Abstract
Complex multiple-component semiconductor photocatalysts can be constructed that display enhanced catalytic efficiency via multiple chargeand energy transfer, mimicking photosystems in nature. In contrast, the efficiency of single-component semiconductor photocatalysts is usually limited due to the fast recombination of the photogenerated excitons. Here, we report the design of an asymmetric covalent triazine framework as an efficient organic single-component semi-conductor photocatalyst. Four different molecular donor–acceptor domains are obtained within the network, leading to enhanced photogenerated chargeseparation via an intramo-lecular energy transfer cascade. The photocatalytic efficiency of the asymmetric covalent triazine framework is superior to that of its symmetric counterparts; this was demonstrated by the visible-light-driven formation of benzophosphole oxides from diphenylphosphine oxide and diphenylacetylene.
Original language | English |
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Pages (from-to) | 8316-8320 |
Journal | Angewandte Chemie - International Edition |
Volume | 57 |
Issue number | 27 |
DOIs | |
Publication status | Accepted/In press - 26 Apr 2018 |
Externally published | Yes |
Funding
We thank the Max Planck Society for financial support. J.B. thanks the Alexander von Humboldt Foundation for a postdoctoral research fellowship. W.H. thanks the China Scholarship Council (CSC) for a fellowship.
Funders | Funder number |
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Alexander von Humboldt-Stiftung | 1188461 |
Max-Planck-Gesellschaft | |
China Scholarship Council | 201406240010 |