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Electrosynthesis of >20 g/L H(2)O(2) from Air

[Image: see text] Hydrogen peroxide (HP) production via electrochemical oxygen reduction reaction (ORR-HP) is a critical reaction for energy storage and environmental remediation. The onsite production of high-concentration H(2)O(2) using gas diffusion electrodes (GDEs) fed by air is especially attr...

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Autores principales: Li, Huihui, Quispe-Cardenas, Estefanny, Yang, Shasha, Yin, Lifeng, Yang, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845047/
https://www.ncbi.nlm.nih.gov/pubmed/35178529
http://dx.doi.org/10.1021/acsestengg.1c00366
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author Li, Huihui
Quispe-Cardenas, Estefanny
Yang, Shasha
Yin, Lifeng
Yang, Yang
author_facet Li, Huihui
Quispe-Cardenas, Estefanny
Yang, Shasha
Yin, Lifeng
Yang, Yang
author_sort Li, Huihui
collection PubMed
description [Image: see text] Hydrogen peroxide (HP) production via electrochemical oxygen reduction reaction (ORR-HP) is a critical reaction for energy storage and environmental remediation. The onsite production of high-concentration H(2)O(2) using gas diffusion electrodes (GDEs) fed by air is especially attractive. However, many studies indicate that the air–GDE combination could not produce concentrated H(2)O(2), as the [H(2)O(2)] leveled off or even decreased with the increasing reaction time. This study proves that the limiting factors are not the oxygen concentration in the air but the anodic and cathodic depletion of the as-formed H(2)O(2). We proved that the anodic depletion could be excluded by adopting a divided electrolytic cell. Furthermore, we demonstrated that applying poly(tetrafluoroethylene) (PTFE) as an overcoating rather than a catalyst binder could effectively mitigate the cathodic decomposition pathways. Beyond that, we further developed a composite electrospun PTFE (E-PTFE)/carbon black (CB)/GDE electrode featuring the electrospun PTFE (E-PTFE) nanofibrous overcoating. The E-PTFE coating provides abundant triphase active sites and excludes the cathodic depletion reaction, enabling the production of >20 g/L H(2)O(2) at a current efficiency of 86.6%. Finally, we demonstrated the efficacy of the ORR-HP device in lake water remediation. Cyanobacteria and microcystin-LR were readily removed along with the onsite production of H(2)O(2).
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spelling pubmed-88450472022-02-15 Electrosynthesis of >20 g/L H(2)O(2) from Air Li, Huihui Quispe-Cardenas, Estefanny Yang, Shasha Yin, Lifeng Yang, Yang ACS ES T Eng [Image: see text] Hydrogen peroxide (HP) production via electrochemical oxygen reduction reaction (ORR-HP) is a critical reaction for energy storage and environmental remediation. The onsite production of high-concentration H(2)O(2) using gas diffusion electrodes (GDEs) fed by air is especially attractive. However, many studies indicate that the air–GDE combination could not produce concentrated H(2)O(2), as the [H(2)O(2)] leveled off or even decreased with the increasing reaction time. This study proves that the limiting factors are not the oxygen concentration in the air but the anodic and cathodic depletion of the as-formed H(2)O(2). We proved that the anodic depletion could be excluded by adopting a divided electrolytic cell. Furthermore, we demonstrated that applying poly(tetrafluoroethylene) (PTFE) as an overcoating rather than a catalyst binder could effectively mitigate the cathodic decomposition pathways. Beyond that, we further developed a composite electrospun PTFE (E-PTFE)/carbon black (CB)/GDE electrode featuring the electrospun PTFE (E-PTFE) nanofibrous overcoating. The E-PTFE coating provides abundant triphase active sites and excludes the cathodic depletion reaction, enabling the production of >20 g/L H(2)O(2) at a current efficiency of 86.6%. Finally, we demonstrated the efficacy of the ORR-HP device in lake water remediation. Cyanobacteria and microcystin-LR were readily removed along with the onsite production of H(2)O(2). American Chemical Society 2021-12-14 2022-02-11 /pmc/articles/PMC8845047/ /pubmed/35178529 http://dx.doi.org/10.1021/acsestengg.1c00366 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Li, Huihui
Quispe-Cardenas, Estefanny
Yang, Shasha
Yin, Lifeng
Yang, Yang
Electrosynthesis of >20 g/L H(2)O(2) from Air
title Electrosynthesis of >20 g/L H(2)O(2) from Air
title_full Electrosynthesis of >20 g/L H(2)O(2) from Air
title_fullStr Electrosynthesis of >20 g/L H(2)O(2) from Air
title_full_unstemmed Electrosynthesis of >20 g/L H(2)O(2) from Air
title_short Electrosynthesis of >20 g/L H(2)O(2) from Air
title_sort electrosynthesis of >20 g/l h(2)o(2) from air
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845047/
https://www.ncbi.nlm.nih.gov/pubmed/35178529
http://dx.doi.org/10.1021/acsestengg.1c00366
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