Correction: Electrochemical investigation and amperometry determination iodate based on ionic liquid/polyoxotungstate/P-doped electrochemically reduced graphene oxide multi-component nanocomposite modified glassy carbon electrode

Correction for ‘Electrochemical investigation and amperometry determination iodate based on ionic liquid/polyoxotungstate/P-doped electrochemically reduced graphene oxide multi-component nanocomposite modified glassy carbon electrode’ by Minoo Sharifi et al., RSC Adv., 2021, 11, 8993–9007, DOI: 10.1039/D1RA00845E.

The authors regret that eqn (3) and (4) were shown incorrectly in the original article.The corrected equations are shown below.3H₄SiW₄^VW₇^VINi(H₂O)O₃₉⁶⁻ + IO₃⁻ → 3H₂SiW₂^VW₉^VINi(H₂O)O₃₉⁶⁻ + I⁻ + 3H₂O (3)3H₆SiW₆^VW₅^VINi(H₂O)O₃₉⁶⁻ + IO₃⁻ → 3H₄SiW₄^VW₇^VINi(H₂O)O₃₉⁶⁻ + I⁻ + 3H₂O (4)The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.     

Fabrication of a polyoxotungstate/metal–organic framework/phosphorus-doped reduced graphene oxide nanohybrid modified glassy carbon electrode by electrochemical reduction and its electrochemical properties

Hybrid nanocomposites based on polyoxometalates (POMs), metal–organic frameworks (MOFs), and graphene oxide (GO) have a unique set of properties. They have specific properties such as high acidity, oxygen-rich surface, and good redox capability from POMs. In contrast, they do not have weaknesses of POMs such as a low surface area, and high solubility in aqueous media. Herein, a novel organic–inorganic nanohybrid compound based on H₃PW₁₂O₄₀ (PW₁₂), a Co-based MOF, and GO was prepared. The prepared hybrid nanocomposite (PW₁₂/MOF/GO) was characterized using different techniques. Then, a PW₁₂/MOF/GO nanocomposite modified glassy carbon electrode (GCE) was fabricated by the drop-casting method and next was dried at room temperature. Then, the PW₁₂/MOF/GO/GCE was subjected to electrochemical reduction at a constant potential of −1.5 V, in 0.1 M H₃PO₄ solution containing 0.10% w/v PW₁₂/MOF/GO additive. The morphology, electrochemical activity, and stability of the modified electrode (PW₁₂/MOF/P@ERGO/GCE) were studied with FE-SEM coupled with EDS, CV, and amperometry. The obtained results confirmed that the PW₁₂/MOF/P@ERGO/GCE could be effective in hydrogen evolution reaction (HER). The electrochemical activity of the PW₁₂/MOF/P@ERGO/GCE due to the desirable microstructure of the electrocatalyst (e.g. high active surface area and homogeneous distribution of the PW₁₂/MOF/P@ERGO), and also the synergistic effect of the blocks, is more than those of PW₁₂/GCE, MOF/GCE, PW₁₂/MOF/GCE, and P@ERGO/GCE. Moreover, the PW₁₂/MOF/P@ERGO/GCE showed an excellent long-term stability under the air atmosphere.

Fabrication of a modified glassy carbon electrode based on a polyoxotungstate/metal–organic framework/phosphorus-doped reduced graphene oxide nanohybrid.     

Simultaneous electrochemical determination of levodopa and piroxicam using a glassy carbon electrode modified with a ZnO–Pd/CNT nanocomposite

A highly conductive electrochemical sensor was constructed for the simultaneous electrochemical determination of levodopa and piroxicam by modification of a glassy carbon electrode with a ZnO–Pd/CNT nanocomposite (GCE/ZnO–Pd/CNTs). The ZnO–Pd/CNT nanocomposite was synthesized by the sol–gel procedure and was characterized by EDAX, MAP and SEM. The sensor was shown to improve the oxidation signal of levodopa and piroxicam by ∼70.2-fold and ∼41.5-fold, respectively. This marks the first time that the electrochemical behavior of levodopa and piroxicam have been investigated at the surface of GCE/ZnO–Pd/CNTs. The voltammogram showed a quasi-reversible signal and an irreversible redox signal for electro-oxidation of levodopa and piroxicam, respectively. The GCE/ZnO–Pd/CNTs showed a linear dynamic range of 0.6 to 100.0 μM (at a potential of ∼180 mV) and 0.1 to 90 μM (at a potential of ∼480 mV) with detection limits of 0.08 and 0.04 μM for the determination of levodopa and piroxicam, respectively. GCE/ZnO–Pd/CNTs were then applied for the determination of levodopa and piroxicam in real samples.

A highly conductive electrochemical sensor was constructed for the simultaneous electrochemical determination of levodopa and piroxicam by modification of a glassy carbon electrode with a ZnO–Pd/CNT nanocomposite (GCE/ZnO–Pd/CNTs).     

Electrosynthesis of electrochemically reduced graphene oxide/polyaniline nanowire/silver nanoflower nanocomposite for development of a highly sensitive electrochemical DNA sensor

A novel nanostructured electrode material based on electrochemically reduced graphene oxide/polyaniline nanowires/silver nanoflowers (ERGO/PANi NWs/AgNFs) was fabricated site-specifically onto a Pt microelectrode (0.80 mm² area) using a three-step electrochemical procedure: electrosynthesis of ERGO, electropolymerization of PANi NWs, and electrodeposition of AgNFs. Synergistic and complementary properties of ERGO, PANi NWs and AgNFs, including high electrochemical activity, large surface area, and high biocompatibility, were obtained. Besides, the electrosynthesis method allowed the direct formation of the desired nanomaterial onto the Pt microelectrode, so the adhesion between the sandwich-structured nanocomposite and the electrode surface was also improved. The optimized ERGO/PANi NWs/AgNFs nanocomposite was used for the first time to develop an electrochemical DNA sensor. As a result, the DNA probe immobilization was facilitated and the electrochemical signals of the DNA sensor were enhanced. The detection limit of the DNA sensor was 2.70 × 10⁻¹⁵ M. Moreover, potential miniaturization for fabrication of a lab-on-a-chip system, direct detection, high sensitivity, and good specificity are the advantages of the fabricated DNA sensor.

A novel nanostructured material based on ERGO/PANi NWs/AgNFs was electrosynthesized on a Pt microelectrode and was used for the first time to develop an electrochemical DNA sensor.     

Electrochemical detection of 2-nitrophenol using a heterostructure ZnO/RuO2 nanoparticle modified glassy carbon electrode

A highly selective chemisensor for 2-nitrophenol detection was fabricated using ZnO/RuO₂ nanoparticles (NPs) synthesized by impregnation method. The as-synthesized NPs were characterized through UV-vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), Energy dispersive X-ray spectroscopy (EDS), FTIR and X-ray diffraction (XRD). A glassy carbon electrode was modified with as-synthesized ZnO/RuO₂ nanoparticles and utilized as a chemical sensor for the detection of 2-nitrophenol. The fabricated sensor exhibited excellent sensitivity (18.20 μA μM⁻¹ cm⁻²), good reproducibility, short response time (8.0 s.), the lowest detection limit (52.20 ± 2.60 pM) and long-term stability in aqueous phase without interference effects. Finally, the fabricated sensor was validated as a 2-NP probe in various environmental water samples at room conditions.

A highly selective chemisensor for 2-nitrophenol detection was fabricated using ZnO/RuO₂ nanoparticles (NPs) synthesized by impregnation method.     

A dopamine electrochemical sensor based on a platinum–silver graphene nanocomposite modified electrode

A platinum–silver graphene (Pt–Ag/Gr) nanocomposite modified electrode was fabricated for the electrochemical detection of dopamine (DA). Electrochemical studies of the Pt–Ag/Gr nanocomposite towards DA detection were performed by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The CV analysis showed that Pt–Ag/Gr/GCE had enhanced electrocatalytic activity towards DA oxidation due to the synergistic effects between the platinum–silver nanoparticles and graphene. The DPV results showed that the modified sensor demonstrated a linear concentration range between 0.1 and 60 μM with a limit of detection of 0.012 μM. The Pt–Ag/Gr/GCE presented satisfactory results for reproducibility, stability and selectivity. The prepared sensor also showed acceptable recoveries for a real sample study.

A platinum–silver graphene nanocomposite was synthesized and characterized. A nanocomposite modified electrode was fabricated in order to investigate the electrochemical detection of dopamine.     

The direct electrochemistry and bioelectrocatalysis of nitrate reductase at a gold nanoparticles/aminated graphene sheets modified glassy carbon electrode

It is rather difficult to achieve the direct electrochemistry of nitrate reductase (NR) as it is a complex homodimeric enzyme. However, in this study, the direct electron transfer between NR''s redox centers and the electrode surface was achieved with the aid of aminated graphene sheets (am-GSs) which could immobilize NR stably and control the orientation of the enzyme molecules on the surface of the modified electrode through electrostatic attractions. Moreover, when the gold nanoparticles (AuNPs) which could act as electronic wire were introduced to the modified electrode, the NR-based enzymatic reduction of nitrate was promoted and a sensitive electrochemical response regarding the electrochemical reduction of nitrate could be obtained at the NR/AuNPs/am-GSs/GC electrode. Under optimized conditions, a wide linear range from 1.0 × 10⁻⁶ mol L⁻¹ to 2.0 × 10⁻³ mol L⁻¹ was acquired with a low detection limit of 7 × 10⁻⁷ mol L⁻¹ (S/N = 3). The biosensor was successfully employed to determine the total nitrogen in environmental water samples and the results were in good accordance with those obtained by ultraviolet-visible spectrophotometry.

The aminated graphene sheets could immobilize nitrate reductase stably and control its orientation through electrostatic attractions, achieving its direct electrochemistry.     

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.     

A label-free immunosensor based on PHEMA/graphene oxide nanocomposite for simultaneous electrochemical determination of alpha fetoprotein

An electrochemical immunosensor based on poly(2-hydroxyethyl methacrylate) (PHEMA)/graphene oxide (GO) nanocomposite was designed in a simple way for the ultrasensitive detection of tumor makers (alpha-fetoprotein, AFP as a model). PHEMA with excellent biocompatibility, provides a large number of sites for connecting signal molecules. After modification with signal molecules, the functional PHEMA significantly improved the sensitivity of electrochemical detection. In order to immobilize antibodies, GO was introduced and used to construct a nanocomposite as a substrate. The designed AFP immunosensor showed favorable selectivity and excellent stability. Meanwhile, it has a low detection limit of 0.403 pg mL⁻¹. Furthermore, the immunosensor was used to detect target AFP in human serum, demonstrating the feasibility of clinical diagnosis.

An electrochemical immunosensor based on poly(2-hydroxyethyl methacrylate) (PHEMA)/graphene oxide (GO) nanocomposite was designed in a simple way for the ultrasensitive detection of tumor makers (alpha-fetoprotein, AFP as a model).     

Electrochemical determination of tetrabromobisphenol A in water samples based on a carbon nanotubes@zeolitic imidazole framework-67 modified electrode

Carbon nanotubes@zeolitic imidazole framework-67 (CNTs@ZIF-67), a conductive composite was prepared from carboxylic carbon nanotubes and a cobalt–imidazole framework. It possesses an excellent adsorption capacity (92.12 mg g⁻¹) for the flame retardant tetrabromobisphenol A (TBBPA). The composite was characterized by transmission and scanning electron microscopy, FTIR and X-ray diffractometry. It was then used to modify an acetylene black electrode. Electrochemical studies showed the current response of the modified electrode to be larger than that of electrodes modified with CNTs-COOH or ZIF-67 only. Electrochemical impedance spectroscopy showed this material combination to improve the conductivity of ZIF-67. The addition of perfluorodecanoic acid further improves the response. The sensor is stable, reproducible, and has a linear range of 0.01–1.5 μM TBBPA concentration, with a 4.2 nM detection limit (at S/N = 3). The sensor was successfully applied to the detection of TBBPA in spiked rain and pool water samples.

Carbon nanotubes@zeolitic imidazole framework-67 (CNTs@ZIF-67), a conductive composite was prepared from carboxylic carbon nanotubes and a cobalt–imidazole framework.     

Ternary 3D reduced graphene oxide/Ni0.5Zn0.5Fe2O4/polyindole nanocomposite for supercapacitor electrode application

A facile two-step strategy has been reported for the preparation of a ternary 3D reduced graphene oxide/Ni_0.5Zn_0.5Fe₂O₄/polyindole nanocomposite (GNP) and this composite is applied as an electrode material for supercapacitor applications. Remarkably, Ni_0.5Zn_0.5Fe₂O₄ nanoparticles (NZF) decorated on reduced graphene oxide (GN2) are achieved by a facile hydrothermal method followed by coating with polyindole (PIN) through an in situ emulsion polymerization process. The structure, porosity, morphology, and thermal stability of the resulting ternary GNP hybrid material were characterized via X-ray diffraction (XRD), Raman spectroscopy, Brunauer–Emmett–Teller (BET) surface area measurements, transmission electron microscopy (TEM), and thermogravimetric analysis (TGA). This combination of hybrid material has a favorable mesoporous structure that enables high exposure of active sites for fast electron transport for supercapacitor applications. We demonstrate here that the ternary GNP hybrid electrode material is capable of delivering a favorable specific capacitance of ∼320 F g⁻¹ at 0.3 A g⁻¹ within the potential range from −0.1 to 1 V, with desirable rate stability and excellent cycling stability in the three-electrode system. Furthermore, an asymmetric supercapacitor (ASC) of a two-electrode configuration was fabricated using 3D RGO and GNP as the negative and positive electrodes, respectively. Such a device manifests a favourable C_sp of 48.9 F g⁻¹ at 0.5 A g⁻¹ and retains stability of 84% even after 2000 cycles. This ASC device exhibits a significant energy density of 16.38 W h kg⁻¹ at a power density of 1784 W kg⁻¹. The synergistic effects of pseudo and double layer capacitive contributions from PIN and GN2 make this ternary GNP hybrid electrode material of great promise in supercapacitor applications.

A facile two-step strategy has been reported for the preparation of a ternary 3D reduced graphene oxide/Ni_0.5Zn_0.5Fe₂O₄/polyindole nanocomposite (GNP) and this composite is applied as an electrode material for supercapacitor applications.     

Photocatalytic activity and antibacterial properties of linen fabric using reduced graphene oxide/silver nanocomposite

Silver nanoparticles were in situ prepared on the surface of linen fabric coated by graphene oxide (GO). In the meantime, the reduction of silver nitrate on the GO-coated fabric led to the synthesis of reduced graphene oxide on the fabric. Two kinds of substrate (cotton and linen) were used. Both RGO/Ag and Ag/GO nanocomposites were added on cotton and linen fabrics through a conventional “pad–dry–cure” method. The chemistry and morphology of the coated surfaces were extensively characterized using Fourier-transformed infrared spectroscopy, energy-dispersive X-ray spectroscopy, and scanning electron microscopy. Resistivity measurements were used for assessing the conductivity. The UV protection properties and the photocatalytic activity of the coated fabrics against methylene blue dye were also investigated. The antibacterial activity was studied against Gram-positive S. aureus and B. subtilis and Gram-negative bacterial strains E. coli and P. aeruginosa by determining the zone of inhibition using the agar diffusion method. Methicillin-resistant Staphylococcus aureus (MRSA) has been responsible for many serious hospital infections worldwide. The fabrics showed superior antibacterial activity and successfully hindered the growth of pathogenic bacterial strains. This outcome suggested that both the RGO/Ag and Ag/GO nanocomposites-coated fabrics could be potentially applied in biomaterials and biomedical fields.

Silver nanoparticles were in situ prepared on the surface of linen fabric coated by graphene oxide (GO).     

Electrochemical behaviour of cellulose/reduced graphene oxide/carbon fiber paper electrodes towards the highly sensitive detection of amitrole

Amitrole is a non-selective triazole herbicide that is widespread used to control a variety of weeds in agriculture, but it may pollute the environment and do harm to organisms. Thus, it is of critical significance to enlist a low-cost, sensitive, stable and renewable method to detect amitrole. In this paper, electrochemical experiments were carried out using carbon fibers/reduced graphene oxide/cellulose paper electrodes, which demonstrated good electrocatalytic performance for amitrole detection. The electrochemical process of amitrole on the surface of the reduced paper electrode was a quasi-reversible reaction controlled by diffusion. Cyclic voltammetry and the amperometric i–t curve method were used for amitrole determination at a micro molar level and higher-concentration range with the following characteristics: linear range 5 × 10⁻⁶ mol L⁻¹ to 3 × 10⁻⁵ mol L⁻¹, detection limit 2.44 × 10⁻⁷ mol L⁻¹. In addition, the relative standard deviation of repeatability is 3.74% and of stability is 4.68%. The reduced paper electrode with high sensitivity, low detection limit, good stability and repeatability provides novel ideas for on-site amitrole detection in food and agriculture.

A cellulose/reduced graphene oxide/carbon fibers paper electrode exhibits high electrocatalytic performance for the oxidation of amitrole, showing high sensitivity, wide linear range and low detection limit.     

Electrocatalytic reduction of oxygen at platinum nanoparticles dispersed on electrochemically reduced graphene oxide/PEDOT:PSS composites

Composites of commercially available graphene oxide (GO) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) with solvent additive ethylene glycol (EG) were investigated as an alternative support for Pt nanoparticles towards the electrocatalytic reduction of oxygen. The surface characteristics of the materials were examined using atomic force microscopy (AFM), X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), and energy dispersive X-ray spectroscopy (EDS). Cyclic voltammetry (CV) and linear sweep voltammetry (LSV) at rotating disk electrodes (RDEs) and rotating ring-disk electrodes (RRDEs) were used to characterise the electrocatalytic activities of the composites materials. The structural and electrochemical studies reveal that the addition of EG favours the homogeneous distribution of Pt particles with reduced particle size and improves the electrocatalytic properties. A 30% and 16% increase in electrochemically active surface area (ECSA), a 1.2 and 1.1 fold increase in specific area activity (SA), and a 1.5 and 1.2 fold increase in mass activity (MA) were observed for 30% and 40% Pt loading on PEDOT:PSS after the addition of EG. A composite of rGO and PEDOT:PSS(EG) was investigated for different (w/w) ratios of PEDOT:PSS and rGO. The 1 : 2 w/w ratio showed an enhanced catalytic activity with high limiting current, more positive onset potential, higher SA and MA with lower H₂O₂ yield compared to PEDOT:PSS(EG) and rGO and previously reported values for PEDOT:PSS.

Composites of commercially available graphene oxide and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) with solvent additive ethylene glycol were investigated as an alternative support for Pt nanoparticles towards the electrocatalytic reduction of oxygen.     

A simple electrochemical immunosensor based on a chitosan/reduced graphene oxide nanocomposite for sensitive detection of biomarkers of malignant melanoma

The sensitive and specific detection of tumor biomarkers is crucial for early diagnosis and treatment of malignant melanoma. Immunoassay with a simple sensing interface and high sensitivity is highly desirable. In this work, a simple electrochemical immunosensor based on a chitosan/reduced graphene oxide (CS–rGO) nanocomposite was developed for sensitive determination of an S-100B protein, a tumor marker of malignant melanoma. CS–rGO nanocomposite were prepared by chemical reduction of graphene oxide in the presence of chitosan and modified on glassy carbon electrode (GCE) to provide a biofriendly, conductive, and easily chemically modified matrix for further immobilization of antibodies. Anti-S-100B antibodies were grafted onto the chitosan molecules to fabricate the immunorecognition interface by a simple glutaraldehyde cross-linking method. Electrochemical determination of S-100B was achieved by measuring the decreased current signal of solution phase electrochemical probes, which originated from the increased steric hindrance and insulation caused by the formation of antigen–antibody complexes at the electrode interface. Due to the good conductivity, high surface area, excellent biocompatibility, and good film-forming ability of CS–rGO, the constructed immunosensor exhibited good stability, high selectivity and sensitivity, a wide dynamic range from 10 fg mL⁻¹ to 1 ng mL⁻¹ and a low limit of detection of 1.9 pg mL⁻¹ (S/N = 3). Moreover, the sensor was also applicable for the sensitive detection of S-100B protein in real human serum samples.

Simple electrochemical immunosensor is easily fabricated based on chitosan/reduce graphene oxide nanocomposite for sensitive determination of a tumor marker of malignant melanoma.     

High electrochemical performance of ink solution based on manganese cobalt sulfide/reduced graphene oxide nano-composites for supercapacitor electrode materials

Large scale supercapacitor electrodes were prepared by 3D-printing directly on a graphite paper substrate from ink solution containing manganese cobalt sulfide/reduced graphene oxide (MCS/rGO) nanocomposites. The MCS/rGO composite solution was synthesized through the dispersion of MCS NPs and rGO in dimethylformamide (DMF) solvent at room temperature. Their morphology and composition were investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray diffraction (EDS). The role of rGO on decreasing charge transfer resistance and enhancing ion exchange was discussed. The MCS/rGO electrode exhibits an excellent specific capacitance of 3812.5 F g⁻¹ at 2 A g⁻¹ and it maintains 1780.8 F g⁻¹ at a high current density of 50 A g⁻¹. The cycling stability of the electrodes reveals capacitance retention of over 92% after 22 000 cycles at 50 A g⁻¹.

Large scale supercapacitor electrodes were prepared by 3D-printing directly on a graphite paper substrate from ink solution containing manganese cobalt sulfide/reduced graphene oxide (MCS/rGO) nanocomposites.     

Rapid and sensitive determination of doxorubicin in human whole blood by vertically-ordered mesoporous silica film modified electrochemically pretreated glassy carbon electrodes

Direct and accurate detection of doxorubicin (DOX) in unprocessed human whole blood is of vital importance in medical diagnosis and monitoring. In this work, we demonstrate the utilization of electrochemically pretreated glassy carbon electrodes (p-GCE) modified with vertically-ordered mesoporous silica films (VMSF) for rapid and sensitive electrochemical detection of DOX. The electrochemically pretreated process is a simple, cost-effective and environmentally friendly approach for improving interface catalytic properties and introducing oxygen-containing groups into the GCE surface, which could be suitable for stably growing VMSF without any adhesive layer simultaneously retaining the underlying electrode activity. Benefiting from the highly sensitive electrode substrate of p-GCE and electrostatic preconcentration effect of VMSF, the present VMSF/p-GCE sensor was able to determine DOX with an ultrahigh sensitivity (23.94 μA μM⁻¹) and a relatively low limit of detection (0.2 nM) and a rather wide linear range (0.5 nM to 23 μM). Furthermore, direct and reliable electrochemical detection of DOX in human whole blood without complicated sample pretreatments was achieved owing to the excellent anti-fouling and anti-interference ability of VMSF.

Direct and accurate detection of doxorubicin (DOX) in unprocessed human whole blood is of vital importance in medical diagnosis and monitoring.     

Synergistic effect of reduced graphene oxide/carbon nanotube hybrid papers on cross-plane thermal and mechanical properties

Graphene paper has attracted great attention as a heat dissipation material due to its excellent thermal conductivity and mechanical properties. However, the thermal conductivity of graphene paper in the normal direction is relatively poor. In this work, the cross-plane thermal conductivities (K_⊥) and mechanical properties of the reduced graphene oxide/carbon nanotube papers with different CNT loadings were studied systematically. It was found that the K_⊥ decreased from 0.0393 W m⁻¹ K⁻¹ for 0 wt% paper to 0.0250 W m⁻¹ K⁻¹ for 3 wt% paper, and then increased to 0.1199 W m⁻¹ K⁻¹ for 20 wt% paper. The papers demonstrated a maximum elastic modulus of 6.1 GPa with 10 wt% CNT loading. The CNTs acted as scaffolds to restrain the graphene sheets from corrugating and to reinforce the mechanical properties of the hybrid papers. The more CNTs that filled the gaps between graphene sheets, the greater the number of channels of the transmission of phonons and the looser the structure in the cross-plane direction. Further mechanism analysis revealed the synergistic effects of CNT loadings and graphene sheets on enhancing the thermal and mechanical performance of the papers.

The top-view SEM images for (a) rGO, (b) rGO/CNT-3%, (c) rGO/CNTs-20% and the corresponding schematic diagram of photon transmission with different spacer CNTs loadings (a-i, b-ii, c-iii).     

Investigation on the role of different conductive polymers in supercapacitors based on a zinc sulfide/reduced graphene oxide/conductive polymer ternary composite electrode

Conductive polymers, such as polyaniline (PANI), polypyrrole (PPy), polythiophene (PTh) and poly 3,4-ethylenedioxythiophene (PEDOT), play an important role in the application of pseudocapacitors. It is necessary to explore the effects of different conductive polymers in electrode composites. Herein, we prepare zinc sulfide/reduced graphene oxide (ZnS/RGO) by the hydrothermal method, and conductive polymers (PANI, PPy, PTh and PEDOT) doped with the same mass ratio (polymer to 70 wt%) via in situ polymerization on the surface of ZnS/RGO composite. For the supercapacitor application, the ZnS/RGO/PANI ternary electrode composite possesses the best capacitance performance and cycle stability out of all of the polymer-coated ZnS/RGO composites. In the three-electrode system, the discharge specific capacitance and cycle stability of ZnS/RGO/PANI are 1045.3 F g⁻¹ and 160% at 1 A g⁻¹ after 1000 loops. In a two-electrode symmetric system, the discharge specific capacitance and cycle stability of ZnS/RGO/PANI are 722.0 F g⁻¹ and 76.1% at 1 A g⁻¹ after 1000 loops, and the greatest energy and power density of the ZnS/RGO/PANI electrode are 349.7 W h kg⁻¹ and 18.0 kW kg⁻¹. In addition, conductive polymers can effectively improve the voltage range of the electrode composites in 6 M KOH electrolyte for the two-electrode system. The discharge voltage ∼1.6 V makes them promising electrode materials for supercapacitors.

Conductive polymers, such as polyaniline (PANI), polypyrrole (PPy), polythiophene (PTh) and poly 3,4-ethylenedioxythiophene (PEDOT), play an important role in the application of pseudocapacitors.