivery systems have recently been explored as an alternative to oral systems, which have many challenges. Due to the limitations of first-generation transdermal systems, second- and third-generation systems have been developed, among which microneedles have been the most remarkable products. Building on the advancements of nanotechnology, nanoneedles have recently been developed. Gene therapy molecules—such as DNA, RNA, siRNA, miRNA, and other nucleic acids—are typically delivered using viral or chemical carriers, but these methods face several challenges. In this context, nanoneedles offer a promising and efficient solution for delivering these large molecules. Nanoneedles are a biocompatible and reliable physical method for gene delivery, enabling transdermal administration by penetrating the skin barrier and delivering nucleic acids directly into cells. Their ability to penetrate cellular barriers with minimal invasiveness makes them advantageous for delivering genetic materials. This review will focus on the potential applications of nanoneedles in pharmaceutical contexts, especially in gene therapy. In addition, information on the properties, structure, and fabrication of nanoneedles is also provided. Full article
(This article belongs to the Special Issue Nanomedicine in Gene Therapy and Immunotherapy)
Show Figures

Figure 1

16 pages, 4779 KiB  
Communication
Binary Solvent Engineering Modulates the Microstructure of Stretchable Organic Field-Effect Transistors for Highly Sensitive NO2 Sensing
by Xiao Jiang, Jiaqi Zeng, Linxuan Zhang, Zhen Zhang and Rongjiao Zhu
Nanomaterials 2025, 15(12), 922; https://doi.org/10.3390/nano15120922 - 13 Jun 2025
Cited by 1 | Viewed by 367
Abstract
Stretchable organic field-effect transistors (OFETs), with inherent flexibility, versatile sensing mechanisms, and signal amplification properties, provide a unique device-level solution for the real-time, in situ detection of trace gaseous pollutants. However, serious challenges remain regarding the synergistic optimization of OFET gas sensor production [...] Read more.
Stretchable organic field-effect transistors (OFETs), with inherent flexibility, versatile sensing mechanisms, and signal amplification properties, provide a unique device-level solution for the real-time, in situ detection of trace gaseous pollutants. However, serious challenges remain regarding the synergistic optimization of OFET gas sensor production preparation, mechano-electrical properties, and gas-sensing performance. Although the introduction of microstructures can theoretically provide OFETs with enhanced sensing performance, the high-precision process required for microstructure fabrication limits scale-up. Herein, a straightforward hybrid solvent strategy is proposed for regulating the intrinsic microstructure of the organic semiconductor layer, with the aim of constructing an ultrasensitive PDVT-10/SEBS fully stretchable OFET NO2 sensor. The binary solvent system induces the formation of nanoneedle-like structures in the PDVT-10/SEBS organic semiconductor, which achieves a maximum mobility of 2.71 cm2 V−1 s−1, a switching current ratio generally exceeding 106, and a decrease in mobility of only 30% at 100% strain. Specifically, the device exhibits a response of up to 77.9 × 106 % within 3 min and a sensitivity of up to 1.4 × 106 %/ppm, and it demonstrates effective interference immunity, with a response of less than 100% to nine interferences. This work paves the way for next-generation wearable smart sensors. Full article
(This article belongs to the Section Nanoelectronics, Nanosensors and Devices)
Show Figures

Figure 1

14 pages, 3101 KiB  
Article
Construction of CuCo2O4@NiFe-LDH Core–Shell Heterostructure for High-Performance Hybrid Supercapacitors
by Yang Chen, Man Li, Chengyu Xue and Fuxiang Wei
Metals 2025, 15(6), 659; https://doi.org/10.3390/met15060659 - 13 Jun 2025
Viewed by 471
Abstract
Transition metal oxides (TMOs) are considered to be highly promising materials for supercapacitor electrodes due to their low cost, multiple convertible valence states, and excellent electrochemical properties. However, inherent limitations, including restricted specific surface area and low electrical conductivity, have largely restricted their [...] Read more.
Transition metal oxides (TMOs) are considered to be highly promising materials for supercapacitor electrodes due to their low cost, multiple convertible valence states, and excellent electrochemical properties. However, inherent limitations, including restricted specific surface area and low electrical conductivity, have largely restricted their application in supercapacitors. In this paper, core–shell heterostructures of nickel–iron layered double hydroxide (NiFe-LDH) nanosheets uniformly grown on CuCo2O4 nanoneedles were synthesized by hydrothermal and calcination methods. It is found that the novel core–shell structure of CuCo2O4@NiFe-LDH improves the electrical conductivity of the electrode materials and optimizes the charge transport path. Under the synergistic effect of the two components and the core–shell heterostructure, the CuCo2O4@NiFe-LDH electrode achieves an ultra-high specific capacity of 323.4 mAh g−1 at 1 A g−1. And the capacity retention after 10,000 cycles at 10 A g−1 is 90.66%. In addition, the assembled CuCo2O4@NiFe-LDH//RGO asymmetric supercapacitor device achieved a considerable energy density (68.7 Wh kg−1 at 856.3 W kg−1). It also has 89.36% capacity retention after 10,000 cycles at 10 A g−1. These properties indicate the great potential application of CuCo2O4@NiFe-LDH in the field of high-performance supercapacitors. Full article
Show Figures

Figure 1

14 pages, 4314 KiB  
Article
Rationally Designed PPy-Coated Fe2O3 Nanoneedles Anchored on N-C Nanoflakes as a High-Performance Anode for Aqueous Supercapacitors
by Zhiqiang Cui, Siqi Zhan, Yatu Luo, Yunfeng Hong, Zexian Liu, Guoqiang Tang, Dongming Cai and Rui Tong
Crystals 2025, 15(4), 346; https://doi.org/10.3390/cryst15040346 - 7 Apr 2025
Cited by 13 | Viewed by 588
Abstract
Flexible supercapacitors have emerged as pivotal energy storage components in wearable smart electronic systems, owing to their exceptional electrochemical performance. However, the widespread application of flexible supercapacitors in smart electronic devices is significantly hindered by the developmental bottleneck of high-performance anode materials. In [...] Read more.
Flexible supercapacitors have emerged as pivotal energy storage components in wearable smart electronic systems, owing to their exceptional electrochemical performance. However, the widespread application of flexible supercapacitors in smart electronic devices is significantly hindered by the developmental bottleneck of high-performance anode materials. In this study, a novel electrode composed of surface-modified Fe2O3 nanoneedles uniformly coated with a polypyrrole (PPy) film and anchored on Co-MOF-derived N-C nanoflake arrays (PPy/Fe2O3/N-C) is designed. This composite electrode, grown in situ on carbon cloth (CC), demonstrated outstanding specific capacity, rate performance, and mechanical flexibility, attributed to its unique hierarchical 3D arrayed structure and the protective PPy layer. The fabricated PPy/Fe2O3/N-C@CC (P-FONC) composite electrode exhibited an excellent specific capacitance of 356.6 mF cm−2 (143 F g−1) at a current density of 2 mA cm−2. The current density increased to 20 mA cm−2, and the composite electrode material preserved a specific capacitance of 278 mF cm−2 (112 F g−1). Furthermore, the assembled quasi-solid-state Mn/Fe asymmetric supercapacitor, configured with P-FONC as the negative electrode and MnO2/N-C@CC as the positive electrode, demonstrated robust chemical stability and notable mechanical flexibility. This study sheds fresh light on the creation of three-dimensional composite electrode materials for highly efficient, flexible energy storage systems. Full article
Show Figures

Figure 1

18 pages, 18008 KiB  
Article
Insights into the Electrochemical Synthesis and Supercapacitive Behaviour of 3D Copper Oxide-Based Nanostructures
by Gintautas Jonkus, Ramunas Levinas, Natalia Tsyntsaru and Henrikas Cesiulis
Solids 2025, 6(2), 15; https://doi.org/10.3390/solids6020015 - 1 Apr 2025
Viewed by 1733
Abstract
In this study, nanostructured copper oxide-based films with crystallite size below 10 nm were electrochemically synthesized on copper foil and foam electrodes and investigated for their supercapacitive behaviour. The synthesis was carried out via cyclic voltammetry (CV) for up to 1000 cycles in [...] Read more.
In this study, nanostructured copper oxide-based films with crystallite size below 10 nm were electrochemically synthesized on copper foil and foam electrodes and investigated for their supercapacitive behaviour. The synthesis was carried out via cyclic voltammetry (CV) for up to 1000 cycles in an alkaline electrolyte. By tuning the upper vertex potential (−0.3 V to 0.65 V vs. Ag/AgCl), both phase composition (Cu2O, Cu(OH)2, CuO) and morphology (grains, nanoneedles, nanoplatelets) were precisely controlled, demonstrating the versatility of this approach. The kinetics of oxide/hydroxide film formation on foil and foam electrodes were analysed based on EIS data that were interpreted in the frame of equivalent electric circuits and their changes with potential. The capacitive properties of the synthesized films were evaluated using CV in the potential range of 0 V–0.65 V, and the optimized CuO film synthesized on Cu foam exhibited a high specific capacitance of 1380 mF cm⁻2. An energy density of 0.061 mWh cm−2 and power density of 1.28 mW cm−2 were obtained at 10 mA cm−2 discharge current. Charge–discharge cycling at 100 mV s−1 for 1000 cycles indicated an initial capacitance increase followed by stable retention, highlighting the structural integrity and electrochemical stability of the films obtained on 3D foam. These findings provide valuable insights into the controlled electrochemical synthesis of copper oxide nanostructures and their potential for high-performance capacitor applications. Full article
Show Figures

Graphical abstract

10 pages, 2095 KiB  
Article
Stable Field Emissions from Zirconium Carbide Nanoneedle Electron Source
by Yimeng Wu, Jie Tang, Shuai Tang, You-Hu Chen, Ta-Wei Chiu, Masaki Takeguchi, Ayako Hashimoto and Lu-Chang Qin
Nanomaterials 2025, 15(2), 93; https://doi.org/10.3390/nano15020093 - 9 Jan 2025
Cited by 1 | Viewed by 913
Abstract
In this study, a single zirconium carbide (ZrC) nanoneedle structure oriented in the <100> direction was fabricated by a dual-beam focused ion beam (FIB-SEM) system, and its field emission characteristics and emission current stability were evaluated. Benefiting from controlled fabrication with real-time observation, [...] Read more.
In this study, a single zirconium carbide (ZrC) nanoneedle structure oriented in the <100> direction was fabricated by a dual-beam focused ion beam (FIB-SEM) system, and its field emission characteristics and emission current stability were evaluated. Benefiting from controlled fabrication with real-time observation, the ZrC nanoneedle has a smooth surface and a tip with a radius of curvature smaller than 20 nm and a length greater than 2 μm. Due to its low work function and well-controlled morphology, the ZrC nanoneedle emitter, positioned in a high-vacuum chamber, was able to generate a single and collimated electron beam with a current of 1.2 nA at a turn-on voltage of 210 V, and the current increased to 100 nA when the applied voltage reached 325 V. After the treatment of the nanoneedle tip, the field emission exhibited a stable emission for 150 min with a fluctuation of 1.4% and an emission current density as high as 1.4 × 1010 A m−2. This work presents an efficient and controllable method for fabricating nanostructures, and this method is applicable to the transition metal compound ZrC as a field emission emitter, demonstrating its potential as an electron source for electron-beam devices. Full article
(This article belongs to the Section Synthesis, Interfaces and Nanostructures)
Show Figures

Figure 1

18 pages, 5326 KiB  
Article
Fabrication of PLA-Based Nanoneedle Patches Loaded with Transcutol-Modified Chitosan Nanoparticles for the Transdermal Delivery of Levofloxacin
by Christina Samiotaki, Ioanna Koumentakou, Evi Christodoulou, Nikolaos D. Bikiaris, Marilena Vlachou, Evangelos Karavas, Konstantina Tourlouki, Nikolaos Kehagias and Panagiotis Barmpalexis
Molecules 2024, 29(18), 4289; https://doi.org/10.3390/molecules29184289 - 10 Sep 2024
Cited by 3 | Viewed by 1772
Abstract
Current transdermal drug delivery technologies, like patches and ointments, effectively deliver low molecular weight drugs through the skin. However, delivering larger, hydrophilic drugs and macromolecules remains a challenge. In the present study, we developed novel transdermal nanoneedle patches containing levofloxacin-loaded modified chitosan nanoparticles. [...] Read more.
Current transdermal drug delivery technologies, like patches and ointments, effectively deliver low molecular weight drugs through the skin. However, delivering larger, hydrophilic drugs and macromolecules remains a challenge. In the present study, we developed novel transdermal nanoneedle patches containing levofloxacin-loaded modified chitosan nanoparticles. Chitosan was chemically modified with transcutol in three ratios (1/1, 1/2, 1/3, w/w), and the optimum ratio was used for nanoparticle fabrication via the ionic gelation method. The successful modification was confirmed using ATR-FTIR spectroscopy, while DLS results revealed that only the 1/3 ratio afforded suitably sized particles of 220 nm. After drug encapsulation, the particle size increased to 435 nm, and the final formulations were examined via XRD and an in vitro dissolution test, which suggested that the nanoparticles reach 60% release in a monophasic pattern at 380 h. We then prepared transdermal patches with pyramidal geometry nanoneedles using different poly(lactic acid)/poly(ethylene adipate) (PLA/PEAd) polymer blends of varying ratios, which were characterized in terms of morphology and mechanical compressive strength. The 90/10 blend exhibited the best mechanical properties and was selected for further testing. Ex vivo permeation studies proved that the nanoneedle patches containing drug-loaded nanoparticles achieved the highest levofloxacin permeation (88.1%). Full article
Show Figures

Graphical abstract

23 pages, 16139 KiB  
Article
Bioarchitectonic Nanophotonics by Replication and Systolic Miniaturization of Natural Forms
by Konstantina Papachristopoulou and Nikolaos A. Vainos
Biomimetics 2024, 9(8), 487; https://doi.org/10.3390/biomimetics9080487 - 13 Aug 2024
Viewed by 2063
Abstract
The mimesis of biological mechanisms by artificial devices constitutes the modern, rapidly expanding, multidisciplinary biomimetics sector. In the broader bioinspiration perspective, however, bioarchitectures may perform independent functions without necessarily mimicking their biological generators. In this paper, we explore such Bioarchitectonic notions and demonstrate [...] Read more.
The mimesis of biological mechanisms by artificial devices constitutes the modern, rapidly expanding, multidisciplinary biomimetics sector. In the broader bioinspiration perspective, however, bioarchitectures may perform independent functions without necessarily mimicking their biological generators. In this paper, we explore such Bioarchitectonic notions and demonstrate three-dimensional photonics by the exact replication of insect organs using ultra-porous silica aerogels. The subsequent conformal systolic transformation yields their miniaturized affine ‘clones’ having higher mass density and refractive index. Focusing on the paradigms of ommatidia, the compound eye of the hornet Vespa crabro flavofasciata and the microtrichia of the scarab Protaetia cuprea phoebe, we fabricate their aerogel replicas and derivative clones and investigate their photonic functionalities. Ultralight aerogel microlens arrays are proven to be functional photonic devices having a focal length f ~ 1000 μm and f-number f/30 in the visible spectrum. Stepwise systolic transformation yields denser and affine functional elements, ultimately fused silica clones, exhibiting strong focusing properties due to their very short focal length of f ~ 35 μm and f/3.5. The fabricated transparent aerogel and xerogel replicas of microtrichia demonstrate a remarkable optical waveguiding performance, delivering light to their sub-100 nm nanotips. Dense fused silica conical clones deliver light through sub-50 nm nanotips, enabling nanoscale light–matter interactions. Super-resolution bioarchitectonics offers new and alternative tools and promises novel developments and applications in nanophotonics and other nanotechnology sectors. Full article
Show Figures

Figure 1

21 pages, 7045 KiB  
Article
Fabrication of Multiple-Channel Electrochemical Microneedle Electrode Array via Separated Functionalization and Assembly Method
by Xin-Shuo Huang, Shuang Huang, Shan-Tao Zheng, Bao-Ming Liang, Tao Zhang, Wan Yue, Fan-Mao Liu, Peng Shi, Xi Xie and Hui-Jiuan Chen
Biosensors 2024, 14(5), 243; https://doi.org/10.3390/bios14050243 - 13 May 2024
Cited by 1 | Viewed by 3097
Abstract
Real-time monitoring of physiological indicators inside the body is pivotal for contemporary diagnostics and treatments. Implantable electrodes can not only track specific biomarkers but also facilitate therapeutic interventions. By modifying biometric components, implantable electrodes enable in situ metabolite detection in living tissues, notably [...] Read more.
Real-time monitoring of physiological indicators inside the body is pivotal for contemporary diagnostics and treatments. Implantable electrodes can not only track specific biomarkers but also facilitate therapeutic interventions. By modifying biometric components, implantable electrodes enable in situ metabolite detection in living tissues, notably beneficial in invasive glucose monitoring, which effectively alleviates the self-blood-glucose-managing burden for patients. However, the development of implantable electrochemical electrodes, especially multi-channel sensing devices, still faces challenges: (1) The complexity of direct preparation hinders functionalized or multi-parameter sensing on a small scale. (2) The fine structure of individual electrodes results in low spatial resolution for sensor functionalization. (3) There is limited conductivity due to simple device structures and weakly conductive electrode materials (such as silicon or polymers). To address these challenges, we developed multiple-channel electrochemical microneedle electrode arrays (MCEMEAs) via a separated functionalization and assembly process. Two-dimensional microneedle (2dMN)-based and one-dimensional microneedle (1dMN)-based electrodes were prepared by laser patterning, which were then modified as sensing electrodes by electrochemical deposition and glucose oxidase decoration to achieve separated functionalization and reduce mutual interference. The electrodes were then assembled into 2dMN- and 1dMN-based multi-channel electrochemical arrays (MCEAs), respectively, to avoid damaging functionalized coatings. In vitro and in vivo results demonstrated that the as-prepared MCEAs exhibit excellent transdermal capability, detection sensitivity, selectivity, and reproducibility, which was capable of real-time, in situ glucose concentration monitoring. Full article
(This article belongs to the Special Issue Recent Advances in Microneedle Array Electrodes in Biomedicine)
Show Figures

Figure 1

12 pages, 3482 KiB  
Article
Chemical Instability-Induced Wettability Patterns on Superhydrophobic Surfaces
by Tianchen Chen and Faze Chen
Micromachines 2024, 15(3), 329; https://doi.org/10.3390/mi15030329 - 27 Feb 2024
Cited by 4 | Viewed by 1498
Abstract
Chemical instability of liquid-repellent surfaces is one of the nontrivial hurdles that hinders their real-world applications. Although much effort has been made to prepare chemically durable liquid-repellent surfaces, little attention has been paid to exploit the instability for versatile use. Herein, we propose [...] Read more.
Chemical instability of liquid-repellent surfaces is one of the nontrivial hurdles that hinders their real-world applications. Although much effort has been made to prepare chemically durable liquid-repellent surfaces, little attention has been paid to exploit the instability for versatile use. Herein, we propose to create hydrophilic patterns on a superhydrophobic surface by taking advantage of its chemical instability induced by acid solution treatment. A superhydrophobic Cu(OH)2 nanoneedle-covered Cu plate that shows poor stability towards HCl solution (1.0 M) is taken as an example. The results show that 2.5 min of HCl solution exposure leads to the etching of Cu(OH)2 nanoneedles and the partial removal of the self-assembled fluoroalkyl silane molecular layer, resulting in the wettability transition from superhydrophobocity to hydrophilicity, and the water contact angle decreases from ~160° to ~30°. Hydrophilic dimples with different diameters are then created on the superhydrophobic surfaces by depositing HCl droplets with different volumes. Afterwards, the hydrophilic dimple-patterned superhydrophobic surfaces are used for water droplet manipulations, including controlled transfer, merging, and nanoliter droplet deposition. The results thereby verify the feasibility of creating wettability patterns on superhydrophobic surfaces by using their chemical instability towards corrosive solutions, which broadens the fabrication methods and applications of functional liquid-repellent surfaces. Full article
Show Figures

Figure 1

14 pages, 5810 KiB  
Article
Electronic Structure Regulated Nickel-Cobalt Bimetal Phosphide Nanoneedles for Efficient Overall Water Splitting
by Heyang Xu, Xilin She, Haolin Li, Chuanhui Wang, Shuai Chen, Lipeng Diao, Ping Lu, Longwei Li, Liwen Tan, Jin Sun and Yihui Zou
Molecules 2024, 29(3), 657; https://doi.org/10.3390/molecules29030657 - 31 Jan 2024
Cited by 4 | Viewed by 1669
Abstract
Transition metal phosphides (TMPs) have been widely studied for water decomposition for their monocatalytic property for anodic or cathodic reactions. However, their bifunctional catalytic activity still remains a major challenge. Herein, hexagonal nickel-cobalt bimetallic phosphide nanoneedles with 1–3 μm length and 15–30 nm [...] Read more.
Transition metal phosphides (TMPs) have been widely studied for water decomposition for their monocatalytic property for anodic or cathodic reactions. However, their bifunctional catalytic activity still remains a major challenge. Herein, hexagonal nickel-cobalt bimetallic phosphide nanoneedles with 1–3 μm length and 15–30 nm diameter supported on NF (NixCo2−xP NDs/NF) with adjusted electron structure have been successfully prepared. The overall alkaline water electrolyzer composed of the optimal anode (Ni0.67Co1.33P NDs/NF) and cathode (Ni1.01Co0.99P NDs/NF) provide 100 mA cm−2 at 1.62 V. Gibbs Free Energy for reaction paths proves that the active site in the hydrogen evolution reaction (HER) is Ni and the oxygen evolution reaction (OER) is Co in NixCo2−xP, respectively. In the HER process, Co-doping can result in an apparent accumulation of charge around Ni active sites in favor of promoting HER activity of Ni sites, and ΔGH* of 0.19 eV is achieved. In the OER process, the abundant electron transfer around Co-active sites results in the excellent ability to adsorb and desorb *O and *OOH intermediates and an effectively reduced ∆GRDS of 0.37 eV. This research explains the regulation of electronic structure change on the active sites of bimetallic materials and provides an effective way to design a stable and effective electrocatalytic decomposition of alkaline water. Full article
(This article belongs to the Special Issue Battery Chemistry: Recent Advances and Future Opportunities)
Show Figures

Figure 1

14 pages, 6311 KiB  
Article
Rapid Growth of Metal–Metal Oxide Core–Shell Structures through Joule Resistive Heating: Morphological, Structural, and Luminescence Characterization
by Juan Francisco Ramos-Justicia, Ana Urbieta and Paloma Fernández
Materials 2024, 17(1), 208; https://doi.org/10.3390/ma17010208 - 30 Dec 2023
Cited by 1 | Viewed by 1511
Abstract
The aim of this study is to prove that resistive heating enables the synthesis of metal/metal oxide composites in the form of core–shell structures. The thickness and morphology of the oxide layer depends strongly on the nature of the metal, but the influences [...] Read more.
The aim of this study is to prove that resistive heating enables the synthesis of metal/metal oxide composites in the form of core–shell structures. The thickness and morphology of the oxide layer depends strongly on the nature of the metal, but the influences of parameters such as the time and current profiles and the presence of an external field have also been investigated. The systems chosen for the present study are Zn/ZnO, Ti/TiO2, and Ni/NiO. The characterization of the samples was performed using techniques based on scanning electron microscopy (SEM). The thicknesses of the oxide layers varied from 10 μm (Zn/ZnO) to 50 μm (Ni/NiO). In the case of Zn- and Ti-based composites, the growth of nanostructures on the oxide layer was observed. Micro- and nanoneedles formed on the ZnO layer while prism-like structures appeared on the TiO2. In the case of the NiO layer, micro- and nanocrystals were observed. Applying an external electric field seemed to align the ZnO needles, whereas its effect on TiO2 and NiO was less appreciable, principally affecting the shape of their grain boundaries. The chemical compositions were analysed using X-ray spectroscopy (EDX), which confirmed the existence of an oxide layer. Structural information was obtained by means of X-ray diffraction (XRD) and was later checked using Raman spectroscopy. The oxide layers seemed to be crystalline and, although some non-stoichiometric phases appeared, the stoichiometric phases were predominant; these were wurtzite, rutile, and cubic for Zn, Ti, and Ni oxides, respectively. The photoluminescence technique was used to study the distribution of defects on the shell, and mainly visible bands (2–2.5 eV), attributed to oxygen vacancies, were present. The near-band edges of ZnO and TiO2 were also observed around 3.2–3.3 eV. Full article
(This article belongs to the Special Issue Advantages and Perspectives of ZnO Nanostructured Materials)
Show Figures

Figure 1

20 pages, 7961 KiB  
Article
Magnetic Carbon Foam Adorned with Co/Fe Nanoneedles as an Efficient Activator of Oxone for Oxidative Environmental Remediation: Roles of Surficial and Chemical Enhancement
by Yi-Chun Chen, Xin-Yu Jiang, Bui Xuan Thanh, Jia-Yin Lin, Haitao Wang, Chao-Wei Huang, Hongta Yang, Afshin Ebrahimi, Sanya Sirivithayapakorn and Kun-Yi (Andrew) Lin
C 2023, 9(4), 107; https://doi.org/10.3390/c9040107 - 13 Nov 2023
Cited by 1 | Viewed by 2413
Abstract
As heterogeneous catalysis is a practical method for activating Oxone, the immobilization of transition metals (e.g., Co, Fe) on carbonaceous supports is a promising platform. Thus, this study attempts to develop a carbon-supported metallic catalyst by growing Co/Fe on carbon foam (CF) via [...] Read more.
As heterogeneous catalysis is a practical method for activating Oxone, the immobilization of transition metals (e.g., Co, Fe) on carbonaceous supports is a promising platform. Thus, this study attempts to develop a carbon-supported metallic catalyst by growing Co/Fe on carbon foam (CF) via adopting melamine foam as a readily available template which could be transferred to nitrogen-doped CF with marcoporous structures. Specifically, a unique adornment of Co/Fe species on this CF is facilely fabricated through a complexation of Co/Fe with a plant extract, tannic acid, on melamine foam, followed by carbonization to produce nano-needle-like Co/Fe on N-doped CF, forming a magnetic CF (MCF). This resultant MCF exhibits a much higher surface area of 54.6 m2/g than CF (9.5 m2/g), and possesses a much larger specific capacitance of 9.7 F/g, than that of CF as 4.0 F/g. These superior features of MCF enable it to accelerate Oxone activation in order to degrade an emerging contaminant, bis(4-hydroxyphenyl)methanone (BHPM). Furthermore, MCF + Oxone exhibits a lower activation energy as 18.6 kJ/mol for BHPM elimination and retains its effectiveness in eliminating BHPM over multiple rounds. More importantly, the CF is also prepared and directly compared with the MCF to study the composition-structure-property relationship to provide valuable insights for further understanding of catalytic behaviors, surficial characteristics, and application of such a functional carbon material. Full article
(This article belongs to the Special Issue Carbon-Based Catalyst (2nd Edition))
Show Figures

Figure 1

11 pages, 6188 KiB  
Article
Gallium-Doped Hydroxyapatite: Shape Transformation and Osteogenesis Activity
by Wei Shuai, Jianguo Zhou, Chen Xia, Sirui Huang, Jie Yang, Lin Liu and Hui Yang
Molecules 2023, 28(21), 7379; https://doi.org/10.3390/molecules28217379 - 1 Nov 2023
Cited by 7 | Viewed by 2061
Abstract
In this study, we employed a chemical precipitation method to successfully synthesize nanoparticles of gallium-doped hydroxyapatite (Ga-HAp). The microstructure of Ga-HAp was precisely tailored by modulating the concentration of gallium ions. Our findings unequivocally demonstrate that gallium ions exert a pronounced inhibitory influence [...] Read more.
In this study, we employed a chemical precipitation method to successfully synthesize nanoparticles of gallium-doped hydroxyapatite (Ga-HAp). The microstructure of Ga-HAp was precisely tailored by modulating the concentration of gallium ions. Our findings unequivocally demonstrate that gallium ions exert a pronounced inhibitory influence on the growth of HAp crystals, and this inhibitory potency exhibits a direct correlation with the concentration of gallium. Furthermore, gallium ions facilitate the metamorphosis of HAp nanoparticles, transitioning them from nanoneedles to nanosheets. It is worth noting, however, that gallium ions exhibit a limited capacity to substitute for calcium ions within the crystal lattice of HAp, with the maximum substitution rate capped at 4.85%. Additionally, gallium plays a pivotal role in constraining the release of ions from HAp, and this behavior remains consistent across samples with varying Ga doping concentrations. Our in vitro experiments confirm that Ga-doped HAp amplifies both the proliferation and osteogenic differentiation of bone marrow mesenchymal stem cells. Full article
(This article belongs to the Special Issue Electroanalysis of Biochemistry and Material Chemistry)
Show Figures

Figure 1

Back to TopTop