4.8 Article

Initiating Hexagonal MoO3 for Superb-Stable and Fast NH4+ Storage Based on Hydrogen Bond Chemistry

期刊

ADVANCED MATERIALS
卷 32, 期 14, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201907802

关键词

ammonium ion batteries; hexagonal MoO3; hydrogen bond chemistry

资金

  1. National Key R&D Program of China [2019YFA0705104]
  2. GRF [N_CityU11305218]
  3. Science Technology and Innovation Committee of Shenzhen Municipality [JCYJ20170818103435068]
  4. City University of Hong Kong [9667165]

向作者/读者索取更多资源

Nonmetallic ammonium (NH4+) ions are applied as charge carriers for aqueous batteries, where hexagonal MoO3 is initially investigated as an anode candidate for NH4+ storage. From experimental and first-principle calculated results, the battery chemistry proceeds with reversible building-breaking behaviors of hydrogen bonds between NH4+ and tunneled MoO3 electrode frameworks, where the ammoniation/deammoniation mechanism is dominated by nondiffusion-controlled pseudocapacitive behavior. Outstanding electrochemical performance of MoO3 for NH4+ storage is delivered with 115 mAh g(-1) at 1 C and can retain 32 mAh g(-1) at 150 C. Furthermore, it remarkably exhibits ultralong and stable cyclic performance up to 100 000 cycle with 94% capacity retention and high power density of 4170 W kg(-1) at 150 C. When coupled with CuFe prussian blue analogous (PBA) cathode, the full ammonium battery can deliver decent energy density 21.3 Wh kg(-1) and the resultant flexible ammonium batteries at device level are also pioneeringly developed for potential realistic applications.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据