4.8 Article

Single Pd atoms in activated carbon fibers and their contribution to hydrogen storage

期刊

CARBON
卷 49, 期 12, 页码 4050-4058

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2011.05.021

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  1. United States Government [DE-AC05-00OR22725]
  2. United States Department of Energy
  3. US Department of Energy, Basic Energy Sciences, Materials Sciences and Engineering Division
  4. Scientific User Facilities Division, DOE Office of Basic Energy Sciences
  5. UC Davis
  6. National Energy Research Scientific Computing Center (NERSC)
  7. Office of Science of US Department of Energy [DE-AC02-05CH11231]

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Palladium-modified activated carbon fibers (Pd-ACF) were synthesized by melt-spinning, carbonization and activation of an isotropic pitch carbon precursor premixed with an organometallic Pd compound. The hydrogen uptake at 25 degrees C and 20 bar on Pd-ACF exceeded the expected capacity based solely on Pd hydride formation and hydrogen physisorption on the microporous carbon support. Aberration-corrected scanning transmission electron microscopy (STEM) with sub-Angstrom spatial resolution provided unambiguous identification of isolated Pd atoms occurring in the carbon matrix that coexist with larger Pd particles. First principles calculations revealed that each single Pd atom can form Kubas-type complexes by binding up to three H-2 molecules in the pressure range of adsorption measurements. Based on Pd atom concentration determined from STEM images, the contribution of various mechanisms to the excess hydrogen uptake measured experimentally was evaluated. With consideration of Kubas binding as a viable mechanism (along with hydride formation and physisorption to carbon support) the role of hydrogen spillover in this system may be smaller than previously thought. (C) 2011 Elsevier Ltd. All rights reserved.

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