Molecular Solar Thermal (MOST) systems are interesting candidates for energy storage in one-photon one-molecule processes. The photoinduced conversion of norbornadiene into its strained valence isome...
Developing norbornadiene–quadricyclane (NBD–QC) systems for molecular solar-thermal (MOST) energy storage is often a process of trial and error. By studying a series of norbornadienes (NBD-R2) doubly substituted at
A series of substituted donor–acceptor norbornadienes with cyano acceptors and ethynyl‐aryl donor units has been synthesized and evaluated in the context of molecular solar‐thermal energy storage. A key step in the synthesis is a procedure for the formation of 2‐cyano‐3‐chloronorbornadiene from readily available starting materials.
Molecular photoswitches of norbornadiene (NBD) derivatives have been effectively applied in molecular solar-thermal energy storage (MOST) by photoisomerization of NBD to a quadricyclane (QC) state. However, a challenge of the NBD-based MOST system is the lack of a reversible two-way photoswitching process, l
A major challenge in the field of molecular solar thermal energy storage is designing visible light-absorbing photoswitches with long energy storage half-lives. Five novel visible light-absorbing norbornadiene dimers
Molecular photoswitches of norbornadiene (NBD) derivatives have been effectively applied in molecular solar-thermal energy storage (MOST) by photoisomerization of NBD to a quadricyclane (QC) state. However, a challenge of the NBD-based MOST system is the lack of a reversible two-way photoswitching process, limiting conversion from QC to thermal
Developing norbornadiene–quadricyclane (NBD–QC) systems for molecular solar-thermal (MOST) energy storage is often a process of trial and error. By studying a series of norbornadienes (NBD-R2) doubly substituted at the C7-position with R = H, Me, and iPr, we untangle the interrelated factors affecting MOST p
Molecular solar thermal energy storage (MOST) systems can convert, store and release solar energy in chemical bonds, i.e., as chemical energy. In this work, phenyl- and naphthyl-linked bis- and tris-norbornadienes are presented as promising MOST systems with very high energy densities.
A general challenge is to combine efficient solar energy capture with high energy densities and energy storage time into a processable composite for device application. Here, norbornadiene (NBD)–quadricyclane (QC) molecular photoswitches are embedded into polymer matrices, with possible applications in energy storing coatings.
Molecular solar thermal energy storage (MOST) systems can convert, store and release solar energy in chemical bonds, i.e., as chemical energy. In this work, phenyl- and naphthyl-linked bis- and tris-norbornadienes
Here, norbornadiene (NBD)–quadricyclane (QC) molecular photoswitches are embedded into polymer matrices, with possible applications in energy storing coatings. The NBD–QC photoswitches that are capable of absorbing sunlight with estimated solar energy storage efficiencies of up to 3.8% combined with attractive energy storage densities of up
So-called molecular solar thermal (MOST) systems[6] combine the light-harvesting process with storage of the gained energy in a single step. Upon irradiation, an energy-lean parent compound is converted into its energy-rich valence isomer. In the latter, the energy difference between the two photoisomers
Molecular Solar Thermal (MOST) systems are interesting candidates for energy storage in one-photon one-molecule processes. The photoinduced conversion of norbornadiene into its strained valence isome...
A major challenge in the field of molecular solar thermal energy storage is designing visible light-absorbing photoswitches with long energy storage half-lives. Five novel visible light-absorbing norbornadiene dimers were prepared, with half-lives up to 23.0 hours, and high energy densities up to 379.3 kJ/kg.
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