Ceper Tolga, Costabel Daniel, Kowalczyk Daniel, Peneva Kalina, Schacher Felix H
Institute of Organic Chemistry and Macromolecular Chemistry, Friedrich Schiller University Jena, Humboldtstraße 10, D-07743 Jena, Germany.
Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, Philosophenweg 7, D-07743 Jena, Germany.
ACS Appl Mater Interfaces. 2024 May 15;16(19):24796-24805. doi: 10.1021/acsami.4c04045. Epub 2024 May 3.
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 evolution catalyst ([MoS]) are electrostatically incorporated. The resulting material exhibits sustained visible-light-driven H 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.
未来利用太阳能并将其转化为化学能的技术,在很大程度上依赖于直接的方法,即在特定环境中制备通用的软物质支架,用于固定催化剂和敏化剂。此外,特别是对于光驱动析氢,迫切需要向无贵金属的光敏剂和催化剂转变。在此,我们报道了一种基于聚两性电解质水凝胶的全有机光捕获软物质网络,其中光敏剂(苝单酰亚胺衍生物)和析氢催化剂([MoS])均通过静电作用掺入。所得材料在抗坏血酸水溶液中表现出持续的可见光驱动析氢,即使在光敏剂负载量较低(0.4%)和催化剂负载量较低(120 ppm)的情况下也是如此。此外,我们对混合水凝胶的长期稳定性提供了初步见解。我们相信,这些结果为在软物质网络中引入无贵金属光驱动催化的通用途径铺平了道路。