State Key Laboratory of Crystal Materials, Shandong University, Jinan, 250100, China.
State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
Adv Mater. 2023 May;35(19):e2208915. doi: 10.1002/adma.202208915. Epub 2023 Mar 29.
Developing a hydrogen economy to replace traditional fossil fuels is essential for sustainable human development. As two promising H 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 production, and simultaneous electrocatalytic I reduction and O production. The efficient charge separation, abundant H production active sites, and a small HI splitting energy barrier contribute to the superior photocatalytic H production activity of MoSe /MAPbBr I (CH NH = MA). Subsequent electrocatalytic I reduction and O 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 (6.99 mmol g ) to O (3.09 mmol g ) produced during the first photocatalytic and electrocatalytic cycle is close to 2:1, and the continuous circulation of I /I between the photocatalytic and electrocatalytic systems can achieve efficient and robust pure water splitting.
发展氢能经济以取代传统的化石燃料,对于可持续的人类发展至关重要。作为两种很有前途的制氢策略,光催化和电催化水分解具有较大的反应能垒,分别面临太阳能到氢气效率差和电化学过电势大的巨大挑战。在此,提出了一种新策略,将困难的纯水分解成两个易于实施的部分,即混合卤化物钙钛矿光催化 HI 分解制氢,以及同时电催化 I 还原和 O 生成。高效的电荷分离、丰富的制氢活性位点和较小的 HI 分解能垒有助于 MoSe/MAPbBr I(CHNH = MA)的优越光催化制氢活性。随后的电催化 I 还原和 O 生成反应只需要 0.92V 的小电压来驱动,远低于电催化纯水分解(>1.23V)。在第一个光催化和电催化循环中产生的 H(6.99mmol g )和 O(3.09mmol g )的摩尔比接近 2:1,光催化和电催化系统之间的 I /I 循环可以实现高效和稳健的纯水分解。