Coordination Number Regulation of Molybdenum Single-Atom Nanozyme Peroxidase-like Specificity

被引:307
作者
Wang, Ying [1 ]
Jia, Guangri [1 ]
Cui, Xiaoqiang [1 ]
Zhao, Xiao [1 ,3 ]
Zhang, Qinghua [4 ]
Gu, Lin [4 ]
Zheng, Lirong [5 ]
Li, Lu Hua [6 ]
Wu, Qiong [1 ]
Singh, David J. [7 ,8 ]
Matsumura, Daiju [9 ]
Tsuji, Takuya [9 ]
Cui, Yi-Tao [10 ]
Zhao, Jingxiang [2 ]
Zheng, Weitao [1 ]
机构
[1] Jilin Univ, Sch Mat Sci & Engn, State Key Lab Automot Simulat & Control, Key Lab Automobile Mat MOE, Changchun 130012, Peoples R China
[2] Harbin Normal Univ, Coll Chem & Chem Engn, Key Lab Photon & Elect Bandgap Mat, Minist Educ, Harbin 150025, Heilongjiang, Peoples R China
[3] Univ Electrocommun, Innovat Res Ctr Fuel Cells, Chofu, Tokyo 1828585, Japan
[4] Chinese Acad Sci, Inst Phys, Lab Adv Mat & Electron Microscopy,Beijing Key Lab, Beijing Natl Lab Condensed Matter Phys,Key Lab Re, Beijing 100190, Peoples R China
[5] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
[6] Deakin Univ, Inst Frontier Mat, Geelong Waurn Ponds Campus, Waurn Ponds, Vic 3216, Australia
[7] Univ Missouri, Dept Phys & Astron, Columbia, MO 65211 USA
[8] Univ Missouri, Dept Chem, Columbia, MO 65211 USA
[9] Japan Atom Energy Agcy SPring 8, Mat Sci Res Ctr, 1-1-1 Kouto, Sayo, Hyogo 6795148, Japan
[10] SANKA High Technol Co Ltd, 90-1 Kurimachi,Shingu Machi, Tatsuno, Hyogo 6795155, Japan
基金
中国国家自然科学基金;
关键词
N-DOPED CARBON; OXYGEN REDUCTION; RATIONAL DESIGN; NANOMATERIALS; ELECTROREDUCTION; CATALYSTS; PLATINUM; HYDROGEN; SILVER; GOLD;
D O I
10.1016/j.chempr.2020.10.023
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanozymes are promising alternatives to natural enzymes, but their use remains limited owing to poor specificity. Overcoming this and controlling the targeted enzyme-like performance of traditional nanozymes is extremely challenging due to the intrinsic structural complexity of these systems. We report theoretical design and experimental realization of a series of heterogeneous molybdenum single-atom nanozymes (named Mo-SA-N-x-C), wherein we find that the peroxidase-like specificity is well regulated by the coordination numbers of single Mo sites. The resulting Mo-SA-N-3-C catalyst shows exclusive peroxidase-like behavior. It achieves this behavior via a homolytic pathway, whereas Mo-SA-N-2-C and Mo-SA-N-4-C catalysts have a different heterolytic pathway. The mechanism of this coordination-number-dependent enzymatic specificity is attributed to geometrical structure differences and orientation relationships of the frontier molecular orbitals toward these Mo-SA-N-x-C peroxidase mimics. This study demonstrates the rational design of peroxidase-specific nanozymes and precise regulation of their enzymatic properties.
引用
收藏
页码:436 / 449
页数:14
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