Metallic molybdenum sulfide nanodots as platinum-alternative co-catalysts for photocatalytic hydrogen evolution

被引:40
|
作者
Xu, Xiaoyong [1 ,2 ]
Pan, Lou [1 ]
Han, Qiutong [3 ]
Wang, Chengzhong [1 ]
Ding, Peng [1 ]
Pan, Jing [1 ]
Hu, Jingguo [1 ]
Zeng, Haibo [2 ]
Zhou, Yong [3 ]
机构
[1] Yangzhou Univ, Coll Phys Sci & Technol, Yangzhou 225002, Jiangsu, Peoples R China
[2] Nanjing Univ Sci & Technol, Coll Mat Sci & Engn, Nanjing 210094, Jiangsu, Peoples R China
[3] Nanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; 1T-phase MoS2; Nanodots; Solar hydrogen production; MOS2 ULTRATHIN NANOSHEETS; H-2; EVOLUTION; CATALYTIC-ACTIVITY; PHASE-TRANSITION; ACTIVE-SITES; WATER; OPTIMIZATION; PERFORMANCE;
D O I
10.1016/j.jcat.2019.04.043
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:237 / 245
页数:9
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