Design and DFT study of nitrogen-rich donor systems for improved photovoltaic performance in dye-sensitized solar cells
| Autor: | Velayudhan V. Divya, Cherumuttathu H. Suresh |
|---|---|
| Rok vydání: | 2021 |
| Předmět: |
Chemistry
Energy conversion efficiency 02 engineering and technology General Chemistry 010402 general chemistry 021001 nanoscience & nanotechnology Photochemistry 01 natural sciences Acceptor Catalysis 0104 chemical sciences law.invention Delocalized electron Dye-sensitized solar cell law Solar cell Materials Chemistry Density functional theory Photosensitizer 0210 nano-technology HOMO/LUMO |
| Zdroj: | New Journal of Chemistry. 45:11585-11595 |
| ISSN: | 1369-9261 1144-0546 |
| DOI: | 10.1039/d1nj00881a |
| Popis: | Eighteen electron-rich nitrogen incorporated donors with a butadiene π-spacer and a cyanoacrylic acid acceptor (A) as photosensitizers (D1–π–A to D18–π–A) for dye-sensitized solar cell (DSSC) applications have been designed for improving the photovoltaic performance. The significance of the nitrogen centres for revamping the donating strength (ΔVmA) of D–π–A is scrutinized using molecular electrostatic potential (MESP) analysis at the B3LYP/cc-pVDZ level of density functional theory (DFT). During the transformation of a donor (D) to D–π–A, a certain delocalization of electron density from D to π–A has occurred, and the change in the MESP minimum (ΔVmA) observed at the cyano region of D–π–A is related to the donating strength of D. Optical and photovoltaic properties are analyzed at the TD/CAM-B3LYP/cc-pVDZ/SMD//B3LYP/cc-pVDZ level. In D1–π–A to D18–π–A, ΔVmA is in the range −7.0 to −19.0 kcal mol−1 and the increase in donating strength is found to be proportional to the number of planar nitrogens in the donors. D12–π–A exhibited the most negative ΔVmA (−19.0 kcal mol−1), indicating the highest electron-donating strength of D12, whereas the least negative ΔVmA (−7.0 kcal mol−1) displayed by D7–π–A is correlated to the weak donating character of D7. By increasing the electron-donating strength of D in D–π–A, a red-shift in the absorption maximum (Δλmax) by 162 to 294 nm is observed. Further, the open-circuit voltage (eVoc) calculated for the D–π–A systems showed a strong linear relationship with ΔVmA. The LUMO (lowest unoccupied molecular orbital) energy of all the D–π–A systems (−1.79 to −2.79 eV) is observed above the conduction band (CB) energy of TiO2 (−4.0 eV), which ensured a desirable electron injection efficiency (ΔGinject) for them. The analysis of the adsorption energy (Eads) of the D–π–A systems on the TiO2 semiconductor (D–π–A/TiO2) showed that D12–π–A has the highest adsorption stability. Improving the adsorption stability is better for improving eVoc and the power conversion efficiency (PCE). The maximum absorption wavelength (λmax) of the D–π–A/TiO2 systems ranges from 513 to 703 nm and all of them display a red-shift with respect to the bare D–π–A systems. The study suggests D12 as the most efficient photosensitizer for DSSC applications. Further, it deepens the understanding of the structure–performance relationship of D–π–A systems as photosensitizers. |
| Databáze: | OpenAIRE |
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