八面体
电化学
材料科学
电极
格子(音乐)
钒
尖晶石
结构稳定性
氧化钒
水溶液
缓冲器(光纤)
电池(电)
储能
氧化物
化学工程
容量损失
压力(语言学)
晶体结构
无机化学
结晶学
纳米技术
化学
试剂
氧化还原
化学物理
作者
Zhongzhuo Yang,Yu Ding,Zhenjun Song,Yuanhao Shen,Chenyang Yang,Wei Peng,Weixiao Wang,Wenchao Shi,Shijie Feng,Lin Xu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-11-28
卷期号:10 (12): 6557-6565
被引量:2
标识
DOI:10.1021/acsenergylett.5c03302
摘要
Ammonium-ion battery (AIB) is an emerging energy storage system, owing to its inherent safety and low cost. However, the large size of NH4+ and its strong interaction with the host lattice lead to severe stress accumulation and undesirable structural evolution. Here, we introduce Al3+ into vanadium oxide to modulate the occupancy of the V t2g orbital, thereby achieving a local chemical coordination manipulation. The electronic adjustment breaks the lattice symmetry and induces a VO6 octahedral distortion. This microdistortion acts as a built-in stress buffer that suppresses lattice breathing and accelerates electron transport. As a result, the AlVO electrode delivers 112 mAh g–1 at 2 A g–1, retains 91% of its capacity over 10000 cycles. The pouch cell also delivers a durable cycling stability, further confirming the feasibility of this strategy. These findings clarify the relationship between local distortion and electrochemical performance, providing a rational route to optimize electrodes through precise regulation of coordination environments.
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