Author:
Hwang Sangyeon,Choi Mingi,Lee Jongseo,Kang Giho,Kim Seo Ju,Seong Baekhoon,Lee Hyungdong,Lee Wonyoung,Byun Doyoung
Abstract
AbstractThe hydrogel of biomolecule-assisted metal/organic complex has the superior ability to form a uniform, continuous, and densely integrated structure, which is necessary for fine thin film fabrication. As a representative of nature-originated polymers with abundant reactive side chains, we select the gelatin molecule as an element for weaving the metal cations. Here, we demonstrate the interaction between the metal cation and gelatin molecules, and associate it with coating quality. We investigate the rheological property of gelatin solutions interacting with metal cation from the view of cross-linking and denaturing of gelatin molecules. Also, we quantitatively compare the corresponding interactions by monitoring the absorbance spectrum of the cation. The coated porous structure is systematically investigated from the infiltration of gelatin-mediated Gd0.2Ce0.8O2−δ (GDC) precursor into Sm0.5Sr0.5CoO3−δ (SSC) porous scaffold. By applying the actively interacting gelatin–GDC system, we achieve a thin film of GDC on SSC with excellent uniformity. Compare to the discrete coating from the typical infiltration process, the optimized thin film coated structure shows enhanced performance and stability.
Funder
National Research Foundation of Korea
Ministry of Science, ICT and Future Planning
Global Frontier R&D Program of the Center for Multiscale Energy System
Publisher
Springer Science and Business Media LLC
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