In this paper, the photodynamics of three chromenes (2,2-spiro-adamantyl-7,8-benzo(2H)chromene, 2,2-diphenyl(2H)chromene and 2,2-diphenyl-5,6-benzo(2H)chromene) has been investigated by nano- and femtosecond time resolved techniques in hydrocarbon solutions at room temperature. Using pump-probe techniques, ultrafast steps of molecular dynamics characterizing the photoresponse of chromenes have been investigated: the breakage of the C-O bond was found to occur within a few hundred femtoseconds producing a short-lived transient that converts to the cisoid-cis open form in less than one picosecond and then to the metastable transoid-cis structure within a few picoseconds. The effect of different excitation wavelengths on the formation rate of the first shortest-lived transient of 5,6DPBC is in agreement with the model previously proposed to explain the wavelength dependence of the reaction and emission quantum yields in photostationary experiments. The results obtained in the nanosecond time domain show that the triplet marginally participates in the photoreaction for only one of the studied compounds (2,2-spiro-adamantyl-7,8-benzo(2H)chromene).
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http://dx.doi.org/10.1039/b407541b | DOI Listing |
Nanoscale
January 2025
Department of Chemistry, Maulana Azad National Institute of Technology, Bhopal-462003, India.
Mixing different metal ions at the B site of ABX perovskites offers a promising approach for addressing challenges related to toxicity, stability and performance in optoelectronic applications. One such example is CsPbSnBr which addresses the toxicity issue posed by lead while allowing us to tune optoelectronic properties such as the band gap. In this work, nearly monodisperse CsPbSnBr quantum dots (QDs) were synthesized with variable Pb/Sn compositions, CsPbBr, CsPbSnBr and CsPbSnBr.
View Article and Find Full Text PDFWe investigate the ultrafast electron correlation effects during non-sequential double ionization (NSDI) of argon subjected to a combined femtosecond field composed of counter-rotating two-color circularly polarized (TCCP) pulse laser using a 3D classical ensemble model (CEM). Our simulation results reveal that manipulation of the carrier-envelope phase (CEP) of the external driving field modulates the dynamical behavior of the two electrons, resulting in a notable sensitivity of their momentum distribution to the relative phase of two components of the counter-rotating TCCP field. Through inversion analysis, we uncover the capability to direct electrons toward a single direction, thereby facilitating focused ion-electron collisions on the attosecond timescale.
View Article and Find Full Text PDFThe intrinsic spontaneous and piezoelectric polarizations of GaN lead to the formation of triangular wells and barriers, resulting in the manifestation of chaotic transport models in GaN quantum well intersubband transition (ISBT) infrared detectors and giving rise to various adverse effects. The APSYS software was utilized to construct a novel GaN quantum well ISBT infrared detector in this study. By endeavoring to modify the quantum well structure, our objective was to precisely adjust the energy level of the first excited state (E1) to align with the apex of the triangular barrier.
View Article and Find Full Text PDFBiological applications using multiphoton microscopy increasingly seek a larger field of view while maintaining sufficient temporal sampling to observe dynamic biological processes. Multiphoton imaging also requires high numerical aperture microscope objectives to realize efficient non-linear excitation and collection of fluorescence. This combination of low-magnification and high-numerical aperture poses a challenge for system design.
View Article and Find Full Text PDFJ Chem Theory Comput
January 2025
Qingdao Institute for Theoretical and Computational Sciences and Center for Optics Research and Engineering, Shandong University, Qingdao 266237, China.
Given a number of data sets for evaluating the performance of single reference methods for the low-lying excited states of closed-shell molecules, a comprehensive data set for assessing the performance of multireference methods for the low-lying excited states of open-shell systems is still lacking. For this reason, we propose an extension (QUEST#4X) of the radical subset of QUEST#4 ( , , 3720) to cover 110 doublet and 39 quartet excited states. Near-exact results obtained by iterative configuration interaction with selection and second-order perturbation correction (iCIPT2) are taken as benchmark to calibrate static-dynamic-static configuration interaction (SDSCI) and static-dynamic-static second-order perturbation theory (SDSPT2), which are minimal MRCI and CI-like perturbation theory, respectively.
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