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Modulating residual ammonium in MnO2 for high-rate aqueous zinc-ion batteries

机译:调节残余铵为高效的汇总水zinc-ion电池

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摘要

Manganese dioxide (MnO2), as a promising cathode candidate, has attracted great attention in aqueous zinc ion batteries (ZIBs). However, the undesirable dissolution of Mn2+ and the sluggish kinetic reaction are still two challenges to overcome before achieving good cycling stability and high-rate performance of ZIBs. Herein, β-MnO2 with chemically residual NH4+ (NMO) was successfully fabricated by controlling the washing condition and utilized as a cathode in a ZIB. Interestingly, NH4+, as a layer pillar in the tunnel structure of NMO, could enhance its conductivity by changing the chemical structure, contributing to accelerating the kinetics of the charge carrier. Moreover, the residual NH4+ in NMO could stabilize the chemical microstructure through the cationic electrostatic shielding effect and the formation of Mn–O⋯H bonds in NMO, promoting the reversible and successive insertion/extraction of H+/Zn2+ in the ZIB. As a result, the Zn/NMO battery exhibits excellent rate performance (up to 8.0 A g−1) and cycling stability (10 000 cycles). This work will pave the way for the design of cathode materials with nonmetallic doping for high-performance ZIB systems.
机译:二氧化锰(汇总),作为一个有前途的阴极候选人,吸引了极大的关注水性锌离子电池(ZIBs)。不良解散Mn2 +和缓慢的动力反应仍两个挑战克服之前实现良好的循环稳定性ZIBs和高效的性能。与化学残留NH4 +(动)成功的通过控制洗涤条件和用作阴极ZIB。动的隧道结构,可以增强其电导率通过改变化学结构,导致加速的动力学电荷载体。动可以稳定的化学微观结构通过阳离子的静电屏蔽效果和形成Mn-O⋯H债券在动,促进可逆和连续插入/提取H + / ZIB Zn2 +。因此,锌/动电池展览优秀的率的性能(8.0 g−1)和骑自行车稳定(10 000次)。为阴极材料的设计为高性能ZIB非金属掺杂系统。

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