Related Experiment Video
Updated: Aug 1, 2026

Probing and Mapping Electrode Surfaces in Solid Oxide Fuel Cells
Published on: September 20, 2012
Phase-dependent electronic structure modulation of nickel selenides by Fe doping for enhanced bifunctional oxygen
Vigneshraaj A S1,2, Siva Kumar Ramesh3, Jinkwon Kim3
1Centre for Nano and Soft Matter Sciences (CeNS), Shivanapura, Bengaluru 562162, India.
Abstract:
Bifunctional oxygen electrocatalysis is a pivotal process that underpins a diverse array of sustainable energy technologies, including electrolyzers and fuel cells. Metal selenides have been identified as highly promising candidates for oxygen electrocatalysts with electronic structure engineering that lies at the heart of catalyst design. Two-phase Fe-doped nitrogen carbon (NC)-supported nickel selenides were synthesized using a coordination polymer template. Fe doping offers significant advantages as it enhances electronic interactions, resulting in higher availability of active sites than nickel selenides and optimizing the adsorption energy for reaction intermediates. Owing to the intriguing compositional and structural features, the obtained NiFe1-Se2-NC@400 electrocatalyst displays better catalytic activity with an overpotential (η10) of 253 mV and a lower Tafel slope of 57.1 mV dec-1 for the Oxygen Evolution Reaction (OER) in 1 M KOH. Likewise, the catalyst demonstrated remarkable efficiency in Oxygen Reduction Reaction (ORR) catalysis, achieving a limiting current density comparable to that of the standard Pt/C catalyst and exhibiting an improved Tafel slope of 35.4 mV dec-1 in 0.1 M KOH. This work reveals the influence of Fe dopants in oxygen electrocatalysis and presents an effective approach to tuning the electronic structure for the development of highly active electrocatalysts in alkaline media.
Related Concept Videos
Properties of Transition Metals
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...
Valence Bond Theory
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
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 eye.
Properties of Organometallic Compounds

