Eddy-resolving Simulation of CAS-LICOM3 for Phase 2 of the Ocean Model Intercomparison Project

A 61-year(1958–2018)global eddy-resolving dataset for phase 2 of the Ocean Model Intercomparison Project has been produced by the version 3 of Chinese Academy of Science,the State Key Laboratory of Numerical Modeling for Atmospheric Sciences and Geophysical Fluid Dynamics/Institute of Atmospheric Physics(LASG/IAP)Climate system Ocean Model(CAS-LICOM3).The monthly and a part of the surface daily data in this study can be accessed on the Earth System Grid Federation(ESGF)node.Besides the details of the model and experiments,the evolutions and spatial patterns of large-scale and mesoscale features are also presented.The mesoscale features are reproduced well in the high-resolution simulation,as the mesoscale activities can contribute up to 50%of the total SST variability in eddy-rich regions.Also,the large-scale circulations are remarkably improved compared with the low-resolution simulation,such as the climatological annual mean SST(the RMSE is reduced from 0.59°C to 0.47°C,globally)and the evolution of Atlantic Meridional Overturning Circulation.The preliminary evaluation also indicates that there are systematic biases in the salinity,the separation location of the western boundary currents,and the magnitude of eddy kinetic energy.All these biases are worthy of further investigation.

Density functional theory study of formaldehyde adsorption and decomposition on Co-doped defective CeO_(2) (110) surface

Formaldehyde as an air pollutant to adverse health effects for humanity has been getting attention.The adsorption and dissociation of formaldehyde(HCHO)on the CoxCe1−xO_(2)−δ(110)surface were investigated by the density functional theory(DFT)calculations.We calculated the oxygen vacancy formation energy as the function of its site around dopant Co in detail.The results showed that Co doping was accompanied by compensating oxygen hole spontaneous formation.The adsorption configurations and bindings of HCHO at different locations on the CoxCe1−xO_(2)(110)were presented.Four possible pathways of oxidation of formaldehyde on the catalytic surface were explored.The results suggested that formaldehyde dissociation at different adsorption sites on the doped CeO_(2)(110)—first forming dioxymethylene(CH2O_(2))intermediate,and then decomposing into H2O,H2,CO_(2),and CO molecules.It was found that the presence of cobalt and oxygen vacancy significantly prompted the surface activity of CeO_(2).

Enhanced electrocaloric effect at room temperature in Mn^(2+) doped lead-free(BaSr)TiO_(3) ceramics via a direct measurement

(Ba_(1-x)Sr_(x))(MnyTi1-y)O_(3)(BSMT)ceramics with x=35,40 mol%and y=0,0.1,0.2,0.3,0.4,0.5 mol%were prepared using a conventional solid-state reaction approach.The dielectric and ferroelectric properties were characterized using impedance analysis and polarization-electric field(P-E)hysteresis loop measurements,respectively.The adiabatic temperature drop was directly measured using a thermocouple when the applied electric field was removed.The results indicate that high permittivity and low dielectric losses were obtained by doping 0.1-0.4 mol%of manganese ions in(BaSr)TiO_(3)(BST)specimens.A maximum electrocaloric effect(ECE)of 2.75 K in temperature change with electrocaloric strength of 0.55 K·(MV/m)^(-1)was directly obtained at~21℃and 50 kV/cm in Ba_(0.6)Sr_(0.4)Mn_(0.001)Ti_(0.999)O_(3) sample,offering a promising ECE material for practical refrigeration devices working at room temperature.

Field-driven merging of polarizations and enhanced electrocaloric effect in BaTiO_(3)-based lead-free ceramics

Solid-state cooling technology based on electrocaloric effect(ECE)has been advanced as an alternative to replace the vapour-compression approach to overcome the releasing of the global warming gases.However,the development in high ECE materials is still a challenge.In this work,polarization merging strategy was proposed to achieve a large ECE in xBa(Sn_(0.07)Ti_(0.93))O_(3)–(1−x)Ba(Hf_(0.1)Ti_(0.9))O_(3) ferroelectric ceramics,where x=0,0.2,0.4,0.6,0.8,and 1.Ba(Sn_(0.07)Ti_(0.93))O_(3) with an orthorhombic phase and Ba(Hf_(0.1)Ti_(0.9))O_(3) with a rhombohedral phase at room temperature were prepared beforehand as precursors,and phase-coexisted xBSnT–(1−x)BHfT ceramics were formed via a solid-state reaction approach.Phase coexisting structures were confirmed using the X-ray diffraction.The merged polarization was confirmed by the dielectric and ferroelectric properties.Optimal ECEs were obtained for 0.2BSnT–0.8BHfT ceramics,i.e.,adiabatic temperature change DT=2.16±0.08 K at 80℃and 5 MV/m,and DT=3.35±0.09 K at 80℃and 7 MV/m.