Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Catalysis02:50

Catalysis

27.0K
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.
27.0K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

3.3K
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...
3.3K
Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

12.1K
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...
12.1K
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide02:44

Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

10.3K
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.
10.3K
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate

11.6K
Alkenes can be dihydroxylated using potassium permanganate.  The method encompasses the reaction of an alkene with a cold, dilute solution of potassium permanganate under basic conditions to form a cis-diol along with a brown precipitate of manganese dioxide.
11.6K
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation02:24

Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation

7.7K
Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
7.7K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

AI-powered risk factor analysis and development of a predictive model for lymphovascular invasion in bladder urothelial carcinoma.

Scientific reports·2026
Same author

Task-Dependent Cortico-Spinal Coupling in the Delta Band During Movement Execution and Inhibitory Control.

IEEE transactions on bio-medical engineering·2026
Same author

Prevalence and psychosocial correlates of depression, anxiety and stress among caregivers of children with childhood-onset systemic lupus erythematosus in China: a cross-sectional study.

BMJ open·2026
Same author

Effectiveness of acceptance and commitment therapy for weight stigma and related psychological outcomes: a systematic review protocol.

Systematic reviews·2026
Same author

<i>CreSAMT1</i> is mainly responsible for the biosynthesis of characteristic aroma compound dimethyl anthranilate in <i>Citrus reticulata</i> 'Chachiensis'.

Horticulture research·2026
Same author

Artificial intelligence applications and the improvement of carbon emission efficiency from the perspective of sustainable development: empirical evidence from China.

Carbon balance and management·2026

Related Experiment Video

Updated: Jul 11, 2025

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
10:21

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions

Published on: October 5, 2019

8.4K

Amorphous-crystalline heterostructure: Efficient catalyst for biomass oxidation coupled with hydrogen evolution.

Jia Wu1, Ke Wang1, Tianqi Yu1

  • 1Guangxi Key Laboratory of Electrochemical Energy Materials, Guangxi Colleges and Universities Key Laboratory of Applied Chemistry Technology and Resource Development, School of Chemistry and Chemical Engineering, Guangxi University, 100 Daxue Road, Nanning 530004, China.

Journal of Colloid and Interface Science
|November 17, 2023
PubMed
Summary

A novel catalyst, NiCo(OH)x/Ni/NiMoO4/NF, efficiently upgrades biomass via 5-hydroxymethylfurfural oxidation and hydrogen evolution. This crystalline-amorphous heterostructure offers enhanced activity and stability for sustainable energy applications.

Keywords:
5-Hydroxymethylfurfural oxidationAmorphous-crystallineCatalystHeterostructureHydrogen evolution reaction

More Related Videos

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
09:21

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether

Published on: August 17, 2019

9.0K
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

3.6K

Related Experiment Videos

Last Updated: Jul 11, 2025

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
10:21

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions

Published on: October 5, 2019

8.4K
Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
09:21

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether

Published on: August 17, 2019

9.0K
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

3.6K

Area of Science:

  • Materials Science
  • Electrochemistry
  • Catalysis

Background:

  • Developing efficient catalysts is crucial for biomass upgrading and hydrogen evolution.
  • Existing catalysts often lack the required activity, selectivity, and stability.

Purpose of the Study:

  • To present a simple method for fabricating crystalline-amorphous phase heterostructures.
  • To develop an efficient electrode for 5-hydroxymethylfurfural oxidation reaction (HMFOR) coupled with hydrogen evolution reaction (HER).

Main Methods:

  • Fabrication of NiCo(OH)x-modified Ni/NiMoO4 nanosheets electrode (NiCo(OH)x/Ni/NiMoO4/NF) using cobalt salt hydrolysis.
  • Utilizing the etching effect of acidic medium to create crystalline-amorphous phase heterostructures.
  • Characterization of the electrode's structure and electrochemical performance.

Main Results:

  • The nanosheets array structure enhances surface area, active site exposure, and mass transfer.
  • Strong coupling interactions at the amorphous-crystalline heterointerface optimize adsorption and charge transfer.
  • The NiCo(OH)x/Ni/NiMoO4/NF catalyst achieves 10 mA cm-2 at 1.34 V for HMFOR-coupled H2 evolution.
  • The catalyst demonstrates stable operation for 13 cycles with good product selectivity.

Conclusions:

  • The study provides a facile method for designing efficient and robust catalysts.
  • The crystalline-amorphous heterostructure design is effective for boosting catalytic activity in HMFOR and HER.
  • This work offers insights into advanced catalyst design for biomass upgrading and hydrogen production.