Direct visualization of hydrogen absorption dynamics in individual palladium nanoparticles

Tarun C. Narayan, Fariah Hayee, Andrea Baldi, Ai Leen Koh, Robert Sinclair, Jennifer A. Dionne

Research output: Contribution to JournalArticleAcademicpeer-review


Many energy storage materials undergo large volume changes during charging and discharging. The resulting stresses often lead to defect formation in the bulk, but less so in nanosized systems. Here, we capture in real time the mechanism of one such transformation-the hydrogenation of single-crystalline palladium nanocubes from 15 to 80 nm-to better understand the reason for this durability. First, using environmental scanning transmission electron microscopy, we monitor the hydrogen absorption process in real time with 3 nm resolution. Then, using dark-field imaging, we structurally examine the reaction intermediates with 1 nm resolution. The reaction proceeds through nucleation and growth of the new phase in corners of the nanocubes. As the hydrogenated phase propagates across the particles, portions of the lattice misorient by 1.5%, diminishing crystal quality. Once transformed, all the particles explored return to a pristine state. The nanoparticles' ability to remove crystallographic imperfections renders them more durable than their bulk counterparts.

Original languageEnglish
Article number14020
JournalNature Communications
Publication statusPublished - 16 Jan 2017


FundersFunder number
Directorate for Mathematical and Physical Sciences1151231


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