An in situ XAS study of the activation of precursor-dependent Pd nanoparticles. Issue 18 (26th April 2018)
- Record Type:
- Journal Article
- Title:
- An in situ XAS study of the activation of precursor-dependent Pd nanoparticles. Issue 18 (26th April 2018)
- Main Title:
- An in situ XAS study of the activation of precursor-dependent Pd nanoparticles
- Authors:
- Lopes, Christian W.
Cerrillo, Jose L.
Palomares, Antonio E.
Rey, Fernando
Agostini, Giovanni - Abstract:
- Abstract : The activation of precursor-dependent Pd nanoparticles was comprehensively followed by in situ X-ray absorption spectroscopy on two inorganic supports for rationalizing the final catalytic activity. Abstract : The activation of precursor-dependent Pd nanoparticles was comprehensively followed by in situ X-ray absorption spectroscopy on two inorganic supports for rationalizing the final catalytic activity. Two series of Pd-based catalysts (7 wt% Pd) were prepared by impregnation of γ-Al2 O3 and activated carbon supports varying the metal precursor (Pd(NO3 )2, PdCl2 and Pd(OAc)2 ). The most relevant physicochemical properties of the studied catalysts were determined by several techniques including ICP-OES, XRD, N2 adsorption and XAS. The results indicate that the thermal stability of the metal precursor plays an important role in the size and speciation of the formed Pd nanoparticles after the activation process. The Cl-based precursor, which presents high thermal stability, passes through a PdO x Cl y mixed phase when submitted to calcination on Pd/Al2 O3 and leaves Cl-species after metal reduction on Pd/C (which can be detrimental to catalytic reactions). Differently, Pd(OAc)2 and Pd(NO3 )2 promote the formation of larger species due to different precursor decomposition pathways. Ordered PdO is observed even before calcination when Pd(NO3 )2 was used as a metallic source, which translates into large nanoparticles after reduction in H2 . By using the averageAbstract : The activation of precursor-dependent Pd nanoparticles was comprehensively followed by in situ X-ray absorption spectroscopy on two inorganic supports for rationalizing the final catalytic activity. Abstract : The activation of precursor-dependent Pd nanoparticles was comprehensively followed by in situ X-ray absorption spectroscopy on two inorganic supports for rationalizing the final catalytic activity. Two series of Pd-based catalysts (7 wt% Pd) were prepared by impregnation of γ-Al2 O3 and activated carbon supports varying the metal precursor (Pd(NO3 )2, PdCl2 and Pd(OAc)2 ). The most relevant physicochemical properties of the studied catalysts were determined by several techniques including ICP-OES, XRD, N2 adsorption and XAS. The results indicate that the thermal stability of the metal precursor plays an important role in the size and speciation of the formed Pd nanoparticles after the activation process. The Cl-based precursor, which presents high thermal stability, passes through a PdO x Cl y mixed phase when submitted to calcination on Pd/Al2 O3 and leaves Cl-species after metal reduction on Pd/C (which can be detrimental to catalytic reactions). Differently, Pd(OAc)2 and Pd(NO3 )2 promote the formation of larger species due to different precursor decomposition pathways. Ordered PdO is observed even before calcination when Pd(NO3 )2 was used as a metallic source, which translates into large nanoparticles after reduction in H2 . By using the average coordination numbers of Pd species obtained from EXAFS data of the as-reduced catalysts, a correlation was observed comparing the three precursors: PdCl2 generates smaller nanoparticles than Pd(OAc)2, which in turn generates smaller nanoparticles than Pd(NO3 )2, regardless of the support used for catalyst preparation. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 20:Issue 18(2018)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 20:Issue 18(2018)
- Issue Display:
- Volume 20, Issue 18 (2018)
- Year:
- 2018
- Volume:
- 20
- Issue:
- 18
- Issue Sort Value:
- 2018-0020-0018-0000
- Page Start:
- 12700
- Page End:
- 12709
- Publication Date:
- 2018-04-26
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8cp00517f ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6903.xml