| Literature DB >> 32080917 |
Guojin Liang1, Yanlei Wang2, Zhaodong Huang1, Funian Mo1, Xinliang Li1, Qi Yang1, Donghong Wang1, Hongfei Li3, Shimou Chen2, Chunyi Zhi1,4.
Abstract
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.Entities:
Keywords: ammonium ion batteries; hexagonal MoO3; hydrogen bond chemistry
Year: 2020 PMID: 32080917 DOI: 10.1002/adma.201907802
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849