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Matthew Laskoski

Bio: Matthew Laskoski is an academic researcher from United States Naval Research Laboratory. The author has contributed to research in topics: Phthalonitrile & Thermosetting polymer. The author has an hindex of 18, co-authored 73 publications receiving 1338 citations. Previous affiliations of Matthew Laskoski include United States Department of the Navy.


Papers
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Journal ArticleDOI
TL;DR: In this article, a multiple aromatic ether linked phthalonitrile was synthesized and characterized, which exhibited good structural integrity upon heating to elevated temperatures and exhibited excellent thermal properties along with long-term oxidative stability.
Abstract: A multiple aromatic ether linked phthalonitrile was synthesized and characterized. The oligomeric phthalonitrile monomer was prepared from the reaction of an excess amount of bisphenol A with 4,4'-difluorobenzophenone in the presence of K 2 CO 3 as the base in an N,N-dimethylformamide/toluene solvent mixture, followed by end capping with 4-nitrophthalonitrile in a two-step, one-pot reaction. The monomer properties were compared to those of the known resin 2,2-bis[4-(3,4-dicyanophenoxylphenyl]propane after being cured in the presence of bis[4-(4-aminophenoxy)-phenyllsulfone. Rheometric measurements and thermogravimetric analysis showed that the oligomeric phthalonitrile resin maintained good structural integrity upon heating to elevated temperatures and exhibited excellent thermal properties along with long-term oxidative stability. The ether-linked phthalonitrile resin absorbed less than 2.5% water by weight after exposure to an aqueous environment for extended periods.

209 citations

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TL;DR: The dry transfer exploits an azide linker molecule to establish a covalent bond to graphene and to generate greater graphene-polymer adhesion compared to that of the graphene-metal foil.
Abstract: In this paper we demonstrate high-quality, uniform dry transfer of graphene grown by chemical vapor deposition on copper foil to polystyrene. The dry transfer exploits an azide linker molecule to e...

132 citations

Journal ArticleDOI
05 Oct 2007-Polymer
TL;DR: A series of multiple aromatic ether-linked phthalonitrile resins containing an aromatic ether phosphine oxide group in the backbone have been synthesized and characterized as discussed by the authors, and the results showed that the phosphorus-containing resins maintained good structural integrity upon heating to elevated temperatures and exhibited excellent thermal properties.

127 citations

Journal ArticleDOI
TL;DR: An improved synthetic method has been developed for oligomeric aromatic ether ketone-based phthalonitrile (PN) resins as discussed by the authors, which lowers the cure temperature of the PN resin to around 150 °C and compared to the traditional high-temperature aromatic diamine.
Abstract: An improved synthetic method has been developed for oligomeric aromatic ether ketone-based phthalonitrile (PN) resins. A new curing additive was studied that lowers the cure temperature of the PN resin to around 150 °C and compared to the traditional high-temperature aromatic diamine. Mechanical and thermo-oxidative analyses of polymeric samples from both systems were determined and compared under various curing conditions. The PN polymer exhibited low water absorption regardless of the chosen cure system. Published 2014. This article is a U.S. Government work and is in the public domain in the USA. J. Polym. Sci., Part A: Polym. Chem. 2014, 52, 1662–1668

104 citations

Journal ArticleDOI
12 Jun 2015-Polymer
TL;DR: In this paper, a versatile scheme to produce a multiple aromatic ether-linked phthalonitrile has been developed and applied to the preparation of two unique resin systems, which exhibited excellent viscosities for molding various shaped articles and were thermally cured to yield crosslinked polymers.

74 citations


Cited by
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TL;DR: Thermal conductivities for both the 5-layer and the 11-layer samples are suppressed at low temperatures, suggesting increasing scattering of low frequency phonons in thin h-BN samples by polymer residue.
Abstract: The thermal conductivity of suspended few-layer hexagonal boron nitride (h-BN) was measured using a microbridge device with built-in resistance thermometers. Based on the measured thermal resistance values of 11-12 atomic layer h-BN samples with suspended lengths ranging between 3 and 7.5 μm, the room-temperature thermal conductivity of a 11-layer sample was found to be about 360 W m(-1) K(-1), approaching the basal plane value reported for bulk h-BN. The presence of a polymer residue layer on the sample surface was found to decrease the thermal conductivity of a 5-layer h-BN sample to be about 250 W m(-1) K(-1) at 300 K. Thermal conductivities for both the 5-layer and the 11-layer samples are suppressed at low temperatures, suggesting increasing scattering of low frequency phonons in thin h-BN samples by polymer residue.

597 citations

Journal ArticleDOI
TL;DR: In this paper, the structural properties of 2D materials, such as defects and dopants, the number of layers, composition, phase, strain, and other structural characteristics, are discussed and analyzed.
Abstract: The exfoliation and identification of the two-dimensional (2D) single atomic layer of carbon have opened the opportunity to explore graphene and related 2D materials due to their unique properties. 2D materials are regarded as one of the most exciting solutions for next generation electronics and optoelectronics in the technological evolution of semiconductor technology. In this review, we focus on the core concept of “structure-property relationships” to explain the state-of-the-art of 2D materials and summarize the unique electrical and light-matter interaction properties in 2D materials. Based on this, we discuss and analyze the structural properties of 2D materials, such as defects and dopants, the number of layers, composition, phase, strain, and other structural characteristics, which could significantly alter the properties of 2D materials and hence affect the performance of semiconductor devices. In particular, the building blocks principles and potential electronic and optoelectronic applications...

469 citations

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TL;DR: The electrical transport properties of CVD-grown graphene are tested in which two important sources of disorder, namely grain boundaries and processing-induced contamination, are substantially reduced, confirming the possibility of achieving high-performance graphene devices based on a scalable synthesis process.
Abstract: While chemical vapor deposition (CVD) promises a scalable method to produce large-area graphene, CVD-grown graphene has heretofore exhibited inferior electronic properties in comparison with exfoliated samples. Here we test the electrical transport properties of CVD-grown graphene in which two important sources of disorder, namely grain boundaries and processing-induced contamination, are substantially reduced. We grow CVD graphene with grain sizes up to 250 μm to abate grain boundaries, and we transfer graphene utilizing a novel, dry-transfer method to minimize chemical contamination. We fabricate devices on both silicon dioxide and hexagonal boron nitride (h-BN) dielectrics to probe the effects of substrate-induced disorder. On both substrate types, the large-grain CVD graphene samples are comparable in quality to the best reported exfoliated samples, as determined by low-temperature electrical transport and magnetotransport measurements. Small-grain samples exhibit much greater variation in quality and...

436 citations

Journal ArticleDOI
TL;DR: The recent advancements in transferring graphene to arbitrary substrates will be extensively reviewed, categorized into mechanical exfoliation, polymer-assisted transfer, continuous transfer by roll-to-roll process, and transfer-free techniques including direct synthesis on insulating substrates.
Abstract: The first micrometer-sized graphene flakes extracted from graphite demonstrated outstanding electrical, mechanical and chemical properties, but they were too small for practical applications. However, the recent advances in graphene synthesis and transfer techniques have enabled various macroscopic applications such as transparent electrodes for touch screens and light-emitting diodes (LEDs) and thin-film transistors for flexible electronics in particular. With such exciting potential, a great deal of effort has been put towards producing larger size graphene in the hopes of industrializing graphene production. Little less than a decade after the first discovery, graphene now can be synthesized up to 30 inches in its diagonal size using chemical vapour deposition methods. In making this possible, it was not only the advances in the synthesis techniques but also the transfer methods that deliver graphene onto target substrates without significant mechanical damage. In this article, the recent advancements in transferring graphene to arbitrary substrates will be extensively reviewed. The methods are categorized into mechanical exfoliation, polymer-assisted transfer, continuous transfer by roll-to-roll process, and transfer-free techniques including direct synthesis on insulating substrates.

430 citations

Journal ArticleDOI
TL;DR: The major "graphene-on-surface" structures are described and the roles of their properties and related phenomena in governing the overall performance for specific applications including optoelectronics, surface catalysis, anti-friction and superlubricity, and coatings and composites are examined.
Abstract: Graphene has demonstrated great potential in next-generation electronics due to its unique two-dimensional structure and properties including a zero-gap band structure, high electron mobility, and high electrical and thermal conductivity. The integration of atom-thick graphene into a device always involves its interaction with a supporting substrate by van der Waals forces and other intermolecular forces or even covalent bonding, and this is critical to its real applications. Graphene films on different surfaces are expected to exhibit significant differences in their properties, which lead to changes in their morphology, electronic structure, surface chemistry/physics, and surface/interface states. Therefore, a thorough understanding of the surface/interface properties is of great importance. In this review, we describe the major “graphene-on-surface” structures and examine the roles of their properties and related phenomena in governing the overall performance for specific applications including optoelectronics, surface catalysis, anti-friction and superlubricity, and coatings and composites. Finally, perspectives on the opportunities and challenges of graphene-on-surface systems are discussed.

285 citations