Hydrogen peroxide (H2O2) electrosynthesis via the 2e(-) Oxygen 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 H2O2 synthesis, 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 2e(-) ORR electrocatalysts.
Metal‐Free Electrocatalysts for the Selective 2 e−Oxygen Reduction Reaction: A Never‐Ending Story? / Tuci, Giulia; Rossin, Andrea; Zhang, Xiong; Truong‐Phuoc, Lai; Berretti, Enrico; Liu, Yuefeng; Pham‐Huu, Cuong; Ali, Sajjad; Jan, Faheem; Poggini, Lorenzo; Giambastiani, Giuliano. - In: CHEMISTRY-A EUROPEAN JOURNAL. - ISSN 0947-6539. - STAMPA. - 29:(2023), pp. e202301036.1-e202301036.10. [10.1002/chem.202301036]
Metal‐Free Electrocatalysts for the Selective 2 e−Oxygen Reduction Reaction: A Never‐Ending Story?
Giambastiani, Giuliano
Conceptualization
2023
Abstract
Hydrogen peroxide (H2O2) electrosynthesis via the 2e(-) Oxygen 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 H2O2 synthesis, 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 2e(-) ORR electrocatalysts.File | Dimensione | Formato | |
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