| Literature DB >> 33206429 |
Rui Xu1, Yu Yao1, Haiyun Wang1, Yifei Yuan2, Jiawei Wang3, Hai Yang1, Yu Jiang1, Pengcheng Shi1, Xiaojun Wu1, Zhangquan Peng3, Zhong-Shuai Wu4,5, Jun Lu2, Yan Yu1,5.
Abstract
The potassium-selenium (K-Se) battery is considered as an alternative solution for stationary energy storage because of abundant resource of K. However, the detailed mechanism of the energy storage process is yet to be unraveled. Herein, the findings in probing the working mechanism of the K-ion storage in Se cathode are reported using both experimental and computational approaches. A flexible K-Se battery is prepared by employing the small-molecule Se embedded in freestanding N -doped porous carbon nanofibers thin film (Se@NPCFs) as cathode. The reaction mechanisms are elucidated by identifying the existence of short-chain molecular Se encapsulated inside the microporous host, which transforms to K2 Se by a two-step conversion reaction via an "all-solid-state" electrochemical process in the carbonate electrolyte system. Through the whole reaction, the generation of polyselenides (K2 Sen , 3 ≤ n ≤ 8) is effectively suppressed by electrochemical reaction dominated by Se2 molecules, thus significantly enhancing the utilization of Se and effecting the voltage platform of the K-Se battery. This work offers a practical pathway to optimize the K-Se battery performance through structure engineering and manipulation of selenium chemistry for the formation of selective species and reveal its internal reaction mechanism in the carbonate electrolyte.Entities:
Keywords: potassium-selenium batteries; reaction mechanism; small-molecular Se
Year: 2020 PMID: 33206429 DOI: 10.1002/adma.202003879
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849