Transparent MoS2/PEDOT Composite Counter Electrodes for Bifacial Dye-Sensitized Solar Cells.

Dye-sensitized solar cells (DSSCs) are solar energy conversion devices with high efficiency and simple fabrication procedures. Developing transparent counter electrode (CE) materials for bifacial DSSCs can address the needs of window-type building-integrated photovoltaics (BIPVs). Herein, transparent organic-inorganic hybrid composite films of molybdenum disulfide and poly(3,4-ethylenedioxythiophene) (MoS2/PEDOT) are prepared to take full advantage of the conductivity and electrocatalytic ability of the two components. MoS2 is synthesized by hydrothermal method and spin-coated to form the MoS2 layer, and then PEDOT films are electrochemically polymerized on top of the MoS2 film to form the composite CEs. The DSSC with the optimized MoS2/PEDOT composite CE shows power conversion efficiency (PCE) of 7% under front illumination and 4.82% under back illumination. Compared with the DSSC made by the PEDOT CE and the Pt CE, the DSSC fabricated by the MoS2/PEDOT composite CE improves the PCE by 10.6% and 6.4% for front illumination, respectively. It proves that the transparent MoS2/PEDOT CE owes superior conductivity and catalytic properties, and it is an excellent candidate for bifacial DSSC in the application of BIPVs.

Self-Polymerized Dopamine Nanoparticles Modified Separators for Improving Electrochemical Performance and Enhancing Mechanical Strength of Lithium-Ion Batteries.

Separators in lithium-ion batteries (LIBs) play an important role for battery safety, so stable electrochemical performance and high mechanical strength of separators will always be of interest. On the basis of the fact that polydopamine (PDA) nanoparticles found in mussel have a strong adhesion ability, biomaterial surface nanoparticles modification methods are developed to increase electrochemical performance and enhance mechanical strength of polypropylene (PP) and polypropylene/polyethylene/polypropylene (PP/PE/PP) separators. The electrolyte uptake performance, ionic conductivities, discharging rate capabilities, yield stresses, and failure strains of PP and PP/PE/PP separators are all enhanced remarkably by PDA modification. Thermal shrinkage results show that thermal stabilities and the shrinkage percentage of PDA-modified separators are improved. The electrochemical testing results conclude that the discharging capacities of PP (increased by 3.77%~187.57%) and PP/PE/PP (increased by 2.31%~92.21%) separators increase remarkably from 0.1 C to 5.0 C. The ionic conductivities of PDA-modified PP and PP/PE/PP separators are 1.5 times and 6.1 times higher than that of unmodified PP and PP/PE/PP separators, which in turn increase the electrolyte uptake and ionic migration. In addition, mechanical properties of PP (yield stresses: 17.48%~100.11%; failure stresses: 13.45%~82.71%; failure strains: 4.08%~303.13%) and PP/PE/PP (yield stresses: 11.77%~296.00%; failure stresses: 12.50%~248.30%; failure strains: 16.53%~32.56%) separators are increased greatly.

[Simulation and analysis of ethanol concentration response to enzyme amount changes in Saccharomyces cerevisiae glycolysis pathway model].

Metabolome has become an important part of Systems Biology, and a large set of data has already gained by applying the methods of metabolome. How to deal with the data and how to combine data of metabolome with data of other omics are problems that can not be ignored. An Enzyme Amount Multiple Factor was imported into the enzyme kinetic equation. When the enzyme amount in the system changed, in silico model, it means to alter the Enzyme Amount Multiple Factor. In order to observe ethanol concentration response to enzyme amount changes in S. cerevisiae glycolysis pathway model, enzyme amount was separately set at high and low level, the corresponding Enzyme Amount Multiple Factor value was 10 and 0.1, relatively. Based on the result of simulation, twelve enzymes in pathway were separated into two classes, class I and class II by cluster analysis. The four enzymes belonging to class I, ADH, HK, PFK and PDC, all catalyze irreversible reactions. The six out of eight enzymes belonging to class II, ALD, GAPDH, GlcTrans, lpPEP, PGI and TIM, catalyze reversible reactions. The other two enzymes belonging to class II, lpGlyc and PK, catalyze irreversible reactions. Based on this method, data of metabolome and proteomics are easily integrated to accomplish relatively overall analysis of system properties.

A complete protein pattern of cellulase and hemicellulase genes in the filamentous fungus Trichoderma reesei.

The complete protein pattern of cellulase and hemicellulase genes was studied through the Genome-wide analysis in Trichoderma reesei. The genome database revealed the presence of 39 ORFs encoding related proteins, including 32 enzymes with a catalysis domain related to cellulases and hemicellulases and 7 related proteins with a cellulose-binding module (CBM). Ten of these encoded yet undescribed enzymes, including six novel beta-glucosidases or xylosidases, two putative xylanases and two undescribed mannases. To better illustrate the relation of these 39 related proteins, four groups were created and analyzed by phylogenetic analysis: group A corresponding to xylanases, group B belonging to mannases and acting to degrade mannan; group C containing all known and putative cellulose-degrading proteins that have highly conserved CBMs; and group D containing beta-glucosidase and beta-xylosidase. Group D was the largest group, in which 8 beta-glucosidases appeared to be non-secreted proteins.