Graphene-Oxide-Based Fluoro- and Chromo-Genic Materials and Their Applications.

Composite materials and their applications constitute a hot field of research nowadays due to the fact that they comprise a combination of the unique properties of each component of which they consist. Very often, they exhibit better performance and properties compared to their combined building blocks. Graphene oxide (GO), as the most widely used derivative of graphene, has attracted widespread attention because of its excellent properties. Abundant oxygen-containing functional groups on GO can provide various reactive sites for chemical modification or functionalization of GO, which in turn can be used to develop novel GO-based composites. This review outlines the most recent advances in the field of novel dyes and pigments encompassing GO as a key ingredient or as an important cofactor. The interactions of graphene with other materials/compounds are highlighted. The special structure and unique properties of GO have a great effect on the performance of fabricated hybrid dyes and pigments by enhancing the color performance of dyes, the anticorrosion properties of pigments, the viscosity and rheology of inks, etc., which further expands the applications of dyes and pigments in dyeing, optical elements, solar-thermal energy storage, sensing, coatings, and microelectronics devices. Finally, challenges in the current development as well as the future prospects of GO-based dyes and pigments are also discussed. This review provides a reference for the further exploration of novel dyes and pigments.

Meissner to ferromagnetic phase transition in La-decorated functionalized Nb2C MXene: an experimental and computational analysis.

This work reports experimental and computational magnetic phase transition from superconducting-diamagnet to ferromagnet in lanthanum (La)-doped functionalized Nb2C MXene. Co-precipitation method is used to synthesize La-doped Nb2C MXene. Structure and morphology of the compound are studied through x-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy and energy dispersion spectroscopy, confirming the successful doping of La while retaining the two-dimensional (2D) structure of MXene. The magnetic properties of doped sample are studied using field-cooled and zero-field-cooled curves as well as from magnetization (M) versus applied magnetic field (H) graphs. Contrary to the superconductivity-like diamagnetic behavior in pristine Nb2C MXene, the La-doped MXene converts the diamagnetism into the ferromagnetic (FM) phases at all temperatures. The ferromagnetism arises due to the pinning of magnetic spins pinned by Lanthanum itself. The computational analysis of pristine Nb2C MXene confirms its diamagnetic behavior and further clarifies the role of La and functional groups (O and F) in the reduction of diamagnetic behavior in La-doped Nb2C MXene while inducing FM nature. This work provides an interesting superconducting-diamagnetic to FM transition with a possibility of its implementation in 2D spintronics.

Synthesis of 3D IrRuMn Sphere as a Superior Oxygen Evolution Electrocatalyst in Acidic Environment.

The design of a three-dimensional structure for an Ir-based catalyst offers a great opportunity to improve the electrocatalytic performance and maximize the use of the precious metal. Herein, a novel wet chemical strategy is reported for the synthesis of an IrRuMn catalyst with a sphere structure and porous features. In the synthetic process, the combined use of citric acid and formamide is requisite for the formation of the sphere structure. This method leads to a favorable 3D IrRuMn sphere structure with many fully exposed active sites. Furthermore, an alloying noble metal, such as Ir or Ru, with the transition metal leads to enhanced oxygen evolution reaction (OER) activity. The doping of a transition metal, such as Mn, is an interesting example, because it exhibits stability and activity in both acidic and alkaline media. For the OER, the IrRuMn sphere catalyst exhibits an overpotential of 260 mV at a current density of 10 mA cm-2 in strongly acidic 0.1 m HClO4 , which is superior to that of a commercial IrO2 /C catalyst. This approach provides a novel way to synthesize an Ir-based multimetallic spherical electrocatalyst, which exhibits exceptional efficiency for the acidic OER. It will pave the way for new approaches to the practical utilization of PEM electrolyzers.

Recent advances in the role of MXene based hybrid architectures as electrocatalysts for water splitting.

The development of non-noble metal based and cost-effective electrocatalysts for water splitting has attracted significant attention due to their potential in production of clean and green hydrogen fuel. Discovered in 2011, a family of two-dimensional transition metal carbides, nitrides, and carbonitrides, have demonstrated promising performance as electro catalysts in the water splitting process due to their high electrical conductivity, very large surface area and abundant catalytic active sites. However, their-long term stability and recyclability are limited due to restacking and agglomeration of MXene flakes. This problem can be solved by combining MXene with other materials to create their hybrid architectures which have demonstrated higher electrocatalytic performance than pristine MXenes. Electrolysis of water encompasses two half-cell reactions, hydrogen evolution reaction (HER) at the cathode and oxygen evolution reaction (OER) at the anode. Firstly, this concise review explains the mechanism of water splitting. Then it provides an overview of the recent advances about applications of MXenes and their hybrid architectures as HER, OER and bifunctional electrocatalysts for overall water splitting. Finally, the recent challenges and potential outlook in the field have been presented. This concise review may provide further understanding about the role of MXene-based hybrid architectures to develop efficient electrocatalysts for water splitting.

A simplified framework for orientation control of synthetic fibers in engineered cementitious composites using magnetic field.

Fiber reinforced concrete (FRC) is attracting many researchers' attention due to its excellent mechanical and fracture properties. However, its widespread implementation is hampered by the issues related to the dispersion and orientation of its fibers. According to the fracture mechanics, the reinforcement would provide maximum bridging when placed perpendicular to the crack propagation. This study is focused on the magnetic-based orientation of synthetic fibers which are mostly used in strain hardening FRC also termed as Engineered Cementitious Composites (ECC). Initially, the PVA fibers were coated with waste iron particles using a hydrothermal synthesis procedure. This was done to make synthetic fibers magnetically responsive by the formation of a physical bond between iron and PVA fibers. A solenoid was used to provide a high-intensity magnetic flux to orient these fibers in the direction of magnetic lines. Three different ECC mixes were prepared and cast in wooden molds. The molds were then placed one by one into the magnetic field for the orientation of the fibers. The fibers were successfully aligned perpendicular to the flexure cracks in only flexure dominant regions with the aid of a magnetic field. The orientation of fibers was verified with the help of microscopic images of the tortured surfaces. As a result of well aligned fibers dispersed in the ECC mix, the flexural strength was increased by 21%.

Intercalation of C60 into MXene Multilayers: A Promising Approach for Enhancing the Electrochemical Properties of Electrode Materials for High-Performance Energy Storage Applications.

In this study, we report on the enhancement of the electrochemical properties of MXene by intercalating C60 nanoparticles between its layers. The aim was to increase the interlayer spacing of MXene, which has a direct effect on capacitance by allowing the electrolyte flow in the electrode. To achieve this, various concentrations of Ti3SiC2 (known as MXene) and C60 nanocomposites were prepared through a hydrothermal process under optimal conditions. The resulting composites were characterized by using X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy, Raman spectroscopy, and cyclic voltammetry. Electrodes were fabricated using different concentrations of MXene and C60 nanocomposites, and current-voltage (I-V) measurements were performed at various scan rates to analyze the capacitance of pseudo supercapacitors. The results showed the highest capacitance of 348 F g1- for the nanocomposite with a composition of 90% MXene and 10% C60. We introduce MXene-C60 composites as promising electrode materials for supercapacitors and highlight their unique properties. Our work provides a new approach to designing high-performance electrode materials for supercapacitors, which can have significant implications for the development of efficient energy storage systems.

2-Dimensional Ti3C2Tx/NaF nano-composites as electrode materials for hybrid battery-supercapacitor applications.

The increasing global demand for energy storage solutions has spurred interest in advanced materials for electrochemical energy storage devices. Transition-metal carbides and nitrides, known as MXenes, are characterized by remarkable conductivity and tunable properties, They have gained significant attention for their potential in energy storage applications. The properties of two-dimensional (2-D) MXenes can be tuned by doping or composite formation. We report a novel Ti3C2Tx/NaF composite prepared via a straightforward hydrothermal process for supercapacitor electrode applications. Three composites with varying NaF concentrations (1%, 3%, and 5%) were synthesized under similar conditions. Structural characterization using X-ray diffraction (XRD) and scanning electron microscopy confirmed the successful formation of the composites, whereas distinct shifts in XRD peaks and new peaks revealed the presence of NaF. Electrochemical performance was evaluated by cyclic voltammetry, galvanostatic charging-discharging, and electrochemical impedance spectroscopy. The composites exhibited pseudo-capacitive behavior with reversible redox reactions during charge and discharge cycles. Specific capacitance of 191 F/g at scan rates of 2 mV/s was measured in 1 M KOH. Electrochemical impedance spectroscopy revealed an escalating impedance factor as NaF content increases within Ti3C2Tx. This study underscores the versatile energy storage potential of Ti3C2Tx/NaF composites, offering insights into their tailored properties and behavior.

Enhanced Electrochemical Performance of MWCNT-Assisted Molybdenum-Titanium Carbide MXene as a Potential Electrode Material for Energy Storage Application.

Two-dimensional (2D) materials such as MXenes have attracted considerable attention owing to their enormous potential for structural flexibility. Here, we prepared a Mo2TiC2Tx-layered structure from parent Mo2TiAlC2Tx MAX by chemically selective etching of the aluminum layer. The prepared MXene was employed in composite formation with CTAB-grafted multiwalled carbon nanotubes (MWCNTs) to have a structure with improved electrochemical performance. The samples were characterized to analyze the structure, morphology, elemental detection, vibrational modes, and surface chemistry, followed by an electrochemical performance of the Mo2TiC2Tx MXene and MWCNTs@Mo2TiC2Tx composite using the GAMRAY Potentiostat under a 1 M KOH electrolyte. The specific capacitance of pristine Mo2TiC2Tx was 425 F g-1, which was enhanced to 1740 F g-1 (almost 4 times) at 5 mV s-1 due to the increase in active surface area and conductive paths between the MXene sheets. The charge storage mechanism was studied by further resolving the cyclic voltammograms. MWCNTs@Mo2TiC2Tx showed much improved electrochemical performance and reaction kinetics, making it an ideal material candidate for supercapacitor applications.

Synergetic Catalytic and Photocatalytic Performances of Tin-Doped BiFeO3/Graphene Nanoplatelet Hybrids under Dark and Light Conditions.

Because of a rapidly growing need for water, it is essential to find new fast and reliable ways of water purification from organic pollutants. For removing organic azo dyes from water, various catalysts and photocatalysts have been designed to meet crucial water needs. In this study tin (Sn) doped bismuth ferrite (BFO) nanoparticles have been synthesized using the sol-gel technique. Further, BFSO/GNP nanohybrids were synthesized by mixing BFSO nanoparticles with graphene nanoplatelets (GNPs) via a simple and cost effective coprecipitation process. XRD and SEM showed that BFSO/GNP nanohybrids are well grown in crystal structure along with uniform and homogeneous morphology. XPS supported the elemental composition and interface bonding of both materials present inside the nanohybrids. DRS and catalytic activities showed that BFSO/GNP nanohybrids are both dark and light active species for performing dye degradation activities during water purification. The as-synthesized nanohybrids provided efficient dye removal from water even in the absence of light owing to the presence of defects and trap-state carriers (electrons) inside the graphene sheets. The optimized nanohybrid BFSO-15/GNP showed 100% dye removal in 60 min with 90% catalytic activity under dark. The recyclability test showed stable and repeatable performance of BFSO/GNP nanohybrids up to 10 cycles of catalytic activities.

Comparative Study between Sulfurized MoS2 from Molybdenum and Molybdenum Trioxide Precursors for Thin-Film Device Applications.

Two-dimensional (2D) materials have been studied as an emerging class of nanomaterials owing to their attractive properties in nearly every field of science and technology. Molybdenum disulfide (MoS2) is one of the more promising candidates of these atomically thin 2D materials for its technological potential. The facile synthesis of MoS2 remains a matter of broad interest. In this study, MoS2 was synthesized by chemical vapor deposition sulfurization at various temperatures (550 °C, 650 °C, and 750 °C) of either precursor molybdenum metal (Mo) or molybdenum trioxide (MoO3) deposited on silicon/silicon dioxide (Si/SiO2) via e-beam evaporation. Monolayer, bilayer, and few layers sulfurized samples have been grown and verified by Raman, photoluminescence spectroscopy, XRD, XPS, and AFM. MoO3 sulfurization provided monolayer growth in comparison to Mo sulfurization under the same conditions and precursor thicknesses. Optical microscopy showed the homogeneous nature of grown samples. A main finding of this work is that MoO3 sulfurization produced higher quality MoS2 as compared to those grown by an Mo precursor. Device characteristics based on monolayer MoO3 sulfurized MoS2-x include nonvolatile resistive switching with Ion/Ioff ≈ 104 at a relatively low operating bias of ±1 V. In addition, field-effect transistor characteristics revealed p-type material growth with a carrier mobility ∼ 41 cm2 V-1 s-1, which is in contrast to typically observed n-type characteristics.

Optimized time dependent exfoliation of graphite for fabrication of Graphene/GO/GrO nanocomposite based pseudo-supercapacitor.

High capacitance devices (Supercapacitors) fabricated using two-dimensional materials such as Graphene and its composites are attracting great attention of the research community, recently. Synthesis of 2D materials and their composites with high quality is desirable for the fabrication of 2D materials-based supercapacitors. Ultrasonic Assisted Liquid Phase Exfoliation (UALPE) is one of the widely used techniques for the synthesis of graphene. In this article, we report the effect of variation in sonication time on the exfoliation of graphite powder to extract a sample with optimal properties well suited for supercapacitors applications. Three different graphite powders (hereafter termed as sample A, sample B, and sample C) were sonicated for duration of 24 h, 48 h and 72 h at 60 °C. The exfoliation of graphite powder into graphene, GO and GrO was studied using XRD and RAMAN. AFM and SEM were further used to examine the layered structure of the synthesized nanocomposite. UV-visible spectroscopy and cyclic voltammetery were used to measure the band gaps, and capacitive behavior of the samples. Sample B exhibited a remarkable specific capacitance of 534.53 F/g with charge specific capacity of 530.1 C/g at 1 A/g and energy density of 66 kW/kg. Power density varied 0.75 kWh/kg to 7.5 kWh/kg for a variation in current density from 1 to 10 A/g. Sample B showed capacitive retention of 94%, the lowest impedance and highest degree of exfoliation and conductivity as compared to the other two samples.

Optimization of bandgap reduction in 2-dimensional GO nanosheets and nanocomposites of GO/iron-oxide for electronic device applications.

In this report we have developed different fabrication parameters to tailor the optical bandgap of graphene oxide (GO) nanosheets to make it operational candidate in electronic industry. Here we performed two ways to reduce the bandgap of GO nanosheets. First, we have optimized the oxidation level of GO by reducing amount of oxidizing agent (i.e. KMnO4) to control the sp2/sp3 hybridization ratio for a series of GO nanosheets samples. We noticed the reduction in primary band edge 3.93-3.2 eV while secondary band edge 2.98-2.2 eV of GO nanosheets as the amount of KMnO4 is decreased from 100 to 30%. Second, we have fabricated a series of 2-dimensional nanocomposites sample containing GO/Iron-oxide by using a novel synthesis process wet impregnation method. XRD analysis of synthesized nanocomposites confirmed the presence of both phases,[Formula: see text]-Fe2O3 and Fe3O4 of iron-oxide with prominent plane (001) of GO. Morphological investigation rules out all the possibilities of agglomerations of iron oxide nanoparticles and coagulation of GO nanosheets. Elemental mapping endorsed the homogeneous distribution of iron oxide nanoparticles throughout the GO nanosheets. Raman spectroscopy confirmed the fairly constant ID/IG ratio and FWHM of D and G peaks, thus proving the fact that the synthesis process of nanocomposites has no effect on the degree of oxidation of GO flakes. Red shift in G peak position of all the nanocomposites samples showed the electronic interaction among the constituents of the nanocomposite. Linear decrease in the intensity of PL (Photoluminescence) spectra with the increasing of Iron oxide nanoparticles points towards the increased interaction among the iron oxide nanoparticles and GO flakes. Optical absorption spectroscopy reveals the linear decrease in primary edge of bandgap from 2.8 to 0.99 eV while secondary edge decrease 3.93-2.2 eV as the loading of [Formula: see text]-Fe2O3 nanoparticles is increased from 0 to 5% in GO nanosheets. Among these nanocomposites samples 5%-iron-oxide/95%-GO nanosheet sample may be a good contestant for electronic devices.

Defects mediated weak ferromagnetism in Zn1-yCyO (0.00 ≤ y ≤ 0.10) nanorods semiconductors for spintronics applications.

A series of carbon-doped ZnO [Zn1-yCyO (0.00 ≤ y ≤ 0.10)] nanorods were synthesized using a cost-effective low-temperature (85 °C) dip coating technique. X-ray diffractometer scans of the samples revealed the hexagonal structure of the C-doped ZnO samples, except for y = 0.10. XRD analysis confirmed a decrease in the unit cell volume after doping C into the ZnO matrix, likely due to the incorporation of carbon at oxygen sites (CO defects) resulting from ionic size differences. The morphological analysis confirmed the presence of hexagonal-shaped nanorods. X-ray photoelectron spectroscopy identified C-Zn-C bonding, i.e., CO defects, Zn-O-C bond formation, O-C-O bonding, oxygen vacancies, and sp2-bonded carbon in the C-doped ZnO structure with different compositions. We analyzed the deconvoluted PL visible broadband emission through fitted Gaussian peaks to estimate various defects for electron transition within the bandgap. Raman spectroscopy confirmed the vibrational modes of each constituent. We observed a stronger room-temperature ferromagnetic nature in the y = 0.02 composition with a magnetization of 0.0018 emu/cc, corresponding to the highest CO defects concentration and the lowest measured bandgap (3.00 eV) compared to other samples. Partial density of states analysis demonstrated that magnetism from carbon is dominant due to its p-orbitals. We anticipate that if carbon substitutes oxygen sites in the ZnO structure, the C-2p orbitals become localized and create two holes at each site, leading to enhanced p-p type interactions and strong spin interactions between carbon atoms and carriers. This phenomenon can stabilize the long-range order of room-temperature ferromagnetism properties for spintronic applications.

Enhancing supercapacitor performance through design optimization of laser-induced graphene and MWCNT coatings for flexible and portable energy storage.

The field of supercapacitors consistently focuses on research and challenges to improve energy efficiency, capacitance, flexibility, and stability. Low-cost laser-induced graphene (LIG) offers a promising alternative to commercially available graphene for next-generation wearable and portable devices, thanks to its remarkable specific surface area, excellent mechanical flexibility, and exceptional electrical properties. We report on the development of LIG-based flexible supercapacitors with optimized geometries, which demonstrate high capacitance and energy density while maintaining flexibility and stability. Three-dimensional porous graphene films were synthesized, and devices with optimized parameters were fabricated and tested. One type of device utilized LIG, while two other types were fabricated on LIG by coating multi-walled carbon nanotubes (MWCNT) at varying concentrations. Characterization techniques, including scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD), Raman spectroscopy, and voltammetry, were employed to analyze the fabricated devices. AFM analysis revealed a surface roughness of 2.03 µm for LIG due to laser treatment. SEM images displayed compact, dense, and porous surface morphology. XRD analysis confirmed the presence of graphene and graphene oxide, which was further supported by energy-dispersive X-ray spectroscopy (EDX) data. Raman spectroscopy indicated that the fabricated samples exhibited distinct D and G bands at 1362 cm-1 and 1579 cm-1, respectively. Cyclic voltammetry (CV) results showed that LIG's capacitance, power density, and energy density were 6.09 mF cm-2, 0.199 mW cm-2, and 3.38 µWh cm-2, respectively, at a current density of 0.2 mA cm-2. The LIG-MWCNT coated electrode exhibited a higher energy density of 6.05 µWh cm-2 and an areal-specific capacitance of 51.975 mF cm-2 compared to the LIG-based devices. The fabricated device has potential applications in smart electronics, nanorobotics, microelectromechanical systems (MEMS), and wearable and portable electronics.

MWCNT-modified MXene as cost-effective efficient bifunctional catalyst for overall water splitting.

Utilization of cost-effective, bifunctional, and efficient electrocatalysts for complete water splitting is desirable for sustainable clean hydrogen energy. In last decade, MXenes, a family of emerging two-dimensional (2D) materials with unique physiochemical properties, enticed scientists because of their use in different applications. However, insufficient electron transport, lower intrinsic chemical activity and limited active site densities are the factors inhibiting their use in electrocatalytic cells for hydrogen production. Here, we have presented material design to address this issue and introduced carbon nanotubes (CNTs) on V2CT x MXene sheets for conductive network channels that enhance the ion diffusion for enhanced electrochemical activity. The SEM reveals the uniform dispersion of the MWCNTs over the MXene surface that resulted in the formation of conductive network channels and enhances reaction kinetics. The as-synthesized electrocatalyst was subjected to linear sweep voltammetry (LSV) measurements for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The hybrid catalyst M2 exhibited an enhanced HER activity with a lower over-potential of 27 mV which is comparable to commercially available Pt-based catalysts (32 mV). Similarly, an enhanced OER activity was observed with a lower over-potential of 469 mV as compared to pristine V2CT x MXene. The electrocatalyst was subjected to a durability test through chronoamperometry and was observed to be stable for 16 hours. Hence, this study opens a new avenue for future cost-effective efficient catalysts for overall water splitting as a solution to produce clean hydrogen.

Enhanced pseudocapacitive energy storage and thermal stability of Sn2+ ion-intercalated molybdenum titanium carbide (Mo2TiC2) MXene.

Electrochemical energy-storage (EES) devices are a major part of energy-storage systems for industrial and domestic applications. Herein, a two-dimensional (2D) transition metal carbide MXene, namely Mo2TiC2, was intercalated with Sn ions to study the structural, morphological, optical, and electrochemical energy-storage effects. The Sn2+-intercalated modified layered structure, prepared via a facile liquid-phase pre-intercalated cetyltrimethylammonium bromide (CTAB) method, showed a higher surface area of 30 m2 g-1, low band gap of 1.3 eV, and large interlayer spacing of 1.47 nm, as compared to the pristine Mo2TiC2. The Sn@Mo2TiC2 electrode showed a high specific capacitance of 670 F g-1, representing a large diffusion control value compared to pure Mo2TiC2 (212 F g-1) at a scan rate of 2 mV s-1. The modified electrode also presented long-term cyclic performance, high-capacity retention and coulombic efficiency measured over 10 000 cycles. The Sn@Mo2TiC2 electrode showed much improved electrocatalytic efficiency, which may open up ways to employ double-transition 2D MXenes in energy-storage devices.

First observation on emergence of strong room-temperature ferroelectricity and multiferroicity in 2D-Ti3C2T x free-standing MXene film.

Two-dimensional (2D) multiferroics are key candidate materials towards advancement of smart technology. Here, we employed a simple synthesis approach to address the long-awaited dream of developing ferroelectric and multiferroic 2D materials, especially in the new class of materials called MXenes. The etched Ti3C2T x MXene was first synthesized after HF-treatment followed by a delamination process for successful synthesis of free-standing Ti3C2T x film. The free-standing film was then exposed to air at room-temperature and heated at different temperatures to form a TiO2 layer derived from the Ti3C2T x MXene itself. The ferroelectric measurement showed a clear polarization hysteresis loop at room-temperature. Also, due to the reported ferromagnetic behavior of Ti3C2T x MXene, our composite could show multiferroic properties at room-temperature. The magnetoelectric coupling test was also performed that showed a clear, switchable spontaneous polarization under applied magnetic field. TiO2 is reported to be an incipient ferroelectric that assumes a ferroelectric phase in composite form. The structural and morphological analysis confirmed successful synthesis of free-standing film and the Raman spectroscopy revealed the formation of different phases of TiO2 and the observed ferroelectricity could be due to structural deformation as a result of the formation of this new phase. The measured value of remanent polarization is 0.5 µC cm-2. This is the first report on the existence of a ferroelectric phase and multiferroic coupling in 2D free-standing MXene film at room-temperature which opens-up the possibility of 2D material-based electric and magnetic data storage applications at room-temperature.

Nickel-adsorbed two-dimensional Nb2C MXene for enhanced energy storage applications.

Owing to the tremendous energy storage capacity of two-dimensional transition metal carbides (MXenes), they have been efficiently utilized as a promising candidate in the field of super-capacitors. The energy storage capacity of MXenes can be further enhanced using metal dopants. Herein, we have reported the synthesis of pristine and nickel doped niobium-carbide (Nb2C) MXenes, their computational and electrochemical properties. Upon introduction of nickel (Ni) the TDOS increases and a continuous DOS pattern is observed which indicates coupling between Ni and pristine MXene. The alterations in the DOS, predominantly in the nearby region of the Fermi level are profitable for our electrochemical applications. Additionally, the Ni-doped sample shows a significant capacitive performance of 666.67 F g-1 which can be attributed to the additional active sites generated by doping with Ni. It is worth noting that doped MXenes exhibited a capacitance retention of 81% up to 10 000 cycles. The current study unveils the opportunities of using MXenes with different metal dopants and hypothesize on their performance for energy storage devices.

Skeletal Fluorosis: A Case of Inhalant Abuse Leading to a Diagnosis of Colon Cancer.

Skeletal fluorosis is a long-term bone disease that develops when prolonged fluoride toxicity leads to osteosclerosis and bone deformities that result in crippling pain and debility. The disease is endemic to many countries due to environmental or industrial exposures. However, rare cases in the United States have been reported from various causes including heavy toothpaste ingestion, excessive tea consumption, voriconazole use, and inhalant abuse. Here, we present a case of a 41-year-old man who presented for weight loss and severe joint pains due to bony sclerotic lesions found on X-rays. Social history revealed that he had been recreationally inhaling compressed air dusters used for cleaning electronics. Owing to concern for malignancy, he underwent an extensive work-up which led to a diagnosis of colon cancer, but positron emission tomography/computed tomography (PET/CT) and bone biopsy were unexpectedly negative for metastatic bone disease. Further characterization of his lesions by skeletal survey led to a diagnosis of skeletal fluorosis secondary to inhalant abuse. As in this patient, the disease can be difficult for clinicians to recognize as it can be mistaken for various boney diseases such as metastatic cancer. However, once there is clinical suspicion for skeletal fluorosis, various tests to help confirm the diagnosis can include serum and urine fluoride levels, skeletal survey, and bone ash fluoride concentration. Treatment of skeletal fluorosis primarily involves cessation of fluoride exposure, and recovery can take years. Ultimately, further study is required to develop recommendations and guidelines for diagnosis, management, and prognosis of the disease in the United States.

An Overview of Recent Advances in the Synthesis and Applications of the Transition Metal Carbide Nanomaterials.

Good stability and reproducibility are important factors in determining the place of any material in their respective field and these two factors also enable them to use in various applications. At present, transition metal carbides (TMCs) have high demand either in the two-dimensional (2D) form (MXene) or as nanocomposites, nanoparticles, carbide films, carbide nano-powder, and carbide nanofibers. They have shown good stability at high temperatures in different environments and also have the ability to show adequate reproducibility. Metal carbides have shown a broad spectrum of properties enabling them to engage the modern approach of multifacet material. Several ways have been routed to synthesize metal carbides in their various forms but few of those gain more attention due to their easy approach and better properties. TMCs find applications in various fields, such as catalysts, absorbents, bio-sensors, pesticides, electrogenerated chemiluminescence (ECL), anti-pollution and anti-bacterial agents, and in tumor detection. This article highlights some recent developments in the synthesis methods and applications of TMCs in various fields.