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具有苯并噻二唑单元的用于光电化学制氢的推挽式有机染料和染料-催化剂组件。

Push-pull organic dyes and dye-catalyst assembly featuring a benzothiadiazole unit for photoelectrochemical hydrogen production.

作者信息

Moinel A, Brochnow M, Aumaître C, Giannoudis E, Fize J, Saint-Pierre C, Pécaut J, Maldivi P, Artero V, Demadrille R, Chavarot-Kerlidou M

机构信息

Univ. Grenoble Alpes, CNRS, CEA, IRIG, SyMMES 17 rue des martyrs 38000 Grenoble France

Univ. Grenoble Alpes, CNRS, CEA, IRIG, Laboratoire de Chimie et Biologie des Métaux 17 rue des Martyrs F-38000 Grenoble France

出版信息

Sustain Energy Fuels. 2022 Jun 29;6(15):3565-3572. doi: 10.1039/d2se00292b. eCollection 2022 Jul 29.

DOI:10.1039/d2se00292b
PMID:35979141
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9337615/
Abstract

In this work, we report the design and the preparation of two new dyes and a molecular dyad for the photoelectrochemical hydrogen production from water in a dye-sensitized photoelectrochemical cell (DSPEC). We designed dyes that include a benzothiadiazole (BTD) and an indacenodithiophene (IDT) units, and we obtained a new molecular dyad by covalent coupling with the cobalt diimine-dioxime catalyst. The introduction of the benzothiadiazole core in the structure improves the absorption properties and leads to an extension of the spectrum in the visible range up to 650 nm. The photoelectrochemical properties of the new dyad were evaluated on pristine and lithium-doped NiO electrodes. We demonstrate that increasing the light harvesting efficiency of the dyad by introducing a IDT-BTD chromophore is clearly beneficial for the photoelectrochemical activity. We also demonstrate that lithium doping of NiO, which improves the electronic conductivity of the mesoporous film, leads to a significant increase in performance, in terms of TON and F.E., more than doubled with our new dyad. This BTD-based molecular system outperforms the results of previously reported dyads using the same catalyst.

摘要

在本工作中,我们报道了两种新型染料和一种分子二元体的设计与制备,用于染料敏化光电化学电池(DSPEC)中从水中进行光电化学制氢。我们设计的染料包含苯并噻二唑(BTD)和茚并二噻吩(IDT)单元,并通过与钴二亚胺 - 二肟催化剂共价偶联获得了一种新的分子二元体。在结构中引入苯并噻二唑核心改善了吸收性能,并使可见光谱范围扩展至650 nm。在原始的和锂掺杂的NiO电极上评估了新二元体的光电化学性质。我们证明,通过引入IDT - BTD发色团提高二元体的光捕获效率对光电化学活性明显有益。我们还证明,NiO的锂掺杂提高了介孔膜的电子导电性,导致在TON和F.E.方面性能显著提高,使用我们的新二元体时性能提高了一倍多。这种基于BTD的分子体系优于先前报道的使用相同催化剂的二元体的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b3/9337615/af5fd44e3ff1/d2se00292b-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b3/9337615/64add7ab932d/d2se00292b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b3/9337615/18ed0bf65c0e/d2se00292b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b3/9337615/43a82ccd7643/d2se00292b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b3/9337615/af5fd44e3ff1/d2se00292b-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b3/9337615/64add7ab932d/d2se00292b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b3/9337615/18ed0bf65c0e/d2se00292b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b3/9337615/43a82ccd7643/d2se00292b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67b3/9337615/af5fd44e3ff1/d2se00292b-f4.jpg

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Influence of Surface and Structural Variations in Donor-Acceptor-Donor Sensitizers on Photoelectrocatalytic Water Splitting.给体-受体-给体敏化剂的表面和结构变化对光电催化水分解的影响
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Towards sustainable and efficient p-type metal oxide semiconductor materials in dye-sensitised photocathodes for solar energy conversion.迈向用于太阳能转换的染料敏化光阴极中可持续且高效的p型金属氧化物半导体材料。
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