镍桥双相碳化钼界面:高性能锂硒电池的协同催化剂。

IF 16.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jiayi Li,Hong Gao,Dingyi Zhang,Li Gao,Shijian Wang,Congcong Li,Xinyao Yuan,Chao Yuan,Xinming Nie,Jinqiang Zhang,Yufei Zhao,Guoxiu Wang,Hao Liu
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引用次数: 0

摘要

过渡金属催化剂是开发高性能锂硒电池的关键。在此,我们报道了一种合理设计的镍桥双相碳化钼(Mo2C),具有多界面结构,暴露了丰富的活性位点,并显着提高了Li-Se电池在大电流工作下的电化学可逆性。催化和导电功能的协同整合促进了Se/Li2Sex的快速沉积和转化,有效防止了在高速和长期循环过程中由于非活性积累而导致的电极钝化。此外,Ni作为连接Mo2C晶格的结构桥梁和电子调制器来优化Mo的d轨道构型,从而最大化功能化Mo2C的催化效率。合理设计的金属碳化物/Se电极通过吸附、解吸和催化的协同作用,不仅可以促进长链Li2Sen物质的快速转化,还可以促进Li2Se2固固转化为Li2Se。因此,该电极在锂硒电池中实现了全过程催化转化,提供了出色的循环稳定性和高倍率性能。即使在高硒负载(5.6 mg cm-2)下,电极在0.1 c下也能提供400 mAh g-1的初始容量。这些结果突出了协同吸附/解吸/催化机制在实现Li-Se电池快速固-固转化途径中的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ni-Bridged Biphasic Molybdenum Carbide Interfaces: A Synergistic Catalyst for High-Performance Lithium-Selenium Batteries.
Transition metal catalysts are key to developing high-performance lithium-selenium (Li-Se) batteries. Herein, we report a rationally designed Ni-bridged biphasic molybdenum carbide (Mo2C) with a multi-interface structure that exposes abundant active sites and significantly enhances the electrochemically reversibility of Li-Se batteries under high current operation. The synergistic integration of catalytic and conductive functions facilitates the rapid deposition and conversion of Se/Li2Sex, effectively preventing electrode passivation caused by inactive accumulation during high-rate and long-term cycling. Furthermore, Ni serves dual roles as a structural bridge to link Mo2C lattice and an electronic modulator to optimize the d-orbital configuration of Mo, thereby maximizing the catalytic efficiency of functionalized Mo2C. The synergistic effects of adsorption, desorption, and catalysis enable the rationally designed metal carbide/Se electrode to promote not only the rapid conversion of long-chain Li2Sen species but also the solid-solid transformation of Li2Se2 into Li2Se. As a result, the electrode achieves full-process catalytic conversion in Li-Se batteries, delivering excellent cycling stability and high-rate performance. Even under high Se loading (5.6 mg cm-2), the electrode delivers an initial capacity of 400 mAh g-1 at 0.1 C. These results highlight the effectiveness of the synergistic adsorption/desorption/catalysis mechanism in enabling a fast solid-solid conversion pathway for Li-Se batteries.
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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