Highly uniform core/double-shell-structured β-NaYF4:Er(3+),Yb(3+)@SiO2@TiO2 hexagonal sub-microprisms are prepared and employed in dye-sensitized solar cells (DSCs) internally. This work paves a facile way to enable the most-efficient upconversion material (β-NaYF4:Er(3+),Yb(3+)) to be used as scattering and upconversion centers in the photoelectrode of a DSC.

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A facile in situ carbonization method was demonstrated to prepare the highly transparent carbon counter electrode (CE) with good mechanical stability for bifacial dye-sensitized solar cells (DSCs). The optical and electrochemical properties of carbon CEs were dramatically affected by the composition and concentration of the precursor. The well-optimized carbon CE exhibited high transparency and sufficient catalytic activity for I3(-) reduction. The bifacial DSC with obtained carbon CE achieved a high power conversion efficiency (PCE) of 5.04% under rear-side illumination, which approaches 85% that of front-side illumination (6.07%). Moreover, the device shows excellent stability as confirmed by the aging test. These promising results reveal the enormous potential of this transparent carbon CE in scaling up and commercialization of low cost and effective bifacial DSCs.

We demonstrate a strategy for incorporating plasmon resonant metallic nanoparticles in the construction of hierarchical TiO(2) spheres. Localized electric fields can be produced by the addition of Au nanoparticles, which can excite dye molecules more effectively than incident far-field light. The synergistic effect of surface plasmon resonance with constructed TiO(2) nanostructures has been investigated, and was confirmed by optical spectroscopy, J-V characteristics, EIS analysis and OCVD measurements. When Au nanoparticles are incorporated into the constructed TiO(2) spheres, the device achieves a power conversion efficiency of 6.62%, a 4.6% increase compared to the device based on constructed TiO(2) spheres without plasmon resonant Au nanoparticles, and a 17.4% increase compared to that without any treatment.

Layer-by-layer self-assembled TiO2 hierarchical nanosheets with exposed {001} facets have been successfully fabricated via a simple one-step solvothermal reaction. The anatase TiO2 layer-by-layer hierarchical nanosheets (TiO2 LHNs) exhibit favorable light scattering effect and large surface area, owing to their layer-by-layer hierarchical structure. When applied to the dye-sensitized solar cells (DSSCs), the layer-by-layer hierarchical structure with exposed {001} facet could effectively enhance light harvesting and dye adsorption, followed by increasing the photocurrent of DSSCs. As a result, the photoelectric conversion efficiency (η) of 7.70% has been achieved for the DSSCs using TiO2 LHNs as the bifunctional layer, indicating 21% improvement compared to the pure Degussa P25 (6.37%) as photoanode. Such enhancement can be mainly ascribed to the better light scattering capability of TiO2 LHNs, higher dye adsorption on TiO2 LHN {001} facets, and longer lifetime of the injected electrons in TiO2 LHNs compared to P25, which are examined by UV-vis spectrophotometry and electrochemical impedance spectroscopy under the same conditions. These remarkable properties of TiO2 LHNs make it a promising candidate as a bifunctional scattering material for DSSCs.

Upconversion materials have been employed as energy relay materials in dye sensitized solar cells (DSCs) to broaden the range of light absorption. However, the origin of the enhancements can be induced by both upconversion and size-dependent light scattering effects. To clarify the role of the upconversion material in the photoelectrode of DSCs, an upconversion induced device was realized here, which has the size-dependent light scattering effect eliminated via the application of NaYF4:Er(3+), Yb(3+)@SiO2 upconversion nanoparticles (β-NYEY@SiO2 UCNPs). An enhancement of 6% in efficiency was observed for the device. This demonstration provided an insight into the possible further employment of upconversion in DSCs.

Controlling over ordered porosity by self-assembly is challenging in the area of materials science. Materials with highly ordered aperture are favorable candidates in catalysis and energy conversion device. Here we describe a facile process to synthesize highly ordered mesoporous carbon (OMC) by direct tri-constituent co-assembly method, which uses resols as the carbon precursor, tri-block copolymer F127 as the soft template and tetraethoxysilane (TEOS) as the inorganic precursor. The obtained products are characterized by small-angle X-ray diffraction (SAXD), Brunauer-Emmett-Teller (BET) nitrogen sorption-desorption measurement and transmission electron microscope (TEM). The results indicate that the OMC possesses high surface areas of 1209 m(2) g(-1), homogeneous pore size of 4.6 nm and a large pore volume of 1.65 cm(3) g(-1). The advantages of high electrochemical active surface area and favorable accessible porosity of OMC benefit the catalysis of I(3)(-) to I(-). As a result, the OMC counter electrode displays a remarkable property when it was applied in dye-sensitized solar cells (DSSCs). For comparison, carbon black (CB) counter electrode and Pt counter electrode have also been prepared. When these different counter electrodes were applied for dye-sensitized solar cells (DSSCs), the power-conversion efficiency (η) of the DSSCs with CB counter electrode are measured to be 5.10%, whereas the corresponding values is 6.39% for the DSSC with OMC counter electrode, which is comparable to 6.84% of the cell with Pt counter electrode under the same experimental conditions.

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