Dual-phase MoS2/MXene/CNT ternary nanohybrids for efficient electrocatalytic hydrogen evolution

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作者
Sichen Wei
Yu Fu
Maomao Liu
Hongyan Yue
Sehwan Park
Young Hee Lee
Huamin Li
Fei Yao
机构
[1] University at Buffalo,Department of Materials Design and Innovation
[2] the State University of New York,Department of Electrical Engineering
[3] University at Buffalo,School of Materials Science and Engineering
[4] the State University of New York,Center for Integrated Nanostructure Physics, Institute for Basic Science, Department of Energy & Department of Physics
[5] Harbin University of Science and Technology,undefined
[6] Sungkyunkwan University,undefined
来源
npj 2D Materials and Applications | / 6卷
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摘要
Two-dimensional (2D) molybdenum disulfide (MoS2) has been recognized as a potential substitution of platinum (Pt) for electrochemical hydrogen evolution reaction (HER). However, the broad adoption of MoS2 is hindered by its limited number of active sites and low inherent electrical conductivity. In this work, we employed a one-step solvothermal synthesis technique to construct a ternary hybrid structure consisting of dual-phase MoS2, titanium carbide (Ti3C2) MXene, and carbon nanotubes (CNTs), and demonstrated synergistic effects for active site exposure, surface area enlargement, and electrical conductivity improvement of the catalyst. The dual-phase MoS2 (DP-MoS2) is directly formed on the MXene with CNTs acting as crosslinks between 2D islands. The existence of edge-enriched metallic phase MoS2, the conductive backbone of MXene along with the crosslink function of CNTs clearly improves the overall HER performance of the ternary nanocomposite. Moreover, the integration of MoS2 with MXene not only increases the interlayer distance of the 2D layers but also partially suppresses the MXene oxidation and the 2D layer restacking, leading to good catalytic stability. As a result, an overpotential of 169 mV and a low Tafel slope of 51 mV/dec was successfully achieved. This work paves a way for 2D-based electrocatalyst engineering and sheds light on the development of the next-generation noble metal-free HER electrocatalysts.
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