电极
材料科学
电池(电)
扩散
锂(药物)
气体扩散电极
离子
储能
比能量
气体扩散
化学工程
分析化学(期刊)
纳米技术
热力学
电化学
化学
功率(物理)
有机化学
物理化学
物理
工程类
医学
内分泌学
作者
Max Jenkins,Daniel Dewar,Marco Lagnoni,Sixie Yang,Gregory J. Rees,Antonio Bertei,Lee Johnson,Xiangwen Gao,Peter G. Bruce
标识
DOI:10.1002/adma.202405715
摘要
Abstract The very high theoretical specific energy of the lithium–air (Li–O 2 ) battery (3500 Wh kg −1 ) compared with other batteries makes it potentially attractive, especially for the electrification of flight. While progress has been made in realizing the Li–air battery, several challenges remain. One such challenge is achieving a high capacity to store charge at the positive electrode at practical current densities, without which Li–air batteries will not outperform lithium‐ion. The capacity is limited by the mass transport of O 2 throughout the porous carbon positive electrode. Here it is shown that by replacing the binder in the electrode by a polymer with the intrinsic ability to transport O 2 , it is possible to reach capacities as high as 31 mAh cm −2 at 1 mA cm −2 in a 300 µm thick electrode. This corresponds to a positive electrode energy density of 2650 Wh L −1 and specific energy of 1716 Wh kg −1 , exceeding significantly Li‐ion batteries and previously reported Li–O 2 cells. Due to the enhanced oxygen diffusion imparted by the gas diffusion polymer, Li 2 O 2 (the product of O 2 reduction on discharge) fills a greater volume fraction of the electrode and is more homogeneously distributed.
科研通智能强力驱动
Strongly Powered by AbleSci AI