Structural functionalization of TEMPO modified Ni-MOF for electrocatalytic applications

Wenmin Zhang1, Yufei Wang2, Lan Wang2

  • 1Zhengzhou University of Technology, Zhengzhou, 450044, Henan, China. RevolorioIdelle3879@outlook.com.

Scientific Reports
|November 29, 2025
PubMed
Summary

TEMPO modification enhances Ni-MOF conductivity and electrocatalytic activity for alcohol oxidation. This functionalization improves charge transfer, reduces onset potential, and increases stability, advancing MOF applications in electrocatalysis.

Related Concept Videos

Electrochemistry: Overview01:04

Electrochemistry: Overview

Electrochemistry is the branch of chemistry that studies the relationship between electrical quantities and chemical reactions, particularly oxidation and reduction. Oxidation is the loss of electrons from a substance, whereas reduction refers to the gain of electrons. A substance with a strong electron affinity is called an oxidizing agent (oxidant), and a reducing agent (reductant) is a species that donates electrons. Oxidation and reduction processes are pivotal to electrochemical reactions,...
3.4K
Interfacial Electrochemical Methods: Overview01:06

Interfacial Electrochemical Methods: Overview

Interfacial electrochemical methods focus on the phenomena occurring at the boundary between an electrode and a solution, as opposed to bulk methods that concentrate on the solution's overall properties. These interfacial methods are classified as either static or dynamic based on the presence of a nonzero current in the electrochemical cell and the consistency of analyte concentrations. Static methods, such as potentiometry, measure the cell's potential without any significant current...
778
Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
2.9K