4.6 Article

Unique three-dimensional heterostructure of MoS2@Co-MOF decorated with Co-Al layered double hydroxide: An effective synergistic alkaline hydrogen evolution electrocatalyst

Journal

ELECTROCHIMICA ACTA
Volume 430, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2022.141072

Keywords

Hydrogen evolution reaction; Layered double hydroxides; Molybdenum disulfide; Electrocatalyst

Funding

  1. Science and Technology Com- mission of Shanghai Municipality Project [18090503800]
  2. Shanghai Natural Science Foundation of Shanghai [17ZR1441700, 14ZR1440500]
  3. Shanghai Associa- tion for Science and Technology Achievements Transformation Alliance Program [LM201851]

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Development of non-platinum based electrocatalysts is crucial for achieving hydrogen economy. In this study, a three-dimensional nanoflower heterostructure composite electrocatalyst was developed for alkaline hydrogen evolution reaction (HER). The catalyst exhibited outstanding electrocatalytic activity, requiring a low overpotential to achieve high current density in 1.0 M KOH solution, surpassing the performance of most reported non-noble-metal HER electrocatalysts.
Development of non-platinum based electrocatalysts with optimized structure is significantly important to realize the blueprint of hydrogen economy. Herein, a three-dimensional (3D) nanoflower heterostructure composite electrocatalyst for alkaline hydrogen evolution reaction (HER) is constructed (MoS2@Co-MOF@CoAl-LDHs/NF), which is composed of CoAl layered double hydroxides (CoAl-LDHs), in-situ Co-MOF and activated molybdenum disulfide (MoS2). Benefiting from the coordination effect between the components, act outs outstanding electrocatalytic activity for HER process, requiring only an overpotential of 96 mV to achieve 10 mA cm-2, a Tafel plot of 73.53 mV dec-1 in 1.0 M potassium hydroxide (KOH) solution, of which the overpotential and the Tafel plot compare favorably to the majority of reported non-noble-metal HER electrocatalyst material. Given the above description, this work breaks new prospects for the development of high-performance electrocatalysts in media that are not conducive to traditional catalyst design.

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