Bioinspired Self-Assembly of Metalloporphyrins and Polyelectrolytes into Hierarchical Supramolecular Nanostructures for Enhanced Photocatalytic H2 Production in Water

IF 16.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2024-01-02 DOI:10.1002/anie.202315599
Qingxuan Tang, Dr. Yifei Han, Lingxuan Chen, Qiaoyan Qi, Dr. Junlai Yu, Dr. Shang-Bo Yu, Dr. Bo Yang, Dr. Hao-Yang Wang, Jiangshan Zhang, Dr. Song-Hai Xie, Dr. Feng Tian, Dr. Zhenhua Xie, Dr. Hanqiu Jiang, Dr. Yubin Ke, Prof. Dr. Guanyu Yang, Prof. Dr. Zhan-Ting Li, Prof. Dr. Jia Tian
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Abstract

Polypeptides, as natural polyelectrolytes, are assembled into tailored proteins to integrate chromophores and catalytic sites for photosynthesis. Mimicking nature to create the water-soluble nanoassemblies from synthetic polyelectrolytes and photocatalytic molecular species for artificial photosynthesis is still rare. Here, we report the enhancement of the full-spectrum solar-light-driven H2 production within a supramolecular system built by the co-assembly of anionic metalloporphyrins with cationic polyelectrolytes in water. This supramolecular photocatalytic system achieves a H2 production rate of 793 and 685 μmol h−1 g−1 over 24 h with a combination of Mg or Zn porphyrin as photosensitizers and Cu porphyrin as a catalyst, which is more than 23 times higher than that of free molecular controls. With a photosensitizer to catalyst ratio of 10000 : 1, the highest H2 production rate of >51,700 μmol h−1 g−1 with a turnover number (TON) of >1,290 per molecular catalyst was achieved over 24 h irradiation. The hierarchical self-assembly not only enhances photostability through forming ordered stackings of the metalloporphyrins but also facilitates both energy and electron transfer from antenna molecules to catalysts, and therefore promotes the photocatalysis. This study provides structural and mechanistic insights into the self-assembly enhanced photostability and catalytic performance of supramolecular photocatalytic systems.

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受生物启发将金属卟啉和聚电解质自组装成层次分明的超分子纳米结构,以增强水中光催化产氢能力
摘要:多肽作为天然的多电解质,被组装成定制的蛋白质,以整合光合作用的发色团和催化位点。模仿自然界,用合成的多电解质和光催化分子物种创造出水溶性纳米组合体来进行人工光合作用的方法还很罕见。在此,我们报告了阴离子金属卟啉与阳离子多电解质在水中共组装而形成的超分子体系,该体系增强了全光谱太阳光驱动的 H2 产率。这种超分子光催化系统以镁或锌卟啉为光敏剂,以铜卟啉为催化剂,在 24 小时内的 H2 产率分别达到 793 和 685 μmol h-1 g-1,是游离分子控制的 23 倍以上。光敏剂与催化剂的比例为 10000:1,在 24 小时的辐照过程中,每个分子催化剂的最高 H2 产率为 51,700 μmol h-1 g-1,周转次数(TON)为 1,290 次。分层自组装不仅通过形成金属卟啉的有序堆积来提高光稳定性,而且有利于能量和电子从天线分子转移到催化剂,从而促进光催化。这项研究从结构和机理上揭示了自组装如何增强超分子光催化系统的光稳定性和催化性能。
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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