| Literature DB >> 32621778 |
Bingqing Lin1, Xi Wu1, Lin Xie2, Yongqiang Kang3, Hongda Du4, Feiyu Kang5, Jia Li5, Lin Gan6.
Abstract
Resolving interstitial hydrogen atoms at the surfaces and interfaces is crucial for understanding the mechanical and physicochemical properties of metal hydrides. Although palladium (Pd) hydrides hold important applications in hydrogen storage and electrocatalysis, the atomic position of interstitial hydrogen at Pd hydride near surfaces still remains undetermined. We report here the first direct imaging of subsurface hydrogen atoms absorbed in Pd nanoparticles by using differentiated and integrated differential phase contrast within aberration-corrected scanning transmission electron microscope. In contrast to the well-established octahedral interstitial sites for hydrogen in the bulk, subsurface hydrogen atoms are directly identified to occupy the tetrahedral interstices. Density functional theory calculations show that the amount and the occupation type of subsurface hydrogen atoms play an indispensable role in fine-tuning the electronic structure and associated chemical reactivity of the Pd surface.Entities:
Keywords: density functional theory calculations; iDPC-STEM; palladium hydrides; subsurface hydrogen
Year: 2020 PMID: 32621778 DOI: 10.1002/anie.202006562
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336