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論文

Wetting induced oxidation of Pt-based nano catalysts revealed by ${{it in situ}}$ high energy resolution X-ray absorption spectroscopy

Cui, Y.-T.*; 原田 慈久*; 丹羽 秀治*; 畑中 達也*; 中村 直樹*; 安藤 雅樹*; 吉田 稔彦*; 石井 賢司*; 松村 大樹; 陰地 宏*; et al.

Scientific Reports (Internet), 7(1), p.1482_1 - 1482_8, 2017/05

https://doi.org/10.1038/s41598-017-00639-1
 被引用回数：19 パーセンタイル：49.58(Multidisciplinary Sciences)

In situ high energy resolution fluorescence detection X-ray absorption spectroscopy (HERFD-XAS) was used to systematically evaluate interactions of H$$_{2}$$O and O$$_{2}$$ adsorbed on Pt and Pt$$_{3}$$Co nanoparticle catalysts in different particle sizes. The systematic increase in oxidation due to adsorption of different species (H$$_{2}$$O adsorption $$<$$ O$$_{2}$$ adsorption $$<$$ O$$_{2}$$ + H$$_{2}$$O coadsorption) suggests that cooperative behavior between O$$_{2}$$ and H$$_{2}$$O adsorptions is responsible for the overpotential induced by hydrated species in fuel cells. From the alloying and particle size effects, it is found that both strength of O$$_{2}$$/H$$_{2}$$O adsorption and their cooperative effect upon coadsorption are responsible for the specific activity of Pt catalysts.

論文

Electronic structure of Pt and Pt-Co nanoparticles with O$$_{2}$$ and O$$_{2}$$/H$$_{2}$$O adsorption revealed by in situ XAFS and hard X-ray photoelectron spectroscopy

Cui, Y.*; 原田 慈久*; 畑中 達也*; 中村 直樹*; 安藤 雅樹*; 吉田 稔彦*; 池永 英司*; 石井 賢司*; 松村 大樹; Li, R.*; et al.

ECS Transactions, 72(8), p.131 - 136, 2016/10

https://doi.org/10.1149/07208.0131ecst
 被引用回数：1 パーセンタイル：48.91(Electrochemistry)

The electronic structures of Pt and Pt-Co nanoparticles with O$$_{2}$$ adsorption and O$$_{2}$$/H$$_{2}$$O co-adsorption were investigated by in situ hard X-ray photoelectron spectroscopy (HAXPES) and in situ high resolution fluorescence detection X-ray absorption spectroscopy (HERFD-XAS) to clarify the effects of water adsorption on fuel cell cathode catalysis surface. The experimental results suggest that under the pressure of 1 mbar, the adsorption of H$$_{2}$$O hinders the successive O$$_{2}$$ adsorption on Pt surface, while under the pressure of 1 bar, the adsorption of H$$_{2}$$O enhances the adsorption of O$$_{2}$$ on Pt surface. This water effect is found to be more significant on Pt surface than on Pt-Co surface. These results would be helpful to understand how the water affects the fuel cell performance and why Pt-Co nanoparticles show higher oxygen reduce reaction (ORR) activity than Pt nanoparticles.

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