过氧化氢酶
吸附
钯
酶
铂金
过氧化物酶
金属
化学工程
组合化学
材料科学
无机化学
纳米技术
化学
催化作用
物理化学
有机化学
冶金
工程类
作者
Junnan Li,Wenqi Liu,Xiaochun Wu,Xingfa Gao
出处
期刊:Biomaterials
[Elsevier]
日期:2015-02-09
卷期号:48: 37-44
被引量:449
标识
DOI:10.1016/j.biomaterials.2015.01.012
摘要
Despite being increasingly used as artificial enzymes, little has been known for the origin of the pH-switchable peroxidase-like and catalase-like activities of metals. Using calculations and experiments, we report the mechanisms for both activities and their pH-switchability for metals Au, Ag, Pd and Pt. The calculations suggest that both activities are intrinsic properties of metals, regardless of the surfaces and intersections of facets exposed to environments. The pre-adsorbed OH groups on the surfaces, which are only favorably formed in basic conditions, trigger the switch between both activities and render the pH-switchability. The adsorption energies between H2O2 and metals can be used as convenient descriptors to predict the relative enzyme-like activities of the metals with similar surface morphologies. The results agree with the enzyme-mimic activities that have been experimentally reported for Au, Ag, Pt and predict that Pd should have the similar properties. The prediction, as well as the predicted activity order for the four metals, has been verified by the experimental tests. The results thus provide an in-depth insight into the peroxidase-like and catalase-like activities of the metals and will guide the de novo design, synthesis and application of artificial enzymes based on inorganic materials.
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