Sun Chaoyang, Cui Xinhang, Xiao Fenglong, Cui Deliang, Wang Qilong, Dang Feng, Yu Haohai, Lian Gang
State Key Laboratory of Crystal Materials, Shandong University, Jinan, 250100, P. R. China.
Department of Physics, National University of Singapore, 2 Science Drive 3, Singapore, 117543, Singapore.
Small. 2024 Aug;20(32):e2400010. doi: 10.1002/smll.202400010. Epub 2024 Mar 12.
Rechargeable Li-O batteries (LOBs) are considered as one of the most promising candidates for new-generation energy storage devices. One of major impediments is the poor cycle stability derived from the sluggish reaction kinetics of unreliable cathode catalysts, hindering the commercial application of LOBs. Therefore, the rational design of efficient and durable catalysts is critical for LOBs. Optimizing surface electron structure via the negative shift of the d-band center offers a reasonable descriptor for enhancing the electrocatalytic activity. In this study, the construction of Ni-incorporating RuO porous nanospheres is proposed as the cathode catalyst to demonstrate the hypothesis. Density functional theory calculations reveal that the introduction of Ni atoms can effectively modulate the surface electron structure of RuO and the adsorption capacities of oxygen-containing intermediates, accelerating charge transfer between them and optimizing the growth pathway of discharge products. Resultantly, the LOBs exhibit a large discharge specific capacity of 19658 mA h g at 200 mA g and extraordinary cycle life of 791 cycles. This study confers the concept of d-band center modulation for efficient and durable cathode catalysts of LOBs.
可充电锂氧电池(LOBs)被认为是新一代储能设备中最有前途的候选者之一。主要障碍之一是不可靠的阴极催化剂反应动力学迟缓导致的循环稳定性差,这阻碍了LOBs的商业应用。因此,合理设计高效耐用的催化剂对LOBs至关重要。通过d带中心的负移优化表面电子结构为提高电催化活性提供了一个合理的描述符。在本研究中,提出构建掺镍RuO多孔纳米球作为阴极催化剂来验证这一假设。密度泛函理论计算表明,引入镍原子可以有效调节RuO的表面电子结构和含氧中间体的吸附能力,加速它们之间的电荷转移并优化放电产物的生长途径。结果,LOBs在200 mA g下表现出19658 mA h g的大放电比容量和791次的超长循环寿命。本研究赋予了LOBs高效耐用阴极催化剂的d带中心调制概念。