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用于混合电解质中高效锂氧电池的(111)平面上CoO的水诱导表面重构

Water-Induced Surface Reconstruction of CoO on the (111) Plane for High-Efficiency Li-O Batteries in a Hybrid Electrolyte.

作者信息

Zhang Wenjing, Gao Rui, Chen Jundong, Wang Junkai, Zheng Jian, Huang Li, Liu Xiangfeng

机构信息

Center of Materials Science and Optoelectronics Engineering, College of Materials Science and Optoelectronic Technology, University of Chinese Academy of Sciences, Beijing 100049, PR China.

CAS Center for Excellence in Topological Quantum Computation, University of Chinese Academy of Sciences, Beijing 100190, China.

出版信息

ACS Appl Mater Interfaces. 2022 Jun 29;14(25):28965-28976. doi: 10.1021/acsami.2c06990. Epub 2022 Jun 15.

Abstract

The crystal plane effect of cobalt oxide has attracted much attention in Li-O batteries (LOBs) and other electrocatalytic fields. However, boosting the catalytic activity of a specific plane still faces significant challenges. Herein, a strategy of adding water into the electrolyte is developed to construct a LiOH-based Li-O battery system using the (111) plane-exposed CoO as a cathode catalyst. The electrochemical performance shows that on the (111) plane, in the presence of water, the overpotential is largely reduced from 1.5 to 1.0 V and the cycling performance is enhanced. It is confirmed that during the discharge process, water reacts to form LiOH and induce the phase transformation of CoO to amorphous CoO(OH). At the recharge stage, LiOH is first decomposed and then CoO(OH) is reduced to CoO. Compared with pristine (111), the newly formed CoO surface exhibits more active sites, which accelerates the following oxygen reduction and oxygen evolution processes. This work not only reveals the reaction mechanism of water-induced reaction on the (111) plane of CoO but also provides a new perspective for further design of hybrid Li-O batteries with a low polarization and a longer cycle life.

摘要

氧化钴的晶面效应在锂氧电池(LOBs)及其他电催化领域备受关注。然而,提高特定晶面的催化活性仍面临重大挑战。在此,开发了一种在电解液中加水的策略,以(111)面暴露的CoO作为阴极催化剂构建基于LiOH的锂氧电池体系。电化学性能表明,在(111)面上,有水存在时,过电位从1.5 V大幅降至1.0 V,循环性能得到增强。证实了在放电过程中,水反应生成LiOH并诱导CoO相转变为非晶态CoO(OH)。在充电阶段,LiOH首先分解,然后CoO(OH)还原为CoO。与原始的(111)相比,新形成的CoO表面表现出更多活性位点,加速了后续的氧还原和析氧过程。这项工作不仅揭示了水在CoO的(111)面上诱导反应的机理,还为进一步设计低极化、长循环寿命的混合锂氧电池提供了新的视角。

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