Origin of high open-circuit voltage in solid state dye-sensitized solar cells employing polymer electrolyte

다국어 초록 (Multilingual Abstract)

<P><B>Abstract</B></P> <P>Herein, the energy level alignment and electron recombination kinetics in solid state dye-sensitized solar cells (DSCs) employing a solid polymer electrolyte (SPE) have been quantitatively characterized. In order to determine the microscopic origin of the enhanced characteristics in polymer electrolytes, we carried out an extensive study of the photovoltaic properties with respect to the electrolyte type and composition, including a liquid electrolyte (LE) and various salt types and concentrations. We observed a smaller downward shift in the conduction band energy of the TiO<SUB>2</SUB> layer upon contact with the SPE as well as a retarded electron recombination rate. These led to an increase in the <I>V</I> <SUB>oc</SUB> for DSCs with an SPE, which is mostly attributable to the coordinative interactions of the ethylene oxide (EO) units in poly(ethylene oxide) (PEO) and poly(ethylene glycol) dimethyl ether (PEGDME) with metallic Li<SUP>+</SUP> ions and Ti atoms. Such coordinative interactions induce 1) the capture of Li<SUP>+</SUP> cations in the bulk of the polymer electrolyte, thereby reducing their effective concentration and 2) the facile formation of a PEO passivation layer on top of the TiO<SUB>2</SUB> layer. Therefore, it was concluded that the high <I>V</I> <SUB>oc</SUB> in solid state DSCs employing a polymer electrolyte is attributable to the coordinative properties of the EO units in PEO and PEGDME in the SPE.</P> <P><B>Highlights</B></P> <P> <UL> <LI> The origin of high open-circuit voltage in solid state dye-sensitized solar cells with PEO-based polymer electrolyte has been firstly unveiled. </LI> <LI> New quantitative analysis of TiO<SUB>2</SUB> conduction band shift was introduced by measuring the change in the Fermi voltage with varying the concentration of the salts. </LI> <LI> PEO containing the EO groups captured cations in electrolyte and also coordinatively adsorbed on the surface of the TiO<SUB>2</SUB> layer. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>