Doping-Assisted Phase Changing Effect on MoS2 Towards Hydrogen Evolution Reaction in Acidic and Alkaline pH

被引:41
作者
Bolar, Saikat [1 ,2 ]
Shit, Subhasis [1 ,2 ]
Murmu, Naresh C. [1 ,2 ]
Kuila, Tapas [1 ,2 ]
机构
[1] Cent Mech Engn Res Inst, CSIR, Surface Engn & Tribol Div, Durgapur 713209, India
[2] Acad Sci & Innovat Res AcSIR, CSIR CMERI Campus, Durgapur 713209, India
关键词
MoS2; anion doping; hydrogen evolution reaction; electrochemical impedance spectroscopy; distribution of relaxation time; OCTAHEDRAL COORDINATION GEOMETRY; ACTIVE EDGE SITES; MOLYBDENUM-DISULFIDE; ELECTROCATALYTIC ACTIVITY; TRANSITION; NANOSHEETS; OPTIMIZATION; CATALYST; DOPANTS;
D O I
10.1002/celc.201901870
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Hydrogen evolution reaction (HER) was improved through nitrogen (N) doping in molybdenum disulfide (MoS2) due to the formation of 1T-metallic phase as compared to the thermodynamically stable 2H-semiconducting phase. Generally, the phase transition of MoS2 from semiconducting 2H to metallic 1T was carried out by chemical intercalation method. A facile solvothermal synthetic procedure is used to organize 1T@2H MoS2 nanoflower by incorporating N in MoS2 crystal lattice which improved the catalytic activity with the generation of metallic property of MoS2. Optimized N doping is an effective strategy for the development of mixed phase MoS2. Physicochemical characterization techniques confirmed the formation of hybrid phase (1T@2H) MoS2 by N incorporation. A tuned dopant concentration in MoS2 crystal lattice effectively enhanced the catalytic performance by modifying the physical and chemical properties. Moreover, optimal N doped MoS2 offered a very low overpotential of similar to 108 and similar to 141 mV to reach the benchmarking current density of 10 mA cm(-2) for HER in acidic and basic medium, respectively. This work elucidated a rational implantation of phase engineering, which is an efficient strategy to develop efficient electrocatalysts, shedding light on the improvement of transition metal-based electrocatalyst in renewable energy technologies.
引用
收藏
页码:336 / 346
页数:11
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