Related Experiment Video
Updated: Nov 17, 2025

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
Published on: October 5, 2019
A Molecular Tetrahedral Cobalt-Seleno-Based Complex as an Efficient Electrocatalyst for Water Splitting
Ibrahim Munkaila Abdullahi1, Jahangir Masud2, Polydoros-Chrisovalantis Ioannou3
1Department of Chemistry, Missouri University of Science & Technology, Rolla, MO 65409, USA.
This study introduces a cobalt-selenium complex for efficient electrocatalysis. The novel complex demonstrates low overpotential for oxygen evolution reactions (OER) and high activity, showing promise for clean energy applications.
Area of Science:
- Inorganic Chemistry
- Electrochemistry
- Materials Science
Background:
- Developing efficient electrocatalysts is crucial for renewable energy technologies.
- Molecular cobalt-based systems show promise for water splitting reactions.
- Cobalt-selenium compounds are emerging as potential catalysts.
Purpose of the Study:
- To synthesize and characterize a novel cobalt-selenium coordination complex.
- To evaluate its catalytic performance in oxygen evolution (OER) and hydrogen evolution (HER) reactions.
- To assess its potential as an efficient electrocatalyst for water splitting.
Main Methods:
- Synthesis of the cobalt-selenium coordination complex [Co{(SePiPr2)2N}2].
- Electrochemical evaluation of OER and HER in alkaline solutions.
- Measurement of overpotential, mass activity, and turnover frequency (TOF).
Main Results:
- The cobalt-selenium complex required an overpotential of 320 mV for OER and 630 mV for HER at 10 mA cm-2.
- The OER overpotential is among the lowest reported for molecular cobalt(II) systems.
- High mass activity (14.15 A g-1) and TOF (0.032 s-1) were observed at 300 mV overpotential for OER.
Conclusions:
- The cobalt-selenium complex exhibits excellent catalytic activity for OER.
- Molecular cobalt-selenium systems are highly promising electrocatalysts for OER.
- Further research into these systems could advance water splitting technologies.
More Related Videos
10:57Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
05:47Preparation of Polyoxometalate-based Photo-responsive Membranes for the Photo-activation of Manganese Oxide Catalysts
Published on: August 7, 2018
Related Concept Videos
Valence Bond Theory
Formation of Complex Ions
Electron Transport Chain: Complex III and IV
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...