Published September 21, 2020 | Version Published + Supplemental Material
Journal Article Open

Proton-assisted electron transfer and hydrogen-atom diffusion in a model system for photocatalytic hydrogen production

  • 1. ROR icon Beijing Normal University
  • 2. ROR icon China University of Geosciences
  • 3. ROR icon California Institute of Technology

Abstract

Solar energy can be converted into chemical energy by photocatalytic water splitting to produce molecular hydrogen. Details of the photo-induced reaction mechanism occurring on the surface of a semiconductor are not fully understood, however. Herein, we employ a model photocatalytic system consisting of single atoms deposited on quantum dots that are anchored on to a primary photocatalyst to explore fundamental aspects of photolytic hydrogen generation. Single platinum atoms (Pt₁) are anchored onto carbon nitride quantum dots (CNQDs), which are loaded onto graphitic carbon nitride nanosheets (CNS), forming a Pt₁@CNQDs/CNS composite. Pt₁@CNQDs/CNS provides a well-defined photocatalytic system in which the electron and proton transfer processes that lead to the formation of hydrogen gas can be investigated. Results suggest that hydrogen bonding between hydrophilic surface groups of the CNQDs and interfacial water molecules facilitates both proton-assisted electron transfer and sorption/desorption pathways. Surface bound hydrogen atoms appear to diffuse from CNQDs surface sites to the deposited Pt₁ catalytic sites leading to higher hydrogen-atom fugacity surrounding each isolated Pt₁ site. We identify a pathway that allows for hydrogen-atom recombination into molecular hydrogen and eventually to hydrogen bubble evolution.

Additional Information

© The Author(s) 2020. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. Received 27 January 2020; Accepted 02 July 2020; Published 21 September 2020. This work was financially supported by the National Natural Science Foundation of China (Grant 21777009), the Bill and Melinda Gates Foundation (BMGF RTTC Grants OPP1111246 and OPP1149755), Beijing Natural Science Foundation (Grant 8182031), and Major Science and Technology Program for Water Pollution Control and Treatment (Grant 2018ZX07109). Data availability: The authors declare that all the data supporting the findings of this study are available within the paper and its Supplementary Information. Author Contributions: Y.Z., Y.D., and H.L. prepared, characterized, and tested the catalysts. Y.D. performed the spectrum related experiments. Y.Z. and L.Y. collected and analyzed the data. Y.Z. and L.Y. wrote the paper in discussion with M.H. L.Y. and M.H. supervised the overall project. The authors declare no competing interests.

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Supplemental Material - 43246_2020_68_MOESM2_ESM.pdf

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Additional details

Identifiers

PMCID
PMC7505813
Eprint ID
105474
Resolver ID
CaltechAUTHORS:20200922-133041984

Funding

National Natural Science Foundation of China
21777009
Bill and Melinda Gates Foundation
OPP1111246
Bill and Melinda Gates Foundation
OPP1149755
Beijing Municipal Natural Science Foundation
8182031
Major Science and Technology Program for Water Pollution Control and Treatment
2018ZX07109

Dates

Created
2020-09-22
Created from EPrint's datestamp field
Updated
2021-11-16
Created from EPrint's last_modified field