142 research outputs found

    Understanding and Controlling Cu-Catalyzed Graphene Nucleation: The Role of Impurities, Roughness, and Oxygen Scavenging

    Get PDF
    The mechanism by which Cu catalyst pretreatments control graphene nucleation density in scalable chemical vapor deposition (CVD) is systematically explored. The intrinsic and extrinsic carbon contamination in the Cu foil is identified by time-of-flight secondary ion mass spectrometry as a major factor influencing graphene nucleation and growth. By selectively oxidizing the backside of the Cu foil prior to graphene growth, a drastic reduction of the graphene nucleation density by 6 orders of magnitude can be obtained. This approach decouples surface roughness effects and at the same time allows us to trace the scavenging effect of oxygen on deleterious carbon impurities as it permeates through the Cu bulk. Parallels to well-known processes in Cu metallurgy are discussed. We also put into context the relative effectiveness and underlying mechanisms of the most widely used Cu pretreatments, including wet etching and electropolishing, allowing a rationalization of current literature and determination of the relevant parameter space for graphene growth. Taking into account the wider CVD growth parameter space, guidelines are discussed for high-throughput manufacturing of "electronic-quality" monolayer graphene films with domain size exceeding 1 mm, suitable for emerging industrial applications, such as electronics and photonics.This research was supported by the ERC under grant InsituNANO (279342), the EPSRC under grant GRAPHTED (EP/K016636/1), and the Innovation R&D programme of the National Measurement System of the U.K. Department of Business, Innovation and Skills (project number 118616)

    Materials Performance of Modified 430 Stainless Steel in Simulated SOFC Stack Environments for Integrated Gasification Fuel Cell System Applications

    Get PDF
    The corrosion behaviors of a low silicon and aluminum 430 stainless steel with and without ceria surface treatment were investigated in a simulated coal syngas at 800 °C and in air. Thermodynamic calculations were made to predict carbon activities for the coal syngas as a function of temperature. At 800 °C, carbon activity is ~1.1, which indicates that carbon that forms could diffuse into the steel and induce carbon corrosion, e.g. carburization and metal dusting. The surface morphology was investigated with X-ray diffraction and scanning electron microscopy. In coal gas, the scale formed on bare steel consisted of Mn 1.5 Cr 1.5 O 4 and Cr 2 O 3 and on ceria treated steel (Fe, Mn)O, FeCr 2 O 4 , Cr 2 O 3 , and CeCrO 3 . Both materials underwent carburization, but not metal dusting. The results of oxidation in air using a thermogravimetric apparatus confirmed that the 430 sample was less resistant to oxidation than the 430 treated with ceria

    A single-label phenylpyrrolocytidine provides a molecular beacon-like response reporting HIV-1 RT RNase H activity

    Get PDF
    6-Phenylpyrrolocytidine (PhpC), a structurally conservative and highly fluorescent cytidine analog, was incorporated into oligoribonucleotides. The PhpC-containing RNA formed native-like duplex structures with complementary DNA or RNA. The PhpC-modification was found to act as a sensitive reporter group being non-disruptive to structure and the enzymatic activity of RNase H. A RNA/DNA hybrid possessing a single PhpC insert was an excellent substrate for HIV-1 RT Ribonuclease H and rapidly reported cleavage of the RNA strand with a 14-fold increase in fluorescence intensity. The PhpC-based assay for RNase H was superior to the traditional molecular beacon approach in terms of responsiveness, rapidity and ease (single label versus dual). Furthermore, the PhpC-based assay is amenable to high-throughput microplate assay format and may form the basis for a new screen for inhibitors of HIV-RT RNase H
    corecore