Mechanism of Hydrogen Storage and Structural Transformation in Bimetallic Pd-Pt Nanoparticles

Akhil Tayal, Okkyun Seo, Jaemyung Kim, Hirokazu Kobayashi, Tomokazu Yamamoto, Syo Matsumura, Hiroshi Kitagawa, Osami Sakata

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)


The hydrogen storage capacity of Pd nanoparticles (NPs) decreases as the particles become smaller; however, this reduced capacity is ameliorated by addition of Pt. In the present work, the hydrogen storage mechanism and structural transformations of core (Pd)-shell (Pt) (CS) and solid-solution (SS) NPs during hydrogen absorption and desorption (PHAD) processes are investigated. In situ X-ray absorption spectroscopy measurements were performed to study the evolution of electronic and local structures around Pd and Pt during PHAD. Under ambient conditions, Pd and Pt have distinct local structures. The Pd atomic pairs are more strained in CS NPs than in SS NPs. A similar behavior has been seen in CS NPs after PHAD. The Pd K-edge extended X-ray absorption fine structure data indicate that in CS and SS NPs a substantial fraction of the signal derives from Pd-Pd atomic pairs, indicating that Pd clusters remain present even after PHAD. PHAD causes a rearrangement of the interfacial structure, which becomes homogeneously distributed. The higher coverage of active bimetallic sites results in a higher observed hydrogen storage capacity in the SS phase.

Original languageEnglish
Pages (from-to)23502-23512
Number of pages11
JournalACS Applied Materials and Interfaces
Issue number20
Publication statusPublished - May 26 2021

All Science Journal Classification (ASJC) codes

  • General Materials Science


Dive into the research topics of 'Mechanism of Hydrogen Storage and Structural Transformation in Bimetallic Pd-Pt Nanoparticles'. Together they form a unique fingerprint.

Cite this