Dong Han Seo

Plasma break-down and re-build: same functional vertical graphenes from diverse natural precursors.

Plasmas, the 4(th) state of matter, uniformly transform natural precursors with different chemical composition in solid, liquid, and gas states into the same functional vertical graphenes in a single-step process within a few minutes. Functional vertical graphenes show reliable biosensing properties, strong binding with proteins, and improved adhesion to substrates.

Synergistic Fusion of Vertical Graphene Nanosheets and Carbon Nanotubes for High‐Performance Supercapacitor Electrodes

Graphene and carbon nanotubes (CNTs) are attractive electrode materials for supercapacitors. However, challenges such as the substrate-limited growth of CNTs, nanotube bundling in liquid electrolytes, under-utilized basal planes, and stacking of graphene sheets have so far impeded their widespread application. Here we present a hybrid structure formed by the direct growth of CNTs onto vertical graphene nanosheets (VGNS). VGNS are fabricated by a green plasma-assisted method to break down and reconstruct a natural precursor into an ordered graphitic structure. The synergistic combination of CNTs and VGNS overcomes the challenges intrinsic to both materials. The resulting VGNS/CNTs hybrids show a high specific capacitance with good cycling stability. The charge storage is based mainly on the non-Faradaic mechanism. In addition, a series of optimization experiments were conducted to reveal the critical factors that are required to achieve the demonstrated high supercapacitor performance.

Plasma-enabled sustainable elemental lifecycles: honeycomb-derived graphenes for next-generation biosensors and supercapacitors

A green and efficient conversion of redundant biomass into functional nanomaterials holds the key to sustainable future technologies. Recently, vertical graphene nanosheets (VGS) have emerged as promising nanomaterials for integration in high-performance biosensors and supercapacitors, owing to their excellent and unique structural, morphological and electrical properties. However, when considering the conventional techniques utilized in nanofabrication, such as thermal or chemical routes, these often involve complex, eco-destructive and resource-consuming processes. Here we report on a single-step, potentially scalable, environmentally-benign and plasma-enabled method to synthesize VGS from an underutilized and natural by-product precursor, honeycomb. The VGS multifunctionality is highlighted by its integration as supercapacitor electrodes for energy storage, and as an electrochemical biosensor for the detection of the neurotoxic Amyloid-beta (Aβ) biomarker of Alzheimers disease. The VGS were employed as binder-free supercapacitor electrodes, and demonstrated high specific capacitance up to 240 F g−1 at a scan rate of 5 mV s−1 and 100% capacitance retention after 2000 charge/discharge cycles. Furthermore, the VGS were functionalized with curcumin bioreceptors, and exhibited good sensitivity and selectivity towards the detection of neurotoxic Aβ species, and demonstrated a detection limit of 0.1 μg mL−1.

Deterministic control of structural and optical properties of plasma-grown vertical graphene nanosheet networks via nitrogen gas variation

The effect of nitrogen on the growth of vertically oriented graphene nanosheets on catalyst-free silicon and glass substrates in a plasma-assisted process is studied. Different concentrations of nitrogen were found to act as versatile control knobs that could be used to tailor the length, number density and structural properties of the nanosheets. Nanosheets with different structural characteristics exhibit markedly different optical properties. The nanosheet samples were treated with a bovine serum albumin protein solution to investigate the effects of this variation on the optical properties for biosensing through confocal micro-Raman spectroscopy and UV-Vis spectrophotometry.

Plasma Catalytic Synthesis of Ammonia Using Functionalized-Carbon Coatings in an Atmospheric-Pressure Non-equilibrium Discharge

We investigate the synthesis of ammonia in a non-equilibrium atmospheric-pressure plasma using functionalized-nanodiamond and diamond-like-carbon coatings on α-Al2O3 spheres as catalysts. Oxygenated nanodiamonds were found to increase the production yield of ammonia, while hydrogenated nanodiamonds decreased the yield. Neither type of nanodiamond affected the plasma properties significantly. Using diffuse-reflectance FT-IR and XPS, the role of different functional groups on the catalyst surface was investigated. Evidence is presented that the carbonyl group is associated with an efficient surface adsorption and desorption of hydrogen in ammonia synthesis on the surface of the nanodiamonds, and an increased production of ammonia. Conformal diamond-like-carbon coatings, deposited by plasma-enhanced chemical vapour deposition, led to a plasma with a higher electron density, and increased the production of ammonia.

High Pseudocapacitive Performance of MnO2 Nanowires on Recyclable Electrodes

Manganese oxides are promising pseudocapacitve materials for achieving both high power and energy densities in pseudocapacitors. However, it remains a great challenge to develop MnO2 -based high-performance electrodes due to their low electrical conductance and poor stability. Here we show that MnO2 nanowires anchored on electrochemically modified graphite foil (EMGF) have a high areal capacitance of 167 mF cm(-2) at a discharge current density of 0.2 mA cm(-2) and a high capacitance retention after 5000 charge/discharge cycles (115 %), which are among the best values reported for any MnO2 -based hybrid structures. The EMGF support can also be recycled and the newly deposited MnO2 -based hybrids retain similarly high performance. These results demonstrate the successful preparation of pseudocapacitors with high capacity and cycling stability, which may open a new opportunity towards a sustainable and environmentally friendly method of utilizing electrochemical energy storage devices.

Multifunctional graphene micro-islands: Rapid, low-temperature plasma-enabled synthesis and facile integration for bioengineering and genosensing applications.

Here, we present a rapid, low-temperature (200°C) plasma-enabled synthesis of graphene micro-islands (GMs). Morphological analyses of GMs by scanning electron microscopy (SEM) and atomic force microscopy (AFM) feature a uniform and open-networked array of aggregated graphene sheets. Structural and surface chemical characterizations by Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) support the presence of thin graphitic edges and reactive oxygen functional groups. We demonstrate that these inherent properties of GMs enable its multifunctional capabilities as a bioactive interface. GMs exhibit a biocompatibility of 80% cell viability with primary fibroblast lung cells after 5 days. Further, GMs were assembled into an impedimetric genosensor, and its performance was characterized by electrochemical impedance spectroscopy (EIS). A dynamic sensing range of 1pM to 1nM is reported, and a limit of quantification (LOQ) of 2.03×10-13M is deduced, with selectivity to single-RNA-base mismatched sequences. The versatile nature of GMs may be explored to enable multi-faceted bioactive platforms for next-generation personalized healthcare technologies.

Different Nanostructures From Different Plasmas: Nanoflowers and Nanotrees on Silicon

Using the advanced radio-frequency plasma-assisted magnetron deposition system, various nanostructures such as nanoflowers of carbon nanotubes, ZnO nanobelts, and silicon nanotrees were successfully synthesized. In this paper, we present the photographs of ICP and magnetron discharges, the photograph of a complex plasma structure, and the SEM images of various nanostructures synthesized in the system with magnetron and ICP sources operating simultaneously.

Anti-fouling graphene-based membranes for effective water desalination

The inability of membranes to handle a wide spectrum of pollutants is an important unsolved problem for water treatment. Here we demonstrate water desalination via a membrane distillation process using a graphene membrane where water permeation is enabled by nanochannels of multilayer, mismatched, partially overlapping graphene grains. Graphene films derived from renewable oil exhibit significantly superior retention of water vapour flux and salt rejection rates, and a superior antifouling capability under a mixture of saline water containing contaminants such as oils and surfactants, compared to commercial distillation membranes. Moreover, real-world applicability of our membrane is demonstrated by processing sea water from Sydney Harbour over 72 h with macroscale membrane size of 4 cm2, processing ~0.5 L per day. Numerical simulations show that the channels between the mismatched grains serve as an effective water permeation route. Our research will pave the way for large-scale graphene-based antifouling membranes for diverse water treatment applications.Intrinsic limitations of nanoporous graphene limit its applications in water treatment. Here the authors produce post-treatment-free, low-cost graphene-based membranes from renewable biomass and demonstrate their high water permeance and antifouling properties using real seawater.

Controlling the adsorption behavior of hydrogen at the interface of polycrystalline CVD graphene

Abstract Polycrystalline graphene films were synthesized from renewable biomaterials in ambient air using a facile and rapid thermal chemical vapour deposition technique. Characterization of the graphene reveals a large surface area, the presence of nanoscale domains and open edges, atomic-level stacking, and high electrical conductivity, which are favorable features for electrochemical hydrogen evolution reactions (HERs). The numerous boundaries and open edges accelerate the gas diffusion process and enlarge the effective reactive surface area for gas evolution, which is responsible for a significant improvement of HER performance and stability compared to a commercial graphene film. The hydrogen adhesion behavior in investigated for both bare Ni foil/foam and graphene grown on Ni foil/foam samples. The hydrogen gas bubbles adhere to the polycrystalline graphene for a long period of time before detaching, in contrast to their behavior on the pristine Ni foil surface. Post treatment of the graphene film using plasma treatment increases the desorption rate of hydrogen bubbles from the surface. The results indicate a wide range of possibilities for use of graphene-based catalysts in electrocatalytic gas evolution reactions.