Special Issue "Noble Metal Nanoparticles in Catalysis"

A special issue of Nanomaterials (ISSN 2079-4991).

Deadline for manuscript submissions: 30 November 2017

Special Issue Editors

Guest Editor
Prof. Dr. Ioannis N. Lykakis

Aristotle University of Thessaloniki, Department of Chemistry, University campus 54124, Thessaloniki, Greece
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Phone: +30 2310 997871
Fax: +30 2310 997871
Interests: catalysis, photocatalysis, green organic transformations, noble metal nanoparticles, polyoxometalate hybrids, kinetic studies
Guest Editor
Prof. Dr. Gerasimos S. Armatas

Department of Materials Science and Technology, University of Crete, Heraklion, 71003, Greece
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Phone: +30 2810 545004
Fax: +30 2810 545197
Interests: mesoporous materials; semiconductor nanoparticles, self-assembly, photocatalysis, water splitting; catalysis

Special Issue Information

Dear Colleagues,

Since the beginning of the millennium, the field of noble-metal nanoparticle catalysis has emerged as one of the top subjects in scientific community. The spectacular properties of these nanoscale elements, such as tunable surface plasmon and photo thermal effects, excellent resistant to corrosion and air oxidation and lesser cytotoxicity, as well as their easy experimental realization make them excellent candidates for biological, opto-electronic and environmental related applications. Among them, Au, Pt and Ag nanoparticles can be taken as examples to demonstrate the relevance and diversity of catalytic functions that can be sustained by noble metals in general. In this Special Issue on “Noble Metal Nanoparticles in Catalysis” a series of original contributions made by leading experts in the field is expected to highlight recent advances and future perspectives of this emerging topic. These research articles are intended to cover various aspects of noble-metal nanoparticle science and technology, including synthesis, structural characterization, theoretical study and catalytic applications in a diverse range of reactions ranging from total synthesis of natural and pharmaceutical products, to water treatment and medicinal area, and to new organic transformations.

Prof. Dr. Ioannis N. Lykakis
Prof. Dr. Gerasimos S.Armatas
Guest Editors

Manuscript Submission Information

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Keywords

  • Gold nanoparticles
  • Silver nanoparticles
  • Platinum nanoparticles
  • Catalysis
  • Green chemistry
  • Nanostructured materials
  • Hydrogen generation
  • Redox organic trasnformations
  • Biological and enviromental applications
  • Medicinal applications

Published Papers (4 papers)

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Research

Open AccessArticle Synthesis of Au-Pd Bimetallic Nanoflowers for Catalytic Reduction of 4-Nitrophenol
Nanomaterials 2017, 7(9), 239; doi:10.3390/nano7090239
Received: 19 July 2017 / Revised: 6 August 2017 / Accepted: 22 August 2017 / Published: 26 August 2017
Cited by 1 | PDF Full-text (3391 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
Due to the great potential to improve catalytic performance, gold (Au) and palladium (Pd) bimetallic catalysts have prompted structure-controlled synthesis of Au-Pd nanoalloys bounded by high-index facets. In this work, we prepared Au-Pd bimetallic nanoflowers (NFs) with a uniform size, well-defined dendritic morphology,
[...] Read more.
Due to the great potential to improve catalytic performance, gold (Au) and palladium (Pd) bimetallic catalysts have prompted structure-controlled synthesis of Au-Pd nanoalloys bounded by high-index facets. In this work, we prepared Au-Pd bimetallic nanoflowers (NFs) with a uniform size, well-defined dendritic morphology, and homogeneous alloy structure in an aqueous solution by seed-mediated synthesis. The prepared bimetallic NFs were fully characterized using a combination of transmission electron microscopy, Ultraviolet-Visible (UV-vis) spectroscopy, inductively coupled plasma optical emission spectroscopy, and cyclic voltammetry measurements. The catalytic activities of the prepared Au-Pd nanoparticles for 4-nitrophenol reduction were also investigated, and the activities are in the order of Au@Pd NFs > Au-Pd NFs (Au1Pd1 core) > Au-Pd NFs (Au core), which could be related to the content and exposed different reactive surfaces of Pd in alloys. This result clearly demonstrates that the superior activities of Au-Pd alloy nanodendrites could be attributed to the synergy between Au and Pd in catalysts. Full article
(This article belongs to the Special Issue Noble Metal Nanoparticles in Catalysis)
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Open AccessArticle Radiolytic Synthesis of Pt-Particle/ABS Catalysts for H2O2 Decomposition in Contact Lens Cleaning
Nanomaterials 2017, 7(9), 235; doi:10.3390/nano7090235
Received: 29 June 2017 / Accepted: 21 August 2017 / Published: 23 August 2017
PDF Full-text (3466 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
A container used in contact lens cleaning requires a Pt plating weight of 1.5 mg for H2O2 decomposition although Pt is an expensive material. Techniques that decrease the amount of Pt are therefore needed. In this study, Pt nanoparticles instead
[...] Read more.
A container used in contact lens cleaning requires a Pt plating weight of 1.5 mg for H2O2 decomposition although Pt is an expensive material. Techniques that decrease the amount of Pt are therefore needed. In this study, Pt nanoparticles instead of Pt plating film were supported on a substrate of acrylonitrile–butadiene–styrene copolymer (ABS). This was achieved by the reduction of Pt ions in an aqueous solution containing the ABS substrate using high-energy electron-beam irradiation. Pt nanoparticles supported on the ABS substrate (Pt-particle/ABS) had a size of 4–10 nm. The amount of Pt required for Pt-particle/ABS was 250 times less than that required for an ABS substrate covered with Pt plating film (Pt-film/ABS). The catalytic activity for H2O2 decomposition was estimated by measuring the residual H2O2 concentration after immersing the catalyst for 360 min. The Pt-particle/ABS catalyst had a considerably higher specific catalytic activity for H2O2 decomposition than the Pt-film/ABS catalyst. In addition, sterilization performance was estimated from the initial rate of H2O2 decomposition over 60 min. The Pt-particle/ABS catalyst demonstrated a better sterilization performance than the Pt-film/ABS catalyst. The difference between Pt-particle/ABS and Pt-film/ABS was shown to reflect the size of the O2 bubbles formed during H2O2 decomposition. Full article
(This article belongs to the Special Issue Noble Metal Nanoparticles in Catalysis)
Figures

Open AccessArticle First-Principles Study of Structural, Electronic and Magnetic Properties of Metal-Centered Tetrahexahedral V15+ Cluster
Nanomaterials 2017, 7(7), 164; doi:10.3390/nano7070164
Received: 30 May 2017 / Revised: 22 June 2017 / Accepted: 27 June 2017 / Published: 30 June 2017
PDF Full-text (1536 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The V-centered bicapped hexagonal antiprism structure (A), as the most stable geometry of the cationic V15+ cluster, is determined by using infrared multiple photo dissociation (IR-MPD) in combination with density functional theory computations. It is found that the A
[...] Read more.
The V-centered bicapped hexagonal antiprism structure (A), as the most stable geometry of the cationic V15+ cluster, is determined by using infrared multiple photo dissociation (IR-MPD) in combination with density functional theory computations. It is found that the A structure can be stabilized by 18 delocalized 3c-2e σ-bonds on outer V3 triangles of the bicapped hexagonal antiprism surface and 12 delocalized 4c-2e σ-bonds on inner trigonal pyramidal V4 moiety, and the features are related to the strong p-d hybridization of the cluster. The total magnetic moments on the cluster are predicted to be 2.0 µB, which come mainly from the central vanadium atom. Full article
(This article belongs to the Special Issue Noble Metal Nanoparticles in Catalysis)
Figures

Open AccessArticle Synthesis of Pt@TiO2@CNTs Hierarchical Structure Catalyst by Atomic Layer Deposition and Their Photocatalytic and Photoelectrochemical Activity
Nanomaterials 2017, 7(5), 97; doi:10.3390/nano7050097
Received: 1 March 2017 / Revised: 20 April 2017 / Accepted: 26 April 2017 / Published: 29 April 2017
Cited by 1 | PDF Full-text (3100 KB) | HTML Full-text | XML Full-text
Abstract
Pt@TiO2@CNTs hierarchical structures were prepared by first functionalizing carbon nanotubes (CNTs) with nitric acid at 140 °C. Coating of TiO2 particles on the CNTs at 300 °C was then conducted by atomic layer deposition (ALD). After the TiO2@CNTs structure was fabricated, Pt particles
[...] Read more.
Pt@TiO2@CNTs hierarchical structures were prepared by first functionalizing carbon nanotubes (CNTs) with nitric acid at 140 °C. Coating of TiO2 particles on the CNTs at 300 °C was then conducted by atomic layer deposition (ALD). After the TiO2@CNTs structure was fabricated, Pt particles were deposited on the TiO2 surface as co-catalyst by plasma-enhanced ALD. The saturated deposition rates of TiO2 on a-CNTs were 1.5 Å/cycle and 0.4 Å/cycle for substrate-enhanced process and linear process, respectively. The saturated deposition rate of Pt on TiO2 was 0.39 Å/cycle. The photocatalytic activities of Pt@TiO2@CNTs hierarchical structures were higher than those without Pt co-catalyst. The particle size of Pt on TiO2@CNTs was a key factor to determine the efficiency of methylene blue (MB) degradation. The Pt@TiO2@CNTs of 2.41 ± 0.27 nm exhibited the best efficiency of MB degradation. Full article
(This article belongs to the Special Issue Noble Metal Nanoparticles in Catalysis)
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