材料科学
不稳定性
放松(心理学)
凝聚态物理
压力(语言学)
阴极
相(物质)
应力松弛
电流(流体)
理论(学习稳定性)
工作(物理)
相变
电流密度
作者
Bingran Liu,Chong Luo,Ruixin Lv,Mingfang Yang,Xiaodong Zhang,Yuhang Zhang,Wenhao Sun,Lihan Zhang,Li Li,Feng Wu,Renjie Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-06-13
卷期号:20 (25): 18263-18273
被引量:1
标识
DOI:10.1021/acsnano.6c03375
摘要
Single-crystal nickel-rich cathodes (SC-NCM) are leading candidates for next-generation high-energy-density lithium-ion batteries (LIBs) due to their structural integrity and thermal stability. However, their practical performance remains constrained by sluggish lithium-ion diffusion, internal stress accumulation, and phase instability under conventional constant-current cycling. Existing bulk or interfacial modification strategies often increase synthesis complexity and limit scalability. Here, we demonstrate that introducing periodic relaxation intervals into constant current, forming a pulse-current (PC) protocol, provides a simple and materials-independent approach to dynamically regulate Li + transport and structural evolution. Pulsed cycling homogenizes ion distribution, enhances insertion/extraction kinetics, and stabilizes critical phase transitions, resulting in a 10.6% increase in initial discharge capacity and improved capacity retention over 300 cycles. Structural characterizations reveal deeper and more reversible H1–M and H2–H3 phase transitions, suppress the formation of rock-salt phases, and reduce localized stress accumulation. Furthermore, this strategy proves robust across practical operating conditions, including low temperature (−20 °C), high voltage (4.6 V), and Ah-level pouch cells. This work uncovers the mechanistic coupling between electrochemical relaxation and structural stability, offering dynamic current modulation as a broadly applicable strategy for unlocking the intrinsic performance of nickel-rich cathodes without chemical modification.
科研通智能强力驱动
Strongly Powered by AbleSci AI