Integrating Mixed Halide Perovskite Photocatalytic HI Splitting and Electrocatalysis into a Loop for Efficient and Robust Pure Water Splitting.
basic_science · Level V
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- Also identified by DOI 10.1002/adma.202208915.
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Abstract
Developing a hydrogen economy to replace traditional fossil fuels is essential for sustainable human development. As two promising H<sub>2</sub> production strategies, photocatalytic and electrocatalytic water splitting with large reaction energy barriers still face the great challenges of poor solar-to-hydrogen efficiency and large electrochemical overpotentials, respectively. Herein, a new strategy is proposed to disassemble the difficult pure water splitting into two parts that are easy to implement, namely mixed halide perovskite photocatalytic HI splitting for H<sub>2</sub> production, and simultaneous electrocatalytic I<sub>3</sub> <sup>-</sup> reduction and O<sub>2</sub> production. The efficient charge separation, abundant H<sub>2</sub> production active sites, and a small HI splitting energy barrier contribute to the superior photocatalytic H<sub>2</sub> production activity of MoSe<sub>2</sub> /MAPbBr<sub>3-</sub> <sub>x</sub> I<sub>x</sub> (CH<sub>3</sub> NH<sub>3</sub> <sup>+</sup> = MA). Subsequent electrocatalytic I<sub>3</sub> <sup>-</sup> reduction and O<sub>2</sub> production reactions only need a small voltage of 0.92 V to drive, which is far lower than that of the electrocatalytic pure water splitting (>1.23 V). The molar ratio of H<sub>2</sub> (6.99 mmol g<sup>-1</sup> ) to O<sub>2</sub> (3.09 mmol g<sup>-1</sup> ) produced during the first photocatalytic and electrocatalytic cycle is close to 2:1, and the continuous circulation of I<sub>3</sub> <sup>-</sup> /I<sup>-</sup> between the photocatalytic and electrocatalytic systems can achieve efficient and robust pure water splitting.