Affiliation:
1. Department of Electrical and Electronic Engineering Graduate School of Engineering Kobe University Rokkodai Kobe 657–8501 Japan
2. JST‐PRESTO Honcho 4‐1‐8 Saitama 332‐0012 Japan
3. Graduate School of Natural Science and Technology Kanazawa University Kanazawa 920–1192 Japan
Abstract
AbstractPhotochemical 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.
Funder
Japan Science and Technology Corporation
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry