Abstract
A new experimental method has been developed to record photoelectron spectra based on the well-established pulsed-field-ionization zero-kinetic-energy photoelectron spectroscopy technique and inspired by the data treatment employed in slow photoelectron spectroscopy. This method has been successfully applied to two well-known systems: the X+2Πg,1/2(v+ = 0) ← X1Σ+g(v = 0) and the X+1Σ+(v+ = 2) ← X2Π1/2(v = 0) ionizing transitions of CO2 and NO, respectively. The first results highlight several advantages of our technique such as an improved signal-to-noise ratio without degrading the spectral resolution and a direct field-free energy determination. The data obtained for NO indicate that this method might be useful for studying field-induced autoionization processes.
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CITATION STYLE
Harper, O. J., Chen, N. L., Boyé-Péronne, S., & Gans, B. (2022). Pulsed-ramped-field-ionization zero-kinetic-energy photoelectron spectroscopy: A methodological advance. Physical Chemistry Chemical Physics, 24(5), 2777–2784. https://doi.org/10.1039/d1cp04569e
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