An azobenzene-based photothermal energy storage system for co-harvesting photon energy and low-grade ambient heat via a photoinduced crystal-to-liquid transition
{"title":"An azobenzene-based photothermal energy storage system for co-harvesting photon energy and low-grade ambient heat via a photoinduced crystal-to-liquid transition","authors":"Liqi Dong, Fei Zhai, Hui Wang, Cong Peng, Yiyu Feng, Wei Feng","doi":"10.20517/energymater.2022.26","DOIUrl":null,"url":null,"abstract":"Ambient heat, slightly above or at room temperature, is a ubiquitous and inexhaustible energy source that has typically been ignored due to difficulties in its utilization. Recent evidence suggests that a class of azobenzene (Azo) photoswitches featuring a reversible photoinduced crystal-to-liquid transition could co-harvest photon energy and ambient heat. Thus, a new horizon has been opened for recovering and regenerating low-grade ambient heat. Here, a series of unilateral para-functionalized photoinduced liquefiable Azo derivatives is presented that can co-harvest and convert photon energy and ambient heat into chemical bond energy and latent heat in molecules and eventually release them in the form of high-temperature utilizable heat. A straightforward crystalline-to-liquid phase transition achieved with ultraviolet light irradiation (365 nm) is enabled by appending a halogen/alkoxy group on the para-position of the Azo photoswitches, and the release of thermal energy is triggered by short-wavelength visible-light irradiation (420 nm). The phase transition properties of the trans- and cis-isomers and the energy density, storage lifetime and heat release performance of the cis-liquid are investigated with differential scanning calorimetry, ultraviolet-visible absorption spectroscopy, and an infrared (IR) thermal camera. The experimental results indicate a high energy density of 335 J/g, a long lifetime of 5 d and a heat release of up to 6.3 °C due to the coupled photochemical-thermophysical mechanism. This work presents a new model for utilizing renewable energy, i.e., the photoinduced conversion of ambient thermal energy.","PeriodicalId":21863,"journal":{"name":"Solar Energy Materials","volume":"16 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Solar Energy Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20517/energymater.2022.26","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
Ambient heat, slightly above or at room temperature, is a ubiquitous and inexhaustible energy source that has typically been ignored due to difficulties in its utilization. Recent evidence suggests that a class of azobenzene (Azo) photoswitches featuring a reversible photoinduced crystal-to-liquid transition could co-harvest photon energy and ambient heat. Thus, a new horizon has been opened for recovering and regenerating low-grade ambient heat. Here, a series of unilateral para-functionalized photoinduced liquefiable Azo derivatives is presented that can co-harvest and convert photon energy and ambient heat into chemical bond energy and latent heat in molecules and eventually release them in the form of high-temperature utilizable heat. A straightforward crystalline-to-liquid phase transition achieved with ultraviolet light irradiation (365 nm) is enabled by appending a halogen/alkoxy group on the para-position of the Azo photoswitches, and the release of thermal energy is triggered by short-wavelength visible-light irradiation (420 nm). The phase transition properties of the trans- and cis-isomers and the energy density, storage lifetime and heat release performance of the cis-liquid are investigated with differential scanning calorimetry, ultraviolet-visible absorption spectroscopy, and an infrared (IR) thermal camera. The experimental results indicate a high energy density of 335 J/g, a long lifetime of 5 d and a heat release of up to 6.3 °C due to the coupled photochemical-thermophysical mechanism. This work presents a new model for utilizing renewable energy, i.e., the photoinduced conversion of ambient thermal energy.