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Hydrogen absorption and desorption on Rh nanoparticles revealed by in situ dispersive X-ray absorption fine structure spectroscopy.


ABSTRACT: To unveil the origin of the hydrogen-storage properties of rhodium nanoparticles (Rh NPs), we investigated the dynamical structural change of Rh NPs using in situ dispersive X-ray absorption fine structure spectroscopy (XAFS). The variation of the Rh-Rh interatomic distance and Debye-Waller factor of Rh NPs with a size of 4.0 and 10.5 nm during hydrogen absorption and desorption suggested that they have a different mechanism for hydrogen absorption, which is that the hydrogen absorption on the inner site has a greater contribution than that on a surface for Rh 4.0 nm. In the case of Rh 10.5 nm, it is opposed to Rh 4.0 nm. This study demonstrates a powerful in situ XAFS method for observing small local structural changes of metal nanoparticles and its importance for understanding of the hydrogen-absorption properties of Rh NPs with an interesting hydrogenation mechanism.

SUBMITTER: Song C 

PROVIDER: S-EPMC9054127 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Hydrogen absorption and desorption on Rh nanoparticles revealed by <i>in situ</i> dispersive X-ray absorption fine structure spectroscopy.

Song Chulho C   Seo Okkyun O   Matsumura Daiju D   Hiroi Satoshi S   Cui Yi-Tao YT   Kim Jaemyung J   Chen Yanna Y   Tayal Akhil A   Kusada Kohei K   Kobayashi Hirokazu H   Kitagawa Hiroshi H   Sakata Osami O  

RSC advances 20200526 34


To unveil the origin of the hydrogen-storage properties of rhodium nanoparticles (Rh NPs), we investigated the dynamical structural change of Rh NPs using <i>in situ</i> dispersive X-ray absorption fine structure spectroscopy (XAFS). The variation of the Rh-Rh interatomic distance and Debye-Waller factor of Rh NPs with a size of 4.0 and 10.5 nm during hydrogen absorption and desorption suggested that they have a different mechanism for hydrogen absorption, which is that the hydrogen absorption o  ...[more]

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