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

Hydroboration-Oxidation of Alkenes03:08

Hydroboration-Oxidation of Alkenes

7.9K
In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
7.9K
Hydrogen Bonds01:04

Hydrogen Bonds

8.0K
A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...
8.0K
Lewis Acids and Bases02:16

Lewis Acids and Bases

13.8K
This lesson delves into Lewis acids and bases in the context of the octet rule for electron-deficient compounds. Here, the concept is discussed, emphasizing the group 13 elements like boron or aluminium. Since group 13 elements possess three valence electrons, they form trivalent compounds with a sextet of electrons and a vacant orbital for the central atom. Consequently, these electron-deficient compounds accept electrons from other species to complete their octet in a chemical reaction. They...
13.8K
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation02:47

Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation

17.8K
Introduction
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
17.8K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

3.2K
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...
3.2K
Regioselectivity and Stereochemistry of Hydroboration02:36

Regioselectivity and Stereochemistry of Hydroboration

8.1K
A significant aspect of hydroboration–oxidation is the regio- and stereochemical outcome of the reaction.
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
8.1K

You might also read

Related Articles

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

Sort by
Same authorSame Topic

Phase Engineering of Iridium Oxides Enables Direct Coupling of Proton Exchange Membrane Water Electrolysis With Intermittent Electrical Energy.

Advanced materials (Deerfield Beach, Fla.)·2026
Same author

Multiscale Magnetic Field Engineering for Advanced Lithium-Based Batteries.

Advanced materials (Deerfield Beach, Fla.)·2026
Same author

Interfacial-Electronegativity-Induced Near-Surface Tetrahedral Reconstruction Enables One-Step Upcycling of Spent LiFePO<sub>4</sub> for High-Rate and Long-Life Pouch Cells.

Advanced materials (Deerfield Beach, Fla.)·2026
Same author

Synergistic interfacial-mechanical binder design for high-areal-capacity and long-lifespan Si-based negative electrodes in practical pouch cells.

Nature communications·2026
Same author

Highly Interdiffused W-Ir Interfaces Enhances Acidic Oxygen Evolution.

Small (Weinheim an der Bergstrasse, Germany)·2026
Same author

Integrated Local-Microstructure Engineering Toward Mechanochemically Robust Ultra-High Nickel Cathodes.

Advanced materials (Deerfield Beach, Fla.)·2026

Related Experiment Video

Updated: Jun 9, 2025

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

3.5K

Practical H2 supply from ammonia borane enabled by amorphous iron domain.

Yufeng Chen1, Zhongling Lang2, Kun Feng1

  • 1Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou, China.

Nature Communications
|October 22, 2024
PubMed
Summary

Amorphous domains on R-Fe2O3 Foam efficiently catalyze ammonia borane (AB) for hydrogen storage. This durable catalyst offers superior performance and stability for hydrogen fuel applications.

More Related Videos

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
06:32

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions

Published on: August 17, 2016

19.5K
Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials
09:05

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials

Published on: May 15, 2015

14.7K

Related Experiment Videos

Last Updated: Jun 9, 2025

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

3.5K
A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
06:32

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions

Published on: August 17, 2016

19.5K
Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials
09:05

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials

Published on: May 15, 2015

14.7K

Area of Science:

  • Materials Science
  • Catalysis
  • Energy Storage

Background:

  • Efficient catalysis of ammonia borane (AB) is crucial for controlled hydrogen release and cost-effective hydrogen storage.
  • Existing benchmarks for AB catalytic performance and stability are often limited, hindering practical applications.
  • Catalyst lifetime is a critical factor for the viability of hydrogen fuel cells.

Purpose of the Study:

  • To develop a highly efficient and stable catalyst for ammonia borane (AB) hydrolysis.
  • To investigate the catalytic mechanism and performance of amorphous domains on metallic Fe crystal structures for hydrogen generation.
  • To evaluate the catalyst's potential for practical hydrogen storage and fuel cell applications.

Main Methods:

  • Synthesis of R-Fe2O3 Foam with amorphous domains on metallic Fe crystal structures.
  • Characterization of catalytic performance, including turnover frequency (TOF) and hydrogen generation rates.
  • Stability testing over extended periods and evaluation in a commercial car fuel cell.

Main Results:

  • R-Fe2O3 Foam achieved a TOF of 113.6 min⁻¹, significantly outperforming reported benchmarks by over 20 times.
  • The catalyst demonstrated exceptional stability, producing approximately 771 L H₂ in 900 h with a high volumetric rate of 43.27 mL/(min·cm²).
  • Stable power outputs (7.8 V, 1.6 A) were maintained for over 5 hours in a driven commercial car fuel cell, with a H₂ supply rate of 180 mL H₂/min.

Conclusions:

  • Amorphous domains on R-Fe2O3 Foam act as highly effective catalytic sites, lowering dissociation barriers for H₂O and AB via Fe-B intermediates.
  • The stable Fe crystal structure contributes to the catalyst's remarkable durability and performance.
  • R-Fe2O3 Foam presents a promising solution for durable, high-performance ammonia borane catalysts and viable chemical hydrogen storage in vehicles.