Skip to main navigation Skip to search Skip to main content

Dye-sensitized solar cells based on organic dyes with naphtho[2,1-b:3,4- b′]dithiophene as the conjugated linker

  • Xiaoxu Wang
  • , Lei Guo
  • , Ping Fang Xia
  • , Fan Zheng
  • , Man Shing Wong*
  • , Zhengtao Zhu
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

30 Citations (Scopus)

Abstract

Naphtho[2,1-b:3,4-b′]dithiophene is used for the first time as the π-spacer for metal-free organic dyes in dye-sensitized solar cells (DSSCs). Four new donor-(π-spacer)-acceptor organic dyes using triarylamine or carbazole as the electron-donating group, cyanoacrylic acid as the electron-withdrawing anchoring moiety, and naphtho[2,1-b:3,4-b′] dithiophene as the linker were synthesized. The absorption, electrochemical, and photovoltaic properties of the dyes were investigated. DSSCs based on these dyes as sensitizers had efficiencies ranging from 3.98% to 4.60%. The highest efficiency was 4.60 ± 0.16% with a Jsc of 10.8 ± 0.4 mA cm-2, a Voc of 657 ± 5 mV, and a fill factor of 64.0 ± 0.2% under 100 mW AM 1.5 irradiation. The incident photon-to-current efficiency (IPCE) measurement showed that these dyes had high quantum efficiency over the visible range, and the long π-spacer of the molecule resulted in broader IPCE at long wavelength and high Jsc. Photovoltage transient was used to understand the electron recombination and the trends of the photovoltaic parameters (e.g. Voc and efficiency) of the DSSCs based on these organic dyes.

Original languageEnglish
Pages (from-to)13328-13336
Number of pages9
JournalJournal of Materials Chemistry A
Volume1
Issue number42
DOIs
Publication statusPublished - 14 Nov 2013

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

Fingerprint

Dive into the research topics of 'Dye-sensitized solar cells based on organic dyes with naphtho[2,1-b:3,4- b′]dithiophene as the conjugated linker'. Together they form a unique fingerprint.

Cite this