H<sub>2</sub> Activation and Adsorbed H Species on Pt‐Based Heterogeneous Catalysts: Fundamentals and Advances

Abstract H 2 activation on heterogeneous catalysts is a fundamental step in numerous chemical processes, with the nature of adsorbed hydrogen (H) species playing a critical role in catalytic performance. In this review, we systematically categorize the formation of different H species based on the coordination environment of active metal sites, distinguishing between homolytic and heterolytic H 2 dissociation pathways. Focusing on Pt‐based heterogeneous catalysts, we provide atomic‐scale insights into adsorbed H species and Pt metal. The experimental detection of Pt─H adducts is then critically evaluated via three key spectroscopic techniques: infrared (IR) spectroscopy, inelastic neutron scattering (INS) spectroscopy, and X‐ray absorption spectroscopy (XAS), highlighting recent advancements in spectral interpretation. Complementary theoretical studies that can provide binding details of Pt─H bonds are also discussed to elucidate Pt─H adsorption configurations, binding energies, dynamic properties, and coverage‐dependent behavior. Finally, we summarize the strengths and limitations of each characterization method and provide perspectives on future research directions for understanding adsorbed H species in catalysis. This review aims to bridge the gap between experimental observations and theoretical modeling, offering a comprehensive foundation for designing more efficient catalysts in hydrogen‐involved reactions.

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Publication Details

Journal
ChemCatChem
Published
2025-08-22
DOI
https://doi.org/10.1002/cctc.202500902
Citations
3
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
1.55

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article

H2 Activation and Adsorbed H Species on Pt‐Based Heterogeneous Catalysts: Fundamentals and Advances

Guangxing Yang, Qiangqiang Wu, Weixiang Xiong
3 citations
ChemCatChem
Catalytic Processes in Materials Science
1.55
article

H2 Activation and Adsorbed H Species on Pt‐Based Heterogeneous Catalysts: Fundamentals and Advances

Guangxing Yang, Qiangqiang Wu, Weixiang Xiong
article en
3 citations

Abstract

Abstract H 2 activation on heterogeneous catalysts is a fundamental step in numerous chemical processes, with the nature of adsorbed hydrogen (H) species playing a critical role in catalytic performance. In this review, we systematically categorize the formation of different H species based on the coordination environment of active metal sites, distinguishing between homolytic and heterolytic H 2 dissociation pathways. Focusing on Pt‐based heterogeneous catalysts, we provide atomic‐scale insights into adsorbed H species and Pt metal. The experimental detection of Pt─H adducts is then critically evaluated via three key spectroscopic techniques: infrared (IR) spectroscopy, inelastic neutron scattering (INS) spectroscopy, and X‐ray absorption spectroscopy (XAS), highlighting recent advancements in spectral interpretation. Complementary theoretical studies that can provide binding details of Pt─H bonds are also discussed to elucidate Pt─H adsorption configurations, binding energies, dynamic properties, and coverage‐dependent behavior. Finally, we summarize the strengths and limitations of each characterization method and provide perspectives on future research directions for understanding adsorbed H species in catalysis. This review aims to bridge the gap between experimental observations and theoretical modeling, offering a comprehensive foundation for designing more efficient catalysts in hydrogen‐involved reactions.

ChemCatChemVol. 17(18)
Guangzhou University (CN), Guangzhou Vocational College of Science and Technology (CN), Guangzhou Electronic Technology (China) (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 16%
Catalytic Processes in Materials Science
1.55
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H<sub>2</sub> Activation and Adsorbed H Species on Pt‐Based Heterogeneous Catalysts: Fundamentals and Advances — Guangxing Yang, Qiangqiang Wu, et al. · ChemCatChem (2025) | TGRS Research Map | TGRS