Related Experiment Video
Updated: Dec 24, 2025

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
Unexpected Correlation Between Boron Chain Condensation and Hydrogen Evolution Reaction (HER) Activity in Highly
Eunsoo Lee1,2, Hyounmyung Park1,2, Hyunkeun Joo1
1Department of Chemical and Environmental Engineering, University of California, Riverside, Riverside, CA, 92521, USA.
Vanadium borides exhibit high electrocatalytic activity for hydrogen evolution. Their activity correlates with boron chain condensation, enabling prediction of performance for known and novel materials.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Transition-metal borides (TMBs) are emerging as efficient electrocatalysts for the hydrogen evolution reaction (HER).
- Understanding the structure-activity relationship is crucial for designing advanced electrocatalytic materials.
Purpose of the Study:
- To investigate the HER electrocatalytic activity of vanadium borides (VB and V3B4).
- To establish a correlation between the crystal structure, specifically boron chain condensation, and HER activity in vanadium borides.
- To develop a predictive model for HER overpotentials in vanadium-boron systems.
Main Methods:
- Electrochemical characterization of VB and V3B4 for HER in sulfuric acid.
- Analysis of structure-activity relationships based on boron chain condensation.
- Development of an exponential equation to predict overpotentials for various VxB_y phases.
Main Results:
- VB and V3B4 demonstrate high electrocatalytic HER activity.
- HER activity increases with enhanced boron chain condensation in vanadium borides.
- Accurate prediction of overpotentials for VB2, V2B3, and hypothetical "V5B8" was achieved.
- An exponential equation was derived to predict overpotentials for VxB_y phases with boron chains.
Conclusions:
- A direct correlation between crystal structure and HER activity in vanadium borides was established.
- The findings facilitate the rational design of novel, high-performance electrocatalysts for HER.
- Structure-activity relationships offer a pathway to optimize electrocatalytic materials.
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Regioselectivity and Stereochemistry of Hydroboration
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 stereochemistry.
Hybridization of Atomic Orbitals I
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Molecular Orbital Theory II
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...

