Abstract

Developing Simple, Affordable, and Environmentally Friendly Water Oxidation Electrocatalysts with High Intrinsic Activity and Low overpotential Continues to Be an Area of Intense Research. in This Article, a Trichromium Diselenide Carbonyl Cluster Complex (Et4N)2[Se2Cr3(CO)10], with a Unique Bonding Structure Comprising Bridging Se Groups, Has Been Identified as a Promising Electrocatalyst for Oxygen Evolution Reaction (OER). This Carbonyl Cluster Exhibits a Promising overpotential of 310 MV and a Low Tafel Slope of 82.0 MV Dec−1 at 10 MAcm−2, with Superior Durability in an Alkaline Medium, for a Prolonged Period of Continuous Oxygen Evolution. the Mass Activity and Turnover Frequency of 62.2 Ag−1 and 0.0174 S−1 Was Achieved, Respectively at 0.390 V vs.. RHE. the Cr-Complex Reported Here Shows Distinctly Different Catalytic Activity based on Subtle Changes in the Ligand Chemistry Around the Catalytically Active Cr Site. Such Dependence Further Corroborates the Critical Influence of Ligand Coordination on the Electron Density Distribution Which Further Affects the Electrochemical Activation and Catalytic Efficiency of the Active Site. Specifically, Even Partial Substitution with More Electronegative Substituents Leads to the Weakening of the Catalytic Efficiency. This Report Further Demonstrates that Metal Carbonyl Chalcogenides Cluster-Type Materials Which Exhibit Partially Occupied Sites and High Valence in their Metal Sites Can Serve as Catalytically Active Centers to Catalyze OER Exhibiting High Intrinsic Activity. the Insight Generated from This Report Can Be Directly Extrapolated to 3-Dimensional Solids Containing Similar Structural Motifs, Thereby Aiding in Optimal Catalyst Design.

Department(s)

Chemistry

Publication Status

Open Access

Comments

National Science Foundation, Grant CAS 2155175

Keywords and Phrases

carbonyl cluster; chromium selenide; molecular complex; oxygen evolution reaction; water splitting

International Standard Serial Number (ISSN)

2073-4344

Document Type

Article - Journal

Document Version

Final Version

File Type

text

Language(s)

English

Rights

© 2023 The Authors, All rights reserved.

Creative Commons Licensing

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.

Publication Date

01 Apr 2023

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