4.8 Article

Atomic Imaging of Subsurface Interstitial Hydrogen and Insights into Surface Reactivity of Palladium Hydrides

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 59, Issue 46, Pages 20348-20352

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202006562

Keywords

density functional calculations; iDPC-STEM; palladium hydrides; subsurface hydrogen

Funding

  1. Natural Science Foundation of China (NSFC) [51622103, 11874036]
  2. Guangdong Natural Science Foundation for Distinguished Young Scholars [2016A030306035]
  3. Basic Research Program of Shenzhen [JCYJ20170412171430026, JCYJ20190809145205497, JCYJ20170817161445322]
  4. Shenzhen Geim Graphene Center at the Tsinghua SIGS
  5. Local Innovative and Research Team Project of Guangdong Pearl River Talents Program [2017BT01N111]

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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 the first direct imaging of subsurface hydrogen atoms absorbed in Pd nanoparticles by using differentiated and integrated differential phase contrast within an 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. DFT 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.

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