Endothermic and Exothermic Energy Transfer Made Equally Efficient for Triplet-Triplet Annihilation Upconversion

被引:38
作者
Isokuortti, Jussi [1 ]
Allu, Srinivasa Rao [2 ,3 ]
Efimov, Alexander [1 ]
Vuorimaa-Laukkanen, Elina [1 ]
Tkachenko, Nikolai V. [1 ]
Vinogradov, Sergei A. [2 ,3 ]
Laaksonen, Timo [1 ,4 ]
Durandin, Nikita A. [1 ]
机构
[1] Tampere Univ, Fac Engn & Nat Sci, Korkeakoulunkatu 8, Tampere 33720, Finland
[2] Univ Penn, Perelman Sch Med, Dept Biochem & Biophys, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Arts & Sci, Dept Chem, Philadelphia, PA 19104 USA
[4] Univ Helsinki, Fac Pharm, Div Pharmaceut Biosci, Viikinkaari 5 E, FIN-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
PHOTODISSOCIATIVE RUTHENIUM COMPLEX; DELAYED FLUORESCENCE; LOW-POWER; LIGHT; RED; NANOCAPSULES; PORPHYRINS; ANTHRACENE; SINGLET; METALLOPORPHYRINS;
D O I
10.1021/acs.jpclett.9b03466
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
Expanding the anti-Stokes shift for triplet-triplet annihilation upconversion (TTA-UC) systems with high quantum yields without compromising power density thresholds (I-th) remains a critical challenge in photonics. Our studies reveal that such expansion is possible by using a highly endothermic TTA-UC pair with an enthalpy difference of +80 meV even in a polymer matrix 1000 times more viscous than toluene. Carrying out efficient endothermic triplet-triplet energy transfer (TET) requires suppression of the reverse annihilator-to-sensitizer TET, which was achieved by using sensitizers with high molar extinction coefficients and long triplet state lifetimes as well as optimized annihilator concentrations. Under these conditions, the sensitizer-to-annihilator forward TET becomes effectively entropy driven, yielding upconversion quantum yields comparable to those achieved with the exothermic TTA-UC pair but with larger anti-Stokes shifts and even lower I-th, a previously unattained achievement.
引用
收藏
页码:318 / 324
页数:13
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