4.7 Article

MOF-derived Co2+-doped TiO2 nanoparticles as photoanodes for dye-sensitized solar cells

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-95844-4

Keywords

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Funding

  1. UAE University strategic research program [31R238]
  2. University of California, Berkeley
  3. UAE University [31N414]
  4. SERB-CRG [CRG/2020/002163]

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The facile synthesis and application of nano-sized semiconductor metal oxides for optoelectronic devices are challenging due to multi-step processes. Semiconductor oxides derived directly from metal-organic frameworks (MOFs) show promise for clean energy conversion and storage devices, with the potential to enhance light absorption in the visible region and improve overall performance.
Facile synthesis and application of nano-sized semiconductor metal oxides for optoelectronic devices have always affected fabrication challenges since it involves multi-step synthesis processes. In this regard, semiconductor oxides derived directly from metal-organic frameworks (MOFs) routes have gained a great deal of scientific interest owing to their high specific surface area, regular and tunable pore structures. Exploring the application potential of these MOF-derived semiconductor oxides systems for clean energy conversion and storage devices is currently a hot topic of research. In this study, titanium-based MIL-125(Ti) MOFs were used as a precursor to synthesize cobalt-doped TiO2-based dye-sensitized solar cells (DSSCs) for the first time. The thermal decomposition of the MOF precursor under an air atmosphere at 400 degrees C resulted in mesoporous anatase-type TiO2 nanoparticles (NPs) of uniform morphology, large surface area with narrow pore distribution. The Co2+ doping in TiO2 leads to enhanced light absorption in the visible region. When used as photoanode in DSSCs, a good power conversion efficiency (PCE) of 6.86% with good photocurrent density (Jsc) of 13.96 mA cm(-2) was obtained with the lowest recombination resistance and the longest electron lifetime, which is better than the performance of the pristine TiO2-based photoanode.

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