Rigid Flexible Pillaring via Synergistic Co‐Doping Stabilizes High‐Capacity Sodium Layered Oxide Cathode
Abstract
ABSTRACT O3‐type layered oxide cathodes offer high energy density but suffer from interlayer gliding and oxygen release at elevated voltages, leading to rapid capacity fade. Here, we propose a rigid–flexible coupled pillaring strategy, where Mg/Li co‐doping offers a versatile route to achieve excellent performance at high voltage. This stems from rigid Mg─O pillaring that suppresses slab gliding, together with compliant Li─O buffering that smooths the in‐plane potential. In tandem, closed‐shell Mg/Li weakens TM─O eg* antibonding and downshifts the O‐2p band center, promoting a tempered, reversible anionic‐redox reaction, thereby avoiding the usual trade‐off in which improvements in durability come at the expense of capacity. Consequently, this pair redirects the high‐voltage response from P3→OP2 to a P3 solid solution, cutting c‐axis breathing to ∼1.7%, and the cathode delivers a capacity of over 160 mAh g −1 at 4.2 V, retains 80% after 500 cycles at 5C. Furthermore, the cathode is scalable to kilogram batches. With excellent coin and Ah‐scale pouch‐cell performance, it shows guidance of design and commercial promise for high‐voltage O3‐type cathodes.
Article Details
Authors (13)
Chenxi Peng
Jun Zeng
Zhen Yang
Conghui Zhang
Fangkun Li
Hongbo Wu
Zhejiang Key Laboratory of Energy Conversion Materials for Advanced Motor College of Materials and Environmental Engineering Hangzhou Dianzi University Hangzhou China
Xiang Tan
School of Materials Science and Engineering Guangdong Provincial Key Laboratory of Advanced Energy Storage Materials South China University of Technology Guangzhou P. R. China
Zhihui Xiong
Hao Yan
Jiarui Wang
School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798, Singapore
Min Zhu
Shuangqiang Chen
College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 P.R. China
Jun Liu