S
Shancheng Yu
Researcher at Nanjing Tech University
Publications - 8
Citations - 113
Shancheng Yu is an academic researcher from Nanjing Tech University. The author has contributed to research in topics: Cathode & Solid oxide fuel cell. The author has an hindex of 5, co-authored 7 publications receiving 85 citations. Previous affiliations of Shancheng Yu include Nanjing Medical University.
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Effect of calcination temperature on oxidation state of cobalt in calcium cobaltite and relevant performance as intermediate-temperature solid oxide fuel cell cathodes
TL;DR: In this paper, the reactivity of CaCO 3 with Co 3 O 4 is evaluated by thermogravimetric analysis (TGA), X-ray powder diffraction (XRD), and X-Ray photoelectron spectroscopy (XPS) for intermediate-temperature solid oxide fuel cells (IT-SOFC) cathode of as-prepared materials.
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Dense thin YSZ electrolyte films prepared by a vacuum slurry deposition technique for SOFCs
TL;DR: In this paper, a novel vacuum deposition technique based on a slurry coating is proposed for the preparation of thin yttria-stabilized zirconia (YSZ) electrolyte films on a porous NiO-YSZ substrate for solid oxide fuel cells (SOFCs).
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Investigation of La 1−x Sm x−y Sr y CoO 3−δ cathode for intermediate temperature solid oxide fuel cells
TL;DR: In this paper, the authors showed that with the linear increase of y in LSSC, the maximum electrical conductivity of the corresponding samples does not alter linearly but reaches a peak when y ≥ 0.35, namely, when y = 0.40.
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Optimization of electrochemical performance of Ca3Co2O6 cathode on yttria-stabilized zirconia electrolyte for intermediate temperature solid oxide fuel cells
TL;DR: In this paper, the chemical compatibility of Ca 3 Co 2 O 6 (CCO) with yttria-stabilized zirconia (YSZ) electrolyte was investigated.
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Performance enhancement for solid oxide fuel cells using electrolyte surface modification
TL;DR: In this article, the yttria-stabilized zirconia electrolyte surface is properly modified to improve the performance of solid oxide fuel cells compared with conventional electrolytes, which can provide more active reaction sites and anchor better to the cathode layer, which is demonstrated in electrochemical impedance spectroscopy studies.