X射线光电子能谱
催化作用
氧气
电子转移
双层
化学
空位缺陷
活性氧
化学工程
纳米技术
光化学
材料科学
结晶学
有机化学
工程类
生物化学
膜
作者
Mengmeng Sun,Shu Huang,Shaojuan Jiang,Gehong Su,Zhiwei Lu,Wu Chun,Qiaobo Ye,Bin Feng,Yong Zhuo,Xuemei Jiang,Shengyu Xu,De Wu,Danni Liu,Xianyang Song,Chang Song,Xiaorong Yan,Hanbing Rao
标识
DOI:10.1016/j.jcis.2023.06.140
摘要
Since the catalyst's surface was the major active location, the inner structure's contribution to catalytic activity was typically overlooked. Here, ZnO–Co3O4−v nanozymes with several surfaces and bulk oxygen vacancies were created. The O atoms of H2O2 moved inward to preferentially fill the oxygen vacancies in the interior and form new "lattice oxygen" by the X-ray photoelectron spectroscopy depth analysis and X-ray absorption fine structure. The internal Co2+ continually transferred electrons to the surface for a continuous catalytic reaction, which generated a significant amount of reactive oxygen species. Inner and outer double-layer electron cycles accompanied this process. A three-dimensional model of ZnO–Co3O4−v was constructed using virtual reality interactive modelling technology to illustrate nanozyme catalysis. Moreover, the bactericidal rate of ZnO–Co3O4−v for Methionine-resistant Staphylococcus aureus and Multiple drug resistant Escherichia coli was as high as 99%. ZnO–Co3O4−v was biocompatible and might be utilized to heal wounds following Methionine-resistant Staphylococcus aureus infection. This work offered a new idea for nanozymes to replace of conventional antibacterial medications.
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