{"title":"Heat trapping with restricted energy dissipation in polyfluorinated supra molecular environment: Wavelength dependency of energy deposition","authors":"Yu Nabetani , Vivek Ramakrishnan , Ryosuke Nakazato , Yuki Iwata , Hiroshi Tachibana , Haruo Inoue , Tsutomu Shiragami","doi":"10.1016/j.jphotochem.2024.116245","DOIUrl":null,"url":null,"abstract":"<div><div>Following our previous report on the heat trapping in organic/inorganic hybrid compound with bilayer structure formed by cationic polyfluorinated surfactant containing azobenzene moiety (C3F-Azo-C6H) in the interlayer of cation-exchangeable synthetic clay (Smecton SA: SSA) nanosheets having been probed by a temperature sensing Rhodamine B (RhB) upon excitation by a fixed wavelength of visible light, a systematic study of the effect of wavelength dependency for the excitation was carried out to get deeper insight into the heat trapping. Evident wavelength effect of excitation on the temperature elevation was observed. Among three components in the fluorescence lifetime (τ<sub>1</sub>, τ<sub>2</sub>, τ<sub>3</sub>) of RhB, the local temperatures <em>T</em><sub>1</sub>, <em>T</em><sub>2</sub> deduced from τ<sub>1</sub>, τ<sub>2</sub> exhibited a systematic temperature elevation upon excitation of RhB with a shorter wavelength of visible light (570–520 nm). Estimation of the energy stored against the energy input indicated that an excess energy initially deposited at Franck-Condon state is retained in a limited number of local modes during the fluorescence lifetime through a pretty slow intramolecular vibrational relaxation (IVR) in the interlayer. Structural analysis by TD-DFT calculation strongly suggested that all the local modes within RhB are classified into four groups (I–IV), which well coincides with the prediction by a comparison analysis in respect to the energy stored against the energy input to rationalize that the IVR of RhB for τ<sub>1</sub> component (<em>T</em><sub>1</sub>) in the interlayer is limited among the local mode groups I (#1–10)–II (#11–21) and τ<sub>2</sub> component (<em>T</em><sub>2</sub>) being restricted up to group III (# 22–36). The systematic study revealed that the hybrid compound C3F-Azo-C6H/SSA provides a unique microenvironment having gaseous/vacuum-like atmosphere to a molecule incorporated in the narrow gap space sandwiched by neighboring C3F-Azo-C6H molecules in the interlayer to allow an inherently slow IVR.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"462 ","pages":"Article 116245"},"PeriodicalIF":4.1000,"publicationDate":"2024-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Photochemistry and Photobiology A-chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1010603024007895","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Following our previous report on the heat trapping in organic/inorganic hybrid compound with bilayer structure formed by cationic polyfluorinated surfactant containing azobenzene moiety (C3F-Azo-C6H) in the interlayer of cation-exchangeable synthetic clay (Smecton SA: SSA) nanosheets having been probed by a temperature sensing Rhodamine B (RhB) upon excitation by a fixed wavelength of visible light, a systematic study of the effect of wavelength dependency for the excitation was carried out to get deeper insight into the heat trapping. Evident wavelength effect of excitation on the temperature elevation was observed. Among three components in the fluorescence lifetime (τ1, τ2, τ3) of RhB, the local temperatures T1, T2 deduced from τ1, τ2 exhibited a systematic temperature elevation upon excitation of RhB with a shorter wavelength of visible light (570–520 nm). Estimation of the energy stored against the energy input indicated that an excess energy initially deposited at Franck-Condon state is retained in a limited number of local modes during the fluorescence lifetime through a pretty slow intramolecular vibrational relaxation (IVR) in the interlayer. Structural analysis by TD-DFT calculation strongly suggested that all the local modes within RhB are classified into four groups (I–IV), which well coincides with the prediction by a comparison analysis in respect to the energy stored against the energy input to rationalize that the IVR of RhB for τ1 component (T1) in the interlayer is limited among the local mode groups I (#1–10)–II (#11–21) and τ2 component (T2) being restricted up to group III (# 22–36). The systematic study revealed that the hybrid compound C3F-Azo-C6H/SSA provides a unique microenvironment having gaseous/vacuum-like atmosphere to a molecule incorporated in the narrow gap space sandwiched by neighboring C3F-Azo-C6H molecules in the interlayer to allow an inherently slow IVR.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.