电场
化学
离解(化学)
静电学
氢
催化作用
极化(电化学)
化学物理
产量(工程)
纳米技术
静电
激发极化
化学工程
静电相互作用
碳纳米管
电位
基质(水族馆)
极化密度
制氢
分解水
动能
电解水
电荷
光化学
作者
Xueyan Yang,Ziming Wang,Zeyang Yu,Ning Wu,Jiajin Liu,Dongjian Jiang,Kaiyang Shi,Xuanli Dong,Yurou Feng,Zhong Lin Wang
摘要
Contact-electrification (CE) is a ubiquitous effect that would render two contact surfaces being reversely charged. These charged surfaces would induce an electric field in space, but polarization caused by this CE-derived electric field has long been ignored. Here, we propose an electrostatic polarization strategy to improve the performance of single-atom catalysts (SACs) based on this CE-derived electric field. Exemplified by Ru 1 /SiO 2, its hydrogen yield could be enhanced by 7.62 times after improving the CE ability of the SiO 2 substrate by fluorination. Such enhancement should mainly be ascribed to the expedited CE effect on fluorinated SiO 2 substrates, which not only facilitates the water dissociation process but also establishes a strong electric field for improving the reduction activity of Ru SAs and the electrostatic attraction of protons. In addition, this strategy is feasible for SACs based on carbon substrates, further suggesting its generalizability. The practicability of Ru 1 /F-SiO 2 was demonstrated through hydrogen evolution from real seawater, achieving a yield of 1.01 mmol·g –1 ·h –1 over 200 h. We expect this electrostatic polarization-based strategy to form a universal route for enhancing the activity of SACs.
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