Catalytic Reforming and Hydrogen Production: From the Past to the Future, 2nd Edition

A special issue of Catalysts (ISSN 2073-4344). This special issue belongs to the section "Industrial Catalysis".

Deadline for manuscript submissions: 31 July 2025 | Viewed by 2157

Special Issue Editors


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Guest Editor
School of Environmental Engineering, Technical University of Crete, GR-73100 Chania, Greece
Interests: methane production; catalyst; synthesis gas; hydrogen production; steam reforming; WGS reaction
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Guest Editor
Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Buffalo, NY 14260, USA
Interests: heterogeneous catalysis; nanoparticle synthesis; surface science; catalysts; environmental processes
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

This is the second edition of the Special Issue, “Catalytic Reforming and Hydrogen Production: From the Past to the Future, 2nd Edition”. In this updated edition, we continue to highlight cutting-edge research in the field of heterogeneous catalysis, with a focus on catalytic reforming and hydrogen production. As the global transition toward clean and sustainable energy accelerates, this issue aspires to advance the discourse on innovative solutions and transformative technologies.

The aim of this edition is not only to provide a platform for sharing groundbreaking scientific discoveries but also to foster interdisciplinary collaboration among researchers, industry experts, and policymakers. By addressing both fundamental science and applied engineering challenges, we hope to bridge the gap between laboratory-scale innovation and large-scale industrial implementation, contributing to a future driven by cleaner energy systems.

We warmly welcome submissions of original research articles and comprehensive reviews that showcase the latest advancements and insights in this dynamic research domain. Contributions may address, but are not limited to, the following key topics:

  • Advanced methane conversion techniques.
  • Dry reforming innovations.
  • CO₂ methanation strategies.
  • Hydrogen production technologies.
  • The water–gas shift (WGS) reaction.
  • Syngas production advancements.
  • Fischer–Tropsch synthesis developments.
  • Utilization of renewable feedstocks for hydrogen generation.
  • Catalytic processes for ammonia decomposition.
  • Integration of catalytic reforming with carbon capture and storage (CCS) technologies.

Dr. Georgios Bampos
Dr. Paraskevi Panagiotopoulou
Dr. Eleni A. Kyriakidou
Guest Editors

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Keywords

  • syngas
  • hydrogen production
  • steam reforming
  • CO₂ methanation
  • water–gas shift (WGS) reaction
  • fuels
  • clean energy
  • hydrocarbons to fuels
  • catalytic hydrogenation
  • carbon-neutral energy systems

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Related Special Issue

Published Papers (4 papers)

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Research

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15 pages, 3237 KiB  
Article
A Simple Fabrication of Tourmaline-Supported Ni-NiAl2O4 Nanocomposites for Enhanced Methane Dry Reforming Activity
by Jin Wang, Xianku Wang, Pengfei Zhou, Liang Bian and Fei Wang
Catalysts 2025, 15(7), 658; https://doi.org/10.3390/catal15070658 - 6 Jul 2025
Viewed by 318
Abstract
Ni-based catalysts have been widely used in catalytic reactions by researchers due to their advantages such as abundant resources, high catalytic activity and lower prices than precious metals. However, the problems of easy agglomeration and poor dispersion of Ni-based catalysts have hindered their [...] Read more.
Ni-based catalysts have been widely used in catalytic reactions by researchers due to their advantages such as abundant resources, high catalytic activity and lower prices than precious metals. However, the problems of easy agglomeration and poor dispersion of Ni-based catalysts have hindered their large-scale application. Therefore, it is necessary to select a suitable preparation method to reduce the agglomeration of the catalyst and improve its dispersion. In this paper, the Ni-NiAl2O4/tourmaline composite material was prepared by using the microwave hydrothermal reduction method. The most favorable conditions for preparing NiAl2O4/tourmaline are as follows: using TEOA as the additive, the microwave hydrothermal temperature is 220 °C, the calcination temperature is 800 °C, and the addition amount of tourmaline is 7.4 wt.%. NiAl2O4 has a good dispersion over the surface of tourmaline support and the optimal NiAl2O4/tourmaline catalyst exhibits a specific surface area of 106.5 m2/g. Metallic nickel was reduced at 650 °C to further obtain Ni-NiAl2O4/tourmaline composites. Finally, the Ni-NiAl2O4/tourmaline composites showed significantly improved catalytic dry reforming of methane (DRM) activity compared to Ni-NiAl2O4 sample under low-temperature conditions (500–600 °C), meaning that the tourmaline carrier could effectively optimize the low-temperature catalytic performance of Ni-NiAl2O4. Full article
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24 pages, 5102 KiB  
Article
Electrocatalytic Investigation of the SOFC Internal CH4 Dry Reforming with Modified Ni/GDC: Effect of Au Content on the Performance Enhancement by Fe-Au Doping
by Evangelia Ioannidou, Stylianos G. Neophytides and Dimitrios K. Niakolas
Catalysts 2025, 15(7), 618; https://doi.org/10.3390/catal15070618 - 23 Jun 2025
Viewed by 358
Abstract
Internal Dry Reforming of Methane (IDRM) in biogas fed Solid Oxide Fuel Cells (SOFCs) was investigated on Fe-Au modified Ni/GDC electrolyte-supported cells at 900 and 850 °C. The aim was to clarify the synergistic interaction between Fe and Au, focusing on the effect [...] Read more.
Internal Dry Reforming of Methane (IDRM) in biogas fed Solid Oxide Fuel Cells (SOFCs) was investigated on Fe-Au modified Ni/GDC electrolyte-supported cells at 900 and 850 °C. The aim was to clarify the synergistic interaction between Fe and Au, focusing on the effect of X wt.% of Au loading (where X = 1 or 3 wt.%) in binary Au-Ni/GDC and ternary 0.5 wt.% Fe-Au-Ni/GDC fuel electrodes. The investigation combined i-V, Impedance Spectroscopy and Gas Chromatography electrocatalytic measurements. It was found that modification with 0.5Fe-Au enhanced significantly the electrocatalytic activity of Ni/GDC for the IDRM reaction, whereas the low wt.% Au content had the most promoting effect. The positive interaction of 0.5 wt.% Fe with 1 wt.% Au increased the conductivity of Ni/GDC and enhanced the corresponding IDRM charge transfer electrochemical processes, especially those in the intermediate frequency region. Comparative long-term measurements, between cells comprising Ni/GDC and 0.5Fe-1Au-Ni/GDC, highlighted the significantly higher IDRM electrocatalytic activity of the modified electrode. The latter operated for almost twice the time (280 h instead of 160 h for Ni/GDC) with a lower degradation rate (0.44 mV/h instead of 0.51 mV/h). Ni/GDC degradation was ascribed to inhibited charge transfer processes in the intermediate frequencies region and to deteriorated ohmic resistance. Stoichiometric analysis on the (post-mortem) surface state of each fuel electrode showed that the wt.% content of reduced nickel on Ni/GDC was lower, compared to 0.5Fe-1Au-Ni/GDC, verifying the lower re-oxidation degree of the latter. This was further correlated to the hindered H2O production during IDRM operation, due to the lower selectivity of the modified electrode for the non-desired RWGS reaction. Full article
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16 pages, 2483 KiB  
Article
H2 Production from Pyrolysis-Steam Reforming of Municipal Solid Waste and Biomass: A Comparative Study When Using the Self-Derived Char-Based Catalysts
by Maijia Qiu, Chenhao Xiang, Yitao Wen, Weichen Hong, Renkai Liu, Dehong Chen and Dezhen Chen
Catalysts 2025, 15(6), 531; https://doi.org/10.3390/catal15060531 - 27 May 2025
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Abstract
This study employed a two-stage fixed-bed pyrolysis-reforming reactor to investigate H2 production behaviors from municipal solid waste (MSW) and biomass with their self-derived catalysts under different operating parameters. The self-derived catalysts are prepared by mechanically mixing pyrolysis-derived chars with CaO and iron [...] Read more.
This study employed a two-stage fixed-bed pyrolysis-reforming reactor to investigate H2 production behaviors from municipal solid waste (MSW) and biomass with their self-derived catalysts under different operating parameters. The self-derived catalysts are prepared by mechanically mixing pyrolysis-derived chars with CaO and iron powders. The main results are as follows: (1) The higher oxygen content in biomass facilitates oxidative dehydrogenation reactions, enabling in situ generation of H2O, which results in a higher H2/CO ratio for biomass compared to MSW under steam-free conditions. (2) There are optimal values for the reforming temperature and steam-to-feedstock ratio (S/F) to achieve best performance. In the presence of steam, MSW generally exhibits superior H2 and syngas production performance to biomass; (3) Both MSW char (MSWC)- and biomass char (BC)-based catalysts showed satisfied H2 production and tar cracking performance at 850–900 °C, and the MSWC-based catalyst demonstrated better catalytic activity than the BC-based catalyst due to its higher contents of several active metals. In addition, the iron powder can be recycled easily, proving the effectiveness of the self-derived convenient and cheap catalysts. Full article
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Review

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28 pages, 3287 KiB  
Review
Recent Progress in Photocatalytic Hydrogen Production Using 2D MoS2 Based Materials
by Khursheed Ahmad and Tae Hwan Oh
Catalysts 2025, 15(7), 648; https://doi.org/10.3390/catal15070648 - 2 Jul 2025
Viewed by 517
Abstract
Due to the increase in energy demand, photocatalytic hydrogen (H2) production has received enormous interest from the scientific community due to its simplicity and cost-effectiveness. The photocatalyst (PC) plays a vital role in H2 evolution, and it is well understood [...] Read more.
Due to the increase in energy demand, photocatalytic hydrogen (H2) production has received enormous interest from the scientific community due to its simplicity and cost-effectiveness. The photocatalyst (PC) plays a vital role in H2 evolution, and it is well understood that an efficient PC should have a larger surface area and better charge separation and transport properties. Previously, extensive efforts were made to prepare the efficient PC for photocatalytic H2 production. In some cases, pristine catalyst could not catalyze the catalytic reactions due to a fast recombination rate or poor catalytic behavior. Thus, cocatalysts can be explored to boost the photocatalytic H2 production. In this regard, a promising cocatalyst should have a large surface area, more active sites, decent conductivity, and improved catalytic properties. Molybdenum disulfide (MoS2) is one of the two-dimensional (2D) layered materials that have excellent optical, electrical, and physicochemical properties. MoS2 has been widely utilized as a cocatalyst for the photocatalytic H2 evolution under visible light. Herein, we have reviewed the progress in the fabrication of MoS2 and its composites with metal oxides, perovskite, graphene, carbon nanotubes, graphitic carbon nitrides, polymers, MXenes, metal-organic frameworks, layered double hydroxides, metal sulfides, etc. for photocatalytic H2 evolution. The reports showed that MoS2 is one of the desirable cocatalysts for photocatalytic H2 production applications. The challenges and future perspectives are also mentioned. This study may be beneficial for the researchers working on the design and fabrication of MoS2-based PCs for photocatalytic H2 evolution applications. Full article
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