材料科学
水溶液
质子
传输(计算)
纳米技术
化学
计算机科学
物理化学
物理
量子力学
并行计算
作者
Lulu Wang,Jie Yan,Yuexian Hong,Zhihao Yu,Jitao Chen,Junrong Zheng
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2023-05-05
卷期号:9 (18)
被引量:25
标识
DOI:10.1126/sciadv.adf4589
摘要
The design of Faradaic battery electrodes with high rate capability and long cycle life comparable to those of supercapacitors is a grand challenge. Here, we bridge this performance gap by taking advantage of a unique ultrafast proton conduction mechanism in vanadium oxide electrode, developing an aqueous battery with untrahigh rate capability up to 1000 C (400 A g-1) and extremely long life of 0.2 million cycles. The mechanism is elucidated by comprehensive experimental and theoretical results. Instead of slow individual Zn2+ transfer or Grotthuss chain transfer of confined H+, the ultrafast kinetics and excellent cyclic stability are enabled by rapid 3D proton transfer in vanadium oxide via the special pair dance switching between Eigen and Zundel configurations with little constraint and low energy barriers. This work provides insight into developing high-power and long-life electrochemical energy storage devices with nonmetal ion transfer through special pair dance topochemistry dictated by hydrogen bond.
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