Xu Rui, Yao Yu, Wang Haiyun, Yuan Yifei, Wang Jiawei, Yang Hai, Jiang Yu, Shi Pengcheng, Wu Xiaojun, Peng Zhangquan, Wu Zhong-Shuai, Lu Jun, Yu Yan
Hefei National Laboratory for Physical Sciences at the Microscale, Department of Materials Science and Engineering, CAS Key Laboratory of Materials for Energy Conversion, University of Science and Technology of China, Hefei, Anhui, 230026, China.
Chemical Sciences and Engineering Division, Argonne National Laboratory, 205-167A, 9700 South, Cass Ave., Lemont, IL, 60439, USA.
Adv Mater. 2020 Dec;32(52):e2003879. doi: 10.1002/adma.202003879. Epub 2020 Nov 18.
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 K 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 (K Se , 3 ≤ n ≤ 8) is effectively suppressed by electrochemical reaction dominated by Se 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.
钾-硒(K-Se)电池因其丰富的钾资源而被视为一种用于固定式储能的替代解决方案。然而,储能过程的详细机制仍有待阐明。在此,我们报告了使用实验和计算方法探究硒阴极中钾离子存储工作机制的研究结果。通过将嵌入独立式氮掺杂多孔碳纳米纤维薄膜(Se@NPCFs)中的小分子硒用作阴极,制备了一种柔性K-Se电池。通过确定微孔主体内部存在的短链分子硒的存在,阐明了反应机制,该短链分子硒在碳酸盐电解质体系中通过“全固态”电化学过程经两步转化反应转变为K₂Se。通过整个反应,由硒分子主导的电化学反应有效抑制了多硒化物(K₂Seₙ,3≤n≤8)的生成,从而显著提高了硒的利用率并影响了K-Se电池的电压平台。这项工作通过结构工程和操纵硒化学以形成选择性物种,为优化K-Se电池性能提供了一条切实可行的途径,并揭示了其在碳酸盐电解质中的内部反应机制。