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Photoinduced Hydration Boosts O2 Evolution on Co-Chelating Covalent Organic Framework
The achievement of artificial photosynthesis relies on successful water oxidation and a detailed mechanistic understanding. Here, we demonstrate a photoinduced hydration pathway for O2 evolution from water oxidation over an imine-linked covalent organic framework (COF) comprising electron-rich benzo...
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Published in: | ACS energy letters 2023-04, Vol.8 (4), p.1857-1863 |
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creator | He, Yajun Liu, Guoyu Liu, Zheyuan Bi, Jinhong Yu, Yan Li, Liuyi |
description | The achievement of artificial photosynthesis relies on successful water oxidation and a detailed mechanistic understanding. Here, we demonstrate a photoinduced hydration pathway for O2 evolution from water oxidation over an imine-linked covalent organic framework (COF) comprising electron-rich benzotrithiophene and electron-deficient benzothiadiazole units with atomically chelated Co sites. The experimental and theoretical results suggest that the water oxidation starts with the photoinduced hydration of imine groups. The subsequent oxidative deprotonation and intramolecular hydroxyl attack lead to O–O bond formation. The hydration path significantly averages the energy barriers of water oxidation, thus promoting O2 evolution. Inspired by this fact, we fabricate a COF-based heterostructure, which realizes overall water splitting with H2 and O2 evolution rates of 450 and 212 μmol·g–1 h–1, respectively. |
doi_str_mv | 10.1021/acsenergylett.3c00228 |
format | article |
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Here, we demonstrate a photoinduced hydration pathway for O2 evolution from water oxidation over an imine-linked covalent organic framework (COF) comprising electron-rich benzotrithiophene and electron-deficient benzothiadiazole units with atomically chelated Co sites. The experimental and theoretical results suggest that the water oxidation starts with the photoinduced hydration of imine groups. The subsequent oxidative deprotonation and intramolecular hydroxyl attack lead to O–O bond formation. The hydration path significantly averages the energy barriers of water oxidation, thus promoting O2 evolution. Inspired by this fact, we fabricate a COF-based heterostructure, which realizes overall water splitting with H2 and O2 evolution rates of 450 and 212 μmol·g–1 h–1, respectively.</description><identifier>ISSN: 2380-8195</identifier><identifier>EISSN: 2380-8195</identifier><identifier>DOI: 10.1021/acsenergylett.3c00228</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>ACS energy letters, 2023-04, Vol.8 (4), p.1857-1863</ispartof><rights>2023 American Chemical Society</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-6748-2620 ; 0000-0002-3066-2991 ; 0000-0002-8141-7742</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>He, Yajun</creatorcontrib><creatorcontrib>Liu, Guoyu</creatorcontrib><creatorcontrib>Liu, Zheyuan</creatorcontrib><creatorcontrib>Bi, Jinhong</creatorcontrib><creatorcontrib>Yu, Yan</creatorcontrib><creatorcontrib>Li, Liuyi</creatorcontrib><title>Photoinduced Hydration Boosts O2 Evolution on Co-Chelating Covalent Organic Framework</title><title>ACS energy letters</title><addtitle>ACS Energy Lett</addtitle><description>The achievement of artificial photosynthesis relies on successful water oxidation and a detailed mechanistic understanding. 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title | Photoinduced Hydration Boosts O2 Evolution on Co-Chelating Covalent Organic Framework |
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