Noble Metal-Free Light-Driven Hydrogen Evolution Catalysis in Polyampholytic Hydrogel Networks

被引:1
|
作者
Ceper, Tolga [1 ,2 ,3 ]
Costabel, Daniel [1 ,2 ,3 ]
Kowalczyk, Daniel [4 ]
Peneva, Kalina [1 ,2 ,3 ]
Schacher, Felix H. [1 ,2 ,3 ]
机构
[1] Friedrich Schiller Univ Jena, Inst Organ Chem & Macromol Chem, D-07743 Jena, Germany
[2] Friedrich Schiller Univ Jena, Jena Ctr Soft Matter JCSM, D-07743 Jena, Germany
[3] Friedrich Schiller Univ Jena, Ctr Energy & Environm Chem Jena CEEC, D-07743 Jena, Germany
[4] Ulm Univ, Inst Chem Engn, D-89081 Ulm, Germany
关键词
hydrogen evolution catalysis; noble metal-free; polyampholyte; hydrogel; scaffold; immobilization; PHOTOCATALYTIC H-2 EVOLUTION; ARTIFICIAL PHOTOSYNTHESIS; WATER; FUEL;
D O I
10.1021/acsami.4c04045
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Future technologies to harness solar energy and to convert this into chemical energy strongly rely on straightforward approaches to prepare versatile soft matter scaffolds for the immobilization of catalysts and sensitizers in a defined environment. In addition, particularly for light-driven hydrogen evolution, a transition to noble metal-free photosensitizers and catalysts is urgently required. Herein, we report a fully organic light-harvesting soft matter network based on a polyampholyte hydrogel where both photosensitizer (a perylene monoimide derivative) and a H-2 evolution catalyst ([Mo3S13](2-)) are electrostatically incorporated. The resulting material exhibits sustained visible-light-driven H-2 evolution in aqueous ascorbic acid solution, even at rather low loadings of photosensitizer (0.4%) and catalyst (120 ppm). In addition, we provide initial insights into the long-term stability of the hybrid hydrogel. We believe that these results pave the way for a generalized route toward the incorporation of noble metal-free light-driven catalysis in soft matter networks.
引用
收藏
页码:24796 / 24805
页数:10
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