Tan Xianfang, Zhang Fangfang, Chen Dongzhi, Gong Jia'ni, Sun Jianguo, Meng Changgong, Zhang Yifu
Hubei Key Laboratory of Radiation Chemistry and Functional Materials, School of Nuclear Technology and Chemistry & Biology, Hubei University of Science and Technology, Xianning 437100, PR China.
State Key Laboratory of New Textile Materials & Advanced Processing Technology, Wuhan Textile University, Wuhan 430073, PR China.
J Colloid Interface Sci. 2024 Sep;669:2-13. doi: 10.1016/j.jcis.2024.04.210. Epub 2024 May 1.
Aqueous nonmetallic ion batteries have garnered significant interest due to their cost-effectiveness, environmental sustainability, and inherent safety features. Specifically, ammonium ion (NH) as a charge carrier has garnered more and more attention recently. However, one of the persistent challenges is enhancing the electrochemical properties of vanadium dioxide (VO) with a tunnel structure, which serves as a highly efficient NH (de)intercalation host material. Herein, a novel architecture, wherein carbon-coated VO nanobelts (VO@C) with a core-shell structure are engineered to augment NH storage capabilities of VO. In detail, VO@C is synthesized via the glucose reduction of vanadium pentoxide under hydrothermal conditions. Experimental results manifest that the introduction of the carbon layer on VO nanobelts can enhance mass transfer, ion transport and electrochemical kinetics, thereby culminating in the improved NH storage efficiency. VO@C core-shell composite exhibits a remarkable specific capacity of ∼300 mAh/g at 0.1 A/g, which is superior to that of VO (∼238 mAh/g) and various other electrode materials used for NH storage. The NH storage mechanism can be elucidated by the reversible NH (de)intercalation within the tunnel of VO, facilitated by the dynamic formation and dissociation of hydrogen bonds. Furthermore, when integrated into a full battery with polyaniline (PANI) cathode, the VO@C//PANI full battery demonstrates robust electrochemical performances, including a specific capacity of ∼185 mAh·g at 0.2 A·g, remarkable durability of 93 % retention after 1500 cycles, as well as high energy density of 58 Wh·kg at 5354 W·kg. This work provides a pioneering approach to design and explore composite materials for efficient NH storage, offering significant implications for future battery technology enhancements.
水系非金属离子电池因其成本效益、环境可持续性和固有的安全特性而备受关注。具体而言,铵离子(NH)作为电荷载体最近越来越受到关注。然而,一个长期存在的挑战是提高具有隧道结构的二氧化钒(VO)的电化学性能,VO用作高效的NH(脱)嵌入主体材料。在此,设计了一种新颖的结构,即具有核壳结构的碳包覆VO纳米带(VO@C),以增强VO的NH存储能力。详细地说,VO@C是在水热条件下通过葡萄糖还原五氧化二钒合成的。实验结果表明,在VO纳米带上引入碳层可以增强传质、离子传输和电化学动力学,从而提高NH存储效率。VO@C核壳复合材料在0.1 A/g时表现出约300 mAh/g的显著比容量,优于VO(约238 mAh/g)和用于NH存储的各种其他电极材料。NH存储机制可以通过VO隧道内可逆的NH(脱)嵌入来解释,这是由氢键的动态形成和解离促进的。此外,当与聚苯胺(PANI)阴极集成到全电池中时,VO@C//PANI全电池表现出强大的电化学性能,包括在0.2 A/g时约185 mAh·g的比容量、1500次循环后93%的显著耐久性以及在5354 W/kg时58 Wh/kg的高能量密度。这项工作为设计和探索用于高效NH存储的复合材料提供了一种开创性的方法,对未来电池技术的改进具有重要意义。