Abstract
LiNi0.5Co0.2Mn0.3O2 (NCM523), as a cathode material for rechargeable lithium-ion batteries, has attracted considerable attention and been successfully commercialized for decades. NCM is also a promising electrocatalyst for the oxygen evolution reaction (OER), and the catalytic activity is highly correlated to its structure. In this paper, we successfully obtain NCM523 with three different structures: spinel NCM synthesized at low temperature (LT-NCM), disordered NCM (DO-NCM) with lithium deficiency obtained at high temperature, and layered hexagonal NCM at high temperature (HT-NCM). By introducing lithium deficiency to tune the valence state of transition metals in NCM from Ni2+ to Ni3+, DO-NCM exhibits the best catalytic activity with the lowest onset potential (∼1.48 V) and Tafel slope (∼85.6 mV dec-1), whereas HT-NCM exhibits the worst catalytic activity with the highest onset potential (∼1.63 V) and Tafel slope (∼241.8 mV dec-1).
Original language | American English |
---|---|
Pages (from-to) | 10496-10502 |
Number of pages | 7 |
Journal | ACS Applied Materials and Interfaces |
Volume | 12 |
Issue number | 9 |
DOIs | |
State | Published - 4 Mar 2020 |
Bibliographical note
Publisher Copyright:Copyright © 2020 American Chemical Society.
NREL Publication Number
- NREL/JA-5K00-75112
Keywords
- cation mixing
- disordered layered hexagonal structure
- lithium deficiency
- NCM523
- OER
- polymer-assisted solution method