A Drive towards Thermodynamic Efficiency for Dissipative Structures in Chemical Reaction Networks

Dissipative accounts of structure formation show that the self-organisation of complex structures is thermodynamically favoured, whenever these structures dissipate free energy that could not be accessed otherwise. These structures therefore open transition channels for the state of the universe to move from a frustrated, metastable state to another metastable state of higher entropy. However, these accounts apply as well to relatively simple, dissipative systems, such as convection cells, hurricanes, candle flames, lightning strikes, or mechanical cracks, as they do to complex biological systems. Conversely, interesting computational properties—that characterize complex biological systems, such as efficient, predictive representations of environmental dynamics—can be linked to the thermodynamic efficiency of underlying physical processes. However, the potential mechanisms that underwrite the selection of dissipative structures with thermodynamically efficient subprocesses is not completely understood. We address these mechanisms by explaining how bifurcation-based, work-harvesting processes—required to sustain complex dissipative structures—might be driven towards thermodynamic efficiency. We first demonstrate a simple mechanism that leads to self-selection of efficient dissipative structures in a stochastic chemical reaction network, when the dissipated driving chemical potential difference is decreased. We then discuss how such a drive can emerge naturally in a hierarchy of self-similar dissipative structures, each feeding on the dissipative structures of a previous level, when moving away from the initial, driving disequilibrium.

Relations between absorption, emission, and excited state chemical potentials from nanocrystal 2D spectra

For quantum-confined nanomaterials, size dispersion causes a static broadening of spectra that has been difficult to measure and invalidates all-optical methods for determining the maximum photovoltage that an excited state can generate. Using femtosecond two-dimensional (2D) spectroscopy to separate size dispersion broadening of absorption and emission spectra allows a test of single-molecule generalized Einstein relations between such spectra for colloidal PbS quantum dots. We show that 2D spectra and these relations determine the thermodynamic standard chemical potential difference between the lowest excited and ground electronic states, which gives the maximum photovoltage. Further, we find that the static line broadening from many slightly different quantum dot structures allows single-molecule generalized Einstein relations to determine the average single-molecule linewidth from Stokes’ frequency shift between ensemble absorption and emission spectra.

Overlayer deposition-induced control of oxide ion concentration in SrFe0.5Co0.5O2.5 oxygen sponges

We form flat oxide-interfaces, i.e. manganite- and titanate-oxygen sponges, and observe peculiar oxygen transport behaviors relying on chemical potential difference at the interfaces. Oxygen transport into oxygen-sponge leads weak ferromagnetism.

Non-Equilibrium Thermodynamic Analysis of Flash Evaporation Process in Vacuum Ice Making

Traditional equilibrium thermodynamics can only solve a few equilibrium processes composed of continuous stable equilibrium states. However, the vacuum flash evaporation process is a typical unsteady process. The study of non-equilibrium thermodynamics of the two-phase flow model is helpful to improve our understanding of the basic law of the flash evaporation process. Based on the theory of non-equilibrium thermodynamics, the flash chamber in the vacuum flash ice making system was studied in this paper, and the possibility of non-equilibrium steady state evaporation with superheat was obtained. The chemical potential difference between liquid water and water vapor under non-equilibrium steady state conditions was determined, and the corresponding evaporation entropy was calculated. It is shown that the results obtained by equilibrium thermodynamics are only related to the temperature difference, while the results obtained by non-equilibrium thermodynamics are not only related to the temperature difference, but also the state of the evaporation process. This is because non-equilibrium thermodynamics considers the cooling of liquid water and the evaporation of water vapor as a whole, taking into account the interaction between the two processes. However, the traditional equilibrium thermodynamics theory divides the steady state evaporation process into two independent processes and ignores the influence of each other.

“Fast” Plasmons Propagating in Graphene Plasmonic Waveguides with Negative Index Metamaterial Claddings

We propose the monolayer graphene plasmonic waveguide (MGPW), which is composed of graphene core sandwiched by two graphene metamaterial (GMM) claddings and investigate the properties of plasmonic modes propagating in the waveguide. The effective refraction index of the GMMs claddings takes negative (or positive) at the vicinity of the Dirac-like point in the band structure. We show that when the effective refraction index of the GMMs is positive, the plasmons travel forward in the MGPW with a positive group velocity (vg > 0, vp > 0). In contrast—for the negative refraction index GMM claddings—a negative group velocity of the fundamental mode (vg < 0, vp > 0) appears in the proposed waveguide structure when the core is sufficiently narrow. A forbidden band appears between the negative and positive group velocity regions, which is enhanced gradually as the width of the core increases. On the other hand, one can overcome this limitation and even make the forbidden band disappear by increasing the chemical potential difference between the nanodisks and the ambient graphene of the GMM claddings. The proposed structure offers a novel scheme of on-chip electromagnetic field and may find significant applications in the future high density plasmonic integrated circuit technique.