Sunlight-activated phase change materials for controlled heat storage and triggered release
We report the design of photo-responsive organic phase change materials that can absorb filtered solar radiation to store both latent heat and photon energy via simultaneous phase transition and photo-isomerization. The activation of photo-switches by long wavelengths ≥530 nm in the visible light ra...
Saved in:
Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 9; no. 15; pp. 9798 - 988 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
01.01.2021
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | We report the design of photo-responsive organic phase change materials that can absorb filtered solar radiation to store both latent heat and photon energy
via
simultaneous phase transition and photo-isomerization. The activation of photo-switches by long wavelengths ≥530 nm in the visible light range at a low irradiance is achieved, in the absence of high-intensity light sources, by the
ortho
-substitution of azobenzene units. The facile transition from crystalline to liquid phase is enabled by appending an aliphatic group on the photochromic moiety. The sunlight-activated liquid phase exhibits an exceptionally long heat storage without crystallization for nearly two months, and the release of energy is triggered by a short irradiation at 430 nm. The successful demonstration of photo-controlled latent heat storage accomplished by solar irradiation opens a new horizon on solar energy harvesting by functional organic materials, as a complementary system to photocatalysts and photovoltaic materials.
Photo-responsive organic phase change materials that can absorb filtered solar radiation in the visible range to store both latent heat and photon energy are demonstrated. |
---|---|
Bibliography: | Electronic Supplementary Information (ESI) available. See DOI 10.1039/d1ta01007g |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d1ta01007g |