分解水
光催化
电催化剂
材料科学
制氢
光催化分解水
卤化物
钙钛矿(结构)
电化学
催化作用
析氧
化学工程
无机化学
纳米技术
电极
化学
物理化学
生物化学
工程类
作者
Xiaolei Liu,Qianqian Zhang,Shengli Zhao,Zeyan Wang,Yuanyuan Liu,Zhaoke Zheng,Hefeng Cheng,Ying Dai,Baibiao Huang,Peng Wang
标识
DOI:10.1002/adma.202208915
摘要
Developing a hydrogen economy to replace traditional fossil fuels is essential for sustainable human development. As two promising H2 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 H2 production, and simultaneous electrocatalytic I3- reduction and O2 production. The efficient charge separation, abundant H2 production active sites, and a small HI splitting energy barrier contribute to the superior photocatalytic H2 production activity of MoSe2 /MAPbBr3-x Ix (CH3 NH3+ = MA). Subsequent electrocatalytic I3- reduction and O2 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 H2 (6.99 mmol g-1 ) to O2 (3.09 mmol g-1 ) produced during the first photocatalytic and electrocatalytic cycle is close to 2:1, and the continuous circulation of I3- /I- between the photocatalytic and electrocatalytic systems can achieve efficient and robust pure water splitting.
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