Cao Tong, Zhang Fan, Chen Mojing, Shao Tong, Li Zhi, Xu Qunjie, Cheng Danhong, Liu Haimei, Xia Yongyao
Shanghai Key Laboratory of Materials Protection and Advanced Materials in Electric Power, College of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090, China.
Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Institute of New Energy, Fudan University, Shanghai 200433, China.
ACS Appl Mater Interfaces. 2021 Jun 16;13(23):26924-26935. doi: 10.1021/acsami.1c04129. Epub 2021 Jun 1.
Aqueous zinc ion batteries (A-ZIBs) have been used as new alternative batteries for grid-scale electrochemical energy storage because of their low cost and environmental protection. Finding a suitable and economical cathode material, which is needed to achieve high energy density and long cycle stability, is one of the most important and arduous challenges at the present stage. Potassium manganese hexacyanoferrate (KMHCF) is a kind of Prussian blue analogue. It has the advantages of a large 3D frame structure that can accommodate the insertion/extraction of zinc ions, and is nontoxic, safe, and easy to prepare. However, regularly synthesized KMHCF has higher water and crystal defects, which reduce the possibility of zinc ions' insertion/extraction, and subsequently the discharge capacity and cycling stability. In this work, a KMHCF material with less water and low defects was obtained by adding polyvinylpyrrolidone during the synthesis process to control the reaction process. The KMHCF serves as the cathode of A-ZIBs and exhibits an excellent electrochemical performance providing a specific capacity of 140 mA h g for the initial cycle at a current density of 100 mA g (1 C). In particular, it can maintain a reversible capacity of 85 mA h g, even after 400 cycles at 1 C. Moreover, unlike the traditional zinc storage mechanism of A-ZIBs, we found that the KMHCF electrode undergoes a phase transition process when the KMHCF electrode was activated by a small current density, which is attributed to part of the Mn on the lattice site being replaced by Zn, thus forming a new stable phase to participate in the subsequent electrochemical reaction.
水系锌离子电池(A-ZIBs)因其低成本和环保特性,已成为用于大规模电化学储能的新型替代电池。寻找一种合适且经济的阴极材料以实现高能量密度和长循环稳定性,是现阶段最重要且艰巨的挑战之一。六氰合铁酸钾锰(KMHCF)是一种普鲁士蓝类似物。它具有大的三维框架结构,能够容纳锌离子的嵌入/脱出,并且无毒、安全且易于制备。然而,常规合成的KMHCF具有较高的含水量和晶体缺陷,这降低了锌离子嵌入/脱出的可能性,进而降低了放电容量和循环稳定性。在这项工作中,通过在合成过程中添加聚乙烯吡咯烷酮来控制反应过程,获得了含水量少且缺陷低的KMHCF材料。该KMHCF用作A-ZIBs的阴极,并表现出优异的电化学性能,在100 mA g(1 C)的电流密度下,初始循环的比容量为140 mA h g。特别是,即使在1 C下循环400次后,它仍能保持85 mA h g的可逆容量。此外,与A-ZIBs传统的锌存储机制不同,我们发现当KMHCF电极通过小电流密度激活时会经历一个相变过程,这是由于晶格位点上的部分Mn被Zn取代,从而形成一个新的稳定相以参与后续的电化学反应。