2006Journal of Polymer Science Part A Polymer ChemistryRequires access

Effect of side‐chain end groups on the optical, electrochemical, and photovoltaic properties of side‐chain conjugated polythiophenes

Erjun Zhou, Chang He, Zhan’ao Tan, Chunhe Yang, Yongfang Li

Open publisher page 72 citations

Abstract

Abstract Three new side‐chain conjugated polythiophene derivatives, poly{3‐[2‐(3‐methoxy‐4‐octyloxy‐phenyl)‐vinyl]‐thiophene} (P3MOPVT), poly{3‐[2‐(3,5‐dimethoxy‐4‐octyloxy‐phenyl)‐vinyl]‐thiophene} (P3DMOPVT), and poly{3‐[2‐(3,4‐dioctyloxy‐phenyl)‐vinyl]‐thiophene} (P3DOPVT), were synthesized by Wittig‐Hornor reaction and GRIM method and compared with poly{3‐[2‐(4‐octyloxy‐phenyl)‐vinyl]‐thiophene} (P3OPVT) for investigating the effect of the end groups of the conjugated side‐chain on the properties of the polymers. Owing to the electron‐donating ability of methoxy groups, the visible absorption peaks of P3MOPVT and P3DMOPVT solutions and films become stronger and red‐shifted compared with P3OPVT. The electrochemical bandgaps of the four polymers are 2.15 eV for P3OPVT, 1.99 eV for P3MOPVT, 1.85 eV for P3DMOPVT, and 2.36 eV for P3DOPVT, respectively, which indicate that the electron‐donating ability of the methoxy end group on the conjugated side chain of P3MOPVT and P3DMOPVT and the large steric hindrance of the two octyloxy end groups on the conjugated side chain of P3DOPVT have obvious influence on the electrochemical properties of the side‐chain conjugated polythiophenes. Polymer solar cells were fabricated with a structure of ITO/PEDOT:PSS/Polymer:PCBM/LiF/Al. The best device, based on P3DMOPVT, shows a power conversion efficiency of 1.63% under the illumination of AM1.5, 80 mW/cm2. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4916–4922, 2006

About this research paper

What this paper is about

Abstract Three new side‐chain conjugated polythiophene derivatives, poly{3‐[2‐(3‐methoxy‐4‐octyloxy‐phenyl)‐vinyl]‐thiophene} (P3MOPVT), poly{3‐[2‐(3,5‐dimethoxy‐4‐octyloxy‐phenyl)‐vinyl]‐thiophene} (P3DMOPVT), and poly{3‐[2‐(3,4‐dioctyloxy‐phenyl)‐vinyl]‐thiophene} (P3DOPVT), were synthesized by Wittig‐Hornor reaction and GRIM method and compared with poly{3‐[2‐(4‐octyloxy‐phenyl)‐vinyl]‐thiophene} (P3OPVT) for investigating the effect of the end groups of the conjugated side‐chain on the properties of the polymers. Owing to the electron‐donating ability of methoxy groups, the visible absorption peaks of P3MOPVT and P3DMOPVT solutions and films become stronger and red‐shifted compared with P3OPVT. The electrochemical bandgaps of the four polymers are 2.15 eV for P3OPVT, 1.99 eV for P3MOPVT, 1.85 eV for P3DMOPVT, and 2.36 eV for P3DOPVT, respectively, which indicate that the electron‐donating ability of the methoxy end group on the conjugated side chain of P3MOPVT and P3DMOPVT and the large steric hindrance of the two octyloxy end groups on the conjugated side chain of P3DOPVT have obvious influence on the electrochemical properties of the side‐chain conjugated polythiophenes. Polymer solar cells were fabricated with a structure of ITO/PEDOT:PSS/Polymer:PCBM/LiF/Al. The best device, based on P3DMOPVT, shows a power conversion efficiency of 1.63% under the illumination of AM1.5, 80 mW/cm2. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4916–4922, 2006

Why it matters

OpenAlex reports 72 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract Three new side‐chain conjugated polythiophene derivatives, poly{3‐[2‐(3‐methoxy‐4‐octyloxy‐phenyl)‐vinyl]‐thiophene} (P3MOPVT), poly{3‐[2‐(3,5‐dimethoxy‐4‐octyloxy‐phenyl)‐vinyl]‐thiophene} (P3DMOPVT), and poly{3‐[2‐(3,4‐dioctyloxy‐phenyl)‐vinyl]‐thiophene} (P3DOPVT), were synthesized by Wittig‐Hornor reaction and GRIM method and compared with poly{3‐[2‐(4‐octyloxy‐phenyl)‐vinyl]‐thiophene} (P3OPVT) for investigating the effect of the end groups of the conjugated side‐chain on the properties of the polymers. Owing to the electron‐donating ability of methoxy groups, the visible absorption peaks of P3MOPVT and P3DMOPVT solutions and films become stronger and red‐shifted compared with P3OPVT. The electrochemical bandgaps of the four polymers are 2.15 eV for P3OPVT, 1.99 eV for P3MOPVT, 1.85 eV for P3DMOPVT, and 2.36 eV for P3DOPVT, respectively, which indicate that the electron‐donating ability of the methoxy end group on the conjugated side chain of P3MOPVT and P3DMOPVT and the large steric hindrance of the two octyloxy end groups on the conjugated side chain of P3DOPVT have obvious influence on the electrochemical properties of the side‐chain conjugated polythiophenes. Polymer solar cells were fabricated with a structure of ITO/PEDOT:PSS/Polymer:PCBM/LiF/Al. The best device, based on P3DMOPVT, shows a power conversion efficiency of 1.63% under the illumination of AM1.5, 80 mW/cm2. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4916–4922, 2006

Key concepts: Conjugated system, Side chain, Thiophene, Polythiophene, PEDOT:PSS, Polymer chemistry, Polymer, Materials science

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of side‐chain end groups on the optical, electrochemical, and photovoltaic properties of side‐chain conjugated polythiophenes — Research Paper | ScholarLens