Adsorption, Ordering, and Metalation of Porphyrins on MgO Nanocube Surfaces: The Directional Role of Carboxylic Anchoring Groups

Beitrag in einer Fachzeitschrift
(Originalarbeit)


Details zur Publikation

Autorinnen und Autoren: Schneider J, Kollhoff F, Schindler T, Bichlmaier S, Bernardi J, Unruh T, Libuda J, Berger T, Diwald O
Zeitschrift: Journal of Physical Chemistry C
Verlag: AMER CHEMICAL SOC
Jahr der Veröffentlichung: 2016
Band: 120
Heftnummer: 47
Seitenbereich: 26879-26888
ISSN: 1932-7447
eISSN: 1932-7455


Abstract


The understanding of porphyrin adsorption on oxide nanoparticles including knowledge about coverages and adsorbate geometries is a prerequisite for the improvement and optimization of hybrid materials. The combination of molecular spectroscopies with small-angle X-ray scattering provides molecular insights into porphyrin adsorption on MgO nanocube dispersions in organic solvents. In particular, we address the influence of terminal carboxyl groups on the adsorption of free base porphyrins, on their chemical binding, on the metalation reaction as well as on the coverage and orientation of adsorbate molecules. We compare the free base form 5,10,15,20-tetraphenyl-21,23H-porphyrin (2HTPP) with the carboxyl-functionalized 5,10,15,20-tetrakis(4-carboxyphenyl)-21,23H-porphyrin (2HTCPP) and show that without carboxylic anchoring groups the free base form metalates on the nanocube surface and adopts a flat-lying adsorbate geometry. The saturation limit for flat-lying adsorption on nanocubes with an average edge length of 6 nm corresponds to 90 14 molecules per particle. This limit is surpassed when 2HTCPP molecules attach via their terminal carboxyl groups to the surface. The resulting upright adsorption geometry suppresses self-metalation, on the one hand, and allows for much higher porphyrin coverages, on the other (at porphyrin concentrations in the stock solution of 2 X 10(-2) mol.L-1). UV-vis diffuse reflectance results are perfectly consistent with conclusions from SAXS data analysis. The experiments reveal concentration dependent 2HTCPP coverages in the range between 0.4 to 1.9 molecules nm(-2) which correspond to the formation of a shell of upright standing porphyrin molecules around the MgO nanocubes. In contrast, after adsorption and metalation of nonfunctionalized 2HTPP the resulting porphyrin shells are in the range of a tenth of a nanometer and thus too thin to be captured by SAXS measurements. Related insights advance our opportunities to prepare well-defined nanohybrids containing highly organized porphyrin films.



FAU-Autorinnen und Autoren / FAU-Herausgeberinnen und Herausgeber

Kollhoff, Fabian
Lehrstuhl für Physikalische Chemie II
Libuda, Jörg Prof. Dr.
Professur für Physikalische Chemie
Schindler, Torben
Lehrstuhl für Kristallographie und Strukturphysik
Unruh, Tobias Prof. Dr.
Professur für Nanomaterialcharakterisierung (Streumethoden)


Zusätzliche Organisationseinheit(en)
Graduiertenkolleg 1896/2 In situ Mikroskopie mit Elektronen, Röntgenstrahlen und Rastersonden
Exzellenz-Cluster Engineering of Advanced Materials
Interdisziplinäres Zentrum, Center for Nanoanalysis and Electron Microscopy (CENEM)


Einrichtungen weiterer Autorinnen und Autoren

Universität Salzburg (Paris Lodron Universität Salzburg)
Vienna University of Technology


Forschungsbereiche

D Catalytic Materials
Exzellenz-Cluster Engineering of Advanced Materials
A1 Functional Particle Systems
Exzellenz-Cluster Engineering of Advanced Materials
A2 Nanoanalysis and Microscopy
Exzellenz-Cluster Engineering of Advanced Materials


Zitierweisen

APA:
Schneider, J., Kollhoff, F., Schindler, T., Bichlmaier, S., Bernardi, J., Unruh, T.,... Diwald, O. (2016). Adsorption, Ordering, and Metalation of Porphyrins on MgO Nanocube Surfaces: The Directional Role of Carboxylic Anchoring Groups. Journal of Physical Chemistry C, 120(47), 26879-26888. https://dx.doi.org/10.1021/acs.jpcc.6b08956

MLA:
Schneider, Johannes, et al. "Adsorption, Ordering, and Metalation of Porphyrins on MgO Nanocube Surfaces: The Directional Role of Carboxylic Anchoring Groups." Journal of Physical Chemistry C 120.47 (2016): 26879-26888.

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Zuletzt aktualisiert 2019-06-08 um 09:04