Related Experiment Video
Updated: Aug 3, 2026

Preparation and Use of Photocatalytically Active Segmented Ag|ZnO and Coaxial TiO2-Ag Nanowires Made by Templated Electrodeposition
Published on: May 2, 2014
Surface and Interface Modulation of V2O5/Ni(OH)2 Nanomaterials for Enhanced Alkaline Water Splitting
Jia Feng1, Yongren Yu1,2, Yinxin Zhang1
1School of New Energy, Shenyang Institute of Engineering, Shenyang 110136, China.
None:
To optimize the electrocatalytic reaction process through the synergistic effects of V and Ni, this study employed a two-step hydrothermal method to successfully construct a V2O5 composite structure grown on a Ni(OH)2 substrate (denoted V2O5/Ni(OH)2-2). Electrochemical evaluation revealed that this catalyst exhibits efficient bifunctional activity in 1.0 M KOH electrolyte. For the hydrogen evolution reaction (HER), it requires a mere 89.6 mV overpotential to achieve a current density of -10 mA cm-2. The catalyst also demonstrates excellent performance in the oxygen evolution reaction (OER), demanding only 198 mV overpotential to drive a current density of 10 mA cm-2, while maintaining low overpotential increases even at high current densities. Furthermore, it exhibits outstanding long-term stability during a 12 h continuous test. When assembled as a dual-electrode overall water splitting device, the system requires a voltage of only 2.82 V to drive a high current density of 100 mA cm-2, showcasing its significant potential for practical applications.
More Related Videos
08:13Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area
Published on: February 19, 2018
10:15Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Aldehydes and Ketones with Water: Hydrate Formation
The formation of hydrates is a reversible reaction. Hydrate formation is influenced by steric and electronic factors accompanying the alkyl substituents on the carbonyl group: The rate of hydrate formation increases with a decrease in the number of alkyl groups attached to the carbonyl carbon. Hence,...