Publications by authors named "Matus E Diveky"

The mass accommodation coefficient of water on aqueous triethylene glycol droplets was determined for water mole fractions in the range = 0.1-0.93 and temperatures between 21 and 26 °C from modulated Mie scattering measurement on single optically-trapped droplets in combination with a kinetic multilayer model.

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The uptake of water vapor by various organic aerosols is important in a number of applications ranging from medical delivery of pharmaceutical aerosols to cloud formation in the atmosphere. The coefficient that describes the probability that the impinging gas-phase molecule sticks to the surface of interest is called the mass accommodation coefficient, α. Despite the importance of this coefficient for the description of water uptake kinetics, accurate values are still lacking for many systems.

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Correction for 'Assessing relative humidity dependent photoacoustics to retrieve mass accommodation coefficients of single optically trapped aerosol particles' by Matus E. Diveky et al., Phys.

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Photoacoustic (PA) spectroscopy enjoys widespread applications across atmospheric sciences. However, experimental biases and limitations originating from environmental conditions and particle size distributions are not fully understood. Here, we combine single-particle photoacoustics with modulated Mie scattering to unravel the fundamental physical processes occurring during PA measurements on aerosols.

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Photoacoustic spectroscopy is widely used to measure the light absorption of aerosols. However, the impact of key factors such as the effect of relative humidity and mass exchange on photoacoustic measurements are still poorly understood. We assess such measurement biases and their physical origin by analysing the photoacoustic signal of single tetraethylene glycol (TEG) particles at varying relative humidities.

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The photocycle of photoactive yellow protein (PYP) begins with small-scale torsional motions of the chromophore leading to large-scale movements of the protein scaffold triggering a biological response. The role of single-bond torsional molecular motions of the chromophore in the initial steps of the PYP photocycle are not fully understood. Here, we employ anion photoelectron spectroscopy measurements and quantum chemistry calculations to investigate the electronic relaxation dynamics following photoexcitation of four model chromophores, para-coumaric acid, its methyl ester, and two analogues with aliphatic bridges hindering torsional motions around the single bonds adjacent to the alkene group.

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