Dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions

Author:

Gao Rui-Ting1ORCID,Nguyen Nhat Truong2ORCID,Nakajima Tomohiko3ORCID,He Jinlu1ORCID,Liu Xianhu4ORCID,Zhang Xueyuan5,Wang Lei1ORCID,Wu Limin16ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.

2. Department of Chemical and Materials Engineering, Gina Cody School of Engineering and Computer Science, Concordia University, Montreal QC H3G 2W1, Canada.

3. Advanced Manufacturing Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba Central 5, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565, Japan.

4. Key Laboratory of Materials Processing and Mold, Ministry of Education, Zhengzhou University, Zhengzhou 450002, China.

5. State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China.

6. Department of Materials Science and State Key Laboratory of Molecular Engineering of Polymers, Fudan University, Shanghai 200433, China.

Abstract

Photoelectrochemical (PEC) water splitting that functions in pH-neutral electrolyte attracts increasing attention to energy demand sustainability. Here, we propose a strategy to in situ form a NiB layer by tuning the composition of the neutral electrolyte with the additions of nickel and borate species, which improves the PEC performance of the BiVO 4 photoanode. The NiB/BiVO 4 exhibits a photocurrent density of 6.0 mA cm −2 at 1.23 V RHE with an onset potential of 0.2 V RHE under 1 sun illumination. The photoanode displays a photostability of over 600 hours in a neutral electrolyte. The additive of Ni 2+ in the electrolyte, which efficiently inhibits the dissolution of NiB, can accelerate the photogenerated charge transfer and enhance the water oxidation kinetics. The borate species with B─O bonds act as a promoter of catalyst activity by accelerating proton-coupled electron transfer. The synergy effect of both species suppresses the surface charge recombination and inhibits the photocorrosion of BiVO 4 .

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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