Highly reversible lithium storage in a conversion-type ZnCo2O4 anode promoted by NiCl2−xFx hydrate. Issue 5 (23rd January 2020)

• Record Type: Journal Article
• Authors: Deng, Jiaojiao; Yu, Xiaoliang; Tang, Jie; Zhang, Lihan; Zhang, Kun; Lin, Shiqi; Li, Baohua
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 5(2020)
• Page Start: 2356
• Page End: 2363
• Publication Date: 2020-01-23
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c9ta13183c
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Highly reversible lithium storage in a conversion-type ZnCo2 O4 anode is achieved by coating ultrafine NiCl2− x F x hydrate on porous ZnCo2 O4 microspheres. Abstract : Transition metal oxides are important conversion-type anodes in lithium ion batteries because of their low cost and high specific capacity. However, the poor conversion-reaction reversibility leads to low coulombic efficiency, sluggish reaction kinetics and unsatisfactory long-term cycling stability, thus severely hindering their practical applications. In this research, we propose a facile strategy to achieve highly reversible lithium storage in a ZnCo2 O4 anode by coating ultrafine NiCl2− x F x hydrate on porous ZnCo2 O4 microspheres. The intimate and well-distributed contact between two components significantly enhances the activity of the reversible conversion reaction. The NiCl2− x F x hydrate also promotes the reversible decomposition of organic components in the as-formed solid electrolyte interface, evidenced from several microstructural analyses. Moreover, the ultrafine hydrated NiCl2− x F x effectively pins ZnCo2 O4 to inhibit the detrimental grain coarsening process during cycling. As a result, the hybrid anode shows significantly increased initial coulombic efficiency from 69.1% to 83%, and the round-trip energy efficiency from 50% to 58.7%. It also demonstrates excellent rate capability and superior cycling stability.