Zhang Ju-An, Xiao Xuedong, Wang Jinyi, Luo Shuai, Lu Yi, Pang Yan-Yu, Tian Wei
Shaanxi Key Laboratory of Macromolecular Science and Technology, Xi'an Key Laboratory of Hybrid Luminescent Materials and Photonic Device, MOE Key Laboratory of Material Physics and Chemistry under Extraordinary Conditions, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an 710072, China.
Department of Chemistry, Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, China.
J Am Chem Soc. 2025 Apr 23;147(16):13447-13460. doi: 10.1021/jacs.5c00204. Epub 2025 Apr 8.
Two-dimensional supramolecular assemblies (2DSAs) with well-defined nanostructures have emerged as promising candidates for diverse applications, particularly in photocatalysis. However, it still remains a significant challenge to simultaneously achieve effective electron transport and multiple active sites in 2DSA, even though this is crucial for enhancing photocatalytic performance. This reason can be attributed to the lack of a suitable structural paradigm that enables both effective intermolecular orbital overlap and increased substrate contact. Inspired by the parallel venation of monocotyledons that can facilitate substrate transfer, we overcome the limitation, in this study, by integrating parallel-arranged one-dimensional (1D) conduits with edge-on packing motifs to construct biomimetic, parallel vein-like two-dimensional supramolecular layers (PV-2DSLs) through the hierarchical self-assembly of cationically modified, rigid multiarmed monomers. The resulting PV-2DSLs exhibit a long-range aromatic cation-π stacking that can facilitate electron transport. Importantly, the unique structural feature of these PV-2DSLs is the orderly and parallel embedding of 1D conduits within the 2D plane, which is significantly different from the conventional channels formed by the vertical stacking of 2D porous materials. These conduits promote multielectron transfer pathways, leading to enhanced charge separation and carrier transport when coupled with long-range aromatic cation-π stacking. As a consequence, these PV-2DSLs exhibit long excited state lifetime, leading to significantly improved hydrogen production rates up to 3.5 mmol g h, which is approximately 17.5 times higher than that of the counterpart without 1D conduits (0.2 mmol g h).
具有明确纳米结构的二维超分子组装体(2DSA)已成为多种应用的有前途的候选者,特别是在光催化领域。然而,在2DSA中同时实现有效的电子传输和多个活性位点仍然是一个重大挑战,尽管这对于提高光催化性能至关重要。其原因可归因于缺乏一种合适的结构范式,该范式既能实现有效的分子间轨道重叠,又能增加底物接触。受单子叶植物平行叶脉可促进底物转移的启发,在本研究中,我们通过将平行排列的一维(1D)管道与边缘堆积 motif 相结合,克服了这一限制,通过阳离子修饰的刚性多臂单体的分级自组装构建了仿生的、平行叶脉状的二维超分子层(PV-2DSL)。所得的PV-2DSL表现出长程芳香阳离子-π堆积,可促进电子传输。重要的是,这些PV-2DSL的独特结构特征是一维管道在二维平面内有序且平行地嵌入,这与二维多孔材料垂直堆叠形成的传统通道有显著不同。这些管道促进了多电子转移途径,当与长程芳香阳离子-π堆积结合时,导致电荷分离和载流子传输增强。因此,这些PV-2DSL表现出长的激发态寿命,导致产氢速率显著提高,高达3.5 mmol g h,约为没有一维管道的对应物(0.2 mmol g h)的17.5倍。