4.5 Article

A facile approach to construct organic D-π-A dyes via sequential condensation reactions for dye-sensitized solar cells

Journal

SUSTAINABLE ENERGY & FUELS
Volume 5, Issue 1, Pages 289-296

Publisher

ROYAL SOC CHEMISTRY

Keywords

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Funding

  1. Natural Science Foundation of Jiangsu Province [BK20191385]
  2. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX20_0860]
  3. High Level Talent Project of Nanjing Forestry University [GXL2018003]
  4. JSPS KAKENHI [18H02079]
  5. King Saud University [RG-1438-041]

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A new strategy for molecular engineering of organic D-pi-A sensitizers has been developed, focusing on constructing D-pi-A backbone via sequential condensation reactions to enhance DSSC performance. The expansion of pi-conjugated spacer in this type of dyes resulted in improved photovoltaic performance, offering a new pathway for designing D-pi-A dyes.
We developed a new strategy for the molecular engineering of organic D-pi-A sensitizers for dye-sensitized solar cell (DSSC) applications. Different from the synthesis of organic D-pi-A dyes by conventional C-C coupling method, the present approach highlights the construction of D-pi-A backbone via sequential condensation reactions. This approach avoids noble metal catalysis as well as harsh reaction conditions. Based on this concept, four organic D-pi-A dyes have been developed as sensitizers for DSSCs, which produced high IPCE values and photovoltage. Moreover, expansion of the pi-conjugated spacer in this type of dyes resulted in enhanced photovoltaic performance, which provided a new pathway for designing D-pi-A dyes.

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