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Related Concept Videos

Heterogeneous Catalysis01:22

Heterogeneous Catalysis

Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...
Catalysis02:50

Catalysis

The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate

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Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the surface of...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide02:44

Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.

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Related Experiment Video

Updated: Jul 13, 2026

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
08:40

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production

Published on: December 6, 2021

Oxygen vacancy-mediated Ru,Fe co-doped Ni(OH)2 for enhanced hydrogen evolution kinetics.

Ruiteng Sun1, Sailong Wang1, Zexing Liang2

  • 1Key Laboratory of Eco-chemical Engineering, International Science and Technology Cooperation Base of Eco-chemical Engineering and Green Manufacturing, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, PR China.

Journal of Colloid and Interface Science
|July 11, 2026
PubMed
Summary

Researchers developed a novel electrocatalyst, RuFeNi-OvH, using oxygen vacancies for efficient hydrogen evolution reactions (HER). This catalyst demonstrates excellent stability and cost-effectiveness for hydrogen production via water electrolysis.

Keywords:
FeHydrogen evolution reactionNi(OH)(2)Oxygen vacancyRu co-doping

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Catalysis

Background:

  • Efficient and stable electrocatalysts are crucial for a hydrogen economy powered by water electrolysis.
  • Developing cost-effective catalysts is essential for practical hydrogen production.

Purpose of the Study:

  • To design and investigate oxygen vacancies mediated Ru, Fe co-doped Ni(OH)2 (RuFeNi-OvH) as an efficient electrocatalyst for the hydrogen evolution reaction (HER).
  • To understand the role of oxygen vacancies in modulating the catalyst's electronic structure and reaction kinetics.

Main Methods:

  • Synthesis of Ru, Fe co-doped Ni(OH)2 with oxygen vacancies (RuFeNi-OvH).
  • Electrochemical characterization of HER performance in 1.0 M KOH.
  • Theoretical calculations to elucidate the mechanism of water adsorption and hydrogen evolution.

Main Results:

  • The RuFeNi-OvH catalyst achieved a current density of 1 A cm-2 at an overpotential of 350 mV.
  • The catalyst demonstrated remarkable stability, operating for 200 hours in a three-electrode system.
  • Theoretical calculations revealed Ru as the active site for water adsorption/dissociation and Ni for hydrogen evolution.

Conclusions:

  • Oxygen vacancies effectively tune the electronic structure and d-band center, reducing the energy barrier for water dissociation and enhancing reaction kinetics.
  • RuFeNi-OvH exhibits superior HER performance and stability, with significant cost-effectiveness for anion exchange membrane (AEM) electrolyzers.
  • This work offers a new strategy for designing efficient and stable HER catalysts by creating vacancies, promoting practical hydrogen production technology.