过电位
电解质
电池(电)
光催化
电化学
材料科学
分解
清除
储能
降级(电信)
纳米技术
化学工程
电极
计算机科学
化学
功率(物理)
催化作用
电信
工程类
有机化学
物理化学
物理
抗氧化剂
量子力学
作者
Yu Qiao,Yang Liu,Kezhu Jiang,Xiang Li,Yibo He,Qi Li,Shichao Wu,Haoshen Zhou
标识
DOI:10.1002/smtd.201700284
摘要
Abstract The development of the nonaqueous Li–O 2 battery, a promising candidate for high‐gravimetric‐energy‐storage techniques, is seriously restrained by the high charge overpotential during electrochemical decomposition of insulating Li 2 O 2 . Benefiting from the photovoltage, photo‐assisted charging is revealed as a feasible method to reduce the charge potential. However, a long period of illumination will inevitably aggravate the degradation of the electrolyte. Herein, composed of contact‐ion‐pairs (CIPs), a newly introduced superconcentrated electrolyte presents superior stability against parasitic photocatalytic decomposition. More significantly, the conventional and photo‐assisted charging processes are rationally integrated as a unique hybrid strategy, in which the highly polarized charging stage is replaced by the photo‐assisted Li 2 O 2 ‐scavenging process. By tuning the photocatalysis and Li 2 O 2 electrochemical oxidization, the hybrid Li 2 O 2 ‐scavenging strategy not only boosts the cycle life of rechargeable Li–O 2 batteries but also opens possibilities in designing photocatalysis‐involved rechargeable energy‐storage battery systems.
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