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一种具有缺电子中心的高度分散钴电催化剂,由硼诱导,用于增强室温钠硫电池的吸附和电催化性能

A Highly Dispersed Cobalt Electrocatalyst with Electron-Deficient Centers Induced by Boron toward Enhanced Adsorption and Electrocatalysis for Room-Temperature Sodium-Sulfur Batteries.

作者信息

Tang Kejian, Peng Xiangqi, Zhang Ziying, Li Guohao, Wang Jie, Wang Yingxinjie, Chen Chi, Zhang Nan, Xie Xiuqiang, Wu Zhenjun

机构信息

College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, P. R. China.

College of Materials Science and Engineering, Hunan University, Changsha, 410082, P. R. China.

出版信息

Small. 2024 Aug;20(31):e2311151. doi: 10.1002/smll.202311151. Epub 2024 Mar 8.

DOI:10.1002/smll.202311151
PMID:38456785
Abstract

As vitally prospective candidates for next-generation energy storage systems, room-temperature sodium-sulfur (RT-Na/S) batteries continue to face obstacles in practical implementation due to the severe shuttle effect of sodium polysulfides and sluggish S conversion kinetics. Herein, the study proposes a novel approach involving the design of a B, N co-doped carbon nanotube loaded with highly dispersed and electron-deficient cobalt (Co@BNC) as a highly conductive host for S, aiming to enhance adsorption and catalyze redox reactions. Crucially, the pivotal roles of the carbon substrate in prompting the electrocatalytic activity of Co are elucidated. The experiments and density functional theory (DFT) calculations both demonstrate that after B doping, stronger chemical adsorption toward polysulfides (NaPSs), lower polarization, faster S conversion kinetics, and more complete S transformation are achieved. Therefore, the as-assembled RT-Na/S batteries with S/Co@BNC deliver a high reversible capacity of 626 mAh g over 100 cycles at 0.1 C and excellent durability (416 mAh g over 600 cycles at 0.5 C). Even at 2 C, the capacity retention remains at 61.8%, exhibiting an outstanding rate performance. This work offers a systematic way to develop a novel Co electrocatalyst for RT-Na/S batteries, which can also be effectively applied to other transition metallic electrocatalysts.

摘要

作为下一代储能系统极具前景的候选者,室温钠硫(RT-Na/S)电池由于多硫化钠严重的穿梭效应和缓慢的硫转化动力学,在实际应用中仍面临障碍。在此,该研究提出了一种新方法,即设计一种负载高度分散且缺电子钴的硼氮共掺杂碳纳米管(Co@BNC)作为硫的高导电主体,旨在增强吸附并催化氧化还原反应。至关重要的是,阐明了碳基底在促进钴的电催化活性方面的关键作用。实验和密度泛函理论(DFT)计算均表明,硼掺杂后,对多硫化物(NaPSs)具有更强的化学吸附、更低的极化、更快的硫转化动力学以及更完全的硫转化。因此,组装的具有S/Co@BNC的RT-Na/S电池在0.1 C下100次循环中提供了626 mAh g的高可逆容量和优异的耐久性(在0.5 C下600次循环中为416 mAh g)。即使在2 C时,容量保持率仍为61.8%,表现出出色的倍率性能。这项工作为开发用于RT-Na/S电池的新型钴电催化剂提供了一种系统方法,该方法也可有效应用于其他过渡金属电催化剂。

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