Singlet Oxygen Mediated Photochemical Upconversion of NIR Light

被引:53
作者
Fueckel, Burkhard [1 ]
Roberts, Derrick A. [1 ]
Cheng, Yuen Yap [1 ]
Clady, Raphael G. C. R. [1 ]
Piper, Roland B. [2 ,3 ]
Ekins-Daukes, N. J. [2 ,3 ]
Crossley, Maxwell J. [1 ]
Schmidt, Timothy W. [1 ]
机构
[1] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[2] Univ London Imperial Coll Sci Technol & Med, Dept Phys, London SW7 2AZ, England
[3] Univ London Imperial Coll Sci Technol & Med, Grantham Inst Climate Change, London SW7 2AZ, England
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2011年 / 2卷 / 09期
基金
澳大利亚研究理事会;
关键词
SENSITIZED DELAYED FLUORESCENCE; TRIPLET-TRIPLET ANNIHILATION; INDOCYANINE GREEN; CYANINE DYES; EXCITATION; CHEMILUMINESCENCE; LUMINESCENCE; TRANSITIONS; MOLECULES; THERAPY;
D O I
10.1021/jz200270w
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report photochemical upconversion (UC) of near-infrared (NIR) light to the visible spectrum mediated by molecular oxygen. Thereby, we address two of the main challenges in the field of photochemical UC, UC of photons above 800 nm and (ii) utilization of molecular oxygen, which is necessarily excluded in conventional photochemical UC systems. In the employed system, singlet oxygen is generated upon photoexcitation of the sensitizer molecules and then acts as an energy transmitter for the UC process. The excitation energy of two singlet oxygen molecules is subsequently harvested by emitter molecules, which in turn gives rise to delayed fluorescence of the emitter species. We discuss strategies for improvement of the currently achieved efficiencies of <= 0.01% to produce excited singlet states in the emitter molecules.
引用
收藏
页码:966 / 971
页数:6
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