Underlying Substrate Effect on Electrochemical Activity for Hydrogen Evolution Reaction with Low-Platinum-Loaded Catalysts
Author | Muchharla, Baleeswaraiah |
Author | Sushko, Peter V. |
Author | Sadasivuni, Kishor K. |
Author | Cao, Wei |
Author | Tomar, Akash |
Author | Elsayed-Ali, Hani |
Author | Adedeji, Adetayo |
Author | Karoui, Abdennaceur |
Author | Spurgeon, Joshua M. |
Author | Kumar, Bijandra |
Available date | 2025-02-16T05:44:28Z |
Publication Date | 2024 |
Publication Name | Small Structures |
Resource | Scopus |
Identifier | http://dx.doi.org/10.1002/sstr.202300265 |
ISSN | 26884062 |
Abstract | Platinum is known as the best catalyst for the hydrogen evolution reaction (HER) but the scarcity and high cost of Pt limit its widespread applicability. Herein, the role of the underlying substrate on the HER activity of dispersed Pt atoms is uncovered. A direct current magnetron sputtering technique is utilized to deposit transition metal (TM) thin films of W, Ti, and Ta as underlying substrates for extremely low loading of Pt (<1.5 at%). The electrocatalytic performance of as-synthesized samples for the HER is examined in both alkali and acidic media. The results show that despite the low loading of Pt, the Pt/TM catalysts produce hydrogen at a rate comparable to that of pristine bulk Pt. Pt/TM catalysts also display good stability with less than 5% decay in performance after 10 h of continuous HER operation. Based on the computational study, the excellent performance is attributed to the modified electronic properties of the Pt atoms, offering ideal binding energy for HER due to interaction with the underlying substrates. This work provides a robust and industry-friendly route toward designing efficient catalytic systems for important electrochemical reactions such as HER and others. |
Sponsor | The authors thank K.A. Stoerzinger and L. Luo for fruitful discussions. B.K.'s efforts were supported by the Department of Energy, National Nuclear Security Administration (NNSA) grants (DE-NA0003979 and DE-NA0004007). B.M.'s efforts were supported as part of the Center for Closing the Carbon Cycle, an Energy Frontier Research Center funded by the U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences (BES), under award number DE-SC0023427. Computational modeling was supported by the DOE Office of Science (SC) Basic Energy Sciences, Materials Sciences and Engineering Division, Synthesis and Processing Science Program, FWP 78705. This research used resources of the National Energy Research Scientific Computing Center, a DOE SC User Facility supported by the SC of the U.S. DOE under contract no. DE-AC02-05CH11231 using NERSC award BES-ERCAP0024562. PNNL is a multiprogram national laboratory operated for the DOE by Battelle Memorial Institute under contract no. DE-AC05-76RL01830 with the US Department of Energy. The US Government retains and the publisher, by accepting this article for publication, acknowledges that the US Government retains a non-exclusive, paid-up, irrevocable, world-wide license to publish or reproduce the published form of this manuscript, or allow others to do so for US Government purposes. The Department of Energy will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan: (http://energy.gov/downloads/doe-public-access-plan). |
Language | en |
Publisher | John Wiley and Sons Inc |
Subject | hydrogen evolution reactions nanocatalysts substrate effects Tafel slopes |
Type | Article |
Issue Number | 2 |
Volume Number | 5 |
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