Hybrid Energy Cell with Hierarchical Nano/Micro-Architectured Polymer Film to Harvest Mechanical, Solar, and Wind Energies Individually/Simultaneously.

We report the creation of hybrid energy cells based on hierarchical nano/micro-architectured polydimethylsiloxane (HNMA-PDMS) films with multifunctionality to simultaneously harvest mechanical, solar, and wind energies. These films consist of nano/micro dual-scale architectures (i.e., nanonipples on inverted micropyramidal arrays) on the PDMS surface. The HNMA-PDMS is replicable by facile and cost-effective soft imprint lithography using a nanoporous anodic alumina oxide film formed on the micropyramidal-structured silicon substrate. The HNMA-PDMS film plays multifunctional roles as a triboelectric layer in nanogenerators and an antireflection layer for dye-sensitized solar cells (DSSCs), as well as a self-cleaning surface. This film is employed in triboelectric nanogenerator (TENG) devices, fabricated by laminating it on indium-tin oxide-coated polyethylene terephthalate (ITO/PET) as a bottom electrode. The large effective contact area that emerged from the densely packed hierarchical nano/micro-architectures of the PDMS film leads to the enhancement of TENG device performance. Moreover, the HNMA-PDMS/ITO/PET, with a high transmittance of >90%, also results in highly transparent TENG devices. By placing the HNMA-PDMS/ITO/PET, where the ITO/PET is coated with zinc oxide nanowires, as the top glass substrate of DSSCs, the device is able to add the functionality of TENG devices, thus creating a hybrid energy cell. The hybrid energy cell can successfully convert mechanical, solar, and wind energies into electricity, simultaneously or independently. To specify the device performance, the effects of external pushing frequency and load resistance on the output of TENG devices are also analyzed, including the photovoltaic performance of the hybrid energy cells.

Enhanced Photovoltaic Performance of Dye-Sensitized Solar Cells by Efficient Near-Infrared Sunlight Harvesting using Upconverting Y2O 3:Er (3+)/Yb (3+) Phosphor Nanoparticles.

We report the efficiency enhancement in dye-sensitized solar cells (DSSCs) using Er(3+)/Yb(3+)-co-doped Y2O3 (i.e., Y2O3:Er(3+)/Yb(3+)) phosphor nanoparticles, prepared by a simple and cost-effective urea-based homogeneous precipitation method, for efficient near-infrared (NIR) sunlight harvesting. Under the light excitation at a wavelength of 980 nm, the as-prepared samples exhibited strong upconversion emissions at green and red visible wavelengths. To investigate the influence of Y2O3:Er(3+)/Yb(3+) nanoparticles on the photovoltaic performance of DSSCs, the phosphor nanoparticles were incorporated into titanium dioxide films to form a composite photoelectrode. For the resulting DSSCs, the increased power conversion efficiency (PCE) of 6.68 % was obtained mainly by the increased photocurrent of J SC = 13.68 mA/cm(2) due to the light harvesting enhancement via the NIR-to-visible upconversion process (cf., PCE = 5.94 %, J SC = 12.74 mA/cm(2) for the reference DSSCs without phosphor nanoparticles), thus, indicating the PCE increment ratio of ~12.4 %.

Improvement in light harvesting of dye-sensitized solar cells with antireflective and hydrophobic textile PDMS coating by facile soft imprint lithography.

We demonstrated the improved conversion efficiency (η) of dye-sensitized solar cells (DSSCs) using the textile-patterned polydimethylsiloxane (PDMS) antireflection layers prepared by metal-coated textile master molds by a simple soft imprint lithography. When light propagates through the textile-patterned surface of PDMS (i.e., textile PDMS) laminated on the outer glass surface deposited with fluorine-doped tin oxide (i.e., FTO/glass), both the transmitted and diffused lights into the photo-anode of DSSCs were simultaneously enhanced. Compared to the bare FTO/glass, the textile PDMS increased the total transmittance from 82.3 to 85.1% and its diffuse transmittance was significantly increased from 5.9 to 78.1% at 550 nm of wavelength. The optical property of textile PDMS was also theoretically analyzed by the finite-difference time-domain simulation. By laminating the textile PDMS onto the outer glass surface of DSSCs, the η was enhanced from 6.04 to 6.51%. Additionally, the fabricated textile PDMS exhibited a hydrophobic surface with water contact angle of ~123.15°.