Publications by authors named "Changsheng Xiang"

Epitaxially grown lanthanide metal-organic frameworks (Ln MOFs) exhibit multicolor and characteristic Ln emission with sharp emission bands, which are of great value in the field of information security and anti-counterfeiting. Epitaxial growth of Ln MOFs is generally achieved by solvothermal or hydrothermal methods, which suffer from challenges such as high reaction temperature and long growth time. Here, we report the fast epitaxial growth of multicolor lanthanide MOFs by an ultrasonic method at room temperature.

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Asphaltene is often regarded as an undesirable by-product of petroleum processing, possesses vast reserves with little market value. The typical routes of consuming asphaltene, namely burning and landfilling, pose significant environmental challenges. In this study, low-value asphaltene is converted into high-value ethylated carbon clusters (ECC) using a supercritical ethanol technique.

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As the world is committed to reach carbon peak by 2030 and net zero by 2050, the use of coal as an energy source is facing unprecedented challenges. According to the International Energy Agency (IEA), global annual coal demand is estimated to drop from more than 5640 million tonnes of coal equivalent (Mtce) in 2021 to 540 Mtce in 2050 under the net zero emission scenario, mostly being replaced by renewable energy such as solar and wind. Therefore, the coal industry is vigorously seeking alternative applications to keep it thriving, and nanotechnology can be one of the contributors.

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Luminescent polymer composite materials, based on poly(vinyl alcohol) (PVA), as a matrix polymer and graphene quantum dots (GQDs) derived from coal, were prepared by casting from aqueous solutions. The coal-derived GQDs impart fluorescent properties to the polymer matrix, and the fabricated composite films exhibit solid state fluorescence. Optical, thermal, and fluorescent properties of the PVA/GQD nanocomposites have been studied.

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Bandgaps of photoluminescent graphene quantum dots (GQDs) synthesized from anthracite have been engineered by controlling the size of GQDs in two ways: either chemical oxidative treatment and separation by cross-flow ultrafiltration, or by a facile one-step chemical synthesis using successively higher temperatures to render smaller GQDs. Using these methods, GQDs were synthesized with tailored sizes and bandgaps. The GQDs emit light from blue-green (2.

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Graphene oxide nanoribbon (GONR) made by the oxidative unzipping of multiwalled carbon nanotube was dispersed in dimethylformamide and mixed with polyacrylonitrile (PAN) to fabricate continuous PAN/GONR composite fibers by gel spinning. Subsequently, PAN/GONR composite fibers were stabilized and carbonized in a batch process to fabricate composite carbon fibers. Structure, processing, and properties of the composite precursor and carbon fibers have been studied.

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A simple method to fabricate edge-oriented MoS2 films with sponge-like morphologies is demonstrated. They are directly fabricated through the reaction of sulfur vapor with anodically formed Mo oxide sponge-like films on flexible Mo substrates. The edge-oriented MoS2 film delivers excellent hydrogen evolution reaction (HER) activity with enhanced kinetics and long-term cycling stability.

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A three-dimensional nanoporous Ni(OH)2 thin-film was hydrothermally converted from an anodically formed porous layer of nickel fluoride/oxide. The nanoporous Ni(OH)2 thin-films can be used as additive-free electrodes for energy storage. The nanoporous layer delivers a high capacitance of 1765 F g(-1) under three electrode testing.

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Nanoporous Ni-Co binary oxide layers were electrochemically fabricated by deposition followed by anodization, which produced an amorphous layered structure that could act as an efficient electrocatalyst for water oxidation. The highly porous morphologies produced higher electrochemically active surface areas, while the amorphous structure supplied abundant defect sites for oxygen evolution. These Ni-rich (10-40 atom % Co) binary oxides have an increased active surface area (roughness factor up to 17), reduced charge transfer resistance, lowered overpotential (∼325 mV) that produced a 10 mA cm(-2) current density, and a decreased Tafel slope (∼39 mV decade(-1)).

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A flexible three-dimensional (3-D) nanoporous NiF2-dominant layer on poly(ethylene terephthalate) has been developed. The nanoporous layer itself can be freestanding without adding any supporting carbon materials or conducting polymers. By assembling the nanoporous layer into two-electrode symmetric devices, the inorganic material delivers battery-like thin-film supercapacitive performance with a maximum capacitance of 66 mF cm(-2) (733 F cm(-3) or 358 F g(-1)), energy density of 384 Wh kg(-1), and power density of 112 kW kg(-1).

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Polyvinyl alcohol functionalized carbon black with H2S-sensor moieties can be pumped through oil and water in porous rock and the H2S content can be determined based on the fluorescent enhancement of the H2S-sensor addends.

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As the cylindrical sp(2)-bonded carbon allotrope, carbon nanotubes (CNTs) have been widely used to reinforce bulk materials such as polymers, ceramics, and metals. However, both the concept demonstration and the fundamental understanding on how 1D CNTs reinforce atomically thin 2D layered materials, such as graphene, are still absent. Here, we demonstrate the successful synthesis of CNT-toughened graphene by simply annealing functionalized CNTs on Cu foils without needing to introduce extraneous carbon sources.

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Bi- and trilayer graphene have attracted intensive interest due to their rich electronic and optical properties, which are dependent on interlayer rotations. However, the synthesis of high-quality large-size bi- and trilayer graphene single crystals still remains a challenge. Here, the synthesis of 100 μm pyramid-like hexagonal bi- and trilayer graphene single-crystal domains on Cu foils using chemical vapor deposition is reported.

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Deicing heating layers are frequently used in covers of large radio-frequency (RF) equipment, such as radar, to remove ice that could damage the structures or make them unstable. Typically, the deicers are made using a metal framework and inorganic insulator; commercial resistive heating materials are often nontransparent to RF waves. The preparation of a sub-skin-depth thin film, whose thickness is very small relative to the RF skin (or penetration) depth, is the key to minimizing the RF absorption.

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Coal is the most abundant and readily combustible energy resource being used worldwide. However, its structural characteristic creates a perception that coal is only useful for producing energy via burning. Here we report a facile approach to synthesize tunable graphene quantum dots from various types of coal, and establish that the unique coal structure has an advantage over pure sp2-carbon allotropes for producing quantum dots.

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A thermoplastic polyurethane (TPU) composite film containing hexadecyl-functionalized low-defect graphene nanoribbons (HD-GNRs) was produced by solution casting. The HD-GNRs were well distributed within the polyurethane matrix, leading to phase separation of the TPU. Nitrogen gas effective diffusivity of TPU was decreased by 3 orders of magnitude with only 0.

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Two types of graphene oxide fibers are spun from high concentration aqueous dopes. Fibers extruded from large flake graphene oxide dope without drawing show unconventional 100% knot efficiency. Fibers spun from small sized graphene oxide dope with stable and continuous drawing yield in good intrinsic alignment with a record high tensile modulus of 47 GPa.

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Precise spatial control of materials is the key capability of engineering their optical, electronic, and mechanical properties. However, growth of graphene on Cu was revealed to be seed-induced two-dimensional (2D) growth, limiting the synthesis of complex graphene spatial structures. In this research, we report the growth of onion ring like three-dimensional (3D) graphene structures, which are comprised of concentric one-dimensional hexagonal graphene ribbon rings grown under 2D single-crystal monolayer graphene domains.

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A composite made from graphene nanoribbons (GNRs) and tin oxide (SnO2) nanoparticles (NPs) is synthesized and used as the anode material for lithium ion batteries (LIBs). The conductive GNRs, prepared using sodium/potassium unzipping of multiwall carbon nanotubes, can boost the lithium storage performance of SnO2 NPs. The composite, as an anode material for LIBs, exhibits reversible capacities of over 1520 and 1130 mAh/g for the first discharge and charge, respectively, which is more than the theoretical capacity of SnO2.

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The solubility of single-walled carbon nanotube (SWCNT) polyelectrolytes [K(THF)]nSWCNT in dimethyl sulfoxide (DMSO) was determined by a combination of centrifugation, UV-vis spectral properties, and solution extraction. The SWCNT formed a liquid crystal at a concentration above 3.8 mg/mL.

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Graphene oxide nanoribbons (GONRs) and chemically reduced graphene nanoribbons (crGNRs) were dispersed at high concentrations in chlorosulfonic acid to form anisotropic liquid crystal phases. The liquid crystal solutions were spun directly into hundreds of meters of continuous macroscopic fibers. The relationship of fiber morphology to coagulation bath conditions was studied.

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Graphene was grown directly on porous nickel films, followed by the growth of controlled lengths of vertical carbon nanotube (CNT) forests that seamlessly emanate from the graphene surface. The metal-graphene-CNT structure is used to directly fabricate field-emitter devices and double-layer capacitors. The three-dimensional nanostructured hybrid materials, with better interfacial contacts and volume utilization, can stimulate the development of several energy-efficient technologies.

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Few-layer graphene, with Bernal stacking order, is of particular interest to the graphene community because of its unique tunable electronic structure. A synthetic method to produce such large area graphene films with precise thickness from 2 to 4 layers would be ideal for chemists and physicists to explore the promising electronic applications of these materials. Here, large-area uniform Bernal-stacked bi-, tri-, and tetralayer graphene films were successfully synthesized on a Cu surface in selective growth windows, with a finely tuned total pressure and CH(4)/H(2) gas ratio.

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In this research, we constructed a controlled chamber pressure CVD (CP-CVD) system to manipulate graphene's domain sizes and shapes. Using this system, we synthesized large (~4.5 mm(2)) single-crystal hexagonal monolayer graphene domains on commercial polycrystalline Cu foils (99.

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