Is Platinum a Proton Blocking Catalyst?
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arXiv
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| Main Authors: | , , , , , |
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| Format: | Preprint |
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2025
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| _version_ | 1866909835452219392 |
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| author | Saksena, Aparna Zhao, Yujun Prabhakar, J. Manoj Raabe, Dierk Gault, Baptiste Joshi, Yug |
| author_facet | Saksena, Aparna Zhao, Yujun Prabhakar, J. Manoj Raabe, Dierk Gault, Baptiste Joshi, Yug |
| contents | Platinum, to date, is the most widely applied electrocatalyst for hydrogen evolution reaction (HER) in acidic media. It is assumed to be a proton-blocking catalyst with only surface-limited adsorption of the reaction intermediates. Here, we critically evaluate the bulk interaction of Pt with hydrogen (H), and its heavier isotope deuterium (D), by monitoring operando mass change of the Pt electrode during galvanostatic heavy/water splitting by employing an electrochemical quartz crystal microbalance. Unexpectedly, we observe an irreversible temporal mass gain and a change in the reaction's overpotential, arising from diffusion of H/D into Pt, confirmed by atom probe tomography and thermal desorption spectroscopy. Sub-surface concentration of at least ca. 15 at. % of D in Pt was observed, diffusing down to a depth of more than 10 nm. Analytical description quantified the diffusion coefficient of D in Pt to be 3.2X10^-18 cm2Xs-1. These findings challenge the existing credence of Pt-proton interaction being limited to the surface, prompting the expansion of the catalyst design strategies to account for property-modifying bulk diffusion of H/D in the Pt matrix |
| format | Preprint |
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arxiv_https___arxiv_org_abs_2510_09522 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Is Platinum a Proton Blocking Catalyst? Saksena, Aparna Zhao, Yujun Prabhakar, J. Manoj Raabe, Dierk Gault, Baptiste Joshi, Yug Chemical Physics Materials Science Platinum, to date, is the most widely applied electrocatalyst for hydrogen evolution reaction (HER) in acidic media. It is assumed to be a proton-blocking catalyst with only surface-limited adsorption of the reaction intermediates. Here, we critically evaluate the bulk interaction of Pt with hydrogen (H), and its heavier isotope deuterium (D), by monitoring operando mass change of the Pt electrode during galvanostatic heavy/water splitting by employing an electrochemical quartz crystal microbalance. Unexpectedly, we observe an irreversible temporal mass gain and a change in the reaction's overpotential, arising from diffusion of H/D into Pt, confirmed by atom probe tomography and thermal desorption spectroscopy. Sub-surface concentration of at least ca. 15 at. % of D in Pt was observed, diffusing down to a depth of more than 10 nm. Analytical description quantified the diffusion coefficient of D in Pt to be 3.2X10^-18 cm2Xs-1. These findings challenge the existing credence of Pt-proton interaction being limited to the surface, prompting the expansion of the catalyst design strategies to account for property-modifying bulk diffusion of H/D in the Pt matrix |
| title | Is Platinum a Proton Blocking Catalyst? |
| topic | Chemical Physics Materials Science |
| url | https://arxiv.org/abs/2510.09522 |