Wang Weikang, Liu Rong, Zhang Jianjun, Kong Tingting, Wang Lele, Yu Xiaohui, Ji Xiaomin, Liu Qinqin, Long Ran, Lu Zhou, Xiong Yujie
Anhui Engineering Research Center of Carbon Neutrality, The Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials, Anhui Normal University, Wuhu, Anhui, 241002, P. R. China.
School of Materials Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu, 212013, P. R. China.
Angew Chem Int Ed Engl. 2025 Jan 15;64(3):e202415800. doi: 10.1002/anie.202415800. Epub 2024 Nov 7.
Two-dimensional (2D) polymeric semiconductors are a class of promising photocatalysts; however, it remains challenging to facilitate their interlayer charge transfer for suppressed in-plane charge recombination and thus improved quantum efficiency. Although some strategies, such as π-π stacking and van der Waals interaction, have been developed so far, directed interlayer charge transfer still cannot be achieved. Herein, we report a strategy of forming asymmetric Zn-N units that can bridge nitrogen (N)-doped carbon layers with polymeric carbon nitride nanosheets (CN-Zn-N(C)) to address this challenge. The symmetry-breaking Zn-N moiety, which has an asymmetric local charge distribution, enables directed interfacial charge transfer between the CN photocatalyst and the N-doped carbon co-catalyst. As evidenced by femtosecond transient absorption spectroscopy, charge separation can be significantly enhanced by the interfacial asymmetric Zn-N bonding bridges. As a result, the designed CN-Zn-N(C) catalyst exhibits dramatically enhanced HO photosynthesis activity, outperforming most of the reported CN-based catalysts. This work highlights the importance of tailoring interfacial chemical bonding channels in polymeric photocatalysts at the molecular level to achieve effective spatial charge separation.
二维(2D)聚合物半导体是一类很有前景的光催化剂;然而,促进其层间电荷转移以抑制面内电荷复合从而提高量子效率仍然具有挑战性。尽管到目前为止已经开发了一些策略,如π-π堆积和范德华相互作用,但定向层间电荷转移仍然无法实现。在此,我们报告了一种形成不对称Zn-N单元的策略,该单元可以将氮(N)掺杂的碳层与聚合物氮化碳纳米片(CN-Zn-N(C))桥接起来,以应对这一挑战。具有不对称局部电荷分布的对称性破缺Zn-N部分能够实现CN光催化剂与N掺杂碳助催化剂之间的定向界面电荷转移。飞秒瞬态吸收光谱表明,界面不对称Zn-N键桥可以显著增强电荷分离。结果,所设计的CN-Zn-N(C)催化剂表现出显著增强的光合成活性,优于大多数已报道的基于CN的催化剂。这项工作突出了在分子水平上定制聚合物光催化剂中的界面化学键通道以实现有效空间电荷分离的重要性。