In the present work, we implement environmentally friendly water-based Quasi-Solid Electrolytes (QSE) for Dye Sensitized Solar Cells (DSSCs), displaying an unprecedent open circuit voltage (VOC) as high as 750 mV. The production of the hydrogel for QSE-DSSCs is achieved by exploiting the concept of fully green design and fabrication, through the selection of components such as the natural polysaccharide galactomannan (GM), biocompatible zinc salts, and the employment of eco-friendly synthetic procedures to produce the hybrid gelating agents. In the process, moderate temperature (<40 °C), only aqueous solutions are employed, and, at most, ethanol is used in some phases of the procedure. Depending on the type of the initial salt, either zinc hydroxysulfate lamellae or zinc oxide nanoparticles are created within the gel matrix, with a more extended nanoporous structure in the latter case. The nanostructures and the gels are investigated by multiple techniques, including X-ray diffraction (XRD), infrared spectroscopy (IR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). Upon ensuing addition of I-/I3- redox mediator and assembling of the device, state-of-the-art aqueous QSE-DSSCs are achieved. The latter couples a 2 % efficiency (limited by charge diffusion as proved by Electrochemical Impedance Spectroscopy) with a good Average Visible Transmittance (AVT), and Light Utilization Efficiency (LUE), a couple of coveted features in wave-selective or semi-transparent devices. Finally, Linear Response-Time Dependent DFT (LR-TDDFT) simulations are carried out on a model iodine/iodide layered zinc hydroxy sulphate structure towards a better understanding of the mechanism responsible for the high AVT.
Green zinc/galactomannan-based hydrogels push up the photovoltage of quasi solid aqueous dye sensitized solar cells
Segura Zarate, Ana YancyMembro del Collaboration Group
;Galliano, SimoneMembro del Collaboration Group
;Barolo, ClaudiaMembro del Collaboration Group
;Bonomo, MatteoMembro del Collaboration Group
;
2024-01-01
Abstract
In the present work, we implement environmentally friendly water-based Quasi-Solid Electrolytes (QSE) for Dye Sensitized Solar Cells (DSSCs), displaying an unprecedent open circuit voltage (VOC) as high as 750 mV. The production of the hydrogel for QSE-DSSCs is achieved by exploiting the concept of fully green design and fabrication, through the selection of components such as the natural polysaccharide galactomannan (GM), biocompatible zinc salts, and the employment of eco-friendly synthetic procedures to produce the hybrid gelating agents. In the process, moderate temperature (<40 °C), only aqueous solutions are employed, and, at most, ethanol is used in some phases of the procedure. Depending on the type of the initial salt, either zinc hydroxysulfate lamellae or zinc oxide nanoparticles are created within the gel matrix, with a more extended nanoporous structure in the latter case. The nanostructures and the gels are investigated by multiple techniques, including X-ray diffraction (XRD), infrared spectroscopy (IR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). Upon ensuing addition of I-/I3- redox mediator and assembling of the device, state-of-the-art aqueous QSE-DSSCs are achieved. The latter couples a 2 % efficiency (limited by charge diffusion as proved by Electrochemical Impedance Spectroscopy) with a good Average Visible Transmittance (AVT), and Light Utilization Efficiency (LUE), a couple of coveted features in wave-selective or semi-transparent devices. Finally, Linear Response-Time Dependent DFT (LR-TDDFT) simulations are carried out on a model iodine/iodide layered zinc hydroxy sulphate structure towards a better understanding of the mechanism responsible for the high AVT.File | Dimensione | Formato | |
---|---|---|---|
1-s2.0-S0038092X24001543-main (1).pdf
Accesso aperto
Tipo di file:
PDF EDITORIALE
Dimensione
3.8 MB
Formato
Adobe PDF
|
3.8 MB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.