化学
电催化剂
异质结
对偶(语法数字)
氢
无机化学
物理化学
电化学
光电子学
电极
有机化学
艺术
物理
文学类
作者
Yaxin Tong,Zengxin Jiang,Lijuan Yu,Yu Bai,Li Gu,Pengkun Wang,Qiaoyun Chen,Mengjia Li,Yongyong Cao,Li Song,Lei Li
标识
DOI:10.1021/acs.inorgchem.5c00107
摘要
Vacancy engineering is widely used to boost the hydrogen evolution reaction (HER) performance. However, dual-vacancy systems are more complex than mono-vacancy structures and remain underexplored. Key challenges involve developing emerging dual-vacancy catalysts, understanding their synergistic effects, and expanding their applications. Here, P/S dual vacancies were fabricated and coupled to heterostructures to improve HER performance. The as-synthesized WP/WS2-H heterostructures rich in P/S dual vacancies exhibit overpotentials of 175 and 170 mV at a current density of 10 mA cm-2 within 1 M KOH and 0.5 M H2SO4, respectively. The ability of P/S dual vacancies to promote HER activity of WP/WS2-H heterostructures is obviously higher than those of P and S mono-vacancy in WP-H and WS2-H. The heterojunctions of WP/WS2-H optimize the charge distribution, enhance the charge transfer rate, and increase the number of electrochemically active sites, thereby improving HER activities. Moreover, the as-fabricated Zn-H2O battery with WP/WS2-H as the cathode presents a maximum power density of up to 6.3 mW cm-2 and a stable discharge capacity of 69 h. This research not only provides a vigorous strategy for fabricating new dual-vacancy catalyst systems but also illustrates a synergistic effect and expands their application.
科研通智能强力驱动
Strongly Powered by AbleSci AI