A new approach exploiting thermally activated delayed fluorescence molecules to optimize solar thermal energy storage
Fan-Yi Meng,
I-Han Chen,
Jiun-Yi Shen,
Kai-Hsin Chang,
Tai-Che Chou,
Yi-An Chen,
Yi-Ting Chen,
Chi-Lin Chen and
Pi-Tai Chou ()
Additional contact information
Fan-Yi Meng: National Taiwan University, R.O.C
I-Han Chen: National Taiwan University, R.O.C
Jiun-Yi Shen: National Taiwan University, R.O.C
Kai-Hsin Chang: National Taiwan University, R.O.C
Tai-Che Chou: National Taiwan University, R.O.C
Yi-An Chen: National Taiwan University, R.O.C
Yi-Ting Chen: National Taiwan University, R.O.C
Chi-Lin Chen: National Taiwan University, R.O.C
Pi-Tai Chou: National Taiwan University, R.O.C
Nature Communications, 2022, vol. 13, issue 1, 1-10
Abstract:
Abstract We propose a new concept exploiting thermally activated delayed fluorescence (TADF) molecules as photosensitizers, storage units and signal transducers to harness solar thermal energy. Molecular composites based on the TADF core phenoxazine–triphenyltriazine (PXZ-TRZ) anchored with norbornadiene (NBD) were synthesized, yielding compounds PZDN and PZTN with two and four NBD units, respectively. Upon visible-light excitation, energy transfer to the triplet state of NBD occurred, followed by NBD → quadricyclane (QC) conversion, which can be monitored by changes in steady-state or time-resolved spectra. The small S1-T1 energy gap was found to be advantageous in optimizing the solar excitation wavelength. Upon tuning the molecule’s triplet state energy lower than that of NBD (61 kcal/mol), as achieved by another composite PZQN, the efficiency of the NBD → QC conversion decreased drastically. Upon catalysis, the reverse QC → NBD reaction occurred at room temperature, converting the stored chemical energy back to heat with excellent reversibility.
Date: 2022
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-28489-0
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DOI: 10.1038/s41467-022-28489-0
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