Morphological Effects on Catalytic Reactions

A special issue of Catalysts (ISSN 2073-4344). This special issue belongs to the section "Catalytic Reaction Engineering".

Deadline for manuscript submissions: closed (30 September 2023) | Viewed by 6081

Special Issue Editors


E-Mail Website
Guest Editor
FNRS, University of Liège, Liège, Belgium
Interests: photocatalysis; adsorption; water treatment; TiO2; SiO2; coating; sol-gel; nanomaterials
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor Assistant
Department of Chemical Engineering, University of Liège, Liège, Belgium
Interests: SiO2; catalysis; sol-gel; nanomaterials; SAXS; ordered mesoporous materials; porosity

Special Issue Information

Dear Colleagues,

It is now well-established that catalytic activity is tremendously affected by the morphological properties of catalytic materials. In its common definition, morphology encompasses both the geometrical structure as well as the chemical nature of a material. Therefore, it is usually more convenient to characterize catalytic activity in terms of apparent and intrinsic activity, each of which are influenced by the geometry and by the chemistry of the catalytic material differently.

Since catalysis is a purely kinetic phenomenon (it does not change the thermodynamical equilibrium of a given reaction), it is known that any changes to the mass or heat transfer would induce notable modifications on the apparent activity. For instance, so-called heterogenized homogeneous catalysts have often shown a drastic decrease in activity that has been attributed to mass transfer, although their intrinsic activity remained unaltered. In some rare cases, intrinsic activity may show an increase, which is the case with some of the enzymes confined in inorganic materials. Additionally, another well-known example concerns the size, the dispersion, and the chemical nature of metal nanoparticles on a support. During the catalysis of automotive exhaust, it is desirable to only dissociate the NO molecule from a mix of NO and CO gas, transfer the O atom, and ensure that N2 and CO2 are at the end. The intrinsic activity is, accordingly, directly influenced by the metal and, because of a compromise between weak and strong dissociative adsorption, it will work better with Rh and Pd than it would with Pt, Fe, Co, Ni, or Ru. Then, to address the issue gases having a short residence time, the metal nanoparticles need to be well dispersed and should be as small in size as possible to increase the specific surface area for contact and hence the number of active sites. However, smaller particles tend to coalesce via an Ostwald ripening phenomenon, which decreases the apparent activity if it is not destroying the catalytic material. This underlines the major role played by the support, whose geometry needs to be tailored to prevent this phenomenon and whose chemical nature needs to be consistent with the operational conditions, such as at sustained high temperatures or in the presence of water vapor.

In this Special Issue titled“Morphological effects on catalytic reactions”, we welcome all kind of papers (research papers, reviews, or communications) where the influence of morphology is linked to catalytic activity. Submitted papers can concern various catalysts for a large range of catalytic reactions where the geometry and/or the chemistry are studied in detail.

Dr. Julien Mahy
Guest Editor

Artium Belet
Guest Editor Assistant

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Catalysts is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • metallic or metallic oxide nanoparticles
  • supported and unsupported catalysts
  • catalytic processes
  • photocatalysis
  • morphology
  • composition
  • biocatalysis
  • heterogeneous catalysis
  • zeolite
  • kinetics
  • sol–gel

Published Papers (3 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

13 pages, 9616 KiB  
Article
Mitigating Co Metal Particle Agglomeration and Enhancing ORR Catalytic Activity through Nitrogen-Enriched Porous Carbon Derived from Biomass
by Yanling Wu, Qinggao Hou, Fangzhou Li, Yuanhua Sang, Mengyang Hao, Xi Tang, Fangyuan Qiu and Haijun Zhang
Catalysts 2023, 13(7), 1118; https://doi.org/10.3390/catal13071118 - 18 Jul 2023
Cited by 1 | Viewed by 1324
Abstract
Biomass-derived porous carbon has gained significant attention as a cost-effective and sustainable material in non-noble metal carbon-based electrocatalysts for the oxygen reduction reaction (ORR). However, during the preparation of transition metal catalysts based on biomass-derived porous carbon, the agglomeration of transition metal atoms [...] Read more.
Biomass-derived porous carbon has gained significant attention as a cost-effective and sustainable material in non-noble metal carbon-based electrocatalysts for the oxygen reduction reaction (ORR). However, during the preparation of transition metal catalysts based on biomass-derived porous carbon, the agglomeration of transition metal atoms often occurs, leading to a notable decline in catalytic activity. In this study, we present a straightforward synthetic approach for the preparation of nitrogen-enriched soybean-derived porous carbon (Co@SP-C-a) as an electrocatalyst for the ORR. To achieve this, we employed a two-step method. In the first step, a chemical activator (KCl) was utilized to enhance the porosity of the self-doped nitrogen biomass carbon material. In the second step, a constant pressure drop funnel technique was employed to uniformly disperse bimetal cobalt/zinc-based zeolitic imidazolium frameworks (ZIF-L and ZIF-67) containing different metal ions (Zn2+ and Co2+) into the activated biomass carbon material. Subsequent high-temperature calcination of the ZIF-L and ZIF-67@SP-C-a composite precursor yielded the Co@SP-C-a catalyst. The obtained catalyst exhibited remarkable ORR activity in an alkaline solution (Eonset = 0.89 V, E1/2 = 0.83 V, JL = −6.13 mA·cm−2) and exceptional long-term stability. This study presents an effective strategy to prevent the agglomeration of metal nanoparticles when integrating them with biomass-based carbon materials, thus leading to enhanced catalytic performance. Full article
(This article belongs to the Special Issue Morphological Effects on Catalytic Reactions)
Show Figures

Graphical abstract

16 pages, 4798 KiB  
Article
Enhanced Decomposition of H2O2 Using Metallic Silver Nanoparticles under UV/Visible Light for the Removal of p-Nitrophenol from Water
by Julien G. Mahy, Marthe Kiendrebeogo, Antoine Farcy and Patrick Drogui
Catalysts 2023, 13(5), 842; https://doi.org/10.3390/catal13050842 - 5 May 2023
Cited by 4 | Viewed by 1580
Abstract
Three Ag nanoparticle (NP) colloids are produced from borohydride reduction of silver nitrate in water by varying the amount of sodium citrate. These nanoparticles are used as photocatalysts with H2O2 to degrade a p-nitrophenol (PNP) solution. X-ray diffraction patterns have [...] Read more.
Three Ag nanoparticle (NP) colloids are produced from borohydride reduction of silver nitrate in water by varying the amount of sodium citrate. These nanoparticles are used as photocatalysts with H2O2 to degrade a p-nitrophenol (PNP) solution. X-ray diffraction patterns have shown the production of metallic silver nanoparticles, whatever the concentration of citrate. The transmission electron microscope images of these NPs highlighted the evolution from spherical NPs to hexagonal/rod-like NPs with broader distribution when the citrate amount increases. Aggregate size in solution has also shown the same tendency. Indeed, the citrate, which is both a capping and a reducing agent, modifies the resulting shape and size of the Ag NPs. When its concentration is low, the pH is higher, and it stabilizes the formation of uniform spherical Ag NPs. However, when its concentration increases, the pH decreases, and the Ag reduction is less controlled, leading to broader distribution and bigger rod-like Ag NPs. This results in the production of three different samples: one with more uniform spherical 20 nm Ag NPs, one intermediate with 30 nm Ag NPs with spherical and rod-like NPs, and one with 50 nm rod-like Ag NPs with broad distribution. These three Ag NPs mixed with H2O2 in water enhanced the degradation of PNP under UV/visible irradiation. Indeed, metallic Ag NPs produce localized surface plasmon resonance under illumination, which photogenerates electrons and holes able to accelerate the production of hydroxyl radicals when in contact with H2O2. The intermediate morphology sample presents the best activity, doubling the PNP degradation compared to the irradiated experiment with H2O2 alone. This better result can be attributed to the small size of the NPs (30 nm) but also to the presence of more defects in this intermediate structure that allows a longer lifetime of the photogenerated species. Recycling experiments on the best photocatalyst sample showed a constant activity of up to 40 h of illumination for a very low concentration of photocatalyst compared to the literature. Full article
(This article belongs to the Special Issue Morphological Effects on Catalytic Reactions)
Show Figures

Graphical abstract

11 pages, 3956 KiB  
Article
Effect of Morphological Modification over g-C3N4 on Photocatalytic Hydrogen Evolution Performance of g-C3N4-Pt Photocatalysts
by Thi Van Anh Hoang, Phuong Anh Nguyen and Eun Woo Shin
Catalysts 2023, 13(1), 92; https://doi.org/10.3390/catal13010092 - 2 Jan 2023
Cited by 7 | Viewed by 2244
Abstract
In this study, the morphological properties of g-C3N4 in g-C3N4-Pt photocatalysts were modified by a simple hydrothermal treatment for photocatalytic hydrogen evolution. In addition, the morphological modification effect of g-C3N4 on the hydrogen [...] Read more.
In this study, the morphological properties of g-C3N4 in g-C3N4-Pt photocatalysts were modified by a simple hydrothermal treatment for photocatalytic hydrogen evolution. In addition, the morphological modification effect of g-C3N4 on the hydrogen evolution performance was investigated. The long-time hydrothermal treatment clearly changed the morphology of g-C3N4 by building extended melem units with more oxygen functional groups at the defect edges of the extended melem units, which was evidenced by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS) measurements. The different morphological features of g-C3N4 resulted in lower photoluminescence (PL) emission intensity in PL spectra and a smaller semicircle radius in electrochemical impedance spectroscopy (EIS) data. This indicates the more efficient charge separation of the g-C3N4-Pt photocatalyst with a modified morphology. Consequently, morphologically modified g-C3N4-Pt showed a higher photocatalytic hydrogen evolution rate due to the better charge separation efficiency. Full article
(This article belongs to the Special Issue Morphological Effects on Catalytic Reactions)
Show Figures

Figure 1

Back to TopTop