溴
卤素
氯
化学
活化能
动力学
氧化还原
电池(电)
化学工程
无机化学
有机化学
热力学
功率(物理)
烷基
物理
量子力学
工程类
作者
Wenting Feng,Jianhang Yang,Xinru Wei,Chenyu Ma,Junwei Han,Guanzhong Ma,Han Wang,Debin Kong,Linjie Zhi
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-06-04
卷期号:64 (32): e202503752-e202503752
被引量:7
标识
DOI:10.1002/anie.202503752
摘要
The development of high-energy-density batteries operable over a wide temperature range is critical for sustainable energy storage. Sodium-chlorine (Na-Cl2) batteries show promising high theoretical energy densities but face significant safety challenges due to gaseous chlorine, particularly at high temperatures. Replacing Cl2 with liquid Br2 to construct a new Na-Br2 battery mitigates gas risks but introduces issues with sluggish reaction kinetics and high-temperature volatility. To overcome these limitations, we developed a revolutionary Na-Br(+) battery based on the activated Br+ by Cl- anions, pioneering a stabilized redox process via Br-/BrCl2 - conversion. The introduction of Cl- enhances the reversibility kinetics of bromine species and facilitating the activation of Br+ through polyanions BrCl2 -, enabling additional electron transfer pathways. The Na-Br(+) battery achieves impressive low polarization (0.18 V) and exhibits wide-temperature functionality (-60 °C to 60 °C) with a cycle life exceeding 400 cycles. This heterogeneous halogen activation strategy addresses key gas safety limitations and advances the practicality of metal-halogen batteries.
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