scispace - formally typeset
K

Klaus Schlichte

Researcher at Max Planck Society

Publications -  51
Citations -  3523

Klaus Schlichte is an academic researcher from Max Planck Society. The author has contributed to research in topics: Catalysis & Nitride. The author has an hindex of 22, co-authored 49 publications receiving 3271 citations.

Papers
More filters
Journal ArticleDOI

Experimental and theoretical investigation of molybdenum carbide and nitride as catalysts for ammonia decomposition.

TL;DR: The relatively high rate of reaction observed for the catalytic decomposition of NH3 is ascribed to highly energetic sites (twin boundaries, stacking faults, steps, and defects) which are observed in both the molybdenum carbide and nitride samples, resulting in a much higher H2 production rate in comparison with that for previously reported Mo-based catalysts.
Journal ArticleDOI

Thermodynamics and dynamics of the Mg–Fe–H system and its potential for thermochemical thermal energy storage

TL;DR: In this article, the reversible Mg 2 FeH 6 and the mixed Mg2 FeH6 and MgH 2 hydride systems were investigated on a micro- or nanoscale level.
Journal ArticleDOI

High-temperature stable, iron-based core-shell catalysts for ammonia decomposition.

TL;DR: High-temperature, stable core-shell catalysts for ammonia decomposition have been synthesized based on α-Fe(2)O(3) nanoparticles coated by porous silica shells based on hematite nanoparticles obtained from the hydrothermal reaction of ferric chlorides, L-lysine, and water.
Journal ArticleDOI

Synthesis and characterisation of titanium nitride based nanoparticles

TL;DR: In this paper, a ligand-assisted ammonolysis reaction of solid TiCl4 complexes at 973 K was used for high surface area titanium nitride-based materials.
Journal ArticleDOI

Catalytic properties of high surface area titanium nitride materials

TL;DR: In this article, the authors used a pyrolysis reaction of donor-stabilized titanium halide precursors in ammonia atmosphere at high temperatures (973-1273 K) for the reduction of diphenylethyne (DPE) to stilbene.