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Coherence in electronically excited dimers. III. The observation of coherence in dimers using optically detected electron spin resonance in zero field and its relationship to coherence in one-dimensional excitons

机译:电子激发二聚体的相干性。三,利用光学检测的电子自旋共振在零场中观察二聚体的相干及其与一维激子相干的关系

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摘要

The observation of coherent dimers in their excited triplet state is reported for a molecular crystal of 1,2,4,5-tetrachlorobenzene at low temperatures (below 4.2 K). Utilizing the theory developed in our previous paper, the coherence time (10^-6 sec) and the anisotropy of the resonance interactions in the excited state were established. The identification of the dimer as translationally equivalent, from the zero-field optically detected magnetic-resonance spectra, establishes the effective dispersion for the triplet exciton band of the neat crystal. Morover, the magnitude of the resonance transfer time was shown to be much less than the coherence time: the dimer is coherent for a period of 10^5 times that associated with the stochastic limit.
机译:据报道,在低温(4.2 K以下)观察到1,2,4,5-四氯苯分子晶体时,在激发三重态下观察到相干二聚体。利用我们以前的论文发展的理论,建立了激发态的相干时间(10 ^ -6 sec)和共振相互作用的各向异性。从零场光学检测到的磁共振光谱中将二聚体确定为平移等效物,可以建立纯晶体三重态激子带的有效色散。此外,共振转移时间的幅度远小于相干时间:二聚体的相干时间是随机极限的10 ^ 5倍。

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    Zewail A. H.; Harris C. B.;

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  • 年度 1975
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