This paper theoretically simulated (using DFT and TD-DFT in N,N-dimethylformamide (DMF) solvent) the photodynamic properties of three non-metallic dye molecules with D-π-A1-π-A2 structure. The total photoelectric conversion efficiency (PCE) could be evaluated by the following parameters: the geometric structures, the electronic structures, and the absorption spectra, the analyses of charge difference density (CDD) and natural bond orbitals (NBO), the analyses of ionization potential (IP) and electron affinity (EA) from electronic contribution capacity, the reorganization energies (λh, λe, and λtotal), and the chemical reaction parameter (h, ω, ω-, and ω+) for intramolecular charge transfer (ICT) processing, the excited lifetime (τ) and the vertical dipole moment (μnormol). The ∆Ginject, the ∆Gdyeregen, the light harvesting efficiencies (LHE) and the excited lifetime (τ) were used to explain experimental JSC. The experimental trend of VOC was explained by the calculation of ∆ECB and μnormol. Moreover, the 15 dyes were designed by adding the electron-donor groups (–OH, –NH2, and –OCH3) and the electron-acceptor groups (–CF3, –F, and −CN) to the LS-387 molecular skeleton, which improved electronic contribution, intramolecular charge transfer (ICT), and optoelectronic performance.
Shape memory polymer network with thermally distinct elasticity and plasticity
