Dye-sensitized solar cells using silicon phthalocyanine photosensitizers with pyridine anchor: Preparation, evaluation of photophysical, electrochemical, and photovoltaic properties


Güzel E., Baş H., BIYIKLIOĞLU Z., Şişman İ.

Applied Organometallic Chemistry, cilt.35, 2021 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 35
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1002/aoc.6214
  • Dergi Adı: Applied Organometallic Chemistry
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aerospace Database, BIOSIS, Chemical Abstracts Core, Chimica, Communication Abstracts, Compendex, Metadex, DIALNET, Civil Engineering Abstracts
  • Anahtar Kelimeler: dye&#8208, sensitized solar cells, photosensitizer, phthalocyanine, pyridine anchor, silicon
  • Karadeniz Teknik Üniversitesi Adresli: Evet

Özet

© 2021 John Wiley & Sons, Ltd.In this study, novel two silicon phthalocyanine photosensitizers (3PY-Si and 4PY-Si) containing pyridine groups as an electron-withdrawing and anchoring group have been prepared and chemically characterized for dye-sensitized solar cells (DSSCs). Photoelectrochemical and photovoltaic properties of the photosensitizers were evaluated. The new photosensitizers elucidated by spectroscopic and electrochemical techniques. As reported by fluorescence measurements, the silicon phthalocyanine photosensitizers exhibited slightly higher fluorescence quantum yield (ΦF = 0.25) than the unsubstituted zinc phthalocyanine which is favorable for photophysical applications. The DSSC based on complex 3PY-Si shows the highest power conversion efficiency (PCE) of 0.53% with the Jsc, Voc and FF values of 1.205 mA cm−2, 0.612 V, and 0.72, respectively, in the presence of the coadsorbent. These silicon phthalocyanine photosensitizers with bulky axial pyridine substituents found to be important materials for (DSSCs) since they show strong absorption in the red region and their ligands hamper the stacking of rings. This situation prevented the formation of aggregates with a common tendency to photosensitizers on the TiO2 surface.