Tunable Pt-MoSx Hybrid Catalysts for Hydrogen Evolution

被引:69
作者
Chia, Xinyi [1 ]
Sutrisnoh, Nur Ayu Afira [1 ]
Pumera, Martin [1 ,2 ]
机构
[1] Nanyang Technol Univ, Sch Phys & Math Sci, Div Chem & Biol Chem, Singapore 637371, Singapore
[2] Brno Univ Technol, Cent European Inst Technol, Purkynova 123, CZ-61200 Brno, Czech Republic
关键词
molybdenum disulfide; platinum; doping; electrodeposition; hydrogen evolution; TRANSITION-METAL DICHALCOGENIDES; VISIBLE-LIGHT IRRADIATION; ACTIVE EDGE SITES; MOLYBDENUM SULFIDE; ELECTROCHEMICAL DEPOSITION; H-2; EVOLUTION; THIN-FILMS; ELECTROCATALYSIS; GENERATION; ELECTRODEPOSITION;
D O I
10.1021/acsami.7b19346
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
Platinum (Pt)-based materials are inevitably among the best-performing electrocatalysts for hydrogen evolution reaction (HER). MoS2 was suggested to be a potent HER catalyst to replace Pt in this reaction by theoretical modeling; however, in practice, this dream remains elusive. Here we show a facile one-pot bottom-up synthesis of Pt-MoSx composites using electrochemical reduction in an electrolytic bath of Pt precursor and ammonium tetrathiomolybdate under ambient conditions. By modifying the millimolar concentration of Pt precursors, composites of different surface elemental composition are fabricated; specifically, Pt1.8MoS2, Pt0.1MoS2.5, Pt0.2MoS0.6, and Pt0.3MoS0.8. All electrodeposited Pt-MoSx hybrids showcase low overpotentials and small Tafel slopes that outperform MoS2 as an electrocatalyst. Tantamount to electrodeposited Pt, the rate-limiting process in the HER mechanism is determined to be the Heyrovsky desorption across Pt-MoSx hybrids and starkly swings from the rate determining Volmer adsorption step in MoS2. The Pt-MoSx composites are equipped with catalytic performance that closely mirrors that of electrodeposited Pt, in particular the HER kinetics for Pt1.8MoS2 and Pt0.1MoS2.5. This work advocates electrosynthesis as a cost-effective method for catalyst design and fabrication of competent composite materials for water splitting applications.
引用
收藏
页码:8702 / 8711
页数:10
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