期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 23, 页码 12891-12896出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202101090
关键词
black phosphorous; energy transfer; excitonic effects; infrared-light-driven photocatalysis; polymeric carbon nitride
资金
- National Key R&D Program of China [2017YFA0207301, 2017YFA0303500]
- Strategic Priority Research Program of Chinese Academy of Sciences [XDB36000000]
- National Natural Science Foundation of China [21922509, 21905262, 21890754, U2032212, U2032160]
- Youth Innovation Promotion Association of CAS [2017493]
- University Synergy Innovation Program of Anhui Province [GXXT-2020-005]
- Key Research Program of Frontier Sciences [QYZDY-SSW-SLH011]
This study proposes an exciton-mediated energy transfer strategy in heterostructures to achieve efficient infrared light response in semiconductors. By utilizing a black phosphorous/polymeric carbon nitride (BP/CN) heterojunction, improved conversion rate and selectivity in amine-amine oxidative coupling reaction under infrared light irradiation were observed. This research opens up a new approach for designing efficient photocatalysts activated by infrared light.
Although a few semiconductors can directly absorb infrared light, their intrinsic properties like improper band-edge position and strong electron-hole interaction restrict further photocatalytic applications. Herein, we propose an exciton-mediated energy transfer strategy for realizing efficient infrared light response in heterostructures. Using black phosphorous/polymeric carbon nitride (BP/CN) heterojunction, CN could be indirectly excited by infrared light with the aid of nonradiatively exciton-based energy transfer from BP. At the same time, excitons are dissociated into free charge carriers at the interface of BP/CN heterojunction, followed by hole injection to BP and electron retainment in CN. As a result of these unique photoexcitation processes, BP/CN heterojunction exhibits promoted conversion rate and selectivity in amine-amine oxidative coupling reaction even under infrared light irradiation. This study opens a new way for the design of efficient infrared light activating photocatalysts.
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