A particularly suitable reactor concept for the continuous dehydrogenation of perhydro-Nethylcarbazole in the context of hydrogen and energy storage applications is described. The concept addresses the fact that dehydrogenation is a highly endothermic gas evolution reaction.Thus, for efficient dehydrogenation a significant amount of reaction heat has to be provided to a reactor that is essentially full of gas. This particular challenge is addressed in our study by the use of a catalyst-coated (Pt on alumina), structured metal reactor obtained by selective electron beam melting. The so-obtained reactor was tested both as a single tube set-up and as a Hydrogen Release Unit (HRU) with ten parallel reactors. In stationary operation, the HRU realized a hydrogen release capacity of 1.75 kW therm (960 W el in a subsequent fuel cell) with up to 1.12 g H 2 min À1 g Pt
À1and a power density of 4.32 kW el L À1 of HRU reactor.
Broader contextThe conversion of our current energy system to a hydrogen-based one requires effective ways to store hydrogen in large amounts over long periods of time using existing infrastructures. Liquid Organic Hydrogen Carrier systems, such as e.g. perhydro-N-ethyl carbazole (H12-NEC)/N-ethyl carbazole (NEC), have the potential to substitute step-by-step liquid fossil fuels as they have attractive energy densities and diesel-like handling. Hydrogen release from H 2 -rich LOHC systems allows the on-demand utilization of regenerative energy equivalents at any time and at any place. However, the hydrogen release from H 2 -rich LOHC systems is challenging due to the endothermic nature of the dehydrogenation reaction combined with the large volume expansion of the reaction mixture. Our contribution shows that 3-D-structured metallic reactors produced via selective electron beam melting and coated with Pt on alumina represent very suitable and efficient dehydrogenation reactors for this catalytic dehydrogenation reaction. Using such reactors, we could demonstrate a power density of up to 4.32 kW el L
À1in the dehydrogenation reaction (assuming a fuel cell efficiency of 55%). The system stability and reproducibility of the dehydrogenation results were found to be excellent over 48 h time-on-stream.