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Nanoporous Pd alloys with compositionally tunable hydrogen storage properties prepared by nanoparticle consolidation

  • Patrick J. Cappillino
  • , Joshua D. Sugar
  • , Michelle A. Hekmaty
  • , Benjamin W. Jacobs
  • , Vitalie Stavila
  • , Paul G. Kotula
  • , Jeffrey M. Chames
  • , Nancy Y. Yang
  • , David B. Robinson

Research output: Contribution to journal › Article › peer-review

32 Scopus citations

Abstract

Nanoporous palladium and palladium alloys are expected to have improved mass transport rates and cycle life compared to bulk materials for energy storage and other applications due to high ratios of surface area to metal volume. Preparation of such materials with high thermal stability and well-controlled metal composition, however, remains a challenge. This work describes a scalable, bottom-up technique for preparing nanoporous palladium alloys based on partial consolidation of dendrimer-encapsulated nanoparticles (DEN). Destabilization of a colloidal suspension of DEN and purification yields high surface area material (60-80 m 2 g -1) with a broad pore size distribution centered between 20 and 50 nm. This approach allows for precise tuning of product composition through adjustment of the composition of the precursor DEN. Nanoporous Pd 0.9Rh 0.1 alloys with uniform composition or with Rh enrichment at pore walls and grain boundaries have been prepared and these structures have been confirmed with high-spatial resolution, aberration corrected quantitative STEM-EDS. Compared to bulk alloys of the same nominal composition, the nanoporous bimetallics show much faster hydrogen uptake kinetics, and store hydrogen at much lower pressure. Pore structure remains intact to temperatures above 300 °C, suggesting that these materials will have long lifetimes at the temperatures used for hydrogen storage applications. © 2012 The Royal Society of Chemistry.
Original languageEnglish
Pages (from-to)14013-14022
Number of pages10
JournalJournal of Materials Chemistry
Volume22
Issue number28
DOIs
StatePublished - Jul 28 2012
Externally publishedYes

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