Interplay of phoresis and self-phoresis in active particles: Transport properties, phoretic, and self-phoretic coefficients.

Self-propelled synthetic particles have attracted scientific interest due to their potential applications as nanomotors in drug delivery and their insight into bacterial taxis. Research on their dynamics has focused on understanding phoresis and self-phoresis in catalytic Janus particles at both the nano- and microscale. This study explores the combined effects of self-diffusiophoresis and self-thermophoresis induced by exothermic chemical reactions on the surface of active particles moving in non-electrolyte media.

Thermodynamic Insights into Symmetry Breaking: Exploring Energy Dissipation across Diverse Scales.

Symmetry breaking is a phenomenon that is observed in various contexts, from the early universe to complex organisms, and it is considered a key puzzle in understanding the emergence of life. The importance of this phenomenon is underscored by the prevalence of enantiomeric amino acids and proteins.The presence of enantiomeric amino acids and proteins highlights its critical role.

Field emission in vacuum resonant tunneling heterostructures with high current densities.

We analyse the steady-state thermal regime of a one-dimensional triode resonant tunnelling structure. The high currents generated by resonant tunnelling produce a large amount of heat that could damage the structure. Establishing the conditions under which it can operate at optimum efficiency is therefore a problem of great relevance for applications.

Variations in activation energy and nuclei size during nucleation explain chiral symmetry breaking.

We show that variations in enantiomer nuclei size and activation energy during the nucleation stage of crystallization are responsible for the chiral symmetry breaking resulting in excess of one of the possible enantiomers with respect to the other. By understanding the crystallisation process as a non-equilibrium self-assembly process, we quantify the enantiomeric excess through the probability distribution of the nuclei size and activation energy variations which are obtained from the free energy involved in the nucleation stage of crystallisation. We validate our theory by comparing it to Kondepudi previous experimental work on sodium chlorate crystallisation.