4.8 Article

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

期刊

CHEM
卷 7, 期 2, 页码 436-449

出版社

CELL PRESS
DOI: 10.1016/j.chempr.2020.10.023

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资金

  1. National Key Research and Development Program of China [2016YFA0200400]
  2. Jilin Province Science and Technology Development Program [20190201233JC]
  3. National Natural Science Foundation of China [51571100, 51872116]
  4. NSF of Heilongjiang Province of China [JJ2020TD0027]
  5. Natural Science Funds for Distinguished Young Scholar of Heilongjiang Province [JC2018004]
  6. Excellent Young Foundation of Harbin Normal University [XKYQ201304]
  7. National Postdoctoral Program for Innovative Talents [BX20180117]
  8. Program for JLU Science and Technology Innovative Research Team (JLUSTIRT) [2017TD-09]
  9. Fundamental Research Funds for the Central Universities

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Researchers have reported on the theoretical design and experimental realization of heterogeneous molybdenum single-atom nanozymes, showing that the coordination number can regulate the peroxidase-like specificity and allow for precise control of their enzymatic properties.
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.

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