催化作用
吸附
悬空债券
材料科学
氧化物
纳米技术
化学工程
化学
冶金
物理化学
工程类
生物化学
硅
作者
Xiao Ge,Sheng‐Song Yu,Rui-Fen Cheng,Wenxing Chen,Fangyao Zhou,Kuang Liang,Jie‐Jie Chen,Han‐Qing Yu,Yuen Shing Wu
标识
DOI:10.1016/j.apcatb.2021.120228
摘要
Precise modulation of local structure will improve the catalytic performance for single-site catalysts (SSCs), by taming electronic structure of supported metals and impacting the adsorption energy of reaction intermediates. In order to modify and strengthen the metal-support interaction, a controllable drilling process induced by atomic Cu1Ox is presented for fabrication of accessible SSCs. First, the bulk Cu2O was thermally driven to migrate and diffuse within the tangent graphene oxide membranes (GOM) interface, drilling plenty of channels in the GOM. Then, the volatile and atomic Cu1Ox species would diffuse through the corroded channels. At last, the Cu1Ox species with strong causticity would corrode the C-N support by breaking the Cu-O bonds and releasing CO2. Hence, the atomic Cu species were eventually anchored in the C-N support by coordination with dangling N-rich defects, forming the Cu SSCs. The fabricated Cu SSCs exhibited an excellent performance in sterilizing bacteria. As our results displayed, Escherichia coli (E. coli.) was almost sterilized by Cu SSCs via activating persulfate. Compared to the traditional approaches employed by wastewater treatment plant, our Cu SSCs exhibit much better antibacterial effect, holding a great potential for practical bacterial disinfection.
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