Superfluidity of flexible chains of polar molecules

We study properties of quantum chains in a gas of polar bosonic molecules confined in a stack of N identical one- and two- dimensional optical lattice layers, with molecular dipole moments aligned perpendicularly to the layers. Quantum Monte Carlo simulations of a single chain (formed by a single molecule on each layer) reveal its quantum roughening transition. The case of finite in-layer density of molecules is studied within the framework of the J-current model approximation, and it is found that N-independent molecular superfluid phase can undergo a quantum phase transition to a rough chain superfluid. A theorem is proven that no superfluidity of chains with length shorter than N is possible. The scheme for detecting chain formation is proposed.Comment: Submitted to Proceedings of the QFS2010 satellite conference "Cold Gases meet Many-Body Theory", Grenoble, August 7, 2010. This is the expanded version of V.

Large specific absorption rates in the magnetic hyperthermia properties of metallic iron nanocubes

We report on the magnetic hyperthermia properties of chemically synthesized ferromagnetic 11 and 16 nm Fe(0) nanoparticles of cubic shape displaying the saturation magnetization of bulk iron. The specific absorption rate measured on 16 nm nanocubes is 1690+-160 W/g at 300 kHz and 66 mT. This corresponds to specific losses-per-cycle of 5.6 mJ/g, largely exceeding the ones reported in other systems. A way to quantify the degree of optimization of any system with respect to hyperthermia applications is proposed. Applied here, this method shows that our nanoparticles are not fully optimized, probably due to the strong influence of magnetic interactions on their magnetic response. Once protected from oxidation and further optimized, such nano-objects could constitute efficient magnetic cores for biomedical applications requiring very large heating power

Unravelling the potential of sustainable aviation fuels to decarbonise the aviation sector

The aviation industry is responsible for approximately 2% of the total anthropogenic greenhouse gas emissions. With an expected four to six-fold growth by 2050, increased attention has been paid to reduce its carbon footprint. In this study, we analyse the requirements to promote Sustainable Aviation Fuels (SAFs) from solar energy to reduce the emissions of the sector. Using a discrete spatio-temporal mathematical description of the region of Spain, we present the key elements required to produce jet fuel via Fischer–Tropsch (FT) and Methanol to fuels (MtF). We have found that solar PV, electricity storage, and alkaline water electrolysis are the key drivers for the performance of solar SAFs while the optimal location of the facilities is driven by the availability of solar radiation, underground H2 storage, and high jet fuel demand. We show that the constant supply of H2 requires an over sizing of technologies, which in turn decreases the utilisation of solar panels and electrolysers. While higher usage rates could be attained by a constant supply of electricity (e.g., via the electricity grid), the use of renewable sources is essential to guarantee a reduction in CO2 emissions compared to fossil-based jet fuel. We found that production costs in 2020 per kgfuel in Spain varied from 3.90 € (MtF) to 4.95 € (FT) using solar radiation as a sole source of energy and a point source of CO2, cutting CO2 life cycle emissions by ∼25% compared to their fossil-based counterpart (2.5–2.7 kgCO2eq per kgfuel). Potential technological improvements could reduce jet fuel production costs to 2.5–3.3 € per kgfuel for CO2 point sources while emissions could reach ∼1.0 kgCO2eq per kgfuel. Ultimately, the impact of these routes in the cost of a flight ticket would result in a minimum increase of 100–150% at present and 40–80% by 2050, accounting for current projections on technologies and carbon prices. This shows that future minimum carbon taxes of 500 € per tCO2 would be required for SAFs to become competitive

Thermodynamics of Dipolar Chain Systems

The thermodynamics of a quantum system of layers containing perpendicularly oriented dipolar molecules is studied within an oscillator approximation for both bosonic and fermionic species. The system is assumed to be built from chains with one molecule in each layer. We consider the effects of the intralayer repulsion and quantum statistical requirements in systems with more than one chain. Specifically, we consider the case of two chains and solve the problem analytically within the harmonic Hamiltonian approach which is accurate for large dipole moments. The case of three chains is calculated numerically. Our findings indicate that thermodynamic observables, such as the heat capacity, can be used to probe the signatures of the intralayer interaction between chains. This should be relevant for near future experiments on polar molecules with strong dipole moments.Comment: 15 pages, 5 figures, final versio

Hydrodynamic interactions in colloidal ferrofluids: A lattice Boltzmann study

We use lattice Boltzmann simulations, in conjunction with Ewald summation methods, to investigate the role of hydrodynamic interactions in colloidal suspensions of dipolar particles, such as ferrofluids. Our work addresses volume fractions $\phi$ of up to 0.20 and dimensionless dipolar interaction parameters $\lambda$ of up to 8. We compare quantitatively with Brownian dynamics simulations, in which many-body hydrodynamic interactions are absent. Monte Carlo data are also used to check the accuracy of static properties measured with the lattice Boltzmann technique. At equilibrium, hydrodynamic interactions slow down both the long-time and the short-time decays of the intermediate scattering function $S(q,t)$, for wavevectors close to the peak of the static structure factor $S(q)$, by a factor of roughly two. The long-time slowing is diminished at high interaction strengths whereas the short-time slowing (quantified via the hydrodynamic factor $H(q)$) is less affected by the dipolar interactions, despite their strong effect on the pair distribution function arising from cluster formation. Cluster formation is also studied in transient data following a quench from $\lambda = 0$; hydrodynamic interactions slow the formation rate, again by a factor of roughly two

Particle interactions in liquid magnetic colloids by zero field cooled measurements: effects on heating efficiency

The influence of magnetic interactions in assemblies formed by either aggregated or disaggregated uniform gamma-Fe_2O_3 particles are investigated as a function of particle size, concentration, and applied field. Hyperthermia and magnetization measurements are performed in the liquid phase of colloids consisting of 8 and 13 nm uniform gamma-Fe_2O_3 particles dispersed in water and hexane. Although hexane allows the disagglomerated obtaining particle system; aggregation is observed in the case of water colloids. The zero field cooled (ZFC) curves show a discontinuity in the magnetization values associated with the melting points of water and hexane. Additionally, for 13 nm gamma-Fe_2O_3 dispersed in hexane, a second magnetization jump is observed that depends on particle concentration and shifts toward lower temperature by increasing applied field. This second jump is related to the strength of the magnetic interactions as it is only present in disagglomerated particle systems with the largest size, i.e., is not observed for 8 nm superparamagnetic particles, and surface effects can be discarded. The specific absorption rate (SAR) decreases with increasing concentration only for the hexane colloid, whereas for aqueous colloids, the SAR is almost independent of particle concentration. Our results suggest that, as a consequence of the magnetic interactions, the dipolar field acting on large particles increases with concentration, leading to a decrease of the SAR