Cui Guodong, Zeng Yinxiang, Wu Jinfang, Guo Yan, Gu Xiaojun, Lou Xiong Wen David
School of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot, 010021, China.
School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Drive, Singapore, 637459, Singapore.
Adv Sci (Weinh). 2022 Apr;9(10):e2106067. doi: 10.1002/advs.202106067. Epub 2022 Feb 10.
The development of MnO as a cathode for aqueous zinc-ion batteries (AZIBs) is severely limited by the low intrinsic electrical conductivity and unstable crystal structure. Herein, a multifunctional modification strategy is proposed to construct N-doped KMn O with abundant oxygen vacancy and large specific surface area (named as N-KMO) through a facile one-step hydrothermal approach. The synergetic effects of N-doping, oxygen vacancy, and porous structure in N-KMO can effectively suppress the dissolution of manganese ions, and promote ion diffusion and electron conduction. As a result, the N-KMO cathode exhibits dramatically improved stability and reaction kinetics, superior to the pristine MnO and MnO with only oxygen vacancy. Remarkably, the N-KMO cathode delivers a high reversible capacity of 262 mAh g after 2500 cycles at 1 A g with a capacity retention of 91%. Simultaneously, the highest specific capacity can reach 298 mAh g at 0.1 A g . Theoretical calculations reveal that the oxygen vacancy and N-doping can improve the electrical conductivity of MnO and thus account for the outstanding rate performance. Moreover, ex situ characterizations indicate that the energy storage mechanism of the N-KMO cathode is mainly a H and Zn co-insertion/extraction process.
MnO作为水系锌离子电池(AZIBs)的阴极,其发展受到低本征电导率和不稳定晶体结构的严重限制。在此,我们提出了一种多功能改性策略,通过简便的一步水热法构建具有丰富氧空位和大比表面积的N掺杂KMnO(命名为N-KMO)。N-KMO中N掺杂、氧空位和多孔结构的协同效应可以有效抑制锰离子的溶解,并促进离子扩散和电子传导。结果,N-KMO阴极表现出显著提高的稳定性和反应动力学,优于原始MnO和仅具有氧空位的MnO。值得注意的是,N-KMO阴极在1 A g下经过2500次循环后,可逆容量高达262 mAh g,容量保持率为91%。同时,在0.1 A g下最高比容量可达298 mAh g。理论计算表明,氧空位和N掺杂可以提高MnO的电导率,从而解释了优异的倍率性能。此外,非原位表征表明,N-KMO阴极的储能机制主要是H和Zn的共嵌入/脱出过程。