Cui Cuixia, Gao Yong, Li Jun, Yang Chao, Liu Meng, Jin Huile, Xia Zhenhai, Dai Liming, Lei Yong, Wang Jichang, Wang Shun
College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang, 325035, China.
School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an, 710072, China.
Angew Chem Int Ed Engl. 2020 May 11;59(20):7928-7933. doi: 10.1002/anie.202000319. Epub 2020 Mar 13.
Although tremendous efforts have been devoted to understanding the origin of boosted charge storage on heteroatom-doped carbons, none of the present studies has shown a whole landscape. Herein, by both experimental evidence and theoretical simulation, it is demonstrated that heteroatom doping not only results in a broadened operating voltage, but also successfully promotes the specific capacitance in aqueous supercapacitors. In particular, the electrolyte cations adsorbed on heteroatom-doped carbon can effectively inhibit hydrogen evolution reaction, a key step of water decomposition during the charging process, which broadens the voltage window of aqueous electrolytes even beyond the thermodynamic limit of water (1.23 V). Furthermore, the reduced adsorption energy of heteroatom-doped carbon consequently leads to more stored cations on the heteroatom-doped carbon surface, thus yielding a boosted charge storage performance.
尽管在理解杂原子掺杂碳上增强电荷存储的起源方面已经付出了巨大努力,但目前的研究都没有展现出全貌。在此,通过实验证据和理论模拟表明,杂原子掺杂不仅导致工作电压拓宽,还成功提高了水系超级电容器中的比电容。特别地,吸附在杂原子掺杂碳上的电解质阳离子能有效抑制析氢反应,这是充电过程中水电解的关键步骤,它拓宽了水系电解质的电压窗口,甚至超过了水的热力学极限(1.23 V)。此外,杂原子掺杂碳吸附能的降低进而导致更多阳离子存储在杂原子掺杂碳表面,从而产生增强的电荷存储性能。