---
_id: '63991'
abstract:
- lang: eng
  text: A series of 1 and 2 nm sized platinum nanoparticles (Pt-NPs) deposited on
    different support materials, namely, gamma-alumina (gamma-Al2O3), titanium dioxide
    (TiO2), silicon dioxide (SiO2) and fumed silica are investigated by solid-state
    NMR and dynamic nuclear polarization enhanced NMR spectroscopy (DNP). DNP signal
    enhancement factors up to 170 enable gaining deeper insight into the surface chemistry
    of Pt-NPs. Carbon monoxide is used as a probe molecule to analyze the adsorption
    process and the surface chemistry on the supported Pt-NPs. The studied systems
    show significant catalytic activity in carbon monoxide oxidation on their surface
    at room temperature. The underlying catalytic mechanism is the water-gas shift
    reaction. In the case of alumina as the support the produced CO2 reacts with the
    surface to form carbonate, which is revealed by solid-state NMR. A similar carbonate
    formation is also observed when physical mixtures of neat alumina with silica,
    fumed silica and titania supported Pt-NPs are studied.
author:
- first_name: V.
  full_name: Klimavicius, V.
  last_name: Klimavicius
- first_name: S.
  full_name: Neumann, S.
  last_name: Neumann
- first_name: S.
  full_name: Kunz, S.
  last_name: Kunz
- first_name: Torsten
  full_name: Gutmann, Torsten
  id: '118165'
  last_name: Gutmann
- first_name: G.
  full_name: Buntkowsky, G.
  last_name: Buntkowsky
citation:
  ama: Klimavicius V, Neumann S, Kunz S, Gutmann T, Buntkowsky G. Room temperature
    CO oxidation catalysed by supported Pt nanoparticles revealed by solid-state NMR
    and DNP spectroscopy. <i>Catalysis Science &#38; Technology</i>. 2019;9(14):3743–3752.
    doi:<a href="https://doi.org/10.1039/c9cy00684b">10.1039/c9cy00684b</a>
  apa: Klimavicius, V., Neumann, S., Kunz, S., Gutmann, T., &#38; Buntkowsky, G. (2019).
    Room temperature CO oxidation catalysed by supported Pt nanoparticles revealed
    by solid-state NMR and DNP spectroscopy. <i>Catalysis Science &#38; Technology</i>,
    <i>9</i>(14), 3743–3752. <a href="https://doi.org/10.1039/c9cy00684b">https://doi.org/10.1039/c9cy00684b</a>
  bibtex: '@article{Klimavicius_Neumann_Kunz_Gutmann_Buntkowsky_2019, title={Room
    temperature CO oxidation catalysed by supported Pt nanoparticles revealed by solid-state
    NMR and DNP spectroscopy}, volume={9}, DOI={<a href="https://doi.org/10.1039/c9cy00684b">10.1039/c9cy00684b</a>},
    number={14}, journal={Catalysis Science &#38; Technology}, author={Klimavicius,
    V. and Neumann, S. and Kunz, S. and Gutmann, Torsten and Buntkowsky, G.}, year={2019},
    pages={3743–3752} }'
  chicago: 'Klimavicius, V., S. Neumann, S. Kunz, Torsten Gutmann, and G. Buntkowsky.
    “Room Temperature CO Oxidation Catalysed by Supported Pt Nanoparticles Revealed
    by Solid-State NMR and DNP Spectroscopy.” <i>Catalysis Science &#38; Technology</i>
    9, no. 14 (2019): 3743–3752. <a href="https://doi.org/10.1039/c9cy00684b">https://doi.org/10.1039/c9cy00684b</a>.'
  ieee: 'V. Klimavicius, S. Neumann, S. Kunz, T. Gutmann, and G. Buntkowsky, “Room
    temperature CO oxidation catalysed by supported Pt nanoparticles revealed by solid-state
    NMR and DNP spectroscopy,” <i>Catalysis Science &#38; Technology</i>, vol. 9,
    no. 14, pp. 3743–3752, 2019, doi: <a href="https://doi.org/10.1039/c9cy00684b">10.1039/c9cy00684b</a>.'
  mla: Klimavicius, V., et al. “Room Temperature CO Oxidation Catalysed by Supported
    Pt Nanoparticles Revealed by Solid-State NMR and DNP Spectroscopy.” <i>Catalysis
    Science &#38; Technology</i>, vol. 9, no. 14, 2019, pp. 3743–3752, doi:<a href="https://doi.org/10.1039/c9cy00684b">10.1039/c9cy00684b</a>.
  short: V. Klimavicius, S. Neumann, S. Kunz, T. Gutmann, G. Buntkowsky, Catalysis
    Science &#38; Technology 9 (2019) 3743–3752.
date_created: 2026-02-07T15:47:21Z
date_updated: 2026-02-17T16:16:33Z
doi: 10.1039/c9cy00684b
extern: '1'
intvolume: '         9'
issue: '14'
keyword:
- Chemistry
- gamma-alumina
- hydrogenation
- silica
- c-13
- interactions
- metal-catalysts
- particle-size
- platinum nanoparticles
- sites
- surface
- water-gas shift
language:
- iso: eng
page: 3743–3752
publication: Catalysis Science & Technology
publication_identifier:
  issn:
  - 2044-4753
status: public
title: Room temperature CO oxidation catalysed by supported Pt nanoparticles revealed
  by solid-state NMR and DNP spectroscopy
type: journal_article
user_id: '100715'
volume: 9
year: '2019'
...
---
_id: '64053'
abstract:
- lang: eng
  text: The utilization and preparation of functional hybrid films for optical sensing
    applications and membranes is of utmost importance. In this work, we report the
    convenient and scalable preparation of self-crosslinking particle-based films
    derived by directed self-assembly of alkoxysilane-based cross-linkers as part
    of a core-shell particle architecture. The synthesis of well-designed monodisperse
    core-shell particles by emulsion polymerization is the basic prerequisite for
    subsequent particle processing via the melt-shear organization technique. In more
    detail, the core particles consist of polystyrene (PS) or poly(methyl methacrylate)
    (PMMA), while the comparably soft particle shell consists of poly(ethyl acrylate)
    (PEA) and different alkoxysilane-based poly(methacrylate)s. For hybrid film formation
    and convenient self-cross-linking, different alkyl groups at the siloxane moieties
    were investigated in detail by solid-state Magic-Angle Spinning Nuclear Magnetic
    Resonance (MAS, NMR) spectroscopy revealing different crosslinking capabilities,
    which strongly influence the properties of the core or shell particle films with
    respect to transparency and iridescent reflection colors. Furthermore, solid-state
    NMR spectroscopy and investigation of the thermal properties by differential scanning
    calorimetry (DSC) measurements allow for insights into the cross-linking capabilities
    prior to and after synthesis, as well as after the thermally and pressure-induced
    processing steps. Subsequently, free-standing and self-crosslinked particle-based
    films featuring excellent particle order are obtained by application of the melt-shear
    organization technique, as shown by microscopy (TEM, SEM).
author:
- first_name: S.
  full_name: Vowinkel, S.
  last_name: Vowinkel
- first_name: S.
  full_name: Paul, S.
  last_name: Paul
- first_name: Torsten
  full_name: Gutmann, Torsten
  id: '118165'
  last_name: Gutmann
- first_name: M.
  full_name: Gallei, M.
  last_name: Gallei
citation:
  ama: Vowinkel S, Paul S, Gutmann T, Gallei M. Free-Standing and Self-Crosslinkable
    Hybrid Films by Core-Shell Particle Design and Processing. <i>Nanomaterials</i>.
    2017;7(11):390. doi:<a href="https://doi.org/10.3390/nano7110390">10.3390/nano7110390</a>
  apa: Vowinkel, S., Paul, S., Gutmann, T., &#38; Gallei, M. (2017). Free-Standing
    and Self-Crosslinkable Hybrid Films by Core-Shell Particle Design and Processing.
    <i>Nanomaterials</i>, <i>7</i>(11), 390. <a href="https://doi.org/10.3390/nano7110390">https://doi.org/10.3390/nano7110390</a>
  bibtex: '@article{Vowinkel_Paul_Gutmann_Gallei_2017, title={Free-Standing and Self-Crosslinkable
    Hybrid Films by Core-Shell Particle Design and Processing}, volume={7}, DOI={<a
    href="https://doi.org/10.3390/nano7110390">10.3390/nano7110390</a>}, number={11},
    journal={Nanomaterials}, author={Vowinkel, S. and Paul, S. and Gutmann, Torsten
    and Gallei, M.}, year={2017}, pages={390} }'
  chicago: 'Vowinkel, S., S. Paul, Torsten Gutmann, and M. Gallei. “Free-Standing
    and Self-Crosslinkable Hybrid Films by Core-Shell Particle Design and Processing.”
    <i>Nanomaterials</i> 7, no. 11 (2017): 390. <a href="https://doi.org/10.3390/nano7110390">https://doi.org/10.3390/nano7110390</a>.'
  ieee: 'S. Vowinkel, S. Paul, T. Gutmann, and M. Gallei, “Free-Standing and Self-Crosslinkable
    Hybrid Films by Core-Shell Particle Design and Processing,” <i>Nanomaterials</i>,
    vol. 7, no. 11, p. 390, 2017, doi: <a href="https://doi.org/10.3390/nano7110390">10.3390/nano7110390</a>.'
  mla: Vowinkel, S., et al. “Free-Standing and Self-Crosslinkable Hybrid Films by
    Core-Shell Particle Design and Processing.” <i>Nanomaterials</i>, vol. 7, no.
    11, 2017, p. 390, doi:<a href="https://doi.org/10.3390/nano7110390">10.3390/nano7110390</a>.
  short: S. Vowinkel, S. Paul, T. Gutmann, M. Gallei, Nanomaterials 7 (2017) 390.
date_created: 2026-02-07T16:15:23Z
date_updated: 2026-02-17T16:12:54Z
doi: 10.3390/nano7110390
extern: '1'
intvolume: '         7'
issue: '11'
keyword:
- Materials Science
- Science & Technology - Other Topics
- solid-state nmr
- spectroscopy
- catalysts
- colloidal crystals
- colloids
- cross-linking
- elastomeric opal films
- emulsion polymerization
- gamma-methacryloxypropyltrimethoxysilane
- hybrid films
- melt-shear organization
- nanoparticles
- particle
- photons
- polymers
- processing
- self-assembly
- transition
language:
- iso: eng
page: '390'
publication: Nanomaterials
publication_identifier:
  issn:
  - 2079-4991
status: public
title: Free-Standing and Self-Crosslinkable Hybrid Films by Core-Shell Particle Design
  and Processing
type: journal_article
user_id: '100715'
volume: 7
year: '2017'
...
---
_id: '63920'
abstract:
- lang: eng
  text: Coordinatively unsaturated sites (CUS) present a key feature of alumina based
    catalysts as they are believed to act as Lewis-acid sites in heterogeneously catalyzed
    reactions. In the present study, the direct observation of active species on a
    fluoride-doped aluminum oxide catalyst is demonstrated. This new fluoride-doped
    aluminum oxide exhibits strong Lewis-acid sites and superior catalytic activity
    as compared to gamma-Al2O3. To emphasize the labile state of Lewis-acid sites,
    two distinctive states of the catalysts surface are addressed using H-1-Al-27
    cross polarization (CP) MAS NMR. On the one hand, the highly dehydrated and active
    state after calcination at 700 degrees C and on the other hand the rehydrated
    and catalytically inactive surface (produced by contact to air) are probed. These
    experiments revealed the presence of significant amounts of coordinatively unsaturated
    sites in the form of 4-and 5-fold coordinated Al-sites on the highly dehydrated
    surface. In contrast to this, the rehydrated sample exhibited a severely restructured
    surface caused by the chemisorption of H2O which is ’constituted in a manner that
    was proposed in earlier models for gamma-Al2O3 surfaces.
author:
- first_name: L.
  full_name: Ahrem, L.
  last_name: Ahrem
- first_name: G.
  full_name: Scholz, G.
  last_name: Scholz
- first_name: Torsten
  full_name: Gutmann, Torsten
  id: '118165'
  last_name: Gutmann
- first_name: B.
  full_name: Calvo, B.
  last_name: Calvo
- first_name: G.
  full_name: Buntkowsky, G.
  last_name: Buntkowsky
- first_name: E.
  full_name: Kemnitz, E.
  last_name: Kemnitz
citation:
  ama: Ahrem L, Scholz G, Gutmann T, Calvo B, Buntkowsky G, Kemnitz E. Direct Observation
    of Coordinatively Unsaturated Sites on the Surface of a Fluoride-Doped Alumina
    Catalyst. <i>Journal of Physical Chemistry C</i>. 2017;121(22):12206–12213. doi:<a
    href="https://doi.org/10.1021/acs.jpcc.7b02535">10.1021/acs.jpcc.7b02535</a>
  apa: Ahrem, L., Scholz, G., Gutmann, T., Calvo, B., Buntkowsky, G., &#38; Kemnitz,
    E. (2017). Direct Observation of Coordinatively Unsaturated Sites on the Surface
    of a Fluoride-Doped Alumina Catalyst. <i>Journal of Physical Chemistry C</i>,
    <i>121</i>(22), 12206–12213. <a href="https://doi.org/10.1021/acs.jpcc.7b02535">https://doi.org/10.1021/acs.jpcc.7b02535</a>
  bibtex: '@article{Ahrem_Scholz_Gutmann_Calvo_Buntkowsky_Kemnitz_2017, title={Direct
    Observation of Coordinatively Unsaturated Sites on the Surface of a Fluoride-Doped
    Alumina Catalyst}, volume={121}, DOI={<a href="https://doi.org/10.1021/acs.jpcc.7b02535">10.1021/acs.jpcc.7b02535</a>},
    number={22}, journal={Journal of Physical Chemistry C}, author={Ahrem, L. and
    Scholz, G. and Gutmann, Torsten and Calvo, B. and Buntkowsky, G. and Kemnitz,
    E.}, year={2017}, pages={12206–12213} }'
  chicago: 'Ahrem, L., G. Scholz, Torsten Gutmann, B. Calvo, G. Buntkowsky, and E.
    Kemnitz. “Direct Observation of Coordinatively Unsaturated Sites on the Surface
    of a Fluoride-Doped Alumina Catalyst.” <i>Journal of Physical Chemistry C</i>
    121, no. 22 (2017): 12206–12213. <a href="https://doi.org/10.1021/acs.jpcc.7b02535">https://doi.org/10.1021/acs.jpcc.7b02535</a>.'
  ieee: 'L. Ahrem, G. Scholz, T. Gutmann, B. Calvo, G. Buntkowsky, and E. Kemnitz,
    “Direct Observation of Coordinatively Unsaturated Sites on the Surface of a Fluoride-Doped
    Alumina Catalyst,” <i>Journal of Physical Chemistry C</i>, vol. 121, no. 22, pp.
    12206–12213, 2017, doi: <a href="https://doi.org/10.1021/acs.jpcc.7b02535">10.1021/acs.jpcc.7b02535</a>.'
  mla: Ahrem, L., et al. “Direct Observation of Coordinatively Unsaturated Sites on
    the Surface of a Fluoride-Doped Alumina Catalyst.” <i>Journal of Physical Chemistry
    C</i>, vol. 121, no. 22, 2017, pp. 12206–12213, doi:<a href="https://doi.org/10.1021/acs.jpcc.7b02535">10.1021/acs.jpcc.7b02535</a>.
  short: L. Ahrem, G. Scholz, T. Gutmann, B. Calvo, G. Buntkowsky, E. Kemnitz, Journal
    of Physical Chemistry C 121 (2017) 12206–12213.
date_created: 2026-02-07T08:56:18Z
date_updated: 2026-02-17T16:19:24Z
doi: 10.1021/acs.jpcc.7b02535
extern: '1'
intvolume: '       121'
issue: '22'
keyword:
- al-27 nmr
- characterization
- Chemistry
- cross-polarization
- dynamic nuclear-polarization
- eta-alumina
- gamma-alumina
- hydroxy fluorides
- ions
- Materials Science
- pentacoordinated al3+
- Science & Technology - Other Topics
- solid-state nmr
- spectroscopic
- structural insights
language:
- iso: eng
page: 12206–12213
publication: Journal of Physical Chemistry C
publication_identifier:
  issn:
  - 1932-7447
status: public
title: Direct Observation of Coordinatively Unsaturated Sites on the Surface of a
  Fluoride-Doped Alumina Catalyst
type: journal_article
user_id: '100715'
volume: 121
year: '2017'
...
