光化学
发色团
激发态
光敏剂
微秒
材料科学
吸收(声学)
可见光谱
超快激光光谱学
光电子学
化学
光学
光谱学
原子物理学
量子力学
复合材料
物理
作者
Qing Li,Leigh Anna Hunt,Kalpani Hirunika Wijesinghe,Christine Curiac,Ashley E. Williams,Amala Dass,Nathan I. Hammer,Jared H. Delcamp
标识
DOI:10.1002/aenm.202203102
摘要
Abstract Strong photoinduced oxidants are important to organic synthesis and solar energy conversion, to chemical fuels or electric. For these applications, visible light absorption is important to solar energy conversion and long‐lived excited states are needed to drive catalysis. With respect to these desirable qualities, a series of five 5,6‐dicyano[2,1,3]benzothiadiazole (DCBT) dyes are examined as organic chromophores that can serve as strong photooxidants in catalytic systems. The series utilizes a DCBT core with aryl groups on the periphery with varying electron donation strengths relative to the core. The dyes are studied via both steady‐state and transient absorption and emission studies. Additionally, computational analysis, voltammetry, crystallography, and absorption spectroelectrochemistry are also used to better understand the behavior of these dyes. Ultimately, a strong photooxidant is arrived at with an exceptionally long excited state lifetime for an organic chromophore of 16 µs. The long‐lived excited state photosensitizer is well‐suited for use in catalysis, and visible light driven photosensitized water oxidation is demonstrated using a water‐soluble photosensitizer.
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