Uniformly dispersed platinum nanoparticles over nitrogen-doped reduced graphene oxide as an efficient electrocatalyst for the oxygen reduction reaction

Oxygen reduction reaction (ORR) with efficient activity and stability is significant for fuel cells. Herein, platinum (Pt) nanoparticles dispersed on nitrogen-doped reduced graphene oxide (N-rGO) were prepared by a hydrothermal and carbonized approach for the electrocatalysis of ORR. Polyvinylpyrrolidone plays a significant role in the reduction and dispersion of platinum particles (about 2 nm). The obtained Pt–N-rGO hybrids exhibited superior activity with an electron transfer number of ∼4.0, onset potential 0.90 eV of ORR, good stability and methanol tolerance in alkaline media. These results reveal the interactions between Pt–N-rGO and oxygen molecules, which may represent an oxygen modified growth in catalyst preparation. The excellent electrocatalysis may lead to the decreased consumption of expensive Pt and open up new opportunities for applications in lithium air batteries.

We developed a facile, yet general approach to prepare ultrafine Pt nanoparticles loaded on N-doped reduced graphene (Pt–N-rGO) composites, which showed excellent oxygen reduction reaction performance.     

PdPbAg alloy NPs immobilized on reduced graphene oxide/In2O3 composites as highly active electrocatalysts for direct ethylene glycol fuel cells

rGO-modified indium oxide (In₂O₃) anchored PdPbAg nanoalloy composites (PdPbAg@rGO/In₂O₃) were prepared by a facile hydrothermal, annealing and reduction method. Electrochemical tests showed that the as-prepared trimetallic catalyst exhibited excellent electrocatalytic activity and high resistance to CO poisoning compared with commercial Pd/C, mono-Pd and different bimetallic catalysts. Specifically, PdPbAg@rGO/In₂O₃ has the highest forward peak current density of 213.89 mA cm⁻², which is 7.89 times that of Pd/C (27.07 mA cm⁻²). After 3600 s chronoamperometry (CA) test, the retained current density of PdPbAg@rGO/In₂O₃ reaches 78.15% of the initial value. Its excellent electrocatalytic oxidation performance is attributed to the support with large specific surface area and the strong synergistic effect of PdPbAg nanoalloys, which provide a large number of interfaces and achievable reactive sites. In addition, the introduction of rGO into the In₂O₃ matrix contributes to its excellent electron transfer and large specific surface area, which is beneficial to improving the catalytic ability of the catalyst. The study of this novel composite material provides a conceptual and applicable route for the development of advanced high electrochemical performance Pd-based electrocatalysts for direct ethylene glycol fuel cells.

rGO-modified indium oxide (In₂O₃) anchored PdPbAg nanoalloy composites (PdPbAg@rGO/In₂O₃) were prepared by a facile hydrothermal, annealing and reduction method.     

Tin disulphide/nitrogen-doped reduced graphene oxide/polyaniline ternary nanocomposites with ultra-high capacitance properties for high rate performance supercapacitor

In this work, tin disulfide/nitrogen-doped reduced graphene oxide/polyaniline ternary composites are synthesized via in situ polymerization of aniline monomers on the surface of tin disulfide/nitrogen-doped reduced graphene oxide nanosheets binary composites with different loading of the conducting polymers. The tin disulfide/nitrogen-doped reduced graphene oxide/polyaniline ternary composites electrode shows much higher specific capacitance, specific energy and specific power values than those of pure polyaniline and tin disulfide/nitrogen-doped reduced graphene oxide binary composites. The highest specific capacitance, specific energy and specific power values of 1021.67 F g⁻¹, 69.53 W h kg⁻¹ and 575.46 W kg⁻¹ are observed for 60% polyaniline deposited onto tin disulfide/nitrogen-doped reduced graphene oxide composites at a current density of 1 A g⁻¹. The above composites also show superior cyclic stability and 78% of the specific capacitance can be maintained after 5000 galvanostatic charge–discharge cycles. The good charge-storage properties of tin disulfide/nitrogen-doped reduced graphene oxide/polyaniline ternary composites is ascribed to the organic–inorganic synergistic effect. This study paves the way to consider tin disulfide/nitrogen-doped reduced graphene oxide/polyaniline ternary composites as excellent electrode materials for energy storage applications.

In this work, SnS₂/NRGO/PANI ternary composites are synthesized via in situ polymerization of aniline monomers on the surface of SnS₂/NRGO nanosheets binary composites with different loading of the conducting polymers.     

A graphene oxide polymer brush based cross-linked nanocomposite proton exchange membrane for direct methanol fuel cells

Functional polymer brush modified graphene oxide (FPGO) with functional linear polysiloxane brushes was synthesized via surface precipitation polymerization (sol–gel) and chemical modification. Then, FPGO was covalently cross-linked to the sulfonated polysulfone (SPSU) matrix to obtain novel SPSU/FPGO cross-linked nanocomposite membranes. Meanwhile, SPSU/GO composite membranes and a pristine SPSU membrane were fabricated as control groups. Reduced agglomeration of the inorganic filler and better interfacial interaction, which are benefit to increase diffusion resistance of methanol and to generate continuous channels for fast proton transportation at elevated temperature, were observed in SPSU/FPGO cross-linked membranes. Moreover, the enhanced membrane stability (thermal, oxidative and dimensional stability) and good mechanical performance also guaranteed their proton conducting durability. It is noteworthy that the SPSU/FPGO-1 cross-linked membrane possesses the best comprehensive properties among all the prepared membranes and Nafion®117, it acquires the highest proton conductivity of 0.462 S cm⁻¹ at 90 °C under hydrated conditions together with a low methanol permeability of 1.71 × 10⁻⁶ cm² s⁻¹ at 30 °C. The resulting high membrane selectivity displays the great potential of the SPSU/FPGO cross-linked membrane for DMFCs application.

A novel proton exchange nanocomposite which was cross-linked by functional graphene oxide polymer brushes shows interesting and comprehensive advantages for DMFCs.     

Antibody-modified reduced graphene oxide film for circulating tumor cell detection in early-stage prostate cancer patients

In recent years, liquid biopsies, especially for detecting circulating tumor cells (CTCs), have received great attention for cancer diagnosis and treatment monitoring. For clinical diagnosis of prostate cancer (PCa), prostate specific antigen (PSA) has been widely used as a standard method for PCa screening. However, PSA diagnostic efficacy within early-stage PCa patients with a PSA level of 4–10 ng mL⁻¹ is always controversial. Therefore, the development of new methods to assist clinical PSA diagnosis is greatly desired. Herein, we report the fabrication of antibody-modified reduced graphene oxide films, which can be used to efficiently detect CTCs in PCa patients with PSA levels of 4–10 ng mL⁻¹. The antibody-modified reduced graphene oxide (rGO) films were fabricated by spray coating reduced graphene oxide solution onto a smooth glass slide and then modifying it with anti-epithelial cell adhesion molecules (anti-EpCAMs) and anti-prostate specific membrane antigen (anti-PSMA). The rGO films exhibited an excellent ability to capture CTCs from the blood of PCa patients with PSA levels of 4–10 ng mL⁻¹ and the efficiency could reach 60% (6/10). Our approach for highly efficient detection of CTCs in early-stage PCa patients may provide great potential in assisting clinical cancer diagnosis.

We report the fabrication of an antibody-modified reduced graphene oxide film, which can be used to efficiently detect CTCs in PCa patients with PSA levels of 4–10 ng mL⁻¹.     

Physicochemical characterisation of reduced graphene oxide for conductive thin films

Graphene is a desirable material for next generation technology. However, producing high yields of single-layer flakes with industrially applicable methods is currently limited. We introduce a combined process for the reduction of graphene oxide (GO) via vitamin C (ascorbic acid) and thermal annealing at temperatures of <150 °C for times of <10 minutes, resulting in electrically conducting thin films with sheet resistances reducing by 8 orders of magnitude to as low as ∼1.3 kΩ □⁻¹, suitable for microelectronics, display technology and optoelectronic applications. The in-depth physicochemical characterisation of the products at different stages of GO preparation and reduction allows for further understanding of the process and demonstrates the suitability for industrial production methodologies due to an environmentally-friendly reducing agent, solution processability and no requirement for high temperatures. The presence of the vitamin C lowers the temperature required to thermally reduce the GO into an electrically conducting thin film, making the technique suitable for thermally sensitive substrates, such as low melting point polymers. Simultaneous spray coating and reduction of GO allows for large area deposition of conductive coatings without sacrificing solution processability, often lost through particle agglomeration, making it compatible with industrial processes, and applicable to, for example, the production of sensors, energy devices and flexible conductive electrodes for touchscreens.

We introduce a combined process for the reduction of graphene oxide (GO) via vitamin C (ascorbic acid) and thermal annealing.     

Benzophenone assisted UV-activated synthesis of unique Pd-nanodendrite embedded reduced graphene oxide nanocomposite: a catalyst for C–C coupling reaction and fuel cell

In this work we report the use of benzophenone (BP) for the synthesis of a palladium (Pd) embedded on reduced graphene oxide (rGO) nanocomposite (Pd/rGO) using a simple aqueous solution and UV irradiation. The simple and facile evolution of thermodynamically unstable branched Pd(0) nanodendrites was achieved by BP photoactivation, circumventing the growth of more stable nanomorphologies. The synthesis of Pd(0)-embedded rGO nanosheets (PRGO-nd) was made possible by the simultaneous reduction of both the GO scaffold and PdCl₂ by introducing BP into the photoactivation reaction. The nanocomposites obtained in the absence of BP were common triangular and twinned Pd(0) structures which were also implanted on the rGO scaffold (PRGO-nt). The disparity in morphologies presumably occurs due to the difference in the kinetics of the reduction of Pd²⁺ to Pd⁰ in the presence and absence of the BP photoinitiator. It was observed that the PRGO-nd was composed of dense arrays of multiple Pd branches around nucleation site which exhibited (111) facet, whereas PRGO-nt showed a mixture of (100) and (111) facets. On comparing the catalytic efficiencies of the as-synthesized nanocatalysts, we observed a superiority in efficiency of the thermodynamically unstable PRGO-nd nanocomposite. This is due to the evolved active facets of the dendritic Pd(0) morphology with its higher surface area, as testified by Brunauer–Emmett–Teller (BET) analysis. Since both PRGO-nd and PRGO-nt contain particles of similar size, the dents and grooves in the structure are the cause of the increase in the effective surface area in the case of nanodendrites. The unique dendritic morphology of the PRGO-nd nanostructures makes them a promising material for superior catalysis, due to their high surface area, and the high density of surface atoms at their edges, corners, and stepped regions. We investigated the efficiency of the as-prepared PRGO-nd catalyst in the Suzuki–Miyaura coupling reaction and showed its proficiency in a 2 h reaction at 60 °C using 2 mol% catalyst containing 0.06 mol% active Pd. Moreover, the electrochemical efficiency for the catalytic hydrogen evolution reaction (HER) was demonstrated, in which PRGO-nd provided a decreased overpotential of 68 mV for a current density of 10 mA cm⁻², a small Tafel slope of 57 mV dec⁻¹ and commendable stability during chronoamperometric testing for 5 h.

Benzophenone photoinitiator aided synthesis of Pd-nanodendrite embedded rGO nanocatalyst possessing superior potential in C–C coupling reaction and fuel cell application.     

NiCo alloy nanoparticles electrodeposited on an electrochemically reduced nitrogen-doped graphene oxide/carbon-ceramic electrode: a low cost electrocatalyst towards methanol and ethanol oxidation

In this work, nickel–cobalt alloy nanoparticles were electrodeposited on/in an electrochemically reduced nitrogen-doped graphene oxide (ErN-GO)/carbon-ceramic electrode (CCE) and the resulting nanocomposite (NiCo/ErN-GO/CCE) was evaluated as a low cost electrocatalyst for methanol and ethanol electrooxidation. Field-emission scanning electron microscopy coupled with energy dispersive X-ray spectroscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy were used for the physical characterization of the electrocatalyst. To study the electrochemical behavior and electrocatalytic activity of the prepared electrocatalyst towards the oxidation of methanol and ethanol in alkaline media, cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy were utilized. Electrochemical investigation of the introduced electrocatalysts (NiCo alloy and Ni nanoparticles alone electrodeposited on/in different substrates) indicated that NiCo/ErN-GO/CCE has highest activity and stability towards methanol (J_p = 88.04 mA cm⁻²) and ethanol (J_p = 64.23 mA cm⁻²) electrooxidation, which highlights its potential use as an anodic material in direct alcohol fuel cells.

NiCo alloy nanoparticles on the electrochemically reduced nitrogen-doped graphene oxide/carbon-ceramic electrode: a low cost electrocatalyst towards methanol and ethanol oxidation.     

Flexible solid-state supercapacitor based on tin oxide/reduced graphene oxide/bacterial nanocellulose

We demonstrate a flexible and light-weight supercapacitor based on bacterial nanocellulose (BNC) incorporated with tin oxide (SnO₂) nanoparticles, graphene oxide (GO) and poly(3,4-ethylenedioxyiophene)-poly(styrenesulfonate) (PEDOT:PSS). The SnO₂ and GO flakes are introduced into the fibrous nanocellulose matrix during bacteria-mediated synthesis. The flexible PEDOT:PSS/SnO₂/rGO/BNC electrodes exhibited excellent electrochemical performance with a capacitance of 445 F g⁻¹ at 2 A g⁻¹ and outstanding cycling stability with 84.1% capacitance retention over 2500 charge/discharge cycles. The flexible solid-state supercapacitors fabricated using PEDOT:PSS/SnO₂/rGO/BNC electrodes and poly(vinyl alcohol) (PVA)-H₂SO₄ coated BNC as a separator exhibited excellent energy storage performance. The fabrication method demonstrated here is highly scalable and opens up new opportunities for the fabrication of flexible cellulose-based energy storage devices.

A novel, simple and scalable method for the incorporation of tin oxide (SnO₂) and graphene oxide (GO) into bacterial nanocellulose during its growth for the fabrication of a flexible, scalable and environmental-friendly energy storage device was reported.     

Free-standing nitrogen-doped graphene paper for lithium storage application

A flexible free-standing nitrogen-doped graphene paper (N-GP) is fabricated via a facile hydrothermal approach with doping reaction occurring at the solid/gas interface of graphene oxide and ammonia vapor. Ammonia not only facilitates the doping of oxidized graphene paper efficiently with a nitrogen doping level of ca. 6.81%, but also promotes its reduction. The electrochemical properties of N-GP as an anode of lithium ion batteries (LIB) are evaluated and N-GP delivers almost doubled reversible discharge capacity compared to the undoped graphene paper (GP) as well as a good cyclic stability and rate performance. The proposed strategy to realize simultaneous reduction and nitrogen doping of graphene oxide via hydrothermal approach at the solid/gas interface offers a green and facile solution to modify graphene paper with desired electrochemical performances for LIB application.

Flexible free-standing nitrogen doped graphene paper produced from a modified hydrothermal reaction at a solid/gas interface with enhanced electrochemical performances.     

Ethylene glycol-based solar-thermal fluids dispersed with reduced graphene oxide

Direct absorption solar collectors, which use optical nanofluids to volumetrically absorb and convert sunlight into heat, have emerged as promising devices to harvest solar-thermal energy for many heat-related applications. Nanofluids, however, generally suffer from aggregation issues and the widely investigated water-based fluids only enable solar-thermal harvesting at relatively low temperatures. Herein, we report a facile way to prepare stably dispersed reduced graphene oxide-ethylene glycol (rGO-EG) fluids for solar-thermal energy harvesting at medium temperatures. Without the use of complex surface modification process, the homogeneous dispersion of rGO-EG fluids was achieved by utilizing the favorable interaction between the oxygen-containing groups on the rGO surfaces and EG molecules. The rGO-EG fluids were prepared by reducing the GO-EG fluids that are uniformly dispersed with ethanol-wetted GO through a single step of heating. The prepared rGO-EG fluids have suitable thermophysical properties for direct solar-thermal energy harvesting, such as broadband absorption of sunlight, high specific heat capacity and low viscosity. The rGO-EG fluids have shown stable uniform dispersion up to 120 °C and have demonstrated consistent solar-thermal energy harvesting performance during repeated solar radiation at ∼110 °C.

Ethylene glycol nanofluids uniformly dispersed with reduced graphene oxide were prepared for medium-temperature direct absorption-based solar-thermal energy harvesting.     

Rational design of large flat nitrogen-doped graphene oxide quantum dots with green-luminescence suitable for biomedical applications

Rational synthesis and simple methodology for the purification of large (35–45 nm in lateral size) and flat (1.0–1.5 nm of height) nitrogen-doped graphene oxide quantum dots (GOQDs) are presented. The methodology allows robust metal-free and acid-free preparation of N-GOQDs with a yield of about 100% and includes hydrothermal treatment of graphene oxide with hydrogen peroxide and ammonia. It was demonstrated that macroscopic impurities can be separated from N-GOQD suspension by their coagulation with 0.9% NaCl solution. Redispersible in water and saline solutions, particles of N-GOQDs were characterized using tip-enhanced Raman spectroscopy (TERS), photoluminescent, XPS, and UV-VIS spectroscopies. The size and morphology of N-GOQDs were studied by dynamic light scattering, AFM, SEM, and TEM. The procedure proposed allows nitrogen-doped GOQDs to be obtained, having 60–51% of carbon, 34–45% of oxygen, and up to 7.2% of nitrogen. The N-GOQD particles obtained in two hours of synthesis contain only pyrrolic defects of the graphene core. The fraction of pyridine moieties grows with the time of synthesis, while the fraction of quaternary nitrogen declines. Application of TERS allows demonstration that the N-GOQDs consist of a graphene core with an average crystallite size of 9 nm and an average distance between nearest defects smaller than 3 nm. The cytotoxicity tests reveal high viability of the monkey epithelial kidney cells Vero in the presence of N-GOQDs in a concentration below 60 mg L⁻¹. The N-GOQDs demonstrate green luminescence with an emission maximum at 505 nm and sedimentation stability in the cell culture medium.

This paper reveals the methodology for robust preparation of purified nitrogen-doped graphene oxide quantum dots with non-cytotoxic activity against monkey epithelial kidney cells (Vero ATCC® CCL-81™).     

Superior quality chemically reduced graphene oxide for high performance EMI shielding materials

The chemical reduction process of graphene oxide combined with a mild and controllable thermal treatment under vacuum at 200 °C for 4 hours provided a cost-effective, scalable, and high-yield route for Reduced Graphene Oxide (RGO) industrial production and became a potential candidate for producing electromagnetic interference (EMI) shielding. We investigated graphite, and RGO using l-ascorbic acid and Sodium borohydride before and after thermal treatment by carefully evaluating the chemical and morphological structures. The thermally treated l-ascorbic Acid reduction route (TCRGOL) conductivity was 2.14 × 10³ S m⁻¹ and total shielding efficiency (SET) based on mass loadings per area of shielding was 94 dB with about one-tenth less graphite weight and surpassing other graphene reduction mechanisms in the frequency range of 8.2–12.4 GHz, i.e., X-band, at room temperature while being tested using the waveguide line technique. The developed treatment represents valuable progress in the path to chemical reduction using a safe reducing agent and offering superior quality RGO rarely achieved with the top-down technique, providing a high EMI shielding performance.

The developed two-step protocol offers a superior reduced graphene oxide TCRGOL quality (7 layers), and its SET was 94 dB over the X-band.     

A novel fabrication method of copper–reduced graphene oxide composites with highly aligned reduced graphene oxide and highly anisotropic thermal conductivity

Recently, metals with graphene and graphene oxide have been extensively used to enhance the mechanical and anisotropic thermal properties of composites. A novel facile fabrication approach of layer by layer self-assembly followed by hot press sintering was adopted to make copper–reduced graphene oxide composites. The microstructure and heat dissipation properties of pure copper and copper–reduced graphene oxide composites were analyzed with the help of SEM and continuous laser machine analysis. Thermal diffusivity of pure copper and copper–reduced graphene oxide composites was examined in different directions to measure the anisotropic thermal properties by using different volumetric percentages of reduced graphene oxide in the composites. Extraordinarily high anisotropic thermal conductivity of the copper–reduced graphene oxide composites was obtained at a very low concentration of 0.8 vol% reduced graphene oxide, with the difference between the thermal conductivity in-plane and through-plane being a factor of 8.82. Laser test results confirmed the highly anisotropic behavior of our copper–reduced graphene oxide composite with the remarkable property of heat dissipation. The three point bending test was also performed to check the flexural strength of the composites. At 0.6 vol% rGO, the flexural strength was noted (∼127 MPa), and it is 22% higher than that of pure sintered Cu. The high value of anisotropic thermal conductivity and higher flexural strength exhibited by the copper–reduced graphene oxide composite produced using a simple two-step fabrication method give us new hope to use these materials as heat sinks in thermal packaging systems.

Highly aligned rGO with anisotropic thermal conductivity was obtained in this work.     

Simultaneous detection of acetaminophen and 4-aminophenol with an electrochemical sensor based on silver–palladium bimetal nanoparticles and reduced graphene oxide

In this paper, Ag–Pd bimetallic nanoparticles uniformly distributed on reduced graphene oxide (rGO) were synthesized by redox reaction between Pd²⁺, Ag⁺and GO, and were characterized by X-ray diffractometry, field emission scanning electron microscopy, electrochemical impedance spectroscopy and thermal gravimetric analyses. A novel electrochemical sensor was constructed based on these nanocomposites using glassy carbon as a substrate. Under optimal conditions, the linear ranges were 0.50–300.00 μM for PA and 1.00–300.00 μM for 4-AP, with the detection limits of 0.23 μM for PA and 0.013 μM for 4-AP, respectively. This sensor was successfully applied to the determination of PA in pharmaceutical formulations and gave satisfactory results with a lower detection limit, wider linear range and good reproducibility.

Simultaneous detection of acetaminophen and 4-aminophenol with a highly sensitive electrochemical sensor based on silver–palladium bimetal nanoparticles and reduced graphene oxide.     

Room-temperature synthesis of water-dispersible sulfur-doped reduced graphene oxide without stabilizers

Sulfur-Doped graphene has attracted significant attention because of its potential uses in sensors, catalysts, and energy storage applications. In conventional approaches, the sulfur-doped graphene is fabricated with graphene oxide and sulfur-containing compounds through thermal annealing or hydrothermal process, which generally involves special equipment and heat treatment, and requires additional stabilizers to make it solution-processable. In this work, we report a facile one-step approach to synthesize water-dispersible sulfur-doped reduced graphene oxide (S-rGO). Graphene oxide (GO) could be readily reduced and converted to S-rGO simultaneously by directly mixing GO dispersion with hydrosulfide hydrate (NaSH·xH₂O) at room temperature. The sulfur doping is confirmed by high resolution S 2p XPS spectrum and element mapping. The colloidal dispersion state of S-rGO is confirmed by the investigation of Tyndall effect, the zeta potential and particle size distribution measurement. Compared with previously reported strategies, NaSH can initiate the reduction and sulfur doping at room temperature, demand no heat treatment, require no equipment and form stable aqueous S-rGO dispersion without using any stabilizer. These advantages will facilitate large-scale production of water-dispersible (sulfur doped) graphene and further boost their applications in sensors, catalysts and energy storage devices.

Room-temperature synthesis of sulfur-doped reduced graphene oxide, which can form stable aqueous dispersion without using any stabilizer.     

Solution-processable reduced graphene oxide template layer for molecular orientation control of organic semiconductors

A reduced graphene oxide (rGO) film is first applied to a surface template layer to control the molecular orientation of crystalline organic semiconductors. The ultrathin and ultrasmooth rGO layer was successfully prepared on a substrate without a transfer process by spin-coating a carefully purified GO aqueous dispersion. This rGO layer exhibited a strong templating effect rivaling monolayer graphene, inducing a face-on orientation of copper phthalocyanine molecules leading to significant improvement of vertical carrier mobilities. The highly-conductive and transparent rGO film does not hamper charge transport at the interface and photoabsorption unlike conventional templating materials. This method can be widely used for vertical organic devices that require high carrier mobilities and strong photoabsorption/emission.

An ultrasmooth reduced graphene oxide (rGO) film indicated a strong templating effect inducing a face-on orientation for copper phthalocyanine.     

Development of hydrophobic reduced graphene oxide as a new efficient approach for photochemotherapy

Nowadays, chemotherapy is one of the crucial and common therapies in the world. So far, it has been revealed to be highly promising, yet patients suffer from the consequences of severe negative medical dosages. In order to overcome these issues, the enhancement of photothermal chemotherapy with reduced graphene oxide (rGO) as a photothermal agent (PTA) is widely utilised in current medical technologies. This is due to its high near-infrared region (NIR) response, in vitro or in vivo organism biocompatibility, low risk of side effects, and effective positive results. Moreover, rGO not only has the ability to ensure that selective cancer cells have a higher mortality rate but can also improve the growth rate of recovering tissues that are untouched by necrosis and apoptosis. These two pathways are specific diverse modalities of cell death that are distinguished by cell membrane disruption and deoxyribonucleic acid (DNA) disintegration of the membrane via phosphatidylserine exposure in the absence of cell membrane damage. Therefore, this review aimed to demonstrate the recent achievements in the modification of rGO nanoparticles as a PTA as well as present a new approach for performing photochemotherapy in the clinical setting.

rGO of QD-rGO nanocomposite could absorb and convert into heat when harvested under NIR radiation, resulting cell death with reduction of fluorescence.     

Lignosulfonate in situ-modified reduced graphene oxide biosensors for the electrochemical detection of dopamine

Lignosulfonate (LS), a biomass by-product from sulfite pulping and the paper-making industry, which has many excellent characteristics, such as renewable, environmentally friendly, amphiphilic nature, and especially the abundant content of hydrophilic functional groups in its architecture, making it highly reactive and can be used as a sensitive material in sensors to show changes in electrical signals. Herein, we report a one-step in situ method to fabricate lignosulfonate-modified reduced graphene oxide (LS–rGO) green biosensors, which can be used for the sensitive electrochemical detection of dopamine without interference from uric acid and ascorbic acid. The modified LS molecular layers act as chemical-sensing layers, while the rGO planar sheets function as electric-transmitting layers in the as-assembled dopamine biosensors. After the in situ-decoration of the LS modifier, the sensing performance of LS–rGO for the detection of dopamine was much higher than that of the pure rGO electrode, and the highest current response of the biosensor toward dopamine greatly improved from 11.2 μA to 52.07 μA. The electrochemical sensitivity of the modified biosensor was optimized to be 0.43 μA μM⁻¹, and the detection limit was as low as 0.035 μM with a wide linear range (0.12–100 μM), which is better than that of most previously reported metal- and organic-based modified graphene electrodes. The newly designed biosensor has unique advantages including rapid, stable, sensitive and selective detection of dopamine without interference, providing a facile pathway for the synthesis of green resource-derived sensing materials instead of the traditional toxic and expensive modifiers.

One-step situ method to fabricate lignosulfonate modified reduced graphene oxide sensors for sensitive, selective and highly repetitive electrochemical detection of dopamine.     

Ultra-wideband self-powered photodetector based on suspended reduced graphene oxide with asymmetric metal contacts

The ultraviolet to terahertz band forms the main focus of optoelectronics research, while light detection in different bands generally requires the use of different materials and processing methods. However, researchers are aiming to realize multi-band detection simultaneously in the same device in certain specific application scenarios and ultra-wideband photoelectric detectors can also realize multi-function and multi-system integration. Therefore, the research and development work on ultra-wideband photoelectric detectors has important practical application value. Here, we produced self-powered suspended Pd-reduced graphene oxide-Ti (Pd-rGO-Ti) photodetectors. We varied the properties of the rGO films by using different annealing temperatures and achieved p-doping and n-doping of the films by evaporating palladium films and titanium films, respectively, thus enabling preparation of photothermoelectric (PTE) photodetectors based on rGO films. The resulting detectors have excellent photoelectric responses over a wideband illumination wavelength range from 375 nm to 118.8 μm (2.52 THz). At the same time, we determined the best experimental conditions and device structure by varying the channel width, the laser spot irradiation position and the experimental atmospheric pressure. The maximum responsivity obtained from our detectors is 142.08 mV W⁻¹, the response time is approximately 100–200 ms and the devices have high detection sensitivity. Based on this work, we assumed in the subsequent experiments that detectors with higher performance can be obtained by reducing the channel width and atmospheric pressure. With advantages that include simple fabrication, low cost, large-scale production potential and ultra-wideband responses, these Pd-rGO-Ti photodetectors have broad application prospects in high-performance integrated optoelectronics.

An ultra-wideband self-powered photodetector based on suspended reduced graphene oxide with asymmetric metal contacts is reported.