A simple and one-pot synthetic procedure using two different sources has been demonstrated to prepare heteroatoms doped reduced graphene oxide such as nitrogen-doped reduced graphene oxide (N-RGO) and sulfur-doped reduced graphene oxide (S-RGO). The N-RGO has been hydrothermally synthesized using urea as nitrogen precursor, wherein the S-RGO has been synthesized using dimethyl sulfoxide (DMSO) as sulfur precursor. The successful N-doping, S-doping and other physicochemical properties of N-RGO and S-RGO have been confirmed with different spectroscopic and electrochemical techniques. The results indicated that doping into the graphene structure exhibits a high conductivity and a better transfer of charge. Moreover, heteroatoms doped graphene (N-RGO and S-RGO) and graphene-related materials (RGO) have been applied for the individual detection of uric acid (UA). Interestingly, the N-RGO exhibited a lower limit of detection (LOD, S/N = 3) of 2.7 10– 5 M for UA (10–1000 μM) compared with undoped RGO and S-RGO. Furthermore, the simultaneous detection of UA in the presence of Xanthine (XA) has been demonstrated a wide linear range of detection for UA: 10–1000 μM, with unchanged concentration of XA to be 200 μM, and exhibited a low limit of detection of 8.7 10− 5 M ( S∕N = 3) for UA. This modified sensor based on N-RGO has revealed a high selectivity and reproducibility thanks to its large surface area, high catalytic properties, and chemical structure. Indeed, the practical applicability of the proposed sensor has been evaluated in milk samples even in the presence of high concentrations of UA with satisfactory results.

본 연구에서는 산화 방지 특성이 있는 가리워진 아민기를 함유한 산화 그래핀(hindered amine grafted graphene oxide, HA-GO)을 합성하여 이를 도입한 나피온(Nafion) 기반의 복합 막을 제조한 후 고분자 전해질 막 연료전지 시스템에 응용하였다. HA-GO는 4-아미노-2, 2, 6, 6-테트라메틸-4-피페리딘(4-amino-2, 2, 6, 6-tetramethyl piperidine)에 존재하는 아민 기와 GO 표면에 존재하는 에폭시기의 개환 반응을 통해 제조하였으며, 합성된 HA-GO의 함량을 달리한 복합 막을 제조하여 순수 Nafion 막과 성능 특성을 비교하였다. HA-GO가 첨가된 복합 막은 Nafion 단일 막에 비해 기계적 물성, 화학적 안정성 및 수소이온 전도 특성이 향상되었다. 특히 HA-GO의 산화 방지 특성으로 인해 HA-GO가 첨가된 복합 막은 펜톤 평가 (Fenton’s test) 이후 수소이온 전도도의 유지 특성이 Nafion 단일 막에 비해 큰 폭으로 향상된 것을 확인할 수 있었다.

This paper evaluates the adsorptive removal of sunset yellow (SY) from aqueous solutions using a new magnetic glycodendrimer (MGD). To synthesize the MGD, chitosan dendrons were cultivated on amine-functionalized magnetic graphene oxide. A number of analytical methods were employed to physicochemically characterize the synthesized MGD. Batch adsorption conditions were optimized using the Box–Behnken design. An optimized initial SY content of 633 mg/L, an optimized contact time of 33.37 min, and an optimized pH of 3.72 maximized the MGD adsorption capacity to 485 mg/g. The Langmuir isotherm was employed to describe adsorption equilibrium, while adsorption kinetics was studied via the Lagergren kinetics model. The SY adsorption onto the MGD was thermodynamically found to be spontaneous (ΔG° < 0) and exothermic (ΔH° = – 19.120 kJ/mol), leading to a decreased disorder (ΔS° = – 54.420 kJ/mol) in the solid–liquid interface. The MGD showed reusability and unique magnetic characteristics. It was concluded that the MGD could be a potential alternative for the adsorptive and magnetic removal of SY from an aqueous solution.

Flexible supercapacitors (FS) are ideal as power backups for upcoming stretchable electronics due to their high power density and good mechanical compliance. However, lacking technology for FS mass manufacturing is still a significant obstacle. The present study describes a novel method for preparing FS based on reduced graphene oxide (RGO) using the N+ plasma technique, in which N+ reduces graphene oxide on the surface of a cotton/polyester substrate. The effect of aloe vera (AV) as a natural reducing & capping agent and carbon nanotubes (CNT) as nanoconductors on the electrochemical performance of the electrodes is studied. FESEM and XPS were employed to investigate the electrodes' structural and chemical composition of electrodes. The galvanostatic charge–discharge curves of electrodes revealed the enhancement of the electrochemical activity of the as-prepared electrode upon additions of AV and CNT. The areal capacitance of the RGO, RGO/AV, and RGO/ AV/CNT supercapacitors at 5 mV/s was 511, 1244.5, and 1879 mF/cm2, respectively. The RGO electrode showed capacitive retention of 80.9% after 2000 cycles enhanced to 89.7% and 92% for RGO/AV and RGO/AV/CNT electrodes, respectively. The equivalent series resistance of the RGO electrode was 126.28 Ω, decreased to 56.62 and 40.06 Ω for RGO/AV and RGO/ AV/CNT electrodes, respectively.

Decabromodiphenyl ether (BDE209) is a persistent aromatic compound widely associated with environmental pollutants. Given its persistence and possible bioaccumulation, exploring a feasible technique to eradicate BDE209 efficiently is critical for today’s environmentally sustainable societies. Herein, an advanced nanocomposite is elaborately constructed, in which a large number of titanium dioxide ( TiO2) nanoparticles are anchored uniformly on two-dimensional graphene oxide (GO) nanosheets ( TiO2/GO) via a modified Hummer’s method and subsequent solvothermal treatment to achieve efficient photocatalytic degradation BDE209. The obtained TiO2/ GO photocatalyst has excellent photocatalytic due to the intense coupling between conductive GO nanosheets and TiO2 nanoparticles. Under the optimal photocatalytic degradation test conditions, the degradation efficiency of BDE209 is more than 90%. In addition, this study also provides an efficient route for designing highly active catalytic materials.

The thermoelectric effect, which converts waste heat into electricity, holds promise as a renewable energy technology. Recently, bismuth telluride (Bi2Te3)-based alloys are being recognized as important materials for practical applications in the temperature range from room temperature to 500 K. However, conventional sintering processes impose limitations on shape-changeable and tailorable Bi2Te3 materials. To overcome these issues, three-dimensional (3D) printing (additive manufacturing) is being adopted. Although some research results have been reported, relatively few studies on 3D printed thermoelectric materials are being carried out. In this study, we utilize extrusion 3D printing to manufacture n-type Bi1.7Sb0.3Te3 (N-BST). The ink is produced without using organic binders, which could negatively influence its thermoelectric properties. Furthermore, we introduce graphene oxide (GO) at the crystal interface to enhance the electrical properties. The formed N-BST composites exhibit significantly improved electrical conductivity and a higher Seebeck coefficient as the GO content increases. Therefore, we propose that the combination of the extrusion 3D printing process (Direct Ink Writing, DIW) and the incorporation of GO into N-BST offers a convenient and effective approach for achieving higher thermoelectric efficiency.

본 연구에서는 PVA(Poly Vinyl Alcohol)섬유와 GO(Graphene Oxide)를 혼입한 섬유보강 콘크리트(FRC)의 역학적 특성 을 평가하고자 하였다. GO와 PVA 섬유를 동시에 혼입한 FRC 각각의 재료를 단일로 사용하였을 때보다 기대효과가 다소 미흡 하였지만, 각 재료의 하이브리드화로 인장강도가 개선되면서 PVA 섬유 혼입률 0.1∼0.3%과 GO 혼입률 0.025%에서 우수한 효 과를 얻을 수 있었다. 특히 PVA 섬유는 0.3%로 혼합하였을 때 부작용을 최소화하면서 최대의 효과를 보였지만, 적절한 GO 배 합비를 조절할 필요가 있으며 FRC내 GO와 PVA 섬유의 최적배합을 구하기 위한 추가적인 연구가 필요할 것으로 사료된다.

환경 오염과 천연 자원의 고갈에 대한 증가하는 우려는 환경적으로 지속 가능한 기술의 개발을 촉진했습니다. 퍼 바포레이션은 낮은 에너지 소비, 환경 영향 및 성능 효율로 인해 최근 수십 년 동안 주목을 받아 왔습니다. 이 방법은 막이 원하는 선택도를 충족하도록 미세 조정될 수 있기 때문에 화학 종을 분리하고 유기 용매를 탈수하는 데 사용되었습니다. 역 삼투 및 증류와 같은 여러 분리 공정은 실험 환경 및 산업 응용 분야에서 모두 활용되고 있습니다. 그러나 퍼바포레이션은 작동 압력 및 온도가 낮고 거부율이 높은 등 여러 이점이 있습니다. 그럼에도 불구하고, 현재 막 기술의 상태만으로는 실용적 인 응용에 대한 요구를 충분하게 할 수 없습니다. 반면, 복합막은 유기 물질과 무기 물질의 장점을 모두 활용할 수 있습니다. 많은 연구들이 현재 한계를 해결하기 위해 그래핀 산화물(GO) 및 MXene (MX)과 같은 무기 나노 물질을 고분자 막에 효과 적으로 통합했습니다. 이 검토는 투과증발에서의 2D 복합막의 최근 발전을 조사하고 성능 향상을 평가합니다.

The present studies explored the possibility of immobilizing phosphocholine (PC) liposomes on the surface of graphene oxide (GO) which was pre-adsorbed with two kinds of enzymes, horseradish peroxidase and glucose oxidase. The transmission electron microscope images showed that the PC liposomes adsorbed onto the GO surface kept integrity. By using 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS)-encapsulated liposomes, a one-step colorimetric assay for glucose was developed. In the presence of glucose, the GO nanocomposites catalyzed the cascade enzymatic reaction producing colorimetric signals directly. Under the optimal conditions, the GO nanocomposites produced linearly increased colorimetric signal with increased concentrations of glucose ranging from 50 to 500 μM. The detection limit was 33 μM. The GO nanocomposites also exhibited good selectivity for the detection of glucose and were able to detect glucose in human serum.

PURPOSES : The purpose of this study is to experimentally analyze the flexural strength characteristics of cement mortar mixtures simultaneously incorporated with graphene oxide (GO) and polyvinyl alcohol (PVA) fibers, and to understand the composite effect of those on enhancing resistance against the initiation and progression of micro-cracks, as well as the control of macro-cracks in flexural behavior. METHODS : Cement mortar(w/c=0.5) specimens for flexural strength test, mixing 6 mm and 12 mm PVA fibers at 1% and 2% volume ratios, were fabricated. Additionally, specimens incorporating GO at a cement weight ratio of 0.05% were prepared for each mixture to analyze the effect of GO. Therefore total eight types of mixture were prepared. The fabricated specimens were subjected to flexural strength tests after curing in waterbath for 7 and 28 days. Concurrently, digital images for analyzing deformation in accordance with loading history were obtained at a rate of 20 Hz using the DIC technique. Through displacement and strain calculation via DIC, the flexural behavior characteristics of the mixtures combined with GO and PVA fibers were precisely analyzed. Furthermore, the composite effect on flexural behavior characteristics when GO and PVA fibers are incorporated was discussed. RESULTS : For the PVA fiber-reinforced cement mortar mixture, the incorporation of 0.05% GO increased the crack initiation load by up to 23%, and the maximum resistive load after cracking by up to 24%. Moreover, introducing GO into the PVA fiber-reinforced mixture increased the flexural strain just before cracking by approximately 30 to 50%, while the maximum resistive load after cracking exhibited similar strain levels with or without GO incorporation. Therefore, under flexural behavior, the integration of GO might delay crack initiation by increasing the strain concurrent with the rise in flexural stress before crack occurrence. It also seems to contribute to reducing crack expansion by synergistically interacting with PVA fibers after crack occurrence. CONCLUSIONS : It was experimentally examined that the flexural strength of PVA fiber reinforced cement mortar is improved by incorporating GO. Moreover, GO enhances resistance of crack occurrance and reduces crack propagation in combination with PVA fibers. This study suggests that simultaneous incorporation of GO and PVA fibers can synergistically improve the performance of cement composites.

Graphene oxide/Iron III oxide (GO: Fe2O3) nanocomposites (NCs) have been topical in recent times owing to the enhanced properties they exhibit. GO acting as a graphene derivative has demonstrated superior features as obtainable in a graphene sheet. Furthermore, the attachment of oxygen functional groups at its basal and edge planes of graphene has allowed for easy metal/oxide functionalization for improved properties harvesting. Fe2O3 nanoparticles (NPs) on the other hand have polymorphic property enabling the degeneracy of Fe2O3 in different phases, thereby resulting in different physical and crystalline properties when used to functionalize GO. The properties of GO: Fe2O3 have been applied to supercapacitor energy harvesting, Li-ion batteries, and biomedicine. The enhanced properties are attributed to the adsorption and electronic structure properties of Fe atoms. In this review, the various synthesis used in the preparation of reduced/graphene oxide: Fe2O3 is discussed. As indicated in the considered literature, the XPS analysis suggests electronic bond interactions between C–C, C–O, C–Fe and Fe–C. The available report on UPS measurements further suggests the formation of mixed states emanating from  and  bonds. The discussed reports further suggest that the various applications based on the harvesting of electronic, electrical, and magnetic properties are due to the ionic and exchange interactions between the different orbital states of carbon, oxygen and iron. The challenges and future prospects of the synthesis and application of GO/Fe2O3 are examined. Graphical abstract showing the process of exfoliation, reduction and functionalization of graphite to produce reduced graphene oxide (rGO).

In this study, graphene oxide (GO) was synthesized by the improved Hummers’ method. The degree of oxidation from graphite (Gi) to GO was determined through interlayer spacing calculated from X–ray diffraction. Besides, the effect of KMnO4: Gi ratios (X1), H2SO4 volume (X2), oxidation temperature (X3), oxidation time of stage 1 (X4), and oxidation time of stage 2 (X5) was screened by the Plackett–Burman model. The simultaneous impact of three factors that influenced the degree of oxidation (X1, X2, and X3) was studied by the Box–Behnken experimental model of response surface methodology to achieve suitable conditions for the GO synthesis process. The characterization of GO product was investigated via the modern analytical methods: X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy, UV–Vis spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, and atomic force microscopy. Inaddition, the study was also carried out on a pilot scale for orientation in industrial application with the yield of 14 g/batch.

In this paper, we presented a hybrid composite of graphene quantum dots (GQDs)-modified three-dimensional graphene nanoribbons (3D GNRs) composite linked by Fe3O4 and CoO nanoparticles through reflux and ultrasonic treatment with GQDs, denoted as 3D GQDs-Fe3O4/CoO@GNRs (3D GFCG). In this hybrid, the 3D GNRs framework strengthened the electrical conductivity and the synergistic effects between GQDs and 3D GFCG enhanced the oxygen reduction reaction (ORR) activity of the nanocomposite. The results imply that decorating GQDs with other electro-catalysts is an effective strategy to synergistically improve their ORR activity.