Rapid Adsorption of Proinflammatory Cytokines by Graphene Nanoplatelets and their Composites for Extracorporeal Detoxification

Sepsis is a complex clinical syndrome that features excessive release of cytokines and other inflammatory mediators that could lead to organ dysfunction. Despite different treatment and management options, sepsis associated high morbidity and mortality rates remain. This has prompted intensive research into alternative therapeutic approaches such as targeted removal of sepsis related molecules using extracorporeal hemoperfusion. In this study, we explore the use of graphene nanoplatelets (GNP) as low-cost alternative hemosorbents for rapid removal of a broad spectrum of proinflammatory cytokine markers. Firstly, the physical characteristics, cytotoxicity, and cytokine marker adsorption profile of GNP were assessed. The results not only confirmed the surface characteristics of GNP and their ability to rapidly remove cytokine markers, but also indicated a low cytotoxicity towards the hepatic cell line HepG2. GNP were then incorporated into a freestanding flexible GNP-poly(tetrafluoroethylene) film with preserved surface characteristics and cytokine adsorption profile for potential use in hemoperfusion applications

MXene: a promising transition metal carbide anode for lithium-ion batteries

Herein we report on Li insertion into a new two-dimensional (2-D) layered Ti₂C-based material (MXene) with an oxidized surface, formed by etching Al from Ti₂AlC in HF at room temperature. Nitrogen sorption of treated powders showed desorption hysteresis consistent with the presence of slit-like pores. At 23 m² g-¹, the specific surface area was an order of magnitude higher than untreated Ti₂AlC. Cyclic voltammetry exhibited lithiation and delithiation peaks at 1.6 V and 2 V vs. Li+/Li, respectively. At C/25, the steady state capacity was 225 mAh g-¹; at 1C, it was 110 mAh g-¹ after 80 cycles; at 3C, it was 80 mAh g-¹ after 120 cycles; at 10C, it was 70 mAh g-¹ after 200 cycles. Since Ti₂C is a member of the MXene family - where M is an early transition metal and X is C and/or N - that to date includes Ti₃C₂, Ta₄C₃, TiNbC, and (V₀.₅,Cr₀.₅)₃C₂, our results suggest that MXenes are promising as anode materials for Li-ion batteries

High capacitance of coarse-grained carbide derived carbon electrodes

We report exceptional electrochemical properties of supercapacitor electrodes composed of large, granular carbide-derived carbon (CDC) particles. Using a titanium carbide (TiC) precursor, we synthesized 70–250 μm sized particles with high surface area and a narrow pore size distribution. Electrochemical cycling of these coarse-grained powders defied conventional wisdom that a small particle size is strictly required for supercapacitor electrodes and allowed high charge storage densities, rapid transport, and good rate handling ability. The material showcased capacitance above 100 F g−1 at sweep rates as high as 250 mV s−1 in organic electrolyte. 250–1000 micron thick dense CDC films with up to 80 mg cm−2 loading showed superior areal capacitances. The material significantly outperformed its activated carbon counterpart in organic electrolytes and ionic liquids. Furthermore, large internal/external surface ratio of coarse-grained carbons allowed the resulting electrodes to maintain high electrochemical stability up to 3.1 V in ionic liquid electrolyte. In addition to presenting novel insights into the electrosorption process, these coarse-grained carbons offer a pathway to low-cost, high-performance implementation of supercapacitors in automotive and grid-storage applications

Rapid Adsorption of Proinflammatory Cytokines by Graphene Nanoplatelets and Their Composites for Extracorporeal Detoxification

Sepsis is a complex clinical syndrome that features excessive release of cytokines and other inflammatory mediators that could lead to organ dysfunction. Despite different treatment and management options, sepsis associated high morbidity and mortality rates remain. This has prompted intensive research into alternative therapeutic approaches such as targeted removal of sepsis related molecules using extracorporeal hemoperfusion. In this study, we explore the use of graphene nanoplatelets (GNP) as low-cost alternative hemosorbents for rapid removal of a broad spectrum of proinflammatory cytokine markers. Firstly, the physical characteristics, cytotoxicity, and cytokine marker adsorption profile of GNP were assessed. The results not only confirmed the surface characteristics of GNP and their ability to rapidly remove cytokine markers, but also indicated a low cytotoxicity towards the hepatic cell line HepG2. GNP were then incorporated into a freestanding flexible GNP-poly(tetrafluoroethylene) film with preserved surface characteristics and cytokine adsorption profile for potential use in hemoperfusion applications

Potential-Induced Electronic Structure Changes in Supercapacitor Electrodes Observed by In Operando Soft X-Ray Spectroscopy

[[abstract]]The dynamic physiochemical response of a functioning graphene-based aerogel supercapacitor is monitored in operando by soft X-ray spectroscopy and interpreted through ab initio atomistic simulations. Unanticipated changes in the electronic structure of the electrode as a function of applied voltage bias indicate structural modifications across multiple length scales via independent pseudocapacitive and electric double layer charge storage channels.[[notice]]補正完畢[[journaltype]]國外[[incitationindex]]SCI[[ispeerreviewed]]Y[[booktype]]電子版[[countrycodes]]US

Factors affecting the nucleus-independent chemical shift in NMR studies of microporous carbon electrode materials

NMR spectroscopy has recently emerged as a powerful method for studying electrolyte species in microporous carbon electrodes used in capacitive energy storage devices. Key to this approach is the nucleus-independent chemical shift (NICS) which enables adsorbed species to be distinguished from those in the bulk electrolyte. The magnitude of the NICS is well known to be dependent on the distance of the adsorbed species from the carbon surface, and has therefore been used in several studies as a probe of the carbon pore size. However, the NICS can also be influenced by a number of other structural and chemical factors which are not always taken into account. To investigate this, we have carried out a systematic study of the factors influencing the NICS of aqueous electrolyte species adsorbed on polymer-derived activated carbon in the absence of an applied potential. We find that a number of effects arising from both the carbon structure as well as the behaviour and chemical properties of the electrolyte species can contribute to the observed NICS. In turn, the measurement of these effects provides important information about ion behaviour and reveals significant differences in the adsorption behaviour of different ions in the absence of an applied potential. In accordance with several computational studies, we find experimental evidence that the local concentration of spontaneously adsorbed alkali ions decreases with the pore size. This has potential implications for understanding the molecular-level mechanism of charge storage in capacitive devices