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The electrochemical production of HO via the two-electron oxygen-reduction reaction (2e ORR) has been actively studied using systems with atomically dispersed metal-nitrogen-carbon (M-N-C) structures. However, the development of well-defined M-N-C structures that restrict the migration and agglomeration of single-metal sites remains elusive. Herein, we demonstrate a Langmuir-Blodgett (LB) monolayer of cobalt phthalocyanine (CoPc) on monolayer graphene (LB CoPc/G) as a single-metal catalyst for the 2e ORR. The as-prepared CoPc LB monolayer has a β-form crystalline structure with a lattice space for the facile adsorption of oxygen molecules on the cobalt active sites. The CoPc LB monolayer system provides highly exposed Co atoms in a well-defined structure without agglomeration, resulting in significantly improved catalytic activity, which is manifested by a very high HO production rate per catalyst (31.04 mol g h) and TOF (36.5 s) with constant production stability for 24 hours. To the best of our knowledge, the CoPc LB monolayer system exhibits the highest HO production rate per active site. This fundamental study suggests that an LB monolayer of molecules with single-metal atoms as a well-defined structure works for single-atom catalysts.
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http://dx.doi.org/10.1021/acsnano.3c08424 | DOI Listing |
J Mater Chem C Mater
August 2025
Institute of Applied Physics, TU Wien 1040 Vienna Austria
Well-ordered organic molecular layers on oxide surfaces are key for organic electronics. Using a combination of scanning tunneling microscopy (STM) and non-contact atomic force microscopy (nc-AFM) we probe the structures of copper phthalocyanine (CuPc) on InO, a model for a prototypical transparent conductive oxide (TCO). These scanning-probe images allow the direct determination of the adsorption site and distortions of the molecules, which are corroborated by DFT calculations.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2024
School of Engineering, Mackenzie Presbyterian University, São Paulo 01302-907, Brazil.
Understanding the interfacial electronic structures of organic semiconductor phthalocyanines (MePc) and graphene is essential for their practical application in various fields. In this study, we investigated the electronic structure and the tuning of the work function of free metal phthalocyanine (Pc4), cobalt phthalocyanine (CoPc), and copper phthalocyanine (CuPc) molecules deposited on a graphene monolayer using X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS). We found that the functionalization of MePc molecules induces p-doping to the graphene substrate due to the charge transfer mechanism with the MePc molecule.
View Article and Find Full Text PDFACS Nano
December 2023
Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), 50 UNIST-gil, Ulsan 44919, Republic of Korea.
The electrochemical production of HO via the two-electron oxygen-reduction reaction (2e ORR) has been actively studied using systems with atomically dispersed metal-nitrogen-carbon (M-N-C) structures. However, the development of well-defined M-N-C structures that restrict the migration and agglomeration of single-metal sites remains elusive. Herein, we demonstrate a Langmuir-Blodgett (LB) monolayer of cobalt phthalocyanine (CoPc) on monolayer graphene (LB CoPc/G) as a single-metal catalyst for the 2e ORR.
View Article and Find Full Text PDFJ Am Chem Soc
November 2022
CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing100190, China.
We report herein the electrochemical scanning tunneling microscopy (ECSTM) study on the synergistic effect of Mg in CO reduction reaction (CORR) catalyzed by cobalt phthalocyanine (CoPc). ECSTM measurement molecularly resolves the self-assembled CoPc monolayer on the Au(111) substrate. In the CO environment, high-contrast species are observed in the adlayer and assigned to the CO adsorption on CoPc.
View Article and Find Full Text PDFACS Appl Mater Interfaces
May 2022
Johannes Kepler University, Institute of Experimental Physics, Surface Science Division, Altenberger Strasse 69, 4040 Linz, Austria.
We report an in situ study of the thin-film growth of cobalt-phthalocyanine on Ag(100) surfaces using photoelectron emission microscopy (PEEM) and the Anderson method. Based on the Fowler-DuBridge theory, we were able to correlate the evolution of the mean electron yield acquired with PEEM for coverages up to two molecular layers of cobalt-phthalocyanine to the global work function changes measured with the Anderson method. For coverages above two monolayers, the transients measured with the Anderson method and those obtained with PEEM show different trends.
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