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在高离子强度下同时进行氧还原和水氧化以实现过氧化氢的可扩展电合成。

Concurrent oxygen reduction and water oxidation at high ionic strength for scalable electrosynthesis of hydrogen peroxide.

作者信息

Kim Changmin, Park Sung O, Kwak Sang Kyu, Xia Zhenhai, Kim Guntae, Dai Liming

机构信息

Australian Carbon Materials Centre (A-CMC), School of Chemical Engineering, University of New South Wales, Sydney, NSW, 2052, Australia.

Department of Energy Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, South Korea.

出版信息

Nat Commun. 2023 Sep 19;14(1):5822. doi: 10.1038/s41467-023-41397-1.

DOI:10.1038/s41467-023-41397-1
PMID:37726271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10509222/
Abstract

Electrosynthesis of hydrogen peroxide via selective two-electron transfer oxygen reduction or water oxidation reactions offers a cleaner, cost-effective alternative to anthraquinone processes. However, it remains a challenge to achieve high Faradaic efficiencies at elevated current densities. Herein, we report that oxygen-deficient PrSrFeZnO perovskite oxides rich of oxygen vacancies can favorably bind the reaction intermediates to facilitate selective and efficient two-electron transfer pathways. These oxides exhibited superior Faradic efficiencies (99%) for oxygen reduction over a wide potential range (0.05 to 0.45 V versus reversible hydrogen electrode) and current densities surpassing 50 mA cm under high ionic strengths. We further found that the oxides perform a high selectivity (80%) for two-electron transfer water oxidation reaction at a low overpotential (0.39 V). Lastly, we devised a membrane-free electrolyser employing bifunctional electrocatalysts, achieving a record-high Faradaic efficiency of 163.0% at 2.10 V and 50 mA cm. This marks the first report of the concurrent oxygen reduction and water oxidation catalysed by efficient bifunctional oxides in a novel membrane-free electrolyser for scalable hydrogen peroxide electrosynthesis.

摘要

通过选择性双电子转移氧还原或水氧化反应电合成过氧化氢,为蒽醌法提供了一种更清洁、更具成本效益的替代方法。然而,在提高电流密度的情况下实现高法拉第效率仍然是一个挑战。在此,我们报告富含氧空位的缺氧PrSrFeZnO钙钛矿氧化物能够有利地结合反应中间体,以促进选择性和高效的双电子转移途径。这些氧化物在较宽的电位范围(相对于可逆氢电极0.05至0.45 V)内表现出优异的氧还原法拉第效率(约99%),并且在高离子强度下电流密度超过50 mA cm。我们进一步发现,这些氧化物在低过电位(0.39 V)下对双电子转移水氧化反应具有高选择性(约80%)。最后,我们设计了一种采用双功能电催化剂的无膜电解槽,在2.10 V和50 mA cm下实现了创纪录的163.0%的高法拉第效率。这标志着在一种用于可扩展过氧化氢电合成的新型无膜电解槽中,首次报道了由高效双功能氧化物同时催化氧还原和水氧化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/325292a6d0e0/41467_2023_41397_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/d3da64aa609b/41467_2023_41397_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/b948a29154ec/41467_2023_41397_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/7334e9b3eddf/41467_2023_41397_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/4f64d5850307/41467_2023_41397_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/33df6b0a6f65/41467_2023_41397_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/325292a6d0e0/41467_2023_41397_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/d3da64aa609b/41467_2023_41397_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/b948a29154ec/41467_2023_41397_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/7334e9b3eddf/41467_2023_41397_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/4f64d5850307/41467_2023_41397_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/33df6b0a6f65/41467_2023_41397_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3821/10509222/325292a6d0e0/41467_2023_41397_Fig6_HTML.jpg

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