MoS2-graphene-CuNi2S4 nanocomposite an efficient electrocatalyst for the hydrogen evolution reaction

被引:25
作者
Adarakatti, Prashanth Shivappa [1 ]
Mahanthappa, Mallappa [2 ]
Hughes, Jack P. [3 ]
Rowley-Neale, Samuel J. [3 ,4 ]
Smith, Graham C. [5 ]
Ashoka, S. [6 ]
Banks, Craig E. [4 ,5 ]
机构
[1] Indian Inst Sci, Solid State & Struct Chem Unit, Bengaluru 560012, India
[2] REVA Univ, Sch Chem Sci, Dept Chem, Bengaluru 560064, India
[3] Manchester Metropolitan Univ, Div Chem & Environm Sci, Sch Sci & Environm, Fac Sci & Engn, Chester St, Manchester M1 5GD, Lancs, England
[4] Manchester Metropolitan Univ, Manchester Fuel Cell Innovat Ctr, Chester St, Manchester M1 5GD, Lancs, England
[5] Univ Chester, Dept Nat Sci, Fac Sci & Engn, Thornton Sci Pk,Pool Lane, Chester CH2 4NU, Cheshire, England
[6] Dayananda Sagar Univ, Sch Engn, Dept Chem, Bengaluru 560068, India
基金
英国工程与自然科学研究理事会;
关键词
Molybdenum disulfide (MoS2); Graphene; Hydrogen evolution reaction; Energy storage; SCREEN-PRINTED ELECTRODES; MOS2; NANOSHEETS; FACILE SYNTHESIS; ACTIVE-SITES; SINGLE-LAYER; GRAPHENE; NANOPARTICLES; CATALYSTS; BULK;
D O I
10.1016/j.ijhydene.2019.05.004
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
We present a facile methodology for the synthesis of a novel 2D-MoS2, graphene and CuNi2S4 (MoS2-g-CuNi2S4) nanocomposite that displays highly efficient electrocatalytic activity towards the production of hydrogen. The intrinsic hydrogen evolution reaction (HER) activity of MoS2 nanosheets was significantly enhanced by increasing the affinity of the active edge sites towards H+ adsorption using transition metal (Cu and Ni-2) dopants, whilst also increasing the edge sites exposure by anchoring them to a graphene framework. Detailed XPS analysis reveals a higher percentage of surface exposed S at 17.04%, of which 48.83% is metal bonded S (sulfide). The resultant MoS2-g-CuNi2S4 nanocomposites are immobilized upon screen-printed electrodes (SPEs) and exhibit a HER onset potential and Tafel slope value of - 0.05 V (vs. RHE) and 29.3 mV dec(-1), respectively. These values are close to that of the polycrystalline Pt electrode (near zero potential (vs. RHE) and 21.0 mV dec(-1), respectively) and enhanced over a bare/unmodified SPE (- 0.43 V (vs. RHE) and 149.1 mV dec(-1), respectively). Given the efficient, HER activity displayed by the novel MoS2-g-CuNi2S4/SPE electrochemical platform and the comparatively low associated cost of production for this nanocomposite, it has potential to be a cost-effective alternative to Pt within electrolyser technologies. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:16069 / 16078
页数:10
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