High-response room-temperature NO2 gas sensor fabricated with thermally reduced graphene oxide-coated commercial cotton fabric.

Electronic textile-based gas sensors with a high response for NO2 gas were fabricated using reduced graphene oxide (rGO)-coated commercial cotton fabric (rGOC). Graphene oxide (GO) was coated on cotton fabric by simply dipping the cotton into a GO solution. To investigate the relationship between the degree of reduction and the sensing response, the GO-coated fabrics were thermally reduced at various temperatures (190, 200, 300, and 400 °C). The change in the amount of oxygen functional groups on the rGOCs was observed by x-ray photoelectron spectroscopy, Raman spectroscopy, and x-ray diffraction patterns. The maximum sensing response of 45.90 % at 10 ppm of NO2 gas at room temperature was exhibited by the rGOC treated at 190 °C, which was the lowest heat-treatment temperature. The high response comes from the greater amount of oxygen functional groups compared to other rGOC samples, and the tubular structure of the cotton.

Thermally modulated multilayered graphene oxide for hydrogen storage.

We have obtained high pressure H(2) isotherms with respect to the interlayer distance of multilayered graphene oxide (GO) modulated by thermal annealing. The maximum storage capacity is 4.8 (0.5) wt% at 77 K (298 K) and at 9.0 MPa pressure. We found the optimum GO interlayer distance for maximum H(2) uptake at 6.5 Å, similar to the predicted distances from first-principles calculations for graphite materials. Our results reveal that multilayered GO can be a practical material of choice to allow the use of graphene as a hydrogen storage material, provided that only small amounts of O and OH functional groups exist as spacers on GO sheets.

Palladium nanoparticle-decorated multi-layer Ti3C2T x dual-functioning as a highly sensitive hydrogen gas sensor and hydrogen storage.

In this work, palladium nanoparticle (PdNP)-decorated Ti3C2T x MXene (Pd-Ti3C2T x ) was synthesized by a simple two-step process. For this, multilayer Ti3C2T x MXene (ML-Ti3C2T x ) was first prepared by a selective HF etching technique, and PdNPs were directly grown on the surface of ML-Ti3C2T x flakes using a polyol method. The relative weight fraction of PdNPs to ML-Ti3C2T x was elaborately controlled to derive the optimal size and distribution of PdNPs, thereby to maximize its performance as a hydrogen sensor. The optimized Pd-Ti3C2T x nanocomposite showed superb hydrogen-sensing capability even at room temperature with sharp, large, reproducible, concentration-dependent, and hydrogen-selective responses. Furthermore, the nanocomposite also unveiled some extent of hydrogen storage capability at room temperature and 77 K, raising a possibility that it can dual-function as a hydrogen sensor and hydrogen storage.

Recyclable aqueous metal adsorbent: Synthesis and Cu(II) sorption characteristics of ternary nanocomposites of Fe3O4 nanoparticles@graphene-poly-N-phenylglycine nanofibers.

Metal pollutant adsorbents are an essential material platform for sustainable environmental remediation, but the adsorbents are typically disposable after sorption, which secondarily contaminates the environment. We report on recyclable Cu(II) adsorbent of deprotonated poly-N-phenylglycine nanofibers (d-PPG NFs)-grafted reduced graphene oxide (rGO) sheets intercalated with Fe3O4 nanoparticles (NPs), which are synthesized via wet chemical process. The adsorption performances of ternary Fe3O4 NPs@rGO-d-PPG NFs and binary Fe3O4 NPs@rGO composites are compared, and the ternary ones exhibit much higher Cu2+-adsorption capacity than binary ones under diverse pH conditions due to both high specific surface area and high cationic affinity of d-PPG NFs that follow the Freundlich adsorption model. Density-functional theory calculation results explain why/how the ternary composites show greater Cu2+ adsorption capability in higher pH environment. The ternary composites present stable, high Cu2+ adsorption capability, irrespective of Co2+ concentration in bimetallic Cu and Co aqueous solution. The Fe3O4 NPs in the ternary composites allow magnet-assisted collection after adsorption batches, whose collection yield is ∼95 % without adsorption capacity degradation in repeated adsorbent reuses over 10 times. This study provides a general, promising pathway to synthesize reusable sorptive materials for water purification/remediation.

Electrical quadruple hysteresis in Pd-doped vanadium pentoxide nanowires due to water adsorption.

Humidity-dependent current-voltage (I-V) characteristics of Pd-doped vanadium pentoxide nanowires (Pd-VONs) were investigated. Electrical quadruple hysteresis (QH) was observed and attributed to the large amount of water molecules adsorbed on the nanowires. Using QH in Pd-VONs, the reaction of water with PdO was interpreted as the water molecules are desorbed and then dissociated with increasing bias voltage. Owing to the dissociated H+ and OH- ions, PdO is reduced and oxidized. As a result, water molecules recombine as the bias voltage is decreased.

Influence of hydrogen incorporation on conductivity and work function of VO2 nanowires.

We report improved conductance by reducing the work function via incorporation of hydrogen into VO2 nanowires. The VO2 nanowires were prepared using the chemical vapor deposition method with V2O5 powder on silicon substrates at 850 °C. Hydrogenation was carried out using the high-pressure hydrogenation method. Raman spectroscopy confirmed that the incorporated hydrogen atoms resulted in a change in the lattice constant of the VO2 nanowires (NWs). To quantitatively measure the work function of the nanowires, Kelvin probe force microscopy (KPFM) was employed at ambient conditions. We found that the work function decreased with increasing H2 pressure, which also resulted in increased conductance. This is associated with hydrogen diffused into the VO2 that acts as a donor to elevate the Fermi level, which was also confirmed by KPFM. From these results, tuning of the reversible electrical properties of VO2 NWs, including the conductance and work function, can be achieved by incorporating hydrogen at relatively moderate temperatures.

Highly stretchable, mechanically stable, and weavable reduced graphene oxide yarn with high NO2 sensitivity for wearable gas sensors.

Stretchable gas sensors are important components of wearable electronic devices used for human safety and healthcare applications. However, the current low stretchability and poor stability of the materials limit their use. Here, we report a highly stretchable, stable, and sensitive NO2 gas sensor composed of reduced graphene oxide (RGO) sheets and highly elastic commercial yarns. To achieve high stretchability and good stability, the RGO sensors were fabricated using a pre-strain strategy (strain-release assembly). The fabricated stretchable RGO gas sensors showed high NO2 sensitivity (55% at 5.0 ppm) under 200% strain and outstanding mechanical stability (even up to 5000 cycles at 400% applied strain), making them ideal for wearable electronic applications. In addition, our elastic graphene gas sensors can also be woven into fabrics and clothes for the creation of smart textiles. Finally, we successfully fabricated wearable gas-sensing wrist-bands from superelastic graphene yarns and stretchable knits to demonstrate a wearable electronic device.

Pyridinic-N-Doped Graphene Paper from Perforated Graphene Oxide for Efficient Oxygen Reduction.

We report a simple approach to fabricate a pyridinic-N-doped graphene film (N-pGF) without high-temperature heat treatment from perforated graphene oxide (pGO). pGO is produced by a short etching treatment with hydrogen peroxide. GO perforation predominated in a short etching time (∼1 h), inducing larger holes and defects compared to pristine GO. The pGO is advantageous to the formation of a pyridinic N-doped graphene because of strong NH3 adsorption on vacancies with oxygen functional groups during the nitrogen-doping process, and the pyridinic-N-doped graphene exhibits good electrocatalytic activity for oxygen reduction reaction (ORR). Using rotating-disk electrode measurements, we confirm that N-pGF undergoes a four-electron-transfer process during the ORR in alkaline and acidic media by possessing sufficient diffusion pathways and readily available ORR active sites for efficient mass transport. A comparison between Pt/N-pGF and commercial Pt/C shows that Pt/N-pGF has superior performance, based on its more positive onset potential and higher limiting diffusion current at -0.5 V.

Visible-light-driven dynamic cancer therapy and imaging using graphitic carbon nitride nanoparticles.

Organic graphitic carbon nitride nanoparticles (NP-g-CN), less than 30 nm in size, were synthesized and evaluated for photodynamic therapy (PDT) and cell imaging applications. NP-g-CN particles were prepared through an intercalation process using a rod-like melamine-cyanuric acid adduct (MCA) as the molecular precursor and a eutectic mixture of LiCl-KCl (45:55 wt%) as the reaction medium for polycondensation. The nano-dimensional NP-g-CN penetrated the malignant tumor cells with minimal hindrance and effectively generated reactive oxygen species (ROS) under visible light irradiation, which could ablate cancer cells. When excited by visible light irradiation (λ > 420 nm), NP-g-CN introduced to HeLa and cos-7 cells generated a significant amount of ROS and killed the cancerous cells selectively. The cytotoxicity of NP-g-CN was manipulated by altering the light irradiation and the BP-g-CN caused more damage to the cancer cells than normal cells at low concentrations. As a potential non-toxic organic nanomaterial, the synthesized NP-g-CN are biocompatible with less cytotoxicity than toxic inorganic materials. The combined effects of the high efficacy of ROS generation under visible light irradiation, low toxicity, and bio-compatibility highlight the potential of NP-g-CN for PDT and imaging without further modification.

Highly conductive and environmentally stable gold/graphene yarns for flexible and wearable electronics.

Here, we fabricated high-performance gold/graphene yarns through a facile method by the electroless deposition of gold nanoparticles onto the surface of graphene yarns. The gold/graphene yarns are fabricated using a completely solution-based process that can be scaled up for practical applications. They possess high electrical conductivity (2.86 × 102 S cm-1) and good gravimetric specific conductivity (6.81 × 102 S cm2 g-1) as well as good reliability under 1000 bending tests with a maximum bending angle of 170° and 10 washing tests with laundry detergents. These stable conducting yarns could also be integrated into textiles and clothes in various forms to create smart fabrics and wearable devices. In addition, this facile approach is easily applicable to various graphene films and devices on soft substrates that are presently used in flexible/wearable electronics.