Multilayer films for photon upconversion-driven photoswitching

Artikel i vetenskaplig tidskrift, 2024

Photoswitchable materials are of significant interest for diverse applications from energy and data storage to additive manufacturing and soft robotics. However, the absorption profile is often a limiting factor for practical applications. This can be overcome using indirect excitation via complementary photophysical pathways, such as triplet sensitisation or photon upconversion. Here, we demonstrate the use of triplet-triplet annihilation upconversion (TTA-UC) to drive photoswitching of the energy storing photoswitch norbornadiene-quadricyclane (NBD-QC) in the solid-state. A photoswitchable bilayer polymer film, incorporating the TTA-UC sensitiser-emitter pair of platinum octaethylporphyrin (PtOEP) and 9,10-diphenylanthracene (DPA), was used to trigger the photoinduced [2+2] cycloaddition of NBD to form QC using visible instead of UV light. The isolated TTA-UC film showed green-to-blue upconversion, with a competitive upconversion efficiency of (1.9 +/- 0.1%) for the solid-state in air. Direct photoswitching of the isolated NBD film was demonstrated with a narrow UV light source (340 nm). However, in the bilayer film, spectral overlap between the upconverted blue emission in the TTA-UC film and the absorbance band of the NBD film resulted in indirect photoswitching using visible green light (532 nm, 1 W cm-2), thus extending the spectral operational window of the photoswitching film. The results demonstrate proof-of-feasibility of TTA-UC-promoted photoswitching in the solid-state, paving the way for potential applications in light-harvesting devices and smart coatings, using a wider selection of irradiation wavelengths.