A graphdiyne nanosheet/Pt nanoparticle composite shows outstanding catalytic activity for the reaction of I3−/I− redox pairs, i.e., the best among rGO/Pt nanoparticle composites, Pt nanoparticles and Pt foils. This is ascribed to enhanced electron transfer resulting from the easier chemical interaction between Pt and the triple bond of graphdiyne.
Pentacene thin film transistors ͑TFTs͒ were fabricated by the organic molecular beam deposition method. The TFTs were characterized in order to study the effect of thermal annealing on the morphology and carrier mobility of the transistors. For all the TFT samples the mobility exhibited an Arrhenius relationship with temperature, indicating a thermally activated transport that could be explained by the carrier trap and thermal release transport mechanism. Therefore, in order to investigate the annealing effect, we tested the data for a significant period of time after annealing until the temperature recovered to room temperature, so that the thermal activation effect was screened and possible effects of thermal expansion and stress were also ruled out. As a result, we found that only with a temperature below a critical temperature of approximately 45°C could annealing improve the mobility, while annealing with T Ͼ 50°C would decrease the mobility compared to the value before annealing. Atomic force microscopy observation and x-ray diffraction ͑XRD͒ data indicated that annealing caused decreased grain size and decreased XRD peak intensity for all samples. Increasing the annealing temperature to 70°C caused obvious desorption because of the low van der Waals intermolecular forces in the organic film. The mobility deterioration after high temperature annealing may be ascribed to the deteriorated microstructure, while the improved mobility may result from the increased crystallinity in the bottom several layers near the substrate film interface. The results also suggested that the influence of possible structure evolution should be distinguished when investigating temperature dependent transport properties.
Ultrathin films of the ferroelectric polymer poly(vinylidene fluoride-trifluoroethylene) [P(VDF-TrFE)] have recently attracted intensive research interest due to their potential applications in emerging organic devices. As special geometry confinement systems, many aspects about their processing, microstructure, and performance are far from being well understood. Here, the cooperative molecular orientation, macroscopic ferroelectric properties, and nanoscale polarization switching behaviors of thermally crystallized ultrathin P(VDF-TrFE) films were investigated. With increasing annealing temperature, the films showed a distinct granule toward layered needle-network (LNN) morphology transition with deteriorated ferroelectricity at a critical point (T(cr)) around 140 °C. Accompanying this is that the polymer backbone first lay more parallel relative to the substrate, and then exactly at T(cr) it showed an abrupt standing-up reorientation. Interestingly, the polarization axis simultaneously showed just opposite orientation and reorientation. Nanoscale polarization switching characterization by using piezoresponse force microscopy and local ferroelectric hysteresis loops revealed a varied molecular orientation in the same needle grain and a polarization reversal constraint effect by the inhomogeneous LNN structure. On the basis of these observations, a tilted-chain lamellae structural model was proposed for the LNN film. The lying down of the polarization axis and the polarization reversal constrain effect well explain the inferior performance of the LNN film despite its higher crystallinity than that of the granular film. The results may shed some light on the understanding of the intercorrelation among the thermal crystallization, microstructure, and macroscopic performance of ultrathin polymer films.
This paper presents a systematic exploration of modifying the electrocaloric effect (ECE) in BaTiO3 ceramics by rare-earth substitution (Ba0.94R0.04TiO3, R = La, Ce, Nd, Sm, Eu, Gd, Dy, Er).
BackgroundConsolidated bioprocessing (CBP) has attracted increasing attention since it can accomplish hydrolytic enzymes production, lignocellulose degradation and microbial fermentation in one single step. Currently, biobutanol is mainly produced by mesophilic and solventogenic clostridia, such as Clostridium beijerinckii and C. acetobutylicum, which cannot directly utilize lignocellulose, an abundant, renewable and economic feedstock. Hence, metabolic construction or isolation of novel cellulolytic/hemicellulolytic and solventogenic bacteria to achieve direct butanol production from lignocellulose offers a promising alternative.ResultsIn this study, a newly isolated Thermoanaerobacterium sp. M5 could directly produce butanol from xylan through CBP at 55 °C via the butanol–ethanol pathway. Further genomic and proteomic analysis showed that the capabilities of efficient xylan degradation and butanol synthesis were attributed to the efficient expression of xylanase, β-xylosidase and the bifunctional alcohol/aldehyde dehydrogenase (AdhE). Process optimization based on the characteristic of AdhE could further improve the final butanol titer to 1.17 g/L from xylan through CBP. Furthermore, a new co-cultivation system consisting of Thermoanaerobacterium sp. M5 which could release xylose from xylan efficiently and C. acetobutylicum NJ4 which possesses the capacity of high butanol production was established. This microbial co-cultivation system could improve the butanol titer to 8.34 g/L, representing the highest butanol titer from xylan through CBP.ConclusionsA newly thermophilic and butanogenic bacterium Thermoanaerobacterium sp. M5 was isolated and key enzymes responsible for butanol production were characterized in this study. High butanol titer was obtained from xylan through process optimization. In addition, the newly set up microbial co-cultivation system, consisting of Thermoanaerobacterium sp. M5 and C. acetobutylicum NJ4, achieved the highest butanol production from xylan compared with the reported co-cultivation systems.
Herein, ultra-small NiFeO hollow particles, with the diameter and wall thickness of only 6 and 1.8 nm, respectively, were anchored on a graphene surface based on the nanoscale Kirkendall effect. The hybrid exhibits an excellent electromagnetic wave absorption property, comparable or superior to that of most reported absorbers. Our strategy may open a way to grow ultra-small hollow particles on graphene for applications in many fields such as eletromagnetic wave absorption and energy storage and conversion.
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