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A cobalt complex redox shuttle for dye-sensitized solar cells with high open-circuit potentials.


ABSTRACT: Dye-sensitized solar cells are a promising alternative to traditional inorganic semiconductor-based solar cells. Here we report an open-circuit voltage of over 1,000 mV in mesoscopic dye-sensitized solar cells incorporating a molecularly engineered cobalt complex as redox mediator. Cobalt complexes have negligible absorption in the visible region of the solar spectrum, and their redox properties can be tuned in a controlled fashion by selecting suitable donor/acceptor substituents on the ligand. This approach offers an attractive alternate to the traditional I(3)(-)/I(-) redox shuttle used in dye-sensitized solar cells. A cobalt complex using tridendate ligands [Co(bpy-pz)(2)](3+/2+)(PF(6))(3/2) as redox mediator in combination with a cyclopentadithiophene-bridged donor-acceptor dye (Y123), adsorbed on TiO(2), yielded a power conversion efficiency of over 10% at 100 mW cm(-2). This result indicates that the molecularly engineered cobalt redox shuttle is a legitimate alternative to the commonly used I(3)(-)/I(-) redox shuttle.

SUBMITTER: Yum JH 

PROVIDER: S-EPMC3272578 | biostudies-other | 2012

REPOSITORIES: biostudies-other

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A cobalt complex redox shuttle for dye-sensitized solar cells with high open-circuit potentials.

Yum Jun-Ho JH   Baranoff Etienne E   Kessler Florian F   Moehl Thomas T   Ahmad Shahzada S   Bessho Takeru T   Marchioro Arianna A   Ghadiri Elham E   Moser Jacques-E JE   Yi Chenyi C   Nazeeruddin Md K MK   Grätzel Michael M  

Nature communications 20120117


Dye-sensitized solar cells are a promising alternative to traditional inorganic semiconductor-based solar cells. Here we report an open-circuit voltage of over 1,000 mV in mesoscopic dye-sensitized solar cells incorporating a molecularly engineered cobalt complex as redox mediator. Cobalt complexes have negligible absorption in the visible region of the solar spectrum, and their redox properties can be tuned in a controlled fashion by selecting suitable donor/acceptor substituents on the ligand.  ...[more]

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