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Related Concept Videos

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

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Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
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Self-supporting nanoporous CoMoP electrocatalyst for hydrogen evolution reaction in alkaline solution.

Weiguo Tang1, Shengli Zhu2, Hui Jiang3

  • 1School of Materials Science and Engineering, Tianjin University, Tianjin 300350, China.

Journal of Colloid and Interface Science
|June 28, 2022
PubMed
Summary

This study presents a novel nanoporous cobalt-molybdenum phosphide (np-CoMoP) catalyst for efficient hydrogen production. This low-cost catalyst demonstrates superior hydrogen evolution reaction (HER) performance and stability in alkaline solutions.

Keywords:
CoMoPDealloyingElectrocatalysisHydrogen evolution reactionNanoporous

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Catalysis

Background:

  • Efficient and low-cost catalysts are crucial for sustainable hydrogen production.
  • Cobalt phosphides show promise but require optimization for enhanced activity and stability.

Purpose of the Study:

  • To develop a novel nanoporous cobalt-molybdenum phosphide (np-CoMoP) catalyst.
  • To investigate the effect of molybdenum (Mo) incorporation on the electronic structure and catalytic performance.
  • To evaluate the hydrogen evolution reaction (HER) activity and stability of the np-CoMoP catalyst.

Main Methods:

  • Electrochemical dealloying method was employed to synthesize the self-supporting nanoporous CoMoP catalyst.
  • Characterization of the catalyst's structure and composition (e.g., nanoporous Co65Mo15P20).
  • Electrochemical testing in alkaline solution to assess HER performance.

Main Results:

  • The np-CoMoP catalyst exhibited enhanced electron transfer and increased active sites due to its unique nanostructure.
  • Superior HER performance was achieved with an overpotential of 40.8 mV at 10 mA cm⁻².
  • A low Tafel slope of 46.2 mV dec⁻¹ and excellent long-term stability were observed.

Conclusions:

  • Molybdenum incorporation effectively tunes the electronic structure of cobalt phosphide, optimizing hydrogen atom desorption.
  • The developed nanoporous CoMoP catalyst offers a promising low-cost and highly efficient solution for hydrogen production.
  • The catalyst demonstrates significant potential for industrial applications in electrocatalytic hydrogen generation.