4.5 Article

Push-pull organic dyes and dye-catalyst assembly featuring a benzothiadiazole unit for photoelectrochemical hydrogen production

Journal

SUSTAINABLE ENERGY & FUELS
Volume 6, Issue 15, Pages 3565-3572

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2se00292b

Keywords

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Funding

  1. French National Research Agency (Labex ARCANE, CBH-EUR-GS) [ANR-17-EURE-0003]
  2. CEA through the DRF-Impulsion program
  3. CEA
  4. European Research Council (ERC)
  5. European Union [832606]
  6. GENCI (CINES) [A0100807648]
  7. GENCI (IDRIS)
  8. European Research Council (ERC) [832606] Funding Source: European Research Council (ERC)

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This work presents the design and preparation of two new dyes and a molecular dyad for photoelectrochemical hydrogen production in a dye-sensitized photoelectrochemical cell (DSPEC). The introduction of a benzothiadiazole core improves the absorption properties and extends the visible spectrum up to 650 nm. The results demonstrate that increasing the light harvesting efficiency of the dyad by introducing an IDT-BTD chromophore is beneficial for the photoelectrochemical activity. Additionally, lithium doping of NiO significantly improves the performance.
In this work, we report the design and the preparation of two new dyes and a molecular dyad for the photoelectrochemical hydrogen production from water in a dye-sensitized photoelectrochemical cell (DSPEC). We designed dyes that include a benzothiadiazole (BTD) and an indacenodithiophene (IDT) units, and we obtained a new molecular dyad by covalent coupling with the cobalt diimine-dioxime catalyst. The introduction of the benzothiadiazole core in the structure improves the absorption properties and leads to an extension of the spectrum in the visible range up to 650 nm. The photoelectrochemical properties of the new dyad were evaluated on pristine and lithium-doped NiO electrodes. We demonstrate that increasing the light harvesting efficiency of the dyad by introducing a IDT-BTD chromophore is clearly beneficial for the photoelectrochemical activity. We also demonstrate that lithium doping of NiO, which improves the electronic conductivity of the mesoporous film, leads to a significant increase in performance, in terms of TON and F.E., more than doubled with our new dyad. This BTD-based molecular system outperforms the results of previously reported dyads using the same catalyst.

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