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通过层层沉积构建具有催化和导电性能的双极膜界面,用于设计膜集成人工光合作用系统。

Catalytic, Conductive Bipolar Membrane Interfaces through Layer-by-Layer Deposition for the Design of Membrane-Integrated Artificial Photosynthesis Systems.

机构信息

Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, MA, 02139, USA.

Department of Chemistry, Florida Institute of Technology, 150 W. University Blvd., Melbourne, FL, 32901, USA.

出版信息

ChemSusChem. 2017 Nov 23;10(22):4599-4609. doi: 10.1002/cssc.201701397. Epub 2017 Nov 7.

DOI:10.1002/cssc.201701397
PMID:29024529
Abstract

In the presence of an electric field, bipolar membranes (BPMs) are capable of initiating water disassociation (WD) within the interfacial region, which can make water splitting for renewable energy in the presence of a pH gradient possible. In addition to WD catalytic efficiency, there is also the need for electronic conductivity in this region for membrane-integrated artificial photosynthesis (AP) systems. Graphene oxide (GO) was shown to catalyze WD and to be controllably reduced, which resulted in electronic conductivity. Layer-by-layer (LbL) film deposition was employed to improve GO film uniformity in the interfacial region to enhance WD catalysis and, through the addition of a conducting polymer in the process, add electronic conductivity in a hybrid film. Three different deposition methods were tested to optimize conducting polymer synthesis with the oxidant in a metastable solution and to yield the best film properties. It was found that an approach that included substrate dipping in a solution containing the expected final monomer/oxidant ratio provided the most predictable film growth and smoothest films (by UV/Vis spectroscopy and atomic force microscopy/scanning electron microscopy, respectively), whereas dipping in excess oxidant or co-spraying the oxidant and monomer produced heterogeneous films. Optimized films were found to be electronically conductive and produced a membrane ohmic drop that was acceptable for AP applications. Films were integrated into the interfacial region of BPMs and revealed superior WD efficiency (≥1.4 V at 10 mA cm ) for thinner films (<10 bilayers≈100 nm) than for either the pure GO catalyst or conducting polymer individually, which indicated that there was a synergistic effect between these materials in the structure configured by the LbL method.

摘要

在电场存在的情况下,双极膜 (BPM) 能够在界面区域引发水离解 (WD),这使得在 pH 梯度存在的情况下有可能进行可再生能源的水分解。除了 WD 催化效率外,对于膜集成人工光合作用 (AP) 系统,该区域还需要电子导电性。已经证明氧化石墨烯 (GO) 可以催化 WD 并被可控还原,从而产生电子导电性。层层 (LbL) 薄膜沉积被用于改善界面区域中 GO 薄膜的均匀性,以增强 WD 催化作用,并通过在该过程中添加导电聚合物来在混合薄膜中添加电子导电性。测试了三种不同的沉积方法,以优化在亚稳溶液中氧化剂与导电聚合物的合成,并获得最佳的薄膜性能。结果发现,包括将基底浸入含有预期最终单体/氧化剂比的溶液中的方法提供了最可预测的薄膜生长和最光滑的薄膜(分别通过紫外/可见光谱和原子力显微镜/扫描电子显微镜),而在过量氧化剂中浸渍或共喷射氧化剂和单体则会产生不均匀的薄膜。优化后的薄膜具有导电性,并产生可接受的 AP 应用的膜欧姆降。将薄膜集成到 BPM 的界面区域中,发现对于较薄的薄膜(<10 层≈100nm),其 WD 效率(在 10mA/cm 时≥1.4V)优于纯 GO 催化剂或导电聚合物单独使用时的效率,这表明在 LbL 方法构建的结构中,这些材料之间存在协同效应。

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