Optimizing graphene content in scaffolds for evenly distributed crumpled MoS2paper wads as anodes for high-performance Li-ion batteries.

Lithium-ion batteries (LIBs) have revolutionized portable electronics, yet their conventional graphite anodes face capacity limitations. Integrating graphene and 3D molybdenum disulfide (MoS2) offers a promising solution. Ensuring a uniform distribution of 3D MoS2nanostructures within a graphene matrix is crucial for optimizing battery performance and preventing issues like agglomeration and capacity degradation. This study focuses on synthesizing a uniformly distributed paper wad structure by optimizing a composite of reduced graphene oxide RGO@MoS2through structural and morphological analyses. Three composites with varying graphene content were synthesized, revealing that the optimized sample containing 30 mg RGO demonstrates beneficial synergy between MoS2and RGO. The interconnected RGO network enhances reactivity and conductivity, addressing MoS2aggregation. Experimental results exhibit an initially superior capacity of 911 mAh g-1, retained at 851 mAh g-1even after 100 cycles at 0.1 A g-1current density, showcasing improved rate efficiency and long-term stability. This research underscores the pivotal role of graphene content in customizing RGO@MoS2composites for enhanced LIB performance.

Angstrom-Scale Transparent Overcoats: Interfacial Nitrogen-Driven Atomic Intermingling Promotes Lubricity and Surface Protection of Ultrathin Carbon.

Lubricity, a phenomenon which enables the ease of motion of objects, and wear resistance, which minimizes material damage or degradation, are important fundamental characteristics for sustainable technology developments. Ultrathin coatings that promote lubricity and wear resistance are of huge importance for a number of applications, including magnetic storage and micro-/nanoelectromechanical systems. Conventional ultrathin coatings have, however, reached their limit. Graphene-based materials that have shown promise to reduce friction and wear have many intrinsic limitations such as high temperature and substrate-specific growth. To address these concerns, a great deal of research is currently ongoing to optimize graphene-based materials. Here we discover that angstrom-thick carbon (8 Å) significantly reduces interfacial friction and wear. This lubricant shows ultrahigh optical transparency and can be directly deposited on a wide range of surfaces at room temperature. Experiments combined with molecular dynamics simulations reveal that the lubricating efficacy of 8 Å carbon is further improved via interfacial nitrogen.

Slippery and Wear-Resistant Surfaces Enabled by Interface Engineered Graphene.

Friction and wear remain the primary cause of mechanical energy dissipation and system failure. Recent studies reveal graphene as a powerful solid lubricant to combat friction and wear. Most of these studies have focused on nanoscale tribology and have been limited to a few specific surfaces. Here, we uncover many unknown aspects of graphene's contact-sliding at micro- and macroscopic tribo-scales over a broader range of surfaces. We discover that graphene's performance reduces for surfaces with increasing roughness. To overcome this, we introduce a new type of graphene/silicon nitride (SiNx, 3 nm) bilayer overcoats that exhibit superior performance compared to native graphene sheets (mono and bilayer), that is, display the lowest microscale friction and wear on a range of tribologically poor flat surfaces. More importantly, two-layer graphene/SiNx bilayer lubricant (<4 nm in total thickness) shows the highest macroscale wear durability on tape-head (topologically variant surface) that exceeds most previous thicker (∼7-100 nm) overcoats. Detailed nanoscale characterization and atomistic simulations explain the origin of the reduced friction and wear arising from these nanoscale coatings. Overall, this study demonstrates that engineered graphene-based coatings can outperform conventional coatings in a number of technologies.

A free-standing, flexible PEDOT:PSS film and its nanocomposites with graphene nanoplatelets as electrodes for quasi-solid-state supercapacitors.

Research and development on all-solid-state, flexible supercapacitors is the prime concern of the scientific community these days due to their various advantages including their easy transportability, miniaturization, and compactness in different appliances. We report the novel configuration of all-solid symmetrical supercapacitors employing free-standing, flexible films of poly(3,4-ethylenedioxythiophene) poly(styrene sulfonate) (PEDOT:PSS) and its nanocomposite electrodes with graphene nanoplatelets (GNPs), separated by ionic liquid (IL) (1-ethyl 3-methylimidazolium trifluoromethanesulfonate (EMITf))-based gel polymer electrolyte (GPE) films. The free-standing and flexible form of PEDOT:PSS/GNP nanocomposite films have been prepared via simple mixing of the two counterparts. Scanning electron microscopy, x-ray diffraction, Raman analysis, and thermal and mechanical characterizations have been performed to ascertain the suitability of pristine and nanocomposite PEDOT:PSS films as potential supercapacitor electrodes. The GPE film, comprising of a solution of NH4CF3SO3 (NH4-triflate or NH4Tf) in IL, entrapped in poly(vinylidine fluoride-co-hexafluoropropylene) (PVdF-HFP), is a promising electrolyte due to its high ionic conductivity and sufficient electrochemical stability window. The supercapacitor with a PEDOT:PSS nanocomposite containing ∼3.8 wt.% of GNP has been found to give an optimum specific capacitance of ∼106 F g-1 (evaluated from electrochemical impedance spectroscopy), and specific energy and power of ∼6.95 Wh kg-1 and 2.58 kW kg-1, respectively (evaluated from galvanostatic charge-discharge). More importantly, the capacitors demonstrate stable performance for more than 2000 charge-discharge cycles, with only ∼10% initial fading in capacitance. Interestingly, the PEDOT:PSS/GNP nanocomposite-based solid-state supercapacitors with the IL-incorporated GPE have shown comparable (even better) performance than other reported PEDOT:PSS-based supercapacitors.

'Bucky gel' of multiwalled carbon nanotubes as electrodes for high performance, flexible electric double layer capacitors.

We report the preparation of a gelled form of multiwalled carbon nanotubes (MWCNTs) with an ionic liquid 1-butyl-1-methyl pyrrolidinium bis(trifluoromethane sulfonyl)imide (BMPTFSI)), referred to as 'bucky gel', to be used as binderless electrodes in electrical double layer capacitors (EDLCs). The characteristics of gelled MWCNTs are compared with pristine MWCNTs using transmission electron microscopy, x-ray diffraction and Raman studies. A gel polymer electrolyte film consisting of a blend of poly(vinylidene fluoride-co-hexafluoropropylene) and BMPTFSI, exhibiting a room temperature ionic conductivity of 1.5 × 10(-3) S cm(-1), shows its suitability as an electrolyte/separator in flexible EDLCs. The performance of EDLCs, assembled with bucky gel electrodes, using impedance spectroscopy, cyclic voltammetry and charge-discharge analyses, are compared with those fabricated with pristine MWCNT-electrodes. An improvement in specific capacitance (from 19.6 to 51.3 F g(-1)) is noted when pristine MWCNTs are replaced by gelled MWCNT-binderless electrodes. Although the rate performance of the EDLCs with gelled MWCNT-electrodes is reduced, the pulse power of the device is sufficiently high (~10.5 kW kg(-1)). The gelled electrodes offer improvements in energy and power densities from 2.8 to 8.0 Wh kg(-1) and 2.0 to 4.7 kW kg(-1), respectively. Studies indicate that the gel formation of MWCNTs with ionic liquid is an excellent route to obtain high-performance EDLCs.

Preparation of nanolignin rich fraction from bamboo stem via green technology: assessment of its antioxidant, antibacterial and UV blocking properties.

This work reports the preparation of nano lignin-rich fraction material via green technology from the holistic use of lignocellulosic biomass bamboo. The bamboo is first chemically treated, followed by acid precipitation to extract bamboo-derived macro lignin-rich fraction material. The nano lignin-rich fraction material was then prepared via ultrasonication technique from the extracted bamboo-derived macro lignin-rich fraction material. The confirmation of the distinct lignin functional groups in the extracted lignin-rich fractions has been done by FTIR. Surface morphology by FESEM and TEM revealed spherical nano-lignin-rich fraction materials from extracted bamboo-derived macro lignin-rich fraction materials. DPPH assays indicated that both the obtained fractions depict beneficial antioxidant characteristics. They were found to be effective in terms of their antibacterial activity against both gram-positive bacteria Staphylococcus aureus (S.aureus) and gram-negative bacteria Escherichia coli (E.coli), using the disc diffusion method. These fractions have UV blocking property, and nano-lignin-rich fraction material acts as a more potential UV blocking agent than others. Thus, the nano-lignin-rich fraction material has great potential as a high antioxidant, antibacterial, and UV blocking agent useful in biomedical applications.Highlights Extraction of macro-lignin rich fraction material using chemical treatment of lignocellulosic biomass bamboo via refluxing followed by acid precipitation.Preparation of nano-lignin rich fraction material from extracted bamboo-derived macro-lignin rich fraction material via ultrasonication technique as a green technology.Structural and surface morphology of the extracted macro-lignin & nano lignin-rich fraction materials have been analyzed by XRD, FTIR, EDX, SEM and TEM.The macro lignin & nano lignin-rich fraction materials showed good antioxidant, antibacterial activity and UV-blocking properties, but the nano-lignin rich fraction material exhibited more efficient properties.

Advances in Nanoarchitectonics of Antimicrobial Tiles and a Quest for Anti-SARS-CoV-2 Tiles.

Design of antimicrobial tiles seems necessary to combat against contagious diseases, especially COVID-19. In addition to personal hygiene, this technology facilitates public hygiene as antimicrobial tiles can be installed at hospitals, schools, banks, offices, lobbies, railway stations, etc. This review is primarily focused on preparing antimicrobial tiles using an antimicrobial layer or coatings that fight against germs. The salient features and working mechanisms of antimicrobial tiles are highlighted. This challenge is a component of the exploratory nature of nanoarchitectonics, that also extends farther than the realm of nanotechnology. This nanoarchitectonics has been successful at the laboratory scale as antimicrobial metal nanoparticles are mainly used as additives in preparing tiles. A detailed description of various materials for developing unique antimicrobial tiles is reported here. Pure metal (Ag, Zn) nanoparticles and a mixture of nanoparticles with other inorganic materials (SiO2,, TiO2, anatase, nepheline) have been predominantly used to combat microbes. The developed antimicrobial tiles have shown excellent activity against a wide range of Gram-positive and Gram-negative bacteria. The last section discussed a hypothetical overview of utilizing the antimicrobial tiles against SARS-CoV-2. Overall, this review gives descriptive knowledge about the importance of antimicrobial tiles to create a clean and sustainable environment.

Unusual High Hardness and Load-Dependent Mechanical Characteristics of Hydrogenated Carbon-Nitrogen Hybrid Films.

Mechanical components are exposed to a rigorous environment in a number of applications including engineering, aerospace, and automobiles. Thus, their service lifetime and reliability are always on the verge of risk. Protective coatings with high hardness are required to enhance their service lifetime and minimize the replacement cost and waste burden. Hydrogenated amorphous carbon including nitrogen-incorporated films, that are commonly deposited by plasma-enhanced chemical vapor deposition, are widely used for commercial protective coating applications. However, their mechanical hardness still falls into the moderate hard regime. This needs to be substantially enhanced for advanced applications. Here, we report the synthesis of very hard nanostructured hydrogenated carbon-nitrogen hybrid (n-C:H:N) films. The optimized n-C:H:N film displays a hardness of about 36 GPa, elastic modulus of 360 GPa, and reasonably good elastic recovery (ER) of 62.7%. The mechanical properties of n-C:H:N films are further tailored when nitrogen pressure is tuned during the growth. The realized remarkably improved mechanical properties are correlated with the films' structural properties and experimental growth conditions. We also conducted density functional theory calculations that show the trend for the elastic modulus of the amorphous carbon films with varying nitrogen concentrations matches well with experimentally measured values. Finally, we probed load-dependent mechanical properties of n-C:H:N films and found an anomalous behavior; some of the mechanical parameters, for instance, ER, reveal an irregular trend with indentation load, which we explain in the framework of the film-substrate composite concept. Overall, this work uncovers many unknown and exciting mechanical phenomena that could pave the way for new technological developments.

Supramolecular assemblies of DNA with neutral nucleoside amphiphiles.

A neutral uridine-based amphiphile is described which condenses plasmid DNA. AFM studies show that the three distinct structural components of the amphiphile (i.e, nucleobase, alkyl chains, and poly(ethylene glycol)) are required for the formation of DNA-amphiphile supramolecular assemblies on a mica surface.

Synthesis and characterization of pi-stacked phenothiazine-labeled oligodeoxynucleotides.

[reaction: see text] A facile procedure for the incorporation of N-methyl phenothiazine as the terminal nucleoside in oligodeoxynucleotides is reported. The phenothiazine nucleoside analogue is synthesized and then incorporated into DNA using an automated DNA solid-phase synthesizer. Phenothiazine-labeled oligodeoxynucleotides form stable B-form duplexes with higher melting temperatures compared to unlabeled DNA duplexes.

High rate performance of flexible pseudocapacitors fabricated using ionic-liquid-based proton conducting polymer electrolyte with poly(3, 4-ethylenedioxythiophene):poly(styrene sulfonate) and its hydrous ruthenium oxide composite electrodes.

We report the studies on all-solid-state flexible pseudocapacitors based on poly (3,4-ethylenedioxythiophene)-poly (styrene sulfonate) (PEDOT-PSS) and PEDOT-PSS/hydrous ruthenium oxide composite electrodes separated by nonaqueous proton conducting polymer electrolyte. Structural, thermal and electrochemical properties including high ionic conductivity (6.2 × 10(-2) S cm(-1) at 20 °C) of the polymer electrolyte, comprising ionic liquid 1-ethyl 3-methyl imidazolium hydrogen sulfate (EMIHSO4) immobilized in the blend of poly (vinyl alcohol) (PVA) and poly (vinyl pyrrolidone) (PVP), demonstrate its excellent suitability in supercapacitor fabrication. A substantial improvement in the specific capacitance (hence the specific energy) has been obtained when the PEDOT-PSS electrodes in the symmetrical pseudocapacitor are replaced by the composite electrodes PEDOT-PSS/RuO2·xH2O. High rate capability of the capacitor cell (with PEDOT-PSS electrodes) has been observed, as evidenced from the high knee frequency (∼966 Hz), low response time (∼70 ms) and high pulse power (∼10.2 kW kg(-1)), observed by impedance analysis. Almost rectangular (capacitive) cyclic voltammetric patterns for high scan rates (up to 15 V s(-1)) confirm the high rate performance of the pseudocapacitor. The PEDOT-PSS/RuO2·xH2O composite electrodes show the lower rate capability (knee frequency ∼312 Hz, response time ∼1 s, pulse power ∼3.2 kW kg(-1) and capacitive CV response up to 500 mV s(-1)) because of slow exchange of charges at the interfaces via RuO2·xH2O. However, the pseudocapacitor with composite electrodes shows higher rate performance relative to many reported RuO2·xH2O systems. About 15% improvement is noticed in the capacitance value when the capacitor with composite electrodes is initially charged and discharged up to ∼200 cycles. Thereafter, the cell shows almost constant value of specific capacitance (∼70 F g(-1)) for 1000 cycles.

Structural and electrochemical properties of succinonitrile-based gel polymer electrolytes: role of ionic liquid addition.

Experimental studies on the novel compositions of gel polymer electrolytes, comprised of plastic crystal succinonitrile (SN) dispersed with pyrrolidinium and imidazolium-based ionic liquids (ILs) entrapped in a host polymer poly(vinylidine fluoride-co-hexafluoropropylene) (PVdF-HFP), are reported. The gel electrolytes are in the form of free-standing films with excellent mechanical, thermal, and electrochemical stability. The introduction of even a small content (~1 wt %) of ionic liquid (1-butyl-1-methylpyrrolidinium bis(trifluoromethyl-sulfonyl)imide (BMPTFSI) or 1-ethyl-3-methylimidazolium trifluoromethanesulfonate (EMITf) in the PVdF-HFP/SN system (1:4 w/w) enhances the electrical conductivity by 4 orders of magnitude, that is, from ~10(-7) to ~10(-3) S cm(-1) at room temperature. The structural changes due to the entrapment of SN or SN/ILs mixtures and ion-SN-polymer interactions are examined by Fourier transform infrared (FTIR)/Raman spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), and differential scanning calorimmetry (DSC). Various physicochemical properties and fast ion conduction in the gel polymer membranes show their promising characteristics as electrolytes in different ionic devices including supercapacitors.

Preparation of highly porous binderless activated carbon electrodes from fibres of oil palm empty fruit bunches for application in supercapacitors.

Fibres from oil palm empty fruit bunches, generated in large quantities by palm oil mills, were processed into self-adhesive carbon grains (SACG). Untreated and KOH-treated SACG were converted without binder into green monolith prior to N2-carbonisation and CO2-activation to produce highly porous binderless carbon monolith electrodes for supercapacitor applications. Characterisation of the pore structure of the electrodes revealed a significant advantage from combining the chemical and physical activation processes. The electrochemical measurements of the supercapacitor cells fabricated using these electrodes, using cyclic voltammetry, electrochemical impedance spectroscopy and galvanostatic charge-discharge techniques consistently found that approximately 3h of activation time, achieved via a multi-step heating profile, produced electrodes with a high surface area of 1704m(2)g(-1) and a total pore volume of 0.889cm(3)g(-1), corresponding to high values for the specific capacitance, specific energy and specific power of 150Fg(-1), 4.297Whkg(-1) and 173Wkg(-1), respectively.