Recent advances and perspectives of electrode materials for emerging ammonium-ion storage: From mechanistic insights to practical applications

被引:19
|
作者
Zheng, Wanying [1 ]
Hu, Xi [1 ]
Wu, Mengcheng [1 ]
Chen, Lingyun [1 ]
Chen, Shaowei [2 ]
机构
[1] Chongqing Univ, Sch Chem & Chem Engn, Dept Appl Chem, Chongqing 401331, Peoples R China
[2] Univ Calif Santa Cruz, Dept Chem & Biochem, 1156 High St, Santa Cruz, CA 95060 USA
基金
中国国家自然科学基金;
关键词
Ammonium-ion storage; Cathode materials; Anode materials; Storage mechanism; Hydrogen bond; PRUSSIAN BLUE ANALOGS; ENERGY-STORAGE; RECENT PROGRESS; VANADIUM-OXIDE; BATTERY; CATHODE; NH4+; INTERCALATION; INSERTION; CAPACITY;
D O I
10.1016/j.cej.2023.143197
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The aggravation of energy and environmental issues forces people to develop sustainable energy storage technologies. In recent years, emerging ammonium-ion storage has been considered a promising energy storage competitor because of NH4+ ions as charge carriers with merits of abundant resources, inherent safety, fast diffusion capability and unique storage mechanism. However, the development of NH4-ion storage devices is still in the initial stage, and finding appropriate electrode materials is one of the most important tasks for fabricating high-performance devices. This article provides a comprehensive review on recent advances of electrode materials for emerging NH4-ion storage devices. Firstly, the ammonium-ion batteries (AIBs) are briefly summarized, and then the cathode materials, anode materials and their NH4-ion storage mechanism based on hydrogen bond are introduced. Furthermore, other NH4-ion storage devices, including NH4-ion supercapacitors (NH4+-SCs), NH4ion capacitors (AICs), ammonium dual-ion batteries (ADIBs) and ammonium-zinc hybrid batteries (AHBs), are also briefly introduced. Finally, a short conclusion and our perspectives on future developments for NH4-ion storage device's electrodes are provided in order to promote their large-scale energy storage applications.
引用
收藏
页数:18
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