Integrating flexible piezoelectric nanogenerators (PENGs) into wearable and portable electronics offers promising prospects for motion monitoring. However, it remains a significant challenge to develop environmentally friendly PENGs using biodegradable and cost-effective natural polymers for mechanical energy harvesting and self-powered sensing. Herein, reduced graphene oxide (rGO) and barium titanate (BTO) were introduced into regenerated cellulose pulp to fabricate a composite porous film-based PENG. The incorporation of rGO not only increased the electrical conductivity of the porous film but also enhanced the dispersibility of BTO. Moreover, the unique pore structure of the composite porous film improved the polarization effect of the air inside the pores, thereby greatly boosting the overall piezoelectric performance. The piezoelectric coefficient of the resulting composite porous film reaches up to 41.5 pC·N-1, which is comparable to or higher than those reported in similar studies. Consequently, the PENG assembled from this cellulose/rGO/BTO composite porous film (CGB-PENG) achieved an output voltage of 47 V, a current of 4.6 μA, and a power density of 30 μW·cm-2, approximately three times the output voltage and ten times the power density of similar studies. This work presents a feasible approach for the fabrication of high-performance cellulose-based PENGs derived from recycled waste cotton textiles.

Central nervous system (CNS) injuries and neurodegenerative diseases have markedly poor prognoses and can result in permanent dysfunction due to the general inability of CNS neurons to regenerate. Differentiation of transplanted stem cells has emerged as a therapeutic avenue to regenerate tissue architecture in damaged areas. Electrical stimulation is a promising approach for directing the differentiation outcomes and pattern of outgrowth of transplanted stem cells, however traditional inorganic bio-electrodes can induce adverse effects such as inflammation. This study demonstrates the implementation of two organic thin films, a polymer/reduced graphene oxide nanocomposite (P(rGO)) and PEDOT:PSS, that have favorable properties for implementation as conductive materials for electrical stimulation, as well as an inorganic indium tin oxide (ITO) conductive film. Transcriptomic analysis reveals that electrical stimulation improves neuronal differentiation of SH-SY5Y cells on all three films, with the greatest effect for P(rGO). Unique material- and electrical stimuli-mediated effects are observed, associated with differentiation, cell-substrate adhesion, and translation. The work demonstrates that P(rGO) and PEDOT:PSS are highly promising organic materials for the development of biocompatible, conductive scaffolds that will enhance electrically-aided stem cell therapeutics for CNS injuries and neurodegenerative diseases.

Accurate assessment of neurological disease through monitoring of biomarkers has been made possible using the antibody-based assays. But these assays suffer from expensive development of antibody probes, reliance on complicated equipments, and high maintenance costs. Here, using the novel reduced graphene oxide/polydopamine-molecularly imprinted polymer (rGO/PDA-MIP) as the probe layer, a robust electrochemical sensing platform is demonstrated for the ultrasensitive detection of glial fibrillary acidic protein (GFAP), a biomarker for a range of neurological diseases. A miniaturized integrated circuit readout system is developed to interface with the electrochemical sensor, which empowers it with the potential to be used as a point-of-care (POC) diagnostic tool in primary clinical settings. This innovative platform demonstrated good sensitivity, selectivity, and stability, with imprinting factor evaluated as 2.8. A record low limit-of-detection (LoD) is down to 754.5 ag mL-1, with a wide dynamic range from 1 to 106 fg mL-1. The sensing platform is validated through the analysis of GFAP in clinical plasma samples, yielding a recovery rate range of 81.6-108.8% compared to Single Molecule Array (Simoa). This cost-effective and user-friendly sensing platform holds the potential to be deployed in primary and resource-limited clinical settings for the assessment of neurological diseases.

Electromagnetic wave absorption materials (EWAMs) have become an effective means to address electromagnetic (EM) radiation and enhance stealth technology, among which aerogels are valued for their lightweight nature and excellent designability. This study utilized environmentally friendly preparation and in-situ reduction techniques to fabricate bacterial cellulose (BC) / reduced graphene oxide (RGO) aerogels, achieving tailored EM wave loss capabilities by controlling the reduction time of ascorbic acid. Benefitting from the effects of freeze-casting, BC winding, hydrogen bond, and RGO layers coupling, the aerogel maintains their original structure after reduction and exhibits satisfactory EM wave absorption. The minimum reflection loss (RLmin) is -38.52 dB, with an effective absorption bandwidth (EAB) of 6.68 GHz and a maximum radar cross section (RCS) reduction of 44.69 dBsm. Additionally, the aerogel\'s lightweight (a low density of 9.03 mg/cm3) and outstanding thermal insulation properties enable it to adapt to complex conditions. Thus, the study provides a novel approach for the construction of industrialized and sustainable RGO-based EWAMs.

The influence of the pH of the reaction medium on the structural characteristics of hydrothermally reduced graphene oxide, synthesized by the tour method, has been investigated. Varying the pH of the reaction medium within the range of 8.0, 10.0 and 12.0 (adjusted with NaOH) has revealed distinct effects on the morphology and properties of the resulting reduced graphene oxide. At a pH of 8.0 the hydrothermal treatment yielded reduced graphene oxide comprising of two particle fractions with a thickness equivalent to 4-5 graphitic layers each. In contrast, pH of 10.0 resulted in two particle fractions corresponding to 2-3 and 4 layers, respectively, while pH of 12.0 produced a single fraction with a particle thickness of 0.70 nm, encompassing 3 graphitic layers. Increasing the pH led to a decrease in the average lateral size of reduced graphene oxide particles to about 8 nm. All rGOs had micro- and mesopores with a specific surface area up to 226 m2g-1, showing a proportional increase in mesopores with increasing pH. Analysis of slit-like micropores revealed a minimum fractal dimension (D= 2.18) at pH = 8.0. The obtained results provide valuable insights into tailoring the structural properties of hydrothermally reduced graphene oxide by controlling the pH of the reaction medium, offering potential applications in various fields, including nanotechnology and materials science.

Nanomaterials with responsiveness to near-infrared light can mediate the photoablation of cancer cells with an exceptional spatio-temporal resolution. However, the therapeutic outcome of this modality is limited by the nanostructures\' poor tumor uptake. To address this bottleneck, it is appealing to develop injectable in situ forming hydrogels due to their capacity to perform a tumor-confined delivery of the nanomaterials with minimal off-target leakage. In particular, injectable in situ forming hydrogels based on Pluronic F127 have been emerging due to their FDA-approval status, biocompatibility, and thermosensitive sol-gel transition. Nevertheless, the application of Pluronic F127 hydrogels has been limited due to their fast dissociation in aqueous media. Such limitation may be addressed by combining the thermoresponsive sol-gel transition of Pluronic F127 with other polymers with crosslinking capabilities. In this work, a novel dual-crosslinked injectable in situ forming hydrogel based on Pluronic F127 (thermosensitive gelation) and Chitosan (ionotropic gelation in the presence of NaHCO3), loaded with Dopamine-reduced graphene oxide (DOPA-rGO; photothermal nanoagent), was developed for application in breast cancer photothermal therapy. The dual-crosslinked hydrogel incorporating DOPA-rGO showed a good injectability (through 21 G needles), in situ gelation capacity and cytocompatibility (viability > 73 %). As importantly, the dual-crosslinking improved the hydrogel\'s porosity and prevented its premature degradation. After irradiation with near-infrared light, the dual-crosslinked hydrogel incorporating DOPA-rGO produced a photothermal heating (ΔT ≈ 22 °C) that reduced the breast cancer cells\' viability to just 32 %. In addition, this formulation also demonstrated a good antibacterial activity by reducing the viability of S. aureus and E. coli to 24 and 33 %, respectively. Overall, the dual-crosslinked hydrogel incorporating DOPA-rGO is a promising macroscale technology for breast cancer photothermal therapy and antimicrobial applications.

Solar-driven interface desalination has emerged as a promising strategy to address the global freshwater shortage crisis. However, the separation and recovery of multicomponent oil-contaminated seawater remain a key challenge. This study reports a novel high-strength Janus photothermal membrane with a unique reverse wettability design. On one side, the membrane has hydrophilic and oleophobic properties, while on the other, it has hydrophobic and oleophilic characteristics. The Janus membrane demonstrates dual functionality: solar desalination and oil-water separation. This dual functionality enables efficient separation and recovery of four components from contaminated seawater: purified water, salt crystals, light oil, and heavy oil. As a result, the Janus membrane achieves an evaporation rate of 2.06 kg m-2 h-1 under 1.0 sun. The ion (Na+, K+, Ca2+, and Mg2+) removal rate approaches 100% with nearly complete recovery of salt crystals. Furthermore, various types of oils can be accurately separated, with separation efficiency approaching 100%. An integrated separation device successfully separates and recovers the four components. This research presents significant potential for efficient separation and recovery of complex components in oil-contaminated seawater.

Material extrusion 3D printing has received enormous attention to potentially overcome its limits by tailoring and designing thick electrodes. In this work, we prepared a thick reduced graphene oxide/carbon nanotube-reduced graphene oxide/carbon nanotubes/manganese oxide@carbon nanotubes (rGC-rGCMC) electrode with controlled lattice architectures, core-sheath structure, and hierarchical porosity by material coaxial extrusion 3D printing, freeze-drying, and thermal treatment. The volume ratios of core to sheath, including 100%-0%, 0%-100%, 20%-80%, 30%-70%, 40%-60%, and 50%-50%, were designed to investigate the influences of the core-sheath structure on thick electrodes. The electrodes with a core-sheath volume ratio of 30%-70% electrodes exhibited an enhanced areal specific capacitance of 588.27 mF cm-2 (39.48 F g-1) at a scan rate of 0.5 mA cm-2. All capacitance decays from core-sheath electrodes (20%-80%, 30%-70%, 40%-60%, and 50%-50%) were smaller than those from rGCMC (0%-100%) electrodes, indicating the improved rate capability from the core-sheath structure. On comparison of 30%-70% core-sheath electrodes with electrodes made of a homogeneous 30% rGC and 70% rGCMC mixture (30%+70%), lower capacitance (382.27 mF cm-2 and 25.66 F g-1 at 0.5 mA cm-2) of the 30%+70% mixture electrode without a core-sheath structure suggested less efficiency to harvest electrons from the redox reactions. Electrochemical impedance spectroscopy (EIS) data further supported and explained the resistances of thick electrodes with different volume ratios.

The elimination of organic substances, such as phenol, in conventional and biological processes, has been considered a challenge for the petroleum industry. In this work, reduced graphene oxide (rGO), obtained from cellulosic biomass (CB-rGO), as cotton waste, was employed as a phenol adsorbent in an aqueous solution simulating refinery effluent. The CB-rGO was characterized using HRTEM, Raman, XRD, FTIR, BET, and zeta analysis. The behavior of variables such as pH, contact time, temperature, CB-rGO mass, and adsorbate concentration on the characteristics of the adsorption process were continuously investigated. These parameters of the adsorption process were evaluated across a range of adsorbent concentrations from 100 to 300 mg/L, pH in the range of 2-11, adsorbent mass 5-25 mg, contact time of 0-180 min, and temperature of 20-60 °C. The adsorption isotherm data were better described by the Freundlich equation compared to the Langmuir and Sips models, despite the small difference in R2 values. Mechanism diffusion was analyzed using the Boyd model and confirmed to be the rate-limiting step in the adsorption process. The endothermic nature of this CB-rGO adsorption process with phenol was confirmed by verifying the thermodynamic data. This successful removal of phenol from synthetic effluents highlights the promising potential of this adsorbent obtained from an industrial residue and being an ecologically more sustainable alternative compared to the synthesis of other materials identified to remove this contaminant.

Bismuth oxyfluoride (BiOF) is an emerging class of material with notable chemical stability, unique layered structure and striking energy band structure. Bi-based semiconductor materials and reduced graphene oxides (rGOs) have attracted considerable attention due to their broad spectrum of potential applications. Herein, we successfully synthesised an efficient photocatalyst comprising BiOF-rGO nanocomposites with embedded Ag nanoparticles using a simple hydrothermal method. The synthesised nanocomposites were characterised through Fourier-transform infrared spectroscopy, X-ray diffraction (XRD), field emission scanning electron microscopy and ultraviolet (UV)-visible spectroscopy. The XRD results indicated the crystalline structures of the BiOF, Ag-doped BiOF and Ag-doped BiOF-rGO composites. Photocatalytic activity assessments focused on the degradation of methylene blue (MB) and methyl orange (MO) dyes under UV-light and sunlight irradiation. The Ag-doped BiOF-rGO composite exhibited significantly enhanced degradation efficiency, achieving 61.81 % and 74.25 % degradation of MB and MO, respectively, after 300 min under UV-light irradiation. On the contrary, pure BiOF demonstrated only 17.63 % and 48.29 % degradation for MB and MO, respectively, under similar conditions. Furthermore, under sunlight irradiation, the Ag-doped BiOF-rGO composite exhibited an MB removal efficiency of 43.87 % after 300 min, whereas pure BiOF showed only 27.47 % under identical conditions. These results underscore the potential of Ag-doped BiOF-rGO composites as highly efficient and adaptable photocatalysts for the photodegradation of organic dyes in industrial wastewater.