Published 2021 | Version v1
Journal article

In situ construction of uniform and robust cathode-electrolyte interphase for Li-rich layered oxides

  • 1. Faculty of Materials and Manufacturing, Beijing University of Technology (China)

Description

High-energy-density Li-rich layered oxides (LLOs) as promising cathodes for Li-ion batteries suffer from the dissolution of transition metals (especially manganese) and severe side reactions in conventional electrolytes, which greatly deteriorate their electrochemical performance. Herein, an in situ "anchoring + pouring" synergistic cathode–electrolyte interphase (CEI) construction is realized by using 1,3,6-hexanetricarbonitrile (HTCN) and tris(trimethylsilyl) phosphate (TMSP) electrolyte additives to alleviate the challenges of an LLO (Li1.13Mn0.517Ni0.256Co0.097O2). HTCN with three nitrile groups can tightly anchor transition metals by coordinative interaction to form the CEI framework, and TMSP will electrochemically decompose to reshape the CEI layer. The uniform and robust in situ constructed CEI layer can suppress the transition metal dissolution, shield the cathode against diverse side reactions, and significantly improve the overall electrochemical performance of the cathod with a discharge voltage decay of only 0.5 mV cycle1. Further investigations based on a series of experimental techniques and theoretical calculations have revealed the composition of in situ constructed CEI layers and their distribution, including the enhanced HTCN anchoring effect after lattice densification of LLOs. This study provides insights into the in situ CEI construction for enhancing the performance of high-energy and high-voltage cathode materials through effective, convenient, and economical electrolyte approaches. (© 2020 Wiley-VCH GmbH)

Availability note (English)

Available from: http://dx.doi.org/10.1002/adfm.202009192

Additional details

Identifiers

Publishing Information

Journal Title
Advanced Functional Materials
Journal Volume
31
Journal Issue
8
Journal Page Range
p. 1-11
ISSN
1616-301X
CODEN
AFMDC6

Optional Information

Notes
AID: 2009192