Metal‐Free Electrocatalysts for the Selective 2 eOxygen Reduction Reaction: A Never‐Ending Story?

Author:

Tuci Giulia1,Rossin Andrea1,Zhang Xiong23,Truong‐Phuoc Lai2,Berretti Enrico1,Liu Yuefeng4,Pham‐Huu Cuong2,Ali Sajjad5,Jan Faheem6,Poggini Lorenzo1,Giambastiani Giuliano1ORCID

Affiliation:

1. Institute of Chemistry of OrganoMetallic Compounds ICCOM-CNR and Consorzio INSTM Via Madonna del Piano, 10 50019, Sesto F.no Florence Italy

2. Institute of Chemistry and Processes for Energy Environment and Health (ICPEES) ECPM UMR 7515 CNRS-University of Strasbourg 25 rue Becquerel 67087 Strasbourg Cedex 02 France

3. CAS Key Laboratory of Science and Technology on Applied Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences 116023 Dalian China

4. Dalian National Laboratory for Clean Energy (DNL) Dalian Institute of Chemical Physics Chinese Academy of Science 457 Zhongshan Road 116023 Dalian China

5. Yangtze Delta Region Institute (Huzhou) University of Electronic Science and Technology of China Huzhou 313001 China

6. Institute of Metal Research Chinese Academy of Sciences Shenyang 110016 China

Abstract

AbstractHydrogen peroxide (H2O2) electrosynthesis via the 2eOxygen Reduction Reaction (ORR) represents a highly challenging, environmentally friendly and cost‐effective alternative to the current anthraquinone‐based technology. Various lightweight element hetero‐doped carbon nanostructures are promising and cheap metal‐free electrocatalysts for H2O2synthesis, particularly those containing O‐functionalities. The exact role of O‐containing functional groups as electroactive sites for the process remains debated if not highly controversial. Herein, we have reported on the covalent exohedral functionalization of the outer surface of extra‐pure multi‐walled carbon nanotubes (MWCNTs) with discrete O‐functional groups as a unique approach to prepare selective electrocatalysts for the process. This kind of decoration has added fundamental tiles to the puzzling structure/reactivity relationship of O‐containing carbon‐based catalysts for ORR, clearing doubts on the controversial role of hydroxyl/phenol groups as key functionalities for the design of more performing 2eORR electrocatalysts.

Funder

Agence Nationale de la Recherche

Ministero dell'Università e della Ricerca

Fellowships for Young International Scientists

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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