Triplet-triplet Annihilation Dynamics of Naphthalene

被引:10
|
作者
Gudem, Mahesh [1 ]
Kowalewski, Markus [1 ]
机构
[1] Stockholm Univ, Albanova Univ Ctr, Dept Phys, SE-10691 Stockholm, Sweden
基金
欧洲研究理事会; 瑞典研究理事会;
关键词
ab initio calculations; conical intersections; polaritonic chemistry; quantum chemistry; quantum dynamics; PHOTON-UP-CONVERSION; PHOTODISSOCIATIVE RUTHENIUM COMPLEX; SILICON SOLAR-CELLS; LIGHT-MATTER STATES; SPACE SCF METHOD; CONICAL INTERSECTIONS; AROMATIC-HYDROCARBONS; DELAYED FLUORESCENCE; SINGLET; NANOCAPSULES;
D O I
10.1002/chem.202200781
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Triplet-triplet annihilation (TTA) is a spin-allowed conversion of two triplet states into one singlet excited state, which provides an efficient route to generate a photon of higher frequency than the incident light. Multiple energy transfer steps between absorbing (sensitizer) and emitting (annihilator) molecular species are involved in the TTA based photon upconversion process. TTA compounds have recently been studied for solar energy applications, even though the maximum upconversion efficiency of 50 % is yet to be achieved. With the aid of quantum calculations and based on a few key requirements, several design principles have been established to develop the well-functioning annihilators. However, a complete molecular level understanding of triplet fusion dynamics is still missing. In this work, we have employed multi-reference electronic structure methods along with quantum dynamics to obtain a detailed and fundamental understanding of TTA mechanism in naphthalene. Our results suggest that the TTA process in naphthalene is mediated by conical intersections. In addition, we have explored the triplet fusion dynamics under the influence of strong light-matter coupling and found an increase of the TTA based upconversion efficiency.
引用
收藏
页数:11
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