Ionically Conductive Tunnels in h‐WO3 Enable High‐Rate NH4+ Storage

• Published in: Advanced science 2022-04, Vol.9 (10), p.e2105158-n/a
• Main Authors: Zhang, Yi‐Zhou, Liang, Jin, Huang, Zihao, Wang, Qian, Zhu, Guoyin, Dong, Shengyang, Liang, Hanfeng, Dong, Xiaochen
• Format: Article
• Language: English
• Subjects: Crystal structure; Electrodes; Electrolytes; energy storage; ionic tunnels; NH4; WO3
• ISSN: 2198-3844; 2198-3844
• DOI: 10.1002/advs.202105158

Compared to the commonly applied metallic ion charge carriers (e.g., Li+ and Na+), batteries using nonmetallic charge carriers (e.g., H+ and NH4+) generally have much faster kinetics and high‐rate capability thanks to the small hydrated ionic sizes and nondiffusion control topochemistry. However, the hosts for nonmetallic charge carriers are still limited. In this work, it is suggested that mixed ionic–electronic conductors can serve as a promising host for NH4+ storage. Using hexagonal tungsten oxide (h‐WO3) as an example, it is shown that the existence of ionic conductive tunnels greatly promotes the high‐rate NH4+ storage. Specifically, a much higher capacity of 82 mAh g–1 at 1 A g–1 is achieved on h‐WO3, in sharp contrast to 14 mAh g–1 of monoclinic tungsten oxide (m‐WO3). In addition, unlike layered materials, the insertion and desertion of NH4+ ions are confined within the tunnels of the h‐WO3, which minimizes the damage to the crystal structure. This leads to outstanding stability of up to 200 000 cycles with 68% capacity retention at a high current of 20 A g–1. Hexagonal tungsten oxide (h‐WO3) with mixed ionically and electronically conductive tunnels can serve as a promising host for high‐rate NH4+ storage. Specifically, a much higher capacity of 82 mAh g–1 at 1 A g–1 is achieved on h‐WO3, in sharp contrast to 14 mAh g–1 of its polymorph monoclinic tungsten oxide (m‐WO3).