Herein, we report a rational method to synthesize a Co3O4 nanobelt array on a conducting substrate and functionalize it in the application of Li-ion battery anodes, which is a novel and facile approach to access the nanobelt array of transition metal oxides. Compared to the previous reports, the as-prepared samples in our experiments exhibited both mesoporosity and single-crystallinity, and meanwhile, good contact with the conducting substrate (via a thin layer of TiO2) provided an express pathway for charge transfer when they were applied in Li-ion batteries without any need to add other ancillary materials (carbon black or binder) to enhance the system's conductivity and stability. Under the condition of high charge-discharge current density of 177 mA/g in Li-ion batteries' testing, the Co3O4 nanobelt array was capable of retaining the specific capacity of 770 mAh/g over 25 cycles. Moreover, even though the charge-discharge rates were increased to 1670 and 3350 mA/g, it still could have reached the stable retention of the specific capacity of 510 and 330 mAh/g beyond 30 cycles, respectively, indicating an obtainable excellent rate capability. More importantly, the improved performance in Li-ion battery testing was definitely ascribed to the unique structures in our samples after elaborate analysis. So the final conclusion would be given that the lab-synthesized Co3O4 nanobelt array potentially could be a highly qualified candidate for Li-ion battery anodes in some practical fields, where high capacity and good capability are strictly required.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/nn9012675 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin 150040, China.
Photoelectrochemical photodetectors (PEC PDs) are promising in underwater optoelectronic devices because of their low cost, good sensitivity, and self-powered characteristics. However, achieving high-performance omnidirectional visible PEC PDs using seawater as the electrolyte is still challenging, hindering their practical application. This work successfully synthesized CuO nanobelt arrays (NAs) on a linear copper wire via a low-temperature solution method with an annealing process.
View Article and Find Full Text PDFTalanta
November 2024
Ministry of Education Key Laboratory for Analytical Science of Food Safety and Biology, Fujian Provincial Key Laboratory of Analysis and Detection Technology for Food Safety, College of Chemistry, Fuzhou University, Fuzhou, 350116, China. Electronic address:
Herein, oxidized 3,3',5,5'-tetramethylbenzidine (oxTMB) nanobelts were developed to enhance the colorimetric and paper-based sensing of HO. It was found that the minor component of Fe in NaSO reagent could catalyze the oxidization of TMB by HO into positively charged oxTMB, which was further assembled into dark blue oxTMB nanobelts via electrostatic interaction with SO. The extinction originating from the absorption and scattering of oxTMB nanobelts was utilized to quantitatively detect HO with a wide linear detection range (1.
View Article and Find Full Text PDFNanotechnology
March 2024
The Collaborative Innovation Center of Advanced Microstructures, School of Electronic Science and Engineering, Nanjing University, Nanjing, 210093, People's Republic of China.
Flexible photodetectors (PDs) have garnered increasing attention for their potential applications in diverse fields, including weather monitoring, smart robotics, smart textiles, electronic eyes, wearable biomedical monitoring devices, and so on. Notably, perovskite nanostructures have emerged as a promising material for flexible PDs due to their distinctive features, such as a large optical absorption coefficient, tunable band gap, extended photoluminescence decay time, high carrier mobility, low defect density, long exciton diffusion lengths, strong self-trapped effect, good mechanical flexibility, and facile synthesis methods. In this review, we first introduce various synthesis methods for perovskite nanostructures and elucidate their corresponding optical and electrical properties, encompassing quantum dots, nanocrystals, nanowires, nanobelts, nanosheets, single-crystal thin films, polycrystalline thin films, and nanostructured arrays.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2023
Department of Applied Chemistry, Petroleum and Chemical Industry Key Laboratory of Organic Electrochemical Synthesis, Zhejiang University of Technology, Hangzhou 310014, P. R. China.
The rational design of high-efficiency, low-cost electrocatalysts for electrochemical water oxidation in alkaline media remains a huge challenge. Herein, combined strategies of metal doping and vacancy engineering are employed to develop unique Mo-doped cobalt oxide nanosheet arrays. The Mo dopants exist in the form of high-valence Mo, and the doping amount has a significant effect on the structure morphology, which transforms from 1D nanowires/nanobelts to 2D nanosheets and finally 3D nanoflowers.
View Article and Find Full Text PDFSmall
December 2023
School of Materials Science and Engineering, National Institute for Advanced Materials, Nankai University, Tianjin, 300350, P. R. China.
Multifunctional electrocatalysts are crucial to cost-effective electrochemical energy conversion and storage systems requiring mutual enhancement of disparate reactions. Embedding noble metal nanoparticles in 2D metal-organic frameworks (MOFs) are proposed as an effective strategy, however, the hybrids usually suffer from poor electrochemical performance and electrical conductivity in operating conditions. Herein, ultrafine Pt nanoparticles strongly anchored on thiophenedicarboxylate acid based 2D Fe-MOF nanobelt arrays (Pt@Fe-MOF) are fabricated, allowing sufficient exposure of active sites with superior trifunctional electrocatalytic activity for hydrogen evolution, oxygen evolution, and oxygen reduction reactions.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!