催化作用
化学
铂金
光催化
贵金属
分解水
制氢
无机化学
氢
硫化物
光催化分解水
纳米点
化学工程
物理化学
有机化学
工程类
作者
Xiaoyong Xu,Lou Pan,Qiutong Han,Chengzhong Wang,Peng Ding,Jing Pan,Jingguo Hu,Haibo Zeng,Yong Zhou
标识
DOI:10.1016/j.jcat.2019.04.043
摘要
Molybdenum sulfide (MoS2) has attracted considerable attention as one of noble-metal-free co-catalysts of hydrogen evolution reaction (HER) for artificial photosynthetic water splitting. There are well-known challenges in optimizing its catalytic activity to pursue the replacement of platinum (Pt) for HER, owing to the edge-limited active sites and intrinsically poor conductivity. Herein, we prepared metallic MoS2 nanodots (MNDs) with 1T-phase occupation and edge-exposure maximum to achieve the simultaneous optimization of electric conductivity and active sites. When integrated as co-catalysts with graphitic carbon nitride (g-CN) for sunlight-driven HER in alkaline electrolyte, the outstanding photocatalytic activity with hydrogen evolution rate of 5.62 mmol g−1 h−1, over 280 times higher than that of pure g-CN, demonstrates the excellent co-catalytic performance of 1T-MoS2 NDs (1T-MNDs) that even comparable to state-of-the-art Pt. The photo-induced charge dynamics describe the role of 1T-MNDs in facilitating charge separation as well as surface catalytic reaction, suggesting a promising potential of 1T-MNDs with more active sites and higher conductivity as Pt-alternative co-catalysts for solar hydrogen production.
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