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    題名: Design of Panchromatic Metalloporphyrin Sensitizers owning Multiple Types of Transitions including D--A and Singlet and Spin-Orbit Coupling Activated Triplet Metal-to-Anchor Charge Transfers for Dye-sensitized Solar Cells
    作者: 林慧絜;Lin, Hui-Jie
    貢獻者: 化學學系
    關鍵詞: DSSC;porphyrin;Spin-Orbit Coupling;Metalloporphyrin
    日期: 2020-07-28
    上傳時間: 2020-09-02 15:11:25 (UTC+8)
    出版者: 國立中央大學
    摘要: 我們使用密度泛函理論(TD-DFT)與spin–orbit coupling effect(SOC effect)來模擬計算把YD2-o-C8作為骨架的porphyrin染料中心金屬Zn換成Ru和Os,使用Cl-或PPh(OMe)2連接中心金屬,成為六配位的porphyrins,研究染料的電子結構和吸收光譜。具有兩個Cl-配位的Ru-和Os-porphyrins在near IR / IR區域邊緣顯示出較弱的吸收,這在原始的YD2-o-C8染料中沒有觀察到的。在長波長邊緣有吸收是源自金屬到受體的電荷轉移(MACT),並進一步由具有重的Ru和Os原子的SOC effect造成紅位移的現象。另一方面,使用PPh(OMe)2 作為ligands的染料在near IR區域不產生吸收,結果可得PPh(OMe)2 ligand能穩定修飾Ru-和Os-porphyrins的“ t2g”軌道。另外也觀察到PPh(OMe)2連接的porphyrins有SOC effect。這項研究表明,將Ru和Os重原子引入以Cl-作為ligands的porphyrins可以誘導在長波長吸收的金屬到受體的電荷轉移,並進一步增強SOC effect,使吸收紅位移。研究結果為設計長波長躍遷提供了一種新方法,同時又保留了原有的染料骨架。;We investigate the electronic structures and absorption spectra for Ru- and
    Os-porphyrins ligated with Cl− or PPh(OMe)2 using an Zn-based YD2-o-C8 skeleton
    as well as YD2-o-C8 and YD2 dyes by time-dependent density functional theory
    (TD-DFT) with spin–orbit coupling (SOC) interactions. The Ru- and Os-porphyrins
    modified with two Cl− as ligands exhibit a weak absorption onset in the near IR/IR
    region, which is not observed in that of original YD2-o-C8 dye. The long wavelength
    absorption edge originates from the metal to acceptor charge transfer MACT and is
    further red-shifted from SOC with heavy Ru and Os atoms. On the other hand, the
    PPh(OMe)2 ligands stabilizing the “t2g” orbitals of the modified Ru- and
    Os-porphyrins do not induce absorption in the near IR region. However, SOC is also
    observed for PPh(OMe)2 ligated Ru- and Os-porphyrins. This study shows that the
    introduction of heavy Ru and Os atoms into porphyrin skeleton with Cl- as ligands can
    induce long wavelength metal-to-acceptor charge transfer and further enhance the
    SOC, red-shifting the absorption. This result offers a new approach for designing long
    wavelength transitions, while remaining the original dye framework.
    顯示於類別:[化學研究所] 博碩士論文

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