Heterogeneous catalysis of large biomolecules: insights from platinum particle size in NAD <sup>+</sup> regeneration

Nicotinamide adenine dinucleotide (NAD<sup>+</sup>) cofactor regeneration is essential for enabling dehydrogenase-promoted biosynthesis for value-added chemicals. Heterogeneous catalytic cofactor regeneration, using supported metal catalysts, is an emerging approach and has shown great promise. However, mechanistic insight remains largely unexplored. In this work, a series of silica-supported platinum (Pt) catalysts have been prepared for NAD<sup>+</sup> cofactor regeneration, to understand the roles of Pt particle size and structure. A turnover frequency (TOF) 'volcano plot' was obtained for Pt clusters in the range of 2.2-7.1 nm, with the maximum TOF (136 h<sup>-1</sup>) observed at 5.6 nm. Selective Pt site blockage with polyvinyl pyrrolidone (PVP) revealed that the significant structure sensitivity originated from the synergistic effect of under- and well-coordinated sites in size-varied Pt clusters. In addition, a facet preference was also identified, where the cofactor regeneration favoured the Pt(100) surface more than Pt(111). These findings provide the first insight into NAD<sup>+</sup> regeneration using heterogeneous Pt catalysts, which will be particularly useful for the rational design of supported metal catalysts.

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Publication Details

Journal
Physical Chemistry Chemical Physics
Published
2025-12-09
DOI
https://doi.org/10.1039/d5cp03860j
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
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article

Heterogeneous catalysis of large biomolecules: insights from platinum particle size in NAD + regeneration

Physical Chemistry Chemical Physics
Enzyme Catalysis and Immobilization
article

Heterogeneous catalysis of large biomolecules: insights from platinum particle size in NAD + regeneration

article en

Abstract

Nicotinamide adenine dinucleotide (NAD<sup>+</sup>) cofactor regeneration is essential for enabling dehydrogenase-promoted biosynthesis for value-added chemicals. Heterogeneous catalytic cofactor regeneration, using supported metal catalysts, is an emerging approach and has shown great promise. However, mechanistic insight remains largely unexplored. In this work, a series of silica-supported platinum (Pt) catalysts have been prepared for NAD<sup>+</sup> cofactor regeneration, to understand the roles of Pt particle size and structure. A turnover frequency (TOF) 'volcano plot' was obtained for Pt clusters in the range of 2.2-7.1 nm, with the maximum TOF (136 h<sup>-1</sup>) observed at 5.6 nm. Selective Pt site blockage with polyvinyl pyrrolidone (PVP) revealed that the significant structure sensitivity originated from the synergistic effect of under- and well-coordinated sites in size-varied Pt clusters. In addition, a facet preference was also identified, where the cofactor regeneration favoured the Pt(100) surface more than Pt(111). These findings provide the first insight into NAD<sup>+</sup> regeneration using heterogeneous Pt catalysts, which will be particularly useful for the rational design of supported metal catalysts.

Physical Chemistry Chemical PhysicsVol. 28(3)
Tianjin University (CN), Missouri University of Science and Technology (US), Lancaster University (GB)
Openalex Percentile: Top 39%
Enzyme Catalysis and Immobilization
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