激发态
偶极子
光敏剂
材料科学
单重态
共振(粒子物理)
磁偶极子跃迁
系统间交叉
分子物理学
单线态氧
原子物理学
光化学
光电子学
磁偶极子
化学
电偶极子跃迁
物理
氧气
有机化学
作者
Hiroaki Hasebe,Hiroshi Sugimoto,Yoshino Katsurayama,Taniyuki Furuyama,Minoru Fujii
出处
期刊:Small
[Wiley]
日期:2023-06-22
卷期号:19 (42)
标识
DOI:10.1002/smll.202302519
摘要
Photochemical reaction exploiting an excited triplet state (T1 ) of a molecule requires two steps for the excitation, i.e., electronic transition from the ground (S0 ) to singlet excited (S1 ) states and intersystem crossing to the T1 state. A dielectric metasurface coupled with photosensitizer that enables energy efficient photochemical reaction via the enhanced S0 →T1 magnetic dipole transition is developed. In the direct S0 →T1 transition, the photon energy of several hundreds of meV is saved compared to the conventional S0 → S1 →T1 transition. To maximize the magnetic field intensity on the surface, a silicon (Si) nanodisk array metasurface with toroidal dipole resonances is designed. The surface of the metasurface is functionalized with ruthenium (Ru(II)) complexes that work as a photosensitizer for singlet oxygen generation. In the coupled system, the rate of the direct S0 →T1 transition of Ru(II) complexes is 41-fold enhanced at the toroidal dipole resonance of a Si nanodisk array. The enhancement of a singlet oxygen generation rate is observed when the toroidal dipole resonance of a Si nanodisk array is matched with the direct S0 →T1 transition wavelength of Ru(II) complexes.
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