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Updated: Dec 28, 2025

Synthesis of Single-Crystalline Core-Shell Metal-Organic Frameworks
Published on: February 10, 2023
Initiating Hexagonal MoO3 for Superb-Stable and Fast NH4 + Storage Based on Hydrogen Bond Chemistry
Guojin Liang1, Yanlei Wang2, Zhaodong Huang1
1Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, China.
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.
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