Flexible and Stackable Laser-Induced Graphene Supercapacitors

In this paper, we demonstrate that by simple laser induction, commercial polyimide films can be readily transformed into porous graphene for the fabrication of flexible, solid-state supercapacitors. Two different solid-state electrolyte supercapacitors are described, namely vertically stacked graphene supercapacitors and in-plane graphene microsupercapacitors, each with enhanced electrochemical performance, cyclability, and flexibility. Devices with a solid-state polymeric electrolyte exhibit areal capacitance of >9 mF/cm² at a current density of 0.02 mA/cm², more than twice that of conventional aqueous electrolytes. Moreover, laser induction on both sides of polyimide sheets enables the fabrication of vertically stacked supercapacitors to multiply its electrochemical performance while preserving device flexibility

Nanocomposite of Polyaniline Nanorods Grown on Graphene Nanoribbons for Highly Capacitive Pseudocapacitors

A facile and cost-effective approach to the fabrication of a nanocomposite material of polyaniline (PANI) and graphene nanoribbons (GNRs) has been developed. The morphology of the composite was characterized by scanning electron microscopy, transmission electron microscopy, X-ray photoelectron microscopy, and X-ray diffraction analysis. The resulting composite has a high specific capacitance of 340 F/g and stable cycling performance with 90% capacitance retention over 4200 cycles. The high performance of the composite results from the synergistic combination of electrically conductive GNRs and highly capacitive PANI. The method developed here is practical for large-scale development of pseudocapacitor electrodes for energy storage

Functionalized Graphene Nanoribbon Films as a Radiofrequency and Optically Transparent Material

We report that conductive films made from hexadecylated graphene nanoribbons (HD-GNRs) can have high transparency to radiofrequency (RF) waves even at very high incident power density. Nanoscale-thick HD-GNR films with an area of several square centimeters were found to transmit up to 390 W (2 × 10⁵ W/m²) of RF power with negligible loss, at an RF transmittance of ∼99%. The HD-GNR films conformed to electromagnetic skin depth theory, which effectively accounts for the RF transmission. The HD-GNR films also exhibited sufficient optical transparency for tinted glass applications, with efficient voltage-induced deicing of surfaces. The dispersion of the HD-GNRs afforded by their edge functionalization enables spray-, spin-, or blade-coating on almost any substrate, thus facilitating flexible, conformal, and large-scale film production. In addition to use in antennas and radomes where RF transparency is crucial, these capabilities bode well for the use of the HD-GNR films in automotive and general glass applications where both optical and RF transparencies are desired

Cobalt Nanoparticles Embedded in Nitrogen-Doped Carbon for the Hydrogen Evolution Reaction

There is great interest in renewable and sustainable energy research to develop low-cost, highly efficient, and stable electrocatalysts as alternatives to replace Pt-based catalysts for the hydrogen evolution reaction (HER). Though nanoparticles encapsulated in carbon shells have been widely used to improve the electrode performances in energy storage devices (e.g., lithium ion batteries), they have attracted less attention in energy-related electrocatalysis. Here we report the synthesis of nitrogen-enriched core–shell structured cobalt–carbon nanoparticles dispersed on graphene sheets and we investigate their HER performances in both acidic and basic media. These catalysts exhibit excellent durability and HER activities with onset overpotentials as low as ∼70 mV in both acidic (0.5 M H₂SO₄) and alkaline (0.1 M NaOH) electrolytes, and the overpotentials needed to deliver 10 mA cm^–2 are determined to be 265 mV in acid and 337 mV in base, further demonstrating their potential to replace Pt-based catalysts. Control experiments reveal that the active sites for HER might come from the synergistic effects between the cobalt nanoparticles and nitrogen-doped carbon

Boron- and Nitrogen-Doped Graphene Quantum Dots/Graphene Hybrid Nanoplatelets as Efficient Electrocatalysts for Oxygen Reduction

The scarcity and high cost of platinum-based electrocatalysts for the oxygen reduction reaction (ORR) has limited the commercial and scalable use of fuel cells. Heteroatom-doped nanocarbon materials have been demonstrated to be efficient alternative catalysts for ORR. Here, graphene quantum dots, synthesized from inexpensive and earth-abundant anthracite coal, were self-assembled on graphene by hydrothermal treatment to form hybrid nanoplatelets that were then codoped with nitrogen and boron by high-temperature annealing. This hybrid material combined the advantages of both components, such as abundant edges and doping sites, high electrical conductivity, and high surface area, which makes the resulting materials excellent oxygen reduction electrocatalysts with activity even higher than that of commercial Pt/C in alkaline media

Enhanced Cycling Stability of Lithium Sulfur Batteries Using Sulfur–Polyaniline–Graphene Nanoribbon Composite Cathodes

A hierarchical nanocomposite material of graphene nanoribbons combined with polyaniline and sulfur using an inexpensive, simple method has been developed. The resulting composite, characterized by scanning electron microscopy, transmission electron microscopy, X-ray photoelectron microscopy, and X-ray diffraction analysis, has a good rate performance and excellent cycling stability. The synergistic combination of electrically conductive graphene nanoribbons, polyaniline, and sulfur produces a composite with high performance. The method developed here is practical for the large-scale development of cathode materials for lithium sulfur batteries

Rebar graphene

As the cylindrical sp2-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. The CNTs act as reinforcing bar (rebar), toughening the graphene through both π–π stacking domains and covalent bonding where the CNTs partially unzip and form a seamless 2D conjoined hybrid as revealed by aberration-corrected scanning transmission electron microscopy analysis. This is termed rebar graphene. Rebar graphene can be free-standing on water and transferred onto target substrates without needing a polymer-coating due to the rebar effects of the CNTs. The utility of rebar graphene sheets as flexible all-carbon transparent electrodes is demonstrated. The in-plane marriage of 1D nanotubes and 2D layered materials might herald an electrical and mechanical union that extends beyond carbon chemistry

Asphalt-Derived High Surface Area Activated Porous Carbons for Carbon Dioxide Capture

Research activity toward the development of new sorbents for carbon dioxide (CO₂) capture have been increasing quickly. Despite the variety of existing materials with high surface areas and high CO₂ uptake performances, the cost of the materials remains a dominant factor in slowing their industrial applications. Here we report preparation and CO₂ uptake performance of microporous carbon materials synthesized from asphalt, a very inexpensive carbon source. Carbonization of asphalt with potassium hydroxide (KOH) at high temperatures (>600 °C) yields porous carbon materials (<b>A-PC</b>) with high surface areas of up to 2780 m² g^–1 and high CO₂ uptake performance of 21 mmol g^–1 or 93 wt % at 30 bar and 25 °C. Furthermore, nitrogen doping and reduction with hydrogen yields active N-doped materials (<b>A-NPC</b> and <b>A-rNPC</b>) containing up to 9.3% nitrogen, making them nucleophilic porous carbons with further increase in the Brunauer–Emmett–Teller (BET) surface areas up to 2860 m² g^–1 for <b>A-NPC</b> and CO₂ uptake to 26 mmol g^–1 or 114 wt % at 30 bar and 25 °C for <b>A-rNPC</b>. This is the highest reported CO₂ uptake among the family of the activated porous carbonaceous materials. Thus, the porous carbon materials from asphalt have excellent properties for reversibly capturing CO₂ at the well-head during the extraction of natural gas, a naturally occurring high pressure source of CO₂. Through a pressure swing sorption process, when the asphalt-derived material is returned to 1 bar, the CO₂ is released, thereby rendering a reversible capture medium that is highly efficient yet very inexpensive