In situ Irradiated XPS Investigation on S‐Scheme TiO<sub>2</sub>@ZnIn<sub>2</sub>S<sub>4</sub> Photocatalyst for Efficient Photocatalytic CO<sub>2</sub> Reduction
Abstract
Reasonable design of efficient hierarchical photocatalysts has gained significant attention. Herein, a step-scheme (S-scheme) core-shell TiO<sub>2</sub> @ZnIn<sub>2</sub> S<sub>4</sub> heterojunction is designed for photocatalytic CO<sub>2</sub> reduction. The optimized sample exhibits much higher CO<sub>2</sub> photoreduction conversion rates (the sum yield of CO, CH<sub>3</sub> OH, and CH<sub>4</sub> ) than the blank control, i.e., ZnIn<sub>2</sub> S<sub>4</sub> and TiO<sub>2</sub> . The improved photocatalytic performance can be attributed to the inhibited recombination of photogenerated charge carriers induced by S-scheme heterojunction. The improvement is also attributed to the large specific surface areas and abundant active sites. Meanwhile, S-scheme photogenerated charge transfer mechanism is testified by in situ irradiated X-ray photoelectron spectroscopy, work function calculation, and electron paramagnetic resonance measurements. This work provides an effective strategy for designing highly efficient heterojunction photocatalysts for conversion of solar fuels.
Funding
- National Natural Science Foundation of China
- Fundamental Research Funds for the Central Universities
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