Hydrated ammonium manganese phosphates by electrochemically induced manganese-defect as cathode material for aqueous zinc ion batteries

IF 9.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Chinese Chemical Letters Pub Date : 2023-04-01 DOI:10.1016/j.cclet.2022.05.054
Xiangsi Wu , Guangli Liu , Sinian Yang , Yuting Li , Hongqiang Wang , Qingyu Li , Xianwen Wu
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引用次数: 2

Abstract

Aqueous zinc ion batteries (AZIBs) with the merits of low cost, low toxicity, high safety, environmental benignity as well as multi-valence properties as the large-scale energy storage devices demonstrate tremendous application prospect. However, the explorations for the most competitive manganese-based cathode materials of AZIBs have been mainly limited to some known manganese oxides. Herein, we report a new type of cathode material NH4MnPO4·H2O (abbreviated as AMPH) for rechargeable AZIBs synthesized through a simple hydrothermal method. An in-situ electrochemical strategy inducing Mn-defect has been used to unlock the electrochemical activity of AMPH through the initial charge process, which can convert poor electrochemical characteristic of AMPH towards Zn2+ and NH4+ into great electrochemically active cathode for AZIBs. It still delivers a reversible discharge capacity up to 90.0 mAh/g at 0.5 A/g even after 1000th cycles, which indicates a considerable capacity and an impressive cycle stability. Furthermore, this cathode reveals an (de)insertion mechanism of Zn2+ and NH4+ without structural collapse during the charge/discharge process. The work not only supplements a new member for the family of manganese-based compound for AZIBs, but also provides a potential direction for developing novel cathode material for AZIBs by introducing defect chemistry.

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电化学诱导锰缺陷水合磷酸锰铵作为水性锌离子电池正极材料
水锌离子电池具有成本低、毒性低、安全性高、环境友好和多价性等优点,作为大规模储能装置具有广阔的应用前景。然而,对最具竞争力的锰基AZIBs正极材料的探索主要局限于一些已知的锰氧化物。本文报道了一种用简单水热法合成的新型可充电azib正极材料NH4MnPO4·H2O(简称AMPH)。采用原位诱导mn缺陷的电化学策略,通过初始充电过程解锁AMPH的电化学活性,将AMPH对Zn2+和NH4+的不良电化学特性转化为azib的高电化学活性阴极。即使在1000次循环后,它仍然提供高达90.0 mAh/g的可逆放电容量,0.5 a /g,这表明相当大的容量和令人印象深刻的循环稳定性。此外,该阴极在充放电过程中显示出Zn2+和NH4+的(de)插入机制,而不会发生结构崩溃。本研究不仅为锰基azib化合物家族补充了一名新成员,而且通过引入缺陷化学为开发新型azib正极材料提供了一个潜在的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chinese Chemical Letters
Chinese Chemical Letters 化学-化学综合
CiteScore
14.10
自引率
15.40%
发文量
8969
审稿时长
1.6 months
期刊介绍: Chinese Chemical Letters (CCL) (ISSN 1001-8417) was founded in July 1990. The journal publishes preliminary accounts in the whole field of chemistry, including inorganic chemistry, organic chemistry, analytical chemistry, physical chemistry, polymer chemistry, applied chemistry, etc.Chinese Chemical Letters does not accept articles previously published or scheduled to be published. To verify originality, your article may be checked by the originality detection service CrossCheck.
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