Operating regimes for second generation luminescent solar concentrators

In this paper, we introduce the concept of first and second generation luminescent solar concentrators. Traditional, first generation devices are characterised by their randomly oriented molecules that absorb sunlight and emit luminescence isotropically. By applying detailed balance to the absorbed and emitted photon fluxes we derive the Shockley–Queisser limit for these devices. It is found that they have inherently low efficiency due to optical losses (the well known reabsorption problem) and also that device performance is strongly affected by the areal ratio between the top and edge surfaces. This latter property makes it very difficult to achieve significant cost reductions because as the edge area is reduced (to lessen the amount of expensive photovoltaic material required for conversion), the efficiency of the system diminishes. First generation concentrators have now approached the fundamental limits which we predict here, thus to achieve a stand‐alone luminescent concentrator that enables significant cost reductions, second generation approaches are now needed. New, second generation devices are characterised by either directional emitters or photonic filters which enhance the waveguiding mechanism, allowing high efficiency and large sizes to be achieved simultaneously. Here we define the fundamental operating regime in which second generation technology must reach to surpass the limit of first generation devices. Copyright © 2011 John Wiley & Sons, Ltd.     

Fabrication and Training of 3D Conductive Polymer Networks for Neuromorphic Wetware

The human brain possesses an exceptional information processing capability owing to the 3D and dense network architecture of numerous neurons and synapses. Brain-inspired neuromorphic hardware can also benefit from 3D architectures, such as high integration of circuits and acquisition of highly complex dynamical systems. In this study, for future 3D neuromorphic engineering, 3D conductive polymer networks consisting of poly(3,4-ethylenedioxy-thiophene) doped with poly(styrene sulfonate) anions (PEDOT:PSS) are successfully and stably fabricated between multiple electrodes from scratch in precursor solution by electropolymerization. The networks efficiently emulate the 3D local connections between neighboring neurons observed in the cortex. This novel technology, which allows 3D conductive wiring only between desired electrodes, is unprecedented and has potential as an underlying technology for 3D integration. Furthermore, the experimental results also conclusively prove that conductance modification can be performed by manipulating the physical and chemical properties of 3D branch-wired conductive polymer wires, thus demonstrating for the first time the feasibility of neuromorphic wetware with enhanced biological plausibility in the subsequent post-Moore era.     

Definition of an Index Parameter To Screen Highly Functional Enzymes Derived from a Biochemical and Thermodynamic Analysis of Ancestral meso-Diaminopimelate Dehydrogenases

Sequence-based protein design approaches are being adopted to generate highly functional enzymes; however, screening the enzymes remains a time-consuming task. In this study, by analyzing the enzymatic properties of four ancestral meso-2,6-diaminopimelate dehydrogenases (AncDAPDHs), AncDAPDH-N1, -N2, -N3, and -N4, we attempted to define a new index parameter that is helpful for efficiently screening the enzymes. Biochemical and thermodynamic analyses indicated that only AncDAPDH-N4 exhibited greater thermal stability than and activity similar to those of native DAPDHs. Structural and sequence comparisons between DAPDH from Corynebacterium glutamicum (CgDAPDH) and the AncDAPDHs suggested that “quality of mutations” is a potential index parameter. In fact, the mutations introduced from CgDAPDH to AncDAPDH-N4 correlated highly with the mutations accumulated during the evolution process from mesophiles to thermophiles. These results suggest that, although there are several exceptions, the correlation coefficient can be used as an index parameter for screening high-functioning enzymes from sequence data.     

Fine dispersion of carbon black in fluorene‐based resin

The dispersion ability of fluorene‐based epoxy resin (FBE), bisphenol A based epoxy resin (PBE), fluorene‐based polyester (FBP), and polycarbonate (PC) in carbon black (CB) was evaluated. CB/FBE composite had a lower L value (reflectance, blackness) than that of CB/PBE composite, for the same CB content. Aggregations of CB in CB/FBE composites were much smaller than those in CB/PBE composites. The strong interaction between fluorene with cardo structure and CB resulted in a fine dispersion of CB in FBE. FBP had much higher dispersion ability of CB than PC. CB (50 wt%) was dispersed into FBP compared with the 10 wt% of CB dispersed in PC by melt blending. The effect of CB on the mechanical properties of FBP was much higher than that on PC due to fine dispersion of CB in FBP. The effect of CB addition on the T_g of FBP was also higher than that of CB on the T_g of PC. Computational simulation indicates that most stable energy between fluorene with a cardo structure and graphite structure was smaller than the energy between bisphenol A and graphite. It was also shown that the minimum energy appeared when the fluorene structure was almost parallel to the graphite plane. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

BAMO/NMMO Copolymer with Polyester Initiation

In order to improve of mechanical properties at low temperature region, 3,3-bis(azidomethyl)oxetan (BAMO), 3-nitratomethyl-3-methyloxetane (NMMO) and polyester (PE) copolymer were synthesized by using polyester initiator with boron trifluoride etherate. The molar ratio of each units in the BAMO/NMMO/PE copolymer was 7.4/2.6/0.39 according to the ¹H-NMR spectrum analysis and was almost exactly the same composition as the monomer fed (7/3/0.33). The relative composition of triad microstructures was same as theoretical value and they were randomly arranged. The PE, which was a replacement of 1,4-butanediol, acted as an excellent soft segment in the copolymer, and the glass transition point of the elastomer was 4.8 degrees lowered by the replacement. This effect was also verified in the mechanical properties of the composite propellant and the tensile elongation was increased from 15% to 40%percnt; at −40 °C.