4.6 Article

Theoretical Studies on Layered Perovskite Photocatalysts Sr2M2O7 (M = Nb and Ta) Modified by NiO Cocatalysts

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 127, Issue 1, Pages 319-327

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.2c07959

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Sr2Nb2O7 and Sr2Ta2O7 with layered perovskite structures are capable of photocatalytic water splitting in the ultraviolet region, which can be enhanced by loading NiO as a cocatalyst. Density functional theory calculations reveal that NiO strongly adsorbs on the semiconductor surfaces of Sr2M2O7 (010) (M = Nb and Ta). NiO acts as the active site for the water oxidation reaction, facilitating the transfer of photoinduced holes from the surface. The formation of interfacial structures between NiO and Sr2M2O7 (010) surfaces has minimal influence on the absorption edge, and H2O tends to molecularly adsorb on the bare surfaces.
Sr2Nb2O7 and Sr2Ta2O7 with layered perovskite structures exhibited abilities to accomplish the photocatalytic water-splitting reaction in the ultraviolet region. Their activities could be much increased by loading NiO as a cocatalyst. In this work, we have applied density functional theory calculations to get insights into the role of NiO in modulating the electronic structure, optical absorption, and photocatalytic reaction mechanism of Sr2M2O7 (010) (M = Nb and Ta) surfaces. The calculated adsorption energies of -3.15 and -3.37 eV indicate the strong adsorption of NiO clusters on the semiconductor surfaces. The energy levels of the cocatalyst cluster in the valence band maximum are higher than those of the surfaces, which is in favor of the transfer of photoinduced holes from the surface to the cocatalyst. Consequently, NiO can serve as the active site of the water oxidation reaction, in accordance with the previous experimental findings. The formation of interfacial structures between NiO and Sr2M2O7 (010) surfaces has seldom influence on the absorption edge of systems, like the experimental observations. The results show that H2O tends to molecularly adsorb on the bare surfaces and the dissociation of water is easy to occur on Ni4O4/Sr2M2O7 (010) surfaces, which lead to the much easier generation of HO* intermediates on the latter than the former. The rate-determining step of the oxygen evolution reaction for Sr2M2O7 photocatalysts is modified by loading the NiO cocatalyst. The computed overpotentials of the oxygen evolution reaction (OER) are 0.58 and 0.53 V for Ni4O4/Sr2M2O7 (010) surfaces and 1.28 and 1.24 V for native Sr2M2O7 (010) surfaces, respectively. The important decrease of overpotentials resulted from loading NiO cluster could be one of the reasons that the remarkable increases in photocatalytic activities were experimentally observed by adding cocatalysts.

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