Institute of Catalysis Research and Technology (IKFT)

The Institute of Catalysis Research and Technology was founded 2011. Its mission is to bridge the gap between fundamental and applied research and the development of new technologies and products in the field of catalysis and process technology of catalyzed processes. The focus of our work is the sustainable utilization of alternative feedstocks and their conversion into energy carriers intermediates. This includes the development of new catalytic systems based on a fundamental understanding of processes on a molecular level. The institute receives basic funding from the Helmholtz Association's program-oriented funding, largely in the Energy research field in the program Materials and Technologies for the Energy Transition.

News

IKFT
IKFT Contributions to DGMK Event on Hydrogen and Syngas

The DGMK event Hydrogen and Syngas - Platform for a sustainable future was jointly organized by the DGMK Divisions "Petrochemistry" and "Conversion of Carbon Carriers", the Division of Industrial Chemistry of the Società Chimica Italiana (SCI) and the ÖGEW Österreichische Gesellschaft für Energiewissenschaften.

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IKFTIKFT
NFDI4Cat Summit 2025

The NFDI4Cat 2.0 kick off meeting took place on 22 and 23 October 2025 at the DECHEMA Haus in Frankfurt (Main). In this second funding period, TT-Prof. Dr. Moritz Wolf joins as a Participant and introduced his activities in data-driven research to the consortium. Together with the established principal investigator Prof. Dr. Olaf Deutschmann and Dr. Sofia Angeli IKFT will shape the future of catalysis-related data and research.

IKFTIKFT
IKFT at EuropaCat 2025 in Trondheim

A large group of researchers from KIT attended the 16th European Congress on Catalysis (EuropaCat 2025) in Trondheim, Norway (31.08 to 05.09.2025). Professors, postdoctoral and doctoral researchers from IKFT, as well as ITCP and ITC, contributed with posters, oral presentations, and a plenary lecture, showcasing the catalysis research at KIT.

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ETOS Research Award for Liana Savintseva

Liana Savintseva won the ETOS Research Award. Congratulations!

WileyWiley

Suspension aging is critical in the synthesis of Cu/Zn-based methanol catalysts, because this process of chemical transformations includes crystallization of different phases. The evolution of these phases within the precipitate is leading along the so-called transitory tipping point to the target phase zincian malachite. More information can be found in the Research Article by Lucas Warmuth and co-workers (DOI: 10.1002/cplu.202500284).

 

 

 

ACS PublicationsACS Publications
Investigation of the particle shape of cobalt-based Fischer–Tropsch catalysts

A recent investigation of the particle shape of cobalt-based Fischer–Tropsch catalysts using Monte Carlo simulations was featured as a front cover in the Journal of Physical Chemistry C.  J. Phys. Chem. C 2025,129,13232−13243.  https://doi.org/10.1021/acs.jpcc.5c02777

 

Veranstaltungskalender

 
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08.Dec
13:00
IKFT, Seminar Room 202, Building 727
Annika Mueller, IKFT
Abschlussvortrag zur Masterarbeit mit Fokus auf Charakterisierung von Methanolkatalysatoren und entsprechenden Modellkatalysatoren nach Reduktion unter verschiedenen Wasserstoffpartialdrücken.
17.Dec
13:00
Seminar Room 202, Building 727
Elisabeth Herzinger, IKFT
Advanced Catalyst and Reactor Engineering for Efficient Hydrogen Release from Perhydro-Benzyltoluene
Hydrogen storage via liquid organic hydrogen carriers (LOHCs) such as perhydro-benzyltoluene (H12-BT) is a promising route for safe, reversible, and compact hydrogen storage under ambient conditions.1 Recent developments in both catalyst design and reactor engineering have significantly enhanced dehydrogenation performance, a critical step for hydrogen release. In this study the performance of bimetallic platinum-rhenium (PtRe) catalysts2 supported on Al₂O₃ was investigated and optimised for dehydrogenation in a continuous three phase slurry reactor. The slurry reactor represents a promising alternative to conventional fixed-bed reactor designs. Superior heat management and rapid separation of released hydrogen mitigate the dewetting effects commonly encountered in endothermic LOHC dehydrogenation processes.
Modification of the PtRe/Al2O3 catalysts focussed on the influence of support morphology, surface chemistry, and synthesis conditions. By tailoring synthesis procedures—including support calcination parameters and the order of metal precursor during sequential impregnation—and analysing the resulting catalysts by ICP-AES, XRD, CO-pulse chemisorption, NH3-TPD, TEM, and N₂ physisorption, observed effects on catalyst productivity and dehydrogenation activity were characterised. Additional selective sulphur poisoning resulted in improved by-product suppression. The findings provide critical insight into the optimisation of metal-support interactions and preparation methods to enhance hydrogen release kinetics and catalyst lifetime.
The slurry reactor demonstrated stable long-term operation at elevated temperatures (330 °C) and pressures (4.7 barg), with high platinum-based productivity and low by-product formation. Operation parameters, such as stirrer speed, temperature, pressure, and feed rate, were systematically varied to optimise space-time-yield and degree of dehydrogenation. Kinetic analyses based on Arrhenius parameters were conducted to deepen mechanistic understanding. Catalyst and reactor performance were benchmarked using both commercial and custom-designed platinum-based catalysts, including S-poisoned Pt/Al₂O₃ and PtRe/Al₂O₃ formulations. Ultimately, the synergy between advanced Pt-based catalysts and optimised slurry reactor design enabled a significant enhancement in hydrogen release efficiency from H12-BT.
This study highlights a holistic approach to LOHC dehydrogenation by combining rational catalyst design with innovative reactor engineering. The integration of tailored PtRe catalysts and continuous slurry reactor operation establishes a robust framework for improving the viability and scalability of hydrogen storage technologies in real-world energy systems.
1. E. Herzinger, M. Wolf, Chem. Ing. Tech. 2024, 96, 65.
2. D. Strauch, P. Weiner, B. B. Sarma, A. Körner, E. Herzinger, P. Wolf, A. Zimina, A. Hutzler, D. E. Doronkin, J.-D. Grunwaldt P. Wasserscheid, M. Wolf, Catal. Sci. Technol. 2024, 7, 1775