4.4 Article

Synthesis of Crosslinked Hydroxypropyl Methylcellulose with Methyl Gallate-Poly(Ethylene Glycol) as a Gel Electrolyte for Dye-Sensitized Solar Cells

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/pssa.202200856

Keywords

conductivity; diffusion coefficient stability; HPMC; hybrid of PEG; MG; quasi-solid-state

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In this study, a polymer gel electrolyte is prepared by blending hydroxypropyl methylcellulose (HPMC) with methyl gallate (MG) encapsulated with poly(ethylene glycol) (PEG) and mixing it with a liquid electrolyte. The structural and physical properties of the prepared polymer gels are analyzed using various analytical instruments. The MG-PEG-HPMC hybrid is capable of entrapping a large amount of liquid electrolyte and is used to fabricate dye-sensitized solar cells (DSSCs). The resulting DSSCs show high ionic conductivity and good triiodide diffusion coefficient, as well as long-term stability.
Hydroxypropyl methylcellulose (HPMC) is blended with methyl gallate (MG) encapsulated with poly(ethylene glycol) (PEG) and then mixed with a liquid electrolyte to prepare a polymer gel electrolyte. The structural and physical properties of prepared polymer gels are analyzed by various analytical instruments. The MG-PEG-HPMC hybrid is found to be able for entrapping a large amount of liquid electrolyte and is used to fabricate dye-sensitized solar cells (DSSCs). This polymer gel electrolyte shows high ionic conductivity (5.43 x 10(-4) S cm(-1)) and good triiodide diffusion coefficient (2.25 x 10(-6) cm(2) s(-1)). The resulting DSSCs show an efficiency of 6.96% at a light intensity of 85 mW cm(-2). The long-term stability test reveals that the fabricated DSSCs will be stable even after 500 h. The benefits of incorporating a gel electrolyte into DSSCs are highlighted along with factors affecting the stability of these devices. The use of these bio-based materials has the potential to make a significant contribution to the widespread exploitation of stable, efficient, and low-cost dye-sensitive solar cells.

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