Sulfonic Acid Functionalization-Boosted Ultrafast, Durable, and Selective Four-Electron Oxygen Reduction Reaction: Evidenced by EC-SHINERS and DFT Studies-Reference-Cited by-同舟云学术

Sulfonic Acid Functionalization-Boosted Ultrafast, Durable, and Selective Four-Electron Oxygen Reduction Reaction: Evidenced by EC-SHINERS and DFT Studies

Published:2023-03-13 Issue:7 Volume:13 Page:4155-4167
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Singh Devesh Kumar¹²,Natchimuthu Karuppusamy Murugasenapathi³⁴^ORCID,Shrivastava Anshu⁵,Palanisamy Tamilarasan³⁴^ORCID,Sinha Indrajit⁵,Ganesan Vellaichamy¹^ORCID

Affiliation:

1. Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi 221005, Uttar Pradesh, India

2. Department of Chemistry, Kutir Post Graduate College, Chakkey, Jaunpur 222146, Uttar Pradesh, India

3. Electrodics and Electrocatalysis Division (EEC), CSIR-Central Electrochemical Research Institute (CECRI), Karaikudi 630003, Tamilnadu, India

4. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India

5. Department of Chemistry, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005, Uttar Pradesh, India

Funder

Banaras Hindu University

Council of Scientific and Industrial Research, India

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.3c00719

Reference26 articles.

1. Molecular Insight of the Critical Role of Ni in Pt-Based Nanocatalysts for Improving the Oxygen Reduction Reaction Probed Using an In Situ SERS Borrowing Strategy

2. In situ Spectroscopic Insight into the Origin of the Enhanced Performance of Bimetallic Nanocatalysts towards the Oxygen Reduction Reaction (ORR)

3. Boosting Electrochemical Oxygen Reduction Performance of Iron Phthalocyanine through Axial Coordination Sphere Interaction

4. Iron phthalocyanine with coordination induced electronic localization to boost oxygen reduction reaction

5. Controlling the Oxygen Reduction Selectivity of Asymmetric Cobalt Porphyrins by Using Local Electrostatic Interactions

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