Related Experiment Video
Updated: Jan 13, 2026

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules
Published on: April 28, 2014
A Biopolymer System Based on Chitosan and an Anisotropic Network of Nickel Fibers in the Hydrogen Evolution Reaction
Guliya R Nizameeva1,2, Elgina M Lebedeva1,2, Viktoria V Vorobieva1
1Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Kazan 420088, Russia.
Abstract:
In this study, we developed a method for creating an active layer based on a composite material consisting of chitosan and an anisotropic network of nickel fibers (Chitosan/Ni + NiFs). Using this chitosan biopolymer matrix and anisotropic network, we achieved a high specific surface area for the catalytic material, high lateral conductivity for the layer, and stable characteristics, ultimately leading to increased overall electrocatalytic activity in the hydrogen evolution reaction (HER). Through linear voltammetry and impedance spectroscopy, we identified the mechanism and kinetics of the HER in the developed system. The overpotential of the electrochemical reaction was 213 mV at a current density of 10 mA/cm2. Chromatographic analysis confirmed the effectiveness of the Chitosan/Ni + NiFs system in the HER. Our results show how the chitosan biopolymer matrix and oriented nickel fiber network influence charge transfer and electrode reactions, as reflected in the activation energies of hydrogen bonds on the electrocatalytic layers. These findings show that it is feasible to combine a biopolymer matrix and an anisotropic nickel fiber network to create effective electrocatalysts. This approach enables the development of environmentally friendly electrolytic hydrogen production technologies.
Related Concept Videos
Catalysis
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
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...

