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用于锂-氧电池的具有开放空心结构的原子分散钌催化剂。

Atomically Dispersed Ruthenium Catalysts with Open Hollow Structure for Lithium-Oxygen Batteries.

作者信息

Chen Xin, Zhang Yu, Chen Chang, Li Huinan, Lin Yuran, Yu Ke, Nan Caiyun, Chen Chen

机构信息

Beijing Advanced Innovation Center for Materials Genome Engineering, Institute of Solid State Chemistry, University of Science and Technology Beijing, Beijing, 100083, People's Republic of China.

Engineering Research Center of Advanced Rare Earth Materials, Department of Chemistry, Tsinghua University, Beijing, 100084, People's Republic of China.

出版信息

Nanomicro Lett. 2023 Nov 21;16(1):27. doi: 10.1007/s40820-023-01240-0.

Abstract

Lithium-oxygen battery with ultra-high theoretical energy density is considered a highly competitive next-generation energy storage device, but its practical application is severely hindered by issues such as difficult decomposition of discharge products at present. Here, we have developed N-doped carbon anchored atomically dispersed Ru sites cathode catalyst with open hollow structure (h-RuNC) for Lithium-oxygen battery. On one hand, the abundance of atomically dispersed Ru sites can effectively catalyze the formation and decomposition of discharge products, thereby greatly enhancing the redox kinetics. On the other hand, the open hollow structure not only enhances the mass activity of atomically dispersed Ru sites but also improves the diffusion efficiency of catalytic molecules. Therefore, the excellent activity from atomically dispersed Ru sites and the enhanced diffusion from open hollow structure respectively improve the redox kinetics and cycling stability, ultimately achieving a high-performance lithium-oxygen battery.

摘要

具有超高理论能量密度的锂氧电池被认为是极具竞争力的下一代储能装置,但目前其实际应用受到诸如放电产物难以分解等问题的严重阻碍。在此,我们开发了用于锂氧电池的具有开放中空结构的氮掺杂碳锚定原子分散钌位点阴极催化剂(h-RuNC)。一方面,大量原子分散的钌位点可有效催化放电产物的形成与分解,从而极大地增强氧化还原动力学。另一方面,开放中空结构不仅提高了原子分散钌位点的质量活性,还提升了催化分子的扩散效率。因此,原子分散钌位点的优异活性与开放中空结构增强的扩散作用分别改善了氧化还原动力学和循环稳定性,最终实现了高性能锂氧电池。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd89/10663429/e4ce9c88ebef/40820_2023_1240_Fig1_HTML.jpg

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