Bicontinuous minimal surface nanostructures for polymer blend solar cells

This paper presents the first examination of the potential for bicontinuous structures such as the gyroid structure to produce high efficiency solar cells based on conjugated polymers. The solar cell characteristics are predicted by a simulation model that shows how the morphology influences device performance through integration of all the processes occurring in organic photocells in a specified morphology. In bicontinuous phases, the surface de. ning the interface between the electron and hole transporting phases divides the volume into two disjoint subvolumes. Exciton loss is reduced because the interface at which charge separation occurs permeates the device so excitons have only a short distance to reach the interface. As each of the component phases is connected, charges will be able to reach the electrodes more easily. In simulations of the current-voltage characteristics of organic cells with gyroid, disordered blend and vertical rod (rods normal to the electrodes) morphologies, we find that gyroids have a lower than anticipated performance advantage over disordered blends, and that vertical rods are superior. These results are explored thoroughly, with geminate recombination, i.e. recombination of charges originating from the same exciton, identified as the primary source of loss. Thus, if an appropriate materials choice could reduce geminate recombination, gyroids show great promise for future research and applications

Oxide chemistry and fluid inclusion constraints on the formation of itabirite-hosted iron ore deposits at the eastern border of the southern Espinhaço Range, Brazil

The Piçarrão and Liberdade deposits contain high-grade iron orebodies (>65% Fe) hosted in the Guanhães Group itabirite, that are associated with pegmatite veins and bodies. Fluid inclusion studies in quartz veins associated with the high-grade orebodies show that medium to high salinities (25–28 wt% NaCl eq.) and temperatures (275–375 °C) fluids are associated with the silica leaching that led to the iron enrichment. Mineral chemistry studies by LA-ICP-MS in the iron oxides demonstrate that metasomatic processes were responsible for the mineralogical transformations of magnetite to hematite and for subsequent hematite recrystallization. These processes are related to the iron upgrade in the itabirite and the formation of high-grade orebodies. The oxidation of the magnetite to martite is associated with an enrichment in P and As, and depletion in Mg, Ti and Co; as observed in martite crystals compared to their matching kenomagnetite rims. On the other hand Ti and Mo are enriched in hematite crystals that recrystallized from martite. In this case Ti behaved as an immobile element, and its enrichment is accompanied by the depletion of most of the trace elements. A second stage of magnetite formation precipitated with quartz in discordant veins and is oxidized to martite-II. These quartz-martite-II veins contain low salinity and temperature fluid inclusions that record an episode of meteoric fluid influx. The results of the LA-ICP-MS analyses on the fluid inclusions from pegmatite and quartz veins associated with the high-grade iron bodies indicate the contribution of anatectic fluids in the evolution of the metasomatic events

The origin and composition of carbonatite-derived carbonate-bearing fluorapatite deposits

Carbonate-bearing fluorapatite rocks occur at over 30 globally distributed carbonatite complexes and represent a substantial potential supply of phosphorus for the fertiliser industry. However, the process(es) involved in forming carbonate-bearing fluorapatite at some carbonatites remain equivocal, with both hydrothermal and weathering mechanisms inferred. In this contribution, we compare the paragenesis and trace element contents of carbonate-bearing fluorapatite rocks from the Kovdor, Sokli, Bukusu, Catalão I and Glenover carbonatites in order to further understand their origin, as well as to comment upon the concentration of elements that may be deleterious to fertiliser production. The paragenesis of apatite from each deposit is broadly equivalent, comprising residual magmatic grains overgrown by several different stages of carbonate-bearing fluorapatite. The first forms epitactic overgrowths on residual magmatic grains, followed by the formation of massive apatite which, in turn, is cross-cut by late euhedral and colloform apatite generations. Compositionally, the paragenetic sequence corresponds to a substantial decrease in the concentration of rare earth elements (REE), Sr, Na and Th, with an increase in U and Cd. The carbonate-bearing fluorapatite exhibits a negative Ce anomaly, attributed to oxic conditions in a surficial environment and, in combination with the textural and compositional commonality, supports a weathering origin for these rocks. Carbonate-bearing fluorapatite has Th contents which are several orders of magnitude lower than magmatic apatite grains, potentially making such apatite a more environmentally attractive feedstock for the fertiliser industry. Uranium and cadmium contents are higher in carbonate-bearing fluorapatite than magmatic carbonatite apatite, but are much lower than most marine phosphorites