The operation of chemical vapor-deposited (CVD) graphene field-effect transistors (GFETs) is highly sensitive to environmental factors such as the substrate, polymer residues, ambient condition, and other species adsorbed on the graphene surface due to their high defect density. As a result, CVD GFETs often exhibit a large hysteresis and time-dependent instability. These problems become a major roadblock in the systematic study of graphene devices. We report a facile process to alleviate these problems, which can be used to fabricate stable high performance CVD GFETs with symmetrical current-voltage (I-V) characteristics and an effective carrier mobility over 6000 cm(2) V(-1) s(-1). This process combined a few steps of processes in sequence including pre-annealing in a vacuum, depositing a passivation layer, and the final annealing in a vacuum, and eliminated ∼50% of charging sources primarily originating from water reduction reactions.
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http://dx.doi.org/10.1039/c4nr06397j | DOI Listing |
Angew Chem Int Ed Engl
December 2024
Nanjing Forestry University, Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, CHINA.
Suboptimal spatial utilization and inefficient access to internal porosity preclude porous carbon cathodes from delivering high energy density in zinc-ion hybrid capacitors (ZIHCs). Inspired by the function of capillaries in biological systems, this study proposes a facile coordination-pyrolysis method to fabricate thin-walled hollow carbon nanofibers (CNFs) with optimized pore structure and surface functional groups for ZHICs. The capillary-like CNFs maximize the electrode/electrolyte interface area, facilitating the optimal utilization of energy storage sites.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
INFN-Laboratori Nazionali di Frascati, 00044 Frascati, Italy.
This study investigates the synthesis of corn starch nanocrystals (SNCs) via sulfuric acid hydrolysis. Esterification of oleic acid (OA) with SNCs was carried out using Maghnite-H as a catalyst, a non-polluting, eco-friendly proton-exchanged montmorillonite-based green catalyst suitable for various chemical processes. Optimization of synthesis parameters, including reaction temperature, duration, and catalyst quantity, was conducted using response surface methodology (RSM) with a central composite design incorporating three factors and three levels.
View Article and Find Full Text PDFNat Commun
December 2024
Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu, 610064, China.
The activation of C-C bond of benzocyclobutenones under mild reaction conditions remains a challenge. We herein report a photoinduced catalyst-free regio-specific C1-C8 bond cleavage of benzocyclobutenones, enabling the generation of versatile ortho-quinoid ketene methides for aza-[4 + 2]-cycloaddition with imines, which offers a facile route to isoquinolinone derivatives, including seven family members of protoberberine alkaloids, gusanlung A, B, D, 8-oxotetrahydroplamatine, tetrahydrothalifendine, tetrahydropalmatine, and xylopinine. Furthermore, the catalytic enantioselective version of this strategy is also realized by merging synergistic photocatalysis and chiral Lewis acid catalysis.
View Article and Find Full Text PDFNat Commun
December 2024
National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui, PR China.
Elucidating the formation mechanism of polycyclic aromatic hydrocarbons (PAHs) is crucial to understand processes in the contexts of combustion, environmental science, astrochemistry, and nanomaterials synthesis. An excited electronic-state pathway has been proposed to account for the formation of 14π aromatic anthracene in the benzyl (b-CH) self-reaction. Here, to improve our understanding of anthracene formation, we investigate CH bimolecular reactions in a tubular SiC microreactor through an isomer-resolved method that combines in situ synchrotron-radiation VUV photoionization mass spectrometry and ex-situ gas chromatography-mass spectrometry.
View Article and Find Full Text PDFJACS Au
December 2024
Department of Chemistry, University of Antwerp, Antwerp 2020, Belgium.
Proton-coupled electron transfer (PCET) is a fundamental redox process and has clear advantages in selectively activating challenging C-H bonds in many biological processes. Intrigued by this activation process, we aimed to develop a facile PCET process in cancer cells by modulating proton tunneling. This approach should lead to the design of an alternative photodynamic therapy (PDT) that depletes the mitochondrial electron transport chain (ETC), the key redox regulator in cancer cells under hypoxia.
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