In order to mitigate the drastic volumetric expansion (>300%) of silicon (Si) during the lithiation process, we demonstrate the synthesis of novel Si nanowire arrays (n-SNWAs) with a coral-like surface on Cu foam via a one-step CVD method, in which the Cu foam can simultaneously act as a catalyst and current collector. The unique coral-like surface endows n-SNWAs with a high structural integrity, which is beneficial for enhancing their electrochemical performance. In addition, the as-prepared n-SNWAs on Cu foam can be directly applied as the anode for lithium-ion batteries (LIBs), exhibiting a very high reversible discharge capacity (2745 mA h g(-1) at 200 mA g(-1)) and a fast charge and discharge capability (884 mA h g(-1) at 3200 mA g(-1)), which is much higher than the conventional SNWAs (c-SNWAs, only 127 mA h g(-1) at 3200 mA g(-1)). Meanwhile, they deliver an improved cycling stability (2178 mA h g(-1) at 400 mA g(-1) after 50 cycles). More significantly, the as-synthesized n-SNWAs on Cu foam also possess a superior specific areal capacity of 4.1 mA h cm(-2) at 0.6 mA cm(-2). Such excellent electrochemical performance is superior, or at least comparable, to the best report for Si anode materials. Combining the cost-effective and facile preparation method, the present n-SNWAs on Cu foam can serve as a promising anode for LIBs.
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http://dx.doi.org/10.1039/c4nr05469e | DOI Listing |
Micromachines (Basel)
December 2024
College of Materials and Metallurgy, Guizhou University, Guiyang 550025, China.
This study introduces the development of a W-M electrochromic film, characterized by a "coral"-like TiO@WO heterostructure, synthesized via a hydrothermal process leveraging the inherent instability of MXene. The film showcases exceptional electrochromic performance, with a coloring response time of 2.8 s, a bleaching response time of 4.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China. Electronic address:
Developing efficient and cost-effective rare earth element-based electrocatalysts for water splitting remains a significant challenge. To address this, interface engineering and charge modulation strategies were employed to create a three-dimensional coral-like CeF/MoO heterostructure electrocatalyst, grown in situ on the multistage porous channels of carbonized sugarcane fiber (CSF). Integrating abundant CeF/MoO heterostructure interfaces and numerous oxygen vacancy defects significantly enhanced the catalyst's active sites and molecular activation capabilities.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
School of Textile Science and Engineering, Xi'an Polytechnic University, Xi'an 710048, Shaanxi, China; Key Laboratory of Functional Textile Material and Product, Xi'an Polytechnic University, Ministry of Education, Xi'an 710048, Shaanxi, China. Electronic address:
Front Microbiol
December 2024
College of Plant Protection, Biocontrol Engineering Laboratory of Crop Diseases and Pests of Gansu Province, Gansu Agricultural University, Lanzhou, China.
J Colloid Interface Sci
January 2025
Key Laboratory of Bioelectrochemistry & Environmental Analysis of Gansu Province, Key Laboratory of Eco-functional Polymer Materials of the Ministry of Education, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070, P. R. China.
Vacancy engineering and heterostructure construction are regarded as potent approaches for synergistically boosting hydrogen production in renewable energy conversion. Herein, a selective phosphorization strategy was implemented to fabricate coral-like ZnO/FeCoP@N-doped carbon hierarchical microspheres (ZnO/FeCoP@NCHMS) via only controllably phosphorizing the Co and Fe atoms in a precursor, which was formed by generating ZnCoFe LDH on the surface of a zinc cobalt coordination polymer microsphere. Then, by adopting a reduction treatment for ZnO/FeCoP@NCHMS, the innovative ZnO/FeCoPv@NCHMS with abundant phosphorus vacancies (Pv) was realized.
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