Interfacial phosphate-like “bridge” mediates bulk charge and surface oxygenated-intermediate migration for efficient photoelectrochemical water splitting

Literature Information

Publication Date 2023-12-02
DOI 10.1039/D3TA06203A
Impact Factor 12.732
Authors

Cheng Wang, Wei Zhang, Shuo Gu, Shengdong Sun, Meng Zhou, Wei Chen, Shikuo Li


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Abstract

Regulating the heterointerface structure is a great challenge to developing an efficient photoelectrode for solar water splitting. Herein, the interfacial phosphate ([PO]) was brought into the ZnIn2S4/CdS interface to modulate the energy band structure by in situ exchange strategy. The interfacial [PO] paved an electronic “bridge” to eliminate the multiphase thermal resistance and promoted the oxygenated-intermediate migration for the surface oxygen evolution reaction (OER). The optimized ZnIn2S4–PO/CdS (ZIS–P/CdS) photoanode presented a prominent PEC activity with a maximum photocurrent density of 5.19 mA cm−2 at 1.23 V vs. reversible hydrogen electrode (RHE) under AM 1.5 G illumination in a neutral solution without a sacrificial agent, which is about 9.8 times higher than that of the pristine ZnIn2S4 (0.53 mA cm−2). Furthermore, the oxygen output of ZIS–P/CdS was as high as 13.1 μmol within 3 h in the neutral solution. The in situ ultrafast spectroscopy and density functional theory simulation confirmed the [PO] promotion of the Z-scheme charge transfer and acceleration of the O–H bond breakage for OER. This work provides a new horizon for understanding the interface structure on the bulk charge migration and the surface reaction kinetics during the PEC reactions.

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Journal of Materials Chemistry A

Journal of Materials Chemistry A
CiteScore: 19.5
Self-citation Rate: 4.7%
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