Transformation of Atomically Dispersed Platinum in SAPO-37 into Platinum Clusters: Catalyst for Ethylene Hydrogenation

Atomically dispersed supported platinum catalysts were synthesized by the reaction of Pt(acac)2 (acac = acetylacetonato) with the silicoaluminophosphate molecular sieve SAPO-37, with infrared spectra showing that the reaction involved SAPO...

Ligand-coordinated Ir single-atom catalysts stabilized on oxide supports for ethylene hydrogenation and their evolution under a reductive atmosphere

Effective, stable, durable, and tunable Ir-ligand single-atom catalysts for ethylene hydrogenation, studied in situ for structural evolution of Ir single-atoms under a reducing atmosphere.

Identification of hydrogen species on Pt/Al2O3 by in situ inelastic neutron scattering and their reactivity with ethylene

Active hydrogen species and their dynamics in ethylene hydrogenation reaction were elucidated by in situ INS and DFT calculations.

Non-Faradaic Promotion of Ethylene Hydrogenation Under Oscillating Potentials

The acceleration of Faradaic reactions by oscillating electric potentials has emerged as a viable tool to enhance electrocatalysis, but the non-Faradaic dynamic promotion of thermal catalytic processes remains to be proven. Here, we present experimental evidence showing that oscillating potentials are capable of enhancing the rate of ethylene hydrogenation despite no promotion effect was observed under static potentials. The non-Faradaic dynamic enhancement reaches up to 553% on a Pd/C electrode when cycling between –0.25 VNHE and 0.55 VNHE under optimized conditions with a frequency of around 0.1 Hz and a duty cycle of 99%. Under those conditions, no stoichiometric electron transfer to ethylene can be observed, confirming the non-Faradaic nature of the process. Experiments in different electrolytes reveal a good correlation between the catalytic enhancement and the doublelayer capacitance – a measure for the interfacial electric field strength. Preliminary kinetic data suggests that cycling to a low potential increases the hydrogen adsorption on the catalyst surface while at higher potential, the ethylene adsorption and hydrogenation becomes relatively more favorable<br>

Non-Faradaic Promotion of Ethylene Hydrogenation Under Oscillating Potentials

The acceleration of Faradaic reactions by oscillating electric potentials has emerged as a viable tool to enhance electrocatalysis, but the non-Faradaic dynamic promotion of thermal catalytic processes remains to be proven. Here, we present experimental evidence showing that oscillating potentials are capable of enhancing the rate of ethylene hydrogenation despite no promotion effect was observed under static potentials. The non-Faradaic dynamic enhancement reaches up to 553% on a Pd/C electrode when cycling between –0.25 VNHE and 0.55 VNHE under optimized conditions with a frequency of around 0.1 Hz and a duty cycle of 99%. Under those conditions, no stoichiometric electron transfer to ethylene can be observed, confirming the non-Faradaic nature of the process. Experiments in different electrolytes reveal a good correlation between the catalytic enhancement and the doublelayer capacitance – a measure for the interfacial electric field strength. Preliminary kinetic data suggests that cycling to a low potential increases the hydrogen adsorption on the catalyst surface while at higher potential, the ethylene adsorption and hydrogenation becomes relatively more favorable<br>