Liu Zhenjie, Ma Lipo, Guo Limin, Peng Zhangquan
State Key Laboratory of Electroanalytical Chemistry , Changchun Institute of Applied Chemistry, Chinese Academy of Science , Changchun 130022 , China.
University of Science and Technology of China , Hefei 230026 , China.
J Phys Chem Lett. 2018 Oct 18;9(20):5915-5920. doi: 10.1021/acs.jpclett.8b02798. Epub 2018 Sep 27.
For years, the aprotic Li-O battery suffered from a severe capacity-current trade-off that would be unacceptable for a beyond Li-ion battery. Recent fundamental study of Li-O electrochemistry revealed that this dilemma is caused by the growth of LiO on the cathode surface and can be solved by discharging LiO in the electrolyte solution. Among the strategies that can promote solution growth of LiO, redox mediators (i.e., soluble catalysts) demonstrate prominent performance. However, soluble redox mediators may shuttle from the cathode to the lithium anode and decompose thereon, causing severe deterioration of the lithium anode and degradation of the mediators' functionality. Here, we report that immobilized redox mediators (e.g., anthraquinone, AQ) in the form of a thin conductive polymer film (PAQ) on the cathode can effectively promote solution growth of LiO even in weakly solvating electrolyte solutions that would otherwise lead to surface film growth and early cell death. The PAQ-catalyzed Li-O battery can deliver a discharge capacity that is up to ∼50 times what its pristine counterpart does at the same current densities and is comparable to the capacity realized by soluble AQ-catalyzed Li-O batteries. Most importantly, the adverse "cross-talk" between the lithium anode and the redox mediators immobilized on the cathode has been completely eliminated.
多年来,非质子锂氧电池一直存在严重的容量-电流权衡问题,这对于超越锂离子电池来说是不可接受的。最近对锂氧电化学的基础研究表明,这种困境是由阴极表面LiO的生长引起的,并且可以通过在电解液中使LiO放电来解决。在能够促进LiO溶液生长的策略中,氧化还原介质(即可溶性催化剂)表现出显著的性能。然而,可溶性氧化还原介质可能会从阴极穿梭到锂阳极并在其上分解,导致锂阳极严重恶化以及介质功能退化。在此,我们报道,以阴极上的薄导电聚合物膜(PAQ)形式固定的氧化还原介质(如蒽醌,AQ)即使在弱溶剂化电解液中也能有效促进LiO的溶液生长,否则这种电解液会导致表面膜生长和电池过早失效。PAQ催化的锂氧电池在相同电流密度下的放电容量比其原始对应电池高出约50倍,并且与可溶性AQ催化的锂氧电池实现的容量相当。最重要的是,锂阳极与固定在阴极上的氧化还原介质之间的不利“串扰”已被完全消除。