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通过原位表征揭示分级纳米Bi@N掺杂碳纳米笼框架的本征钾存储行为

Unveiling Intrinsic Potassium Storage Behaviors of Hierarchical Nano Bi@N-Doped Carbon Nanocages Framework via In Situ Characterizations.

作者信息

Sun Zehang, Liu Yang, Ye Weibin, Zhang Jinyang, Wang Yuyan, Lin Yue, Hou Linrui, Wang Ming-Sheng, Yuan Changzhou

机构信息

School of Materials Science & Engineering, University of Jinan, Jinan, 250022, P. R. China.

State Key Lab of Physical Chemistry of Solid Surfaces, College of Materials, Xiamen University, Xiamen, 361005, China.

出版信息

Angew Chem Int Ed Engl. 2021 Mar 22;60(13):7180-7187. doi: 10.1002/anie.202016082. Epub 2021 Feb 17.

Abstract

Metallic bismuth has drawn attention as a promising alloying anode for advanced potassium ion batteries (PIBs). However, serious volume expansion/electrode pulverization and sluggish kinetics always lead to its inferior cycling and rate properties for practical applications. Therefore, advanced Bi-based anodes via structural/compositional optimization and sur-/interface design are needed. Herein, we develop a bottom-up avenue to fabricate nanoscale Bi encapsulated in a 3D N-doped carbon nanocages (Bi@N-CNCs) framework with a void space by using a novel Bi-based metal-organic framework as the precursor. With elaborate regulation in annealing temperatures, the optimized Bi@N-CNCs electrode exhibits large reversible capacities and long-duration cyclic stability at high rates when evaluated as competitive anodes for PIBs. Insights into the intrinsic K -storage processes of the Bi@N-CNCs anode are put forward from comprehensive in situ characterizations.

摘要

金属铋作为一种有前景的先进钾离子电池(PIBs)合金负极受到了关注。然而,严重的体积膨胀/电极粉化以及缓慢的动力学总是导致其在实际应用中的循环性能和倍率性能较差。因此,需要通过结构/成分优化以及表面/界面设计来制备先进的铋基负极。在此,我们开发了一种自下而上的方法,以一种新型铋基金属有机框架为前驱体,制备出封装在具有空隙空间的三维氮掺杂碳纳米笼(Bi@N-CNCs)框架中的纳米级铋。通过对退火温度的精心调控,优化后的Bi@N-CNCs电极在作为PIBs的竞争性负极进行评估时,展现出高倍率下的大可逆容量和长时间的循环稳定性。通过全面的原位表征,对Bi@N-CNCs负极的本征钾存储过程进行了深入研究。

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