光催化
化学
半导体
电子转移
催化作用
氢
接受者
分解水
光化学
化学工程
光电子学
材料科学
生物化学
物理
有机化学
凝聚态物理
工程类
作者
Zhijian Wang,Bingbao Mei,Jiazang Chen
标识
DOI:10.1016/j.jcat.2022.03.014
摘要
Sunlight-driven photocatalytic hydrogen evolution represents a promising strategy to sustainable clean energy supply. This approach, however, is limited due to low rate even after replacing the sluggish oxygen evolution with efficient hole-extraction, because the very high barrier severely slows the supply of photogenerated electrons to the cocatalysts. Here, we bridge semiconductor-cocatalyst contact with metals that are of appropriate work function. This measure lowers the barrier for interfacial electron transfer by ∼800 meV in our demonstrated Pt/CdS photocatalyst. By this merit, the photocatalyst with intermediate metal delivers an unprecedented hydrogen evolution rate of 1.87 mmol dm−2 h−1 (37.4 mmol g−1 h−1) under sunlight (AM 1.5G, 100 mW/cm2) and linearly increases to 18.39 mmol dm−2 h−1 (367.8 mmol g−1 h−1) by intensifying the illumination to 940 mW/cm2 (AM 1.5G).
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