C<sub>60</sub>-Supported Single Pt Atom for Selective CH<sub>4</sub> Activation

Supported single-atom catalysts (SACs) exhibit great potential for the selective activation of C-H bonds, enabling the direct conversion of methane (CH<sub>4</sub>) into high value-added chemical products. Herein, benefiting from state-of-the-art mass spectrometry coupled with newly designed variable-temperature double ion trap reactors, we successfully immobilized a single Pt<sup>-</sup> atom on a unique zero-dimensional carbon support (C<sub>60</sub>) and observed a significantly enhanced reactivity of C<sub>60</sub>Pt<sup>-</sup> toward CH<sub>4</sub> activation at room temperature compared to inert bare Pt<sup>-</sup>. The crucial role of the C<sub>60</sub> support in modifying the electronic state of the single metal site (Pt<sup>-</sup> → Pt<sup>0</sup>) was highlighted as a key factor in enhancing orbital interactions with CH<sub>4</sub>. Furthermore, the electron-buffering capability of C<sub>60</sub> also facilitates selective CH<sub>4</sub> activation by cleaving only one C-H bond. This finding not only provides atomic-scale insights into supported SACs for CH<sub>4</sub> activation but also underscores the importance of considering the positive support effects of C<sub>60</sub> in designing related catalysts for direct CH<sub>4</sub> conversion.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2025-06-17
DOI
https://doi.org/10.1021/acs.jpclett.5c01340
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
0.00

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article

C60-Supported Single Pt Atom for Selective CH4 Activation

Xi‐Guan Zhao, Sheng‐Gui He, H. Y. Jia, Xunlei Ding et al.
The Journal of Physical Chemistry Letters
Catalytic Processes in Materials Science
article

C60-Supported Single Pt Atom for Selective CH4 Activation

Xi‐Guan Zhao, Sheng‐Gui He, H. Y. Jia, Xunlei Ding, B. Zang, Jiao-Jiao Chen, Qing‐Yu Liu
article en

Abstract

Supported single-atom catalysts (SACs) exhibit great potential for the selective activation of C-H bonds, enabling the direct conversion of methane (CH<sub>4</sub>) into high value-added chemical products. Herein, benefiting from state-of-the-art mass spectrometry coupled with newly designed variable-temperature double ion trap reactors, we successfully immobilized a single Pt<sup>-</sup> atom on a unique zero-dimensional carbon support (C<sub>60</sub>) and observed a significantly enhanced reactivity of C<sub>60</sub>Pt<sup>-</sup> toward CH<sub>4</sub> activation at room temperature compared to inert bare Pt<sup>-</sup>. The crucial role of the C<sub>60</sub> support in modifying the electronic state of the single metal site (Pt<sup>-</sup> → Pt<sup>0</sup>) was highlighted as a key factor in enhancing orbital interactions with CH<sub>4</sub>. Furthermore, the electron-buffering capability of C<sub>60</sub> also facilitates selective CH<sub>4</sub> activation by cleaving only one C-H bond. This finding not only provides atomic-scale insights into supported SACs for CH<sub>4</sub> activation but also underscores the importance of considering the positive support effects of C<sub>60</sub> in designing related catalysts for direct CH<sub>4</sub> conversion.

The Journal of Physical Chemistry LettersVol. 16(25)
North China Electric Power University (CN), Chinese Academy of Sciences (CN), Beijing National Laboratory for Molecular Sciences (CN), State Key Laboratory for Structural Chemistry of Unstable and Stable Species
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 90%
Catalytic Processes in Materials Science
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