Related Experiment Video
Updated: Jan 3, 2026

Simple Methods for the Preparation of Non-noble Metal Bulk-electrodes for Electrocatalytic Applications
Published on: June 21, 2017
Flower-like platinum-cobalt-ruthenium alloy nanoassemblies as robust and highly efficient electrocatalyst for
Hong-Yan Chen1, Hua-Jie Niu1, Xiaohong Ma2
1Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Life Sciences, College of Geography and Environmental Sciences, Zhejiang Normal University, Jinhua 321004, China.
Abstract:
Exploring hydrogen evolution reaction (HER) catalyst with highly catalytic features in alkaline conditions is considered as significance for water splitting. In this study, a general and simple method was developed to prepare flower-like platinum-cobalt-ruthenium alloy nanoassemblies (PtCoRu NAs) by using murexide and cetyltrimethylammonium chloride (CTAC) as the co-structure-directing agents. Benefiting from the structural advantages and multimetallic compositions, the as-prepared PtCoRu NAs displayed remarkably enhanced electrocatalytic performance for the HER in 1.0 M KOH, with a low overpotential (η, 22 mV) to drive 10 mA cm-2, small Tafel slope (46 mV dec-1), and high exchange current density (j0, 3.30 mA cm-2) during the long-term electrolysis. The as-developed strategy sheds some valuable guidelines for preparing advanced multimetallic catalysts for production of hydrogen in fuel cells.
More Related Videos
08:40Synthesis 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
09:02Synthesis of Platinum-nickel Nanowires and Optimization for Oxygen Reduction Performance
Published on: April 27, 2018
Related Concept Videos
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...
Catalysis