Einstein founded statistical physics on an important generalization of the Boltzmann principle: Einstein's reversion, where not the model but the law of entropy is placed first. The advantage is that it assures the 2nd Law and requires no model assumptions. In particular, the existence of a complete molecular mechanism is not necessary. However, if the empirical behavior of a system is known, the entropy and the corresponding probability of the thermodynamic states can be directly derived. With his approach Einstein successfully explained Brownian motion, wave-particle dualism, quantum transitions as well as the Bose-Einstein condensation. Impossible to find in any textbook, we outline Einstein's approach and apply it to soft interfaces. The introduction of their proper entropy potential, its first, and its second derivatives predicts interfacial nonequilibrium excitation, propagation, and fluctuations, respectively. Experimental observations of the phenomenology of the membrane susceptibilities allow quantitative predictions. The propagation of waves as well as the existence of channel-like current fluctuations are experimentally confirmed and compared to measurements on living systems. Finally, we present experiments that confirm Einstein's approach to the interfacial reaction coordinate. Here the phenomenology of the system is derived from a proper entropy law even though hidden from direct observation. Not structure of molecules but entropy of the aqueous interfaces turns out to be the origin of catalysis and the associated surprising increase in reaction rate. Simultaneous specificity and activity appears now predictable and no more paradox. The theory derived from K.K. in 1999 is briefly outlined and confirmed in experiments on Acetylcholinesterases incorporated in lipid monolayers. Since enzyme activity is controlled from remote by these continuous layers, our results predict the ubiquitous, integrative action in biology of the excitable hydration interface.
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