C. J. Bondue

TL;DR: In this paper, the electrochemical reduction of CO2 at gold electrodes under mildly acidic conditions was investigated, and the authors derived a general design principle for acid CO2 electrolyzers to suppress hydrogen evolution from proton reduction: the rate of CO/OH- formation must be high enough to match or compensate the mass transfer of protons to the electrode surface.

TL;DR: In this article, the authors report a study on acetone reduction at platinum single-crystal electrodes using online electrochemical mass spectroscopy, in situ Fourier transform infrared spectrograms and density functional theory calculations.

TL;DR: This paper studies the electrochemical hydrogenation of the carbonyl functional group of acetophenone and 4-acetylpyridine at platinum single-crystal electrodes to determine the selective electroreduction of functionalized ketones.

TL;DR: Results of Electrospray ionization (ESI) results show that any effect of water in the Li(+) containing electrolyte is not due to an altered solvation of the cation, which suggests an influence of the double layer at the interface between the electrode and the electrolyte on oxygen reduction in addition to the well-known higher stability of Na2 O2 and K2O2.

TL;DR: Differential electrochemical mass spectrometry (DEMS) has become an indispensable tool for qualitative and quantitative detection of volatile products or intermediates of continuous Faradaic reactions, but also determination of the amount of adsorbates (sub-layer or monolayer) at different electrode surfaces by means of their desorption as mentioned in this paper.