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  • 1
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2023
    In:  Journal of Materials Chemistry A Vol. 11, No. 10 ( 2023), p. 5166-5178
    In: Journal of Materials Chemistry A, Royal Society of Chemistry (RSC), Vol. 11, No. 10 ( 2023), p. 5166-5178
    Abstract: The oxygen evolution reaction (OER) requires electrodes that are not only catalytically active, but also stable under harsh electrochemical environments to enable efficient, durable technologies. Our recent report of a stable amorphous Ni 0.5 Sb 0.5 O z OER photoanode established Ni–Sb–O as an important system for computational understanding of both the structural and catalytic behavior of these complex oxides. In the present work we show that Ni x Sb 1− x O z with x 〉 0.33 crystallizes into a previously unknown phase. Guided by experimental X-ray diffraction, we use density functional theory calculations to perform a prototype phase search to identify a broad family of stable and metastable mixed rutile and hexagonal-like phases for x = 0.33, 0.50, and 0.66 compositions. For the identified phases, we predict favorable oxygen vacancy formation energies for Ni-rich compositions under the reducing synthesis conditions which match measured Ni K-edge X-ray absorption spectra. The calculated overpotential for the most active site decreases with increasing Ni content, from 0.91 V ( x = 0.33) to 0.49 V ( x = 0.66), which captures the experimentally observed trend. We find the active site changes from the Ni–O–Sb bridge to a Ni–O–Ni bridge at increasing Ni concentrations, rather than the commonly studied singly under-coordinated sites. Finally, detailed Pourbaix analysis of the identified phases show excellent electrochemical stability, consistent with experimentally measured low metal ion concentrations in the electrolyte of photoelectrochemical cells. Collectively, our consideration of an ensemble of structures enables identification of the most catalytically prolific structural motifs, aiding the understanding of crystalline and amorphous catalysts and elucidating the co-optimization of activity and durability in nickel antimonates.
    Type of Medium: Online Resource
    ISSN: 2050-7488 , 2050-7496
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2702232-8
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  • 2
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 116, No. 24 ( 2019-06-11), p. 11630-11639
    Abstract: A major challenge to the implementation of artificial photosynthesis (AP), in which fuels are produced from abundant materials (water and carbon dioxide) in an electrochemical cell through the action of sunlight, is the discovery of active, inexpensive, safe, and stable catalysts for the oxygen evolution reaction (OER). Multimetallic molecular catalysts, inspired by the natural photosynthetic enzyme, can provide important guidance for catalyst design, but the necessary mechanistic understanding has been elusive. In particular, fundamental transformations for reactive intermediates are difficult to observe, and well-defined molecular models of such species are highly prone to decomposition by intermolecular aggregation. Here, we present a general strategy for stabilization of the molecular cobalt-oxo cubane core (Co 4 O 4 ) by immobilizing it as part of metal–organic frameworks, thus preventing intermolecular pathways of catalyst decomposition. These materials retain the OER activity and mechanism of the molecular Co 4 O 4 analog yet demonstrate unprecedented long-term stability at pH 14. The organic linkers of the framework allow for chemical fine-tuning of activity and stability and, perhaps most importantly, provide “matrix isolation” that allows for observation and stabilization of intermediates in the water-splitting pathway.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2019
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 3
    In: Chemistry of Materials, American Chemical Society (ACS), Vol. 33, No. 15 ( 2021-08-10), p. 5872-5884
    Type of Medium: Online Resource
    ISSN: 0897-4756 , 1520-5002
    Language: English
    Publisher: American Chemical Society (ACS)
    Publication Date: 2021
    detail.hit.zdb_id: 1500399-1
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  • 4
    In: Cell Reports Physical Science, Elsevier BV, Vol. 3, No. 7 ( 2022-07), p. 100959-
    Type of Medium: Online Resource
    ISSN: 2666-3864
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2022
    detail.hit.zdb_id: 3015727-4
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  • 5
    Online Resource
    Online Resource
    The Electrochemical Society ; 2023
    In:  ECS Meeting Abstracts Vol. MA2023-01, No. 37 ( 2023-08-28), p. 2125-2125
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2023-01, No. 37 ( 2023-08-28), p. 2125-2125
    Abstract: Renewable generation of fuels via solar energy offers promising pathways towards sustainable energy future. Its deployment hinges on the discovery of electrochemically durable materials with good solar-to-chemical conversion efficiency. Necessary visible spectrum photoresponse from electrochemically stable materials is however quite rare. On the other hand, the oxygen evolution reaction (OER) requires electrodes that are not only catalytically active, but also stable under harsh electrochemical environments. In this talk, we report on and theoretical understanding of photo-electrochemical behavior an amorphous and crystaline versions of Ni-Sb-Ox and Co-Sb-Ox oxide photoanodes discovered via high-throughput experimental screening [1,2]. The newly discovered amorphous phases meet the requirements of operational stability, visible photoresponse, and appreciable photovoltage. Guided by experimental X-ray absorption characterization of these systems we use density functional theory calculations to perform a prototype phase search to identify a broad family of stable and metastable mixed rutile and hexagonal-like phases for other compositions [3] . Detailed Pourbaix analysis of the identified phases show excellent electrochemical stability, consistent with experimentally measured electrolyte concentrations of photoelectrochemical cells. We analyze when he identified phases form favorable oxygen vacancies formation energies under the reducing synthesis conditions which match measured Ni K-edge x-ray absorption spectra. The calculated OER overpotentials for the most active sites decreases with increasing Ni/Co content, which captures the experimentally observed trend. Stable amorphous metal-antimonates photoanodes are important systems for computational understanding of both the structural and catalytic behavior of these complex oxides and elucidating the co-optimization of photo-electrochemical activity and durability. This material is based on work performed by the Liquid Sunlight Alliance, which is supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, Fuels from Sunlight Hub under award DE-SC0021266. [1] Zhou, L., Peterson, E. A., Rao, K. K., Lu, Y., Li, X., Lai, Y., Bauers, S. R., Richter, M. H., Kan, K., Wang, Y., Newhouse, P. F., Yano, J., Neaton, J. B., Bajdich, M., & Gregoire, J. M. Addressing solar photochemistry durability with an amorphous nickel antimonate photoanode. Cell Reports Physical Science , 3 (7), 100959. (2022). [2] Zhou, L., Wang, Y., Kan, K., Lucana, D. M., Guevarra, D., Lai, Y., & Gregoire, J. M. Surveying Metal Antimonate Photoanodes for Solar Fuel Generation. ACS Sustainable Chemistry and Engineering , 21 , 33. (2022). [3] Rao, K. K., Zhou, L., Lai, Y., Richter, M. H., Li, X., Lu, Y., Yano, J., Gregoire, J. M. Bajdich, M., Resolving Atomistic Structure and Oxygen Evolution Activity in Nickel Antimonates, (under review).
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2023
    detail.hit.zdb_id: 2438749-6
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