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Showing papers in "ACS Nano in 2010"


Journal ArticleDOI
22 Jul 2010-ACS Nano
TL;DR: An improved method for the preparation of graphene oxide (GO) is described, finding that excluding the NaNO(3), increasing the amount of KMnO(4), and performing the reaction in a 9:1 mixture of H(2)SO(4)/H(3)PO(4) improves the efficiency of the oxidation process.
Abstract: An improved method for the preparation of graphene oxide (GO) is described. Currently, Hummers’ method (KMnO4, NaNO3, H2SO4) is the most common method used for preparing graphene oxide. We have found that excluding the NaNO3, increasing the amount of KMnO4, and performing the reaction in a 9:1 mixture of H2SO4/H3PO4 improves the efficiency of the oxidation process. This improved method provides a greater amount of hydrophilic oxidized graphene material as compared to Hummers’ method or Hummers’ method with additional KMnO4. Moreover, even though the GO produced by our method is more oxidized than that prepared by Hummers’ method, when both are reduced in the same chamber with hydrazine, chemically converted graphene (CCG) produced from this new method is equivalent in its electrical conductivity. In contrast to Hummers’ method, the new method does not generate toxic gas and the temperature is easily controlled. This improved synthesis of GO may be important for large-scale production of GO as well as the ...

9,812 citations


Journal ArticleDOI
14 Apr 2010-ACS Nano
TL;DR: This work exemplifies the evolution of structural parameters in layered materials in changing from the three-dimensional to the two-dimensional regime by characterized by Raman spectroscopy.
Abstract: Molybdenum disulfide (MoS2) of single- and few-layer thickness was exfoliated on SiO2/Si substrate and characterized by Raman spectroscopy. The number of S−Mo−S layers of the samples was independently determined by contact-mode atomic force microscopy. Two Raman modes, E12g and A1g, exhibited sensitive thickness dependence, with the frequency of the former decreasing and that of the latter increasing with thickness. The results provide a convenient and reliable means for determining layer thickness with atomic-level precision. The opposite direction of the frequency shifts, which cannot be explained solely by van der Waals interlayer coupling, is attributed to Coulombic interactions and possible stacking-induced changes of the intralayer bonding. This work exemplifies the evolution of structural parameters in layered materials in changing from the three-dimensional to the two-dimensional regime.

3,969 citations


Journal ArticleDOI
15 Feb 2010-ACS Nano
TL;DR: The resultant N-graphene was demonstrated to act as a metal-free electrode with a much better electrocatalytic activity, long-term operation stability, and tolerance to crossover effect than platinum for oxygen reduction via a four-electron pathway in alkaline fuel cells.
Abstract: Nitrogen-doped graphene (N-graphene) was synthesized by chemical vapor deposition of methane in the presence of ammonia. The resultant N-graphene was demonstrated to act as a metal-free electrode with a much better electrocatalytic activity, long-term operation stability, and tolerance to crossover effect than platinum for oxygen reduction via a four-electron pathway in alkaline fuel cells. To the best of our knowledge, this is the first report on the use of graphene and its derivatives as metal-free catalysts for oxygen reduction. The important role of N-doping to oxygen reduction reaction (ORR) can be applied to various carbon materials for the development of other metal-free efficient ORR catalysts for fuel cell applications, even new catalytic materials for applications beyond fuel cells.

3,604 citations


Journal ArticleDOI
Hao Zhang1, Xiao-Jun Lv1, Yueming Li1, Ying Wang1, Jinghong Li1 
26 Jan 2010-ACS Nano
TL;DR: A chemically bonded TiO(2) (P25)-graphene nanocomposite photocatalyst with graphene oxide and P25, using a facile one-step hydrothermal method could provide new insights into the fabrication of a TiO (2)-carbon composite as high performance photocatalysts and facilitate their application in the environmental protection issues.
Abstract: Herein we obtained a chemically bonded TiO2 (P25)-graphene nanocomposite photocatalyst with graphene oxide and P25, using a facile one-step hydrothermal method. During the hydrothermal reaction, both of the reduction of graphene oxide and loading of P25 were achieved. The as-prepared P25-graphene photocatalyst possessed great adsorptivity of dyes, extended light absorption range, and efficient charge separation properties simultaneously, which was rarely reported in other TiO2−carbon photocatalysts. Hence, in the photodegradation of methylene blue, a significant enhancement in the reaction rate was observed with P25-graphene, compared to the bare P25 and P25-CNTs with the same carbon content. Overall, this work could provide new insights into the fabrication of a TiO2−carbon composite as high performance photocatalysts and facilitate their application in the environmental protection issues.

2,944 citations


Journal ArticleDOI
30 Jun 2010-ACS Nano
TL;DR: This paper prepares a self-assembled graphene hydrogel (SGH) via a convenient one-step hydrothermal method and shows that the high-performance SGH with inherent biocompatibility of carbon materials is attractive in the fields of biotechnology and electrochemistry.
Abstract: Self-assembly of two-dimensional graphene sheets is an important strategy for producing macroscopic graphene architectures for practical applications, such as thin films and layered paperlike materials. However, construction of graphene self-assembled macrostructures with three-dimensional networks has never been realized. In this paper, we prepared a self-assembled graphene hydrogel (SGH) via a convenient one-step hydrothermal method. The SGH is electrically conductive, mechanically strong, and thermally stable and exhibits a high specific capacitance. The high-performance SGH with inherent biocompatibility of carbon materials is attractive in the fields of biotechnology and electrochemistry, such as drug-delivery, tissue scaffolds, bionic nanocomposites, and supercapacitors.

2,931 citations


Journal ArticleDOI
10 May 2010-ACS Nano
TL;DR: Wu, Zhong-Shuai; Ren, Wencai; Wen, Lei; Gao, Libo; Zhao, Jinping; Chen, Zongping; Zhou, Guangmin; Li, Feng; Cheng, Hui-Ming.
Abstract: [Wu, Zhong-Shuai; Ren, Wencai; Wen, Lei; Gao, Libo; Zhao, Jinping; Chen, Zongping; Zhou, Guangmin; Li, Feng; Cheng, Hui-Ming] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China;Ren, WC (reprint author), Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, 72 Wenhua Rd, Shenyang 110016, Peoples R China;wcren@imraccn cheng@imraccn

2,272 citations


Journal ArticleDOI
06 Oct 2010-ACS Nano
TL;DR: It was found that the cell membrane damage of the bacteria caused by direct contact of theacteria with the extremely sharp edges of the nanowalls was the effective mechanism in the bacterial inactivation.
Abstract: Bacterial toxicity of graphene nanosheets in the form of graphene nanowalls deposited on stainless steel substrates was investigated for both Gram-positive and Gram-negative models of bacteria. The graphene oxide nanowalls were obtained by electrophoretic deposition of Mg2+-graphene oxide nanosheets synthesized by a chemical exfoliation method. On the basis of measuring the efflux of cytoplasmic materials of the bacteria, it was found that the cell membrane damage of the bacteria caused by direct contact of the bacteria with the extremely sharp edges of the nanowalls was the effective mechanism in the bacterial inactivation. In this regard, the Gram-negative Escherichia coli bacteria with an outer membrane were more resistant to the cell membrane damage caused by the nanowalls than the Gram-positive Staphylococcus aureus lacking the outer membrane. Moreover, the graphene oxide nanowalls reduced by hydrazine were more toxic to the bacteria than the unreduced graphene oxide nanowalls. The better antibacteri...

2,148 citations


Journal ArticleDOI
Qiong Wu1, Yuxi Xu1, Zhiyi Yao1, Anran Liu1, Gaoquan Shi1 
31 Mar 2010-ACS Nano
TL;DR: Supercapacitor devices based on this conductive flexible composite film showed large electrochemical capacitance at a discharge rate of 0.3 A g(-1) and exhibited greatly improved electrochemical stability and rate performances.
Abstract: Composite films of chemically converted graphene (CCG) and polyaniline nanofibers (PANI-NFs) were prepared by vacuum filtration the mixed dispersions of both components. The composite film has a layered structure, and PANI-NFs are sandwiched between CCG layers. Furthermore, it is mechanically stable and has a high flexibility; thus, it can be bent into large angles or be shaped into various desired structures. The conductivity of the composite film containing 44% CCG (5.5 × 102 S m−1) is about 10 times that of a PANI-NF film. Supercapacitor devices based on this conductive flexible composite film showed large electrochemical capacitance (210 F g−1) at a discharge rate of 0.3 A g−1. They also exhibited greatly improved electrochemical stability and rate performances.

2,089 citations


Journal ArticleDOI
12 May 2010-ACS Nano
TL;DR: This review gives an introduction to the rich BN nanotube/nanosheet field, including the latest achievements in the synthesis, structural analyses, and property evaluations, and presents the purpose and significance of this direction in the light of the general nanotubes/ nanosheet developments.
Abstract: Hexagonal boron nitride (h-BN) is a layered material with a graphite-like structure in which planar networks of BN hexagons are regularly stacked. As the structural analogue of a carbon nanotube (CNT), a BN nanotube (BNNT) was first predicted in 1994; since then, it has become one of the most intriguing non-carbon nanotubes. Compared with metallic or semiconducting CNTs, a BNNT is an electrical insulator with a band gap of ca. 5 eV, basically independent of tube geometry. In addition, BNNTs possess a high chemical stability, excellent mechanical properties, and high thermal conductivity. The same advantages are likely applicable to a graphene analogue-a monatomic layer of a hexagonal BN. Such unique properties make BN nanotubes and nanosheets a promising nanomaterial in a variety of potential fields such as optoelectronic nanodevices, functional composites, hydrogen accumulators, electrically insulating substrates perfectly matching the CNT, and graphene lattices. This review gives an introduction to the rich BN nanotube/nanosheet field, including the latest achievements in the synthesis, structural analyses, and property evaluations, and presents the purpose and significance of this direction in the light of the general nanotube/nanosheet developments.

1,990 citations


Journal ArticleDOI
12 Apr 2010-ACS Nano
TL;DR: This method provides a facile and straightforward approach to deposit MnO(2) nanoparticles onto the graphene oxide sheets (single layer of graphite oxide) and may be readily extended to the preparation of other classes of hybrids based on GO sheets for technological applications.
Abstract: A composite of graphene oxide supported by needle-like MnO2 nanocrystals (GO−MnO2 nanocomposites) has been fabricated through a simple soft chemical route in a water−isopropyl alcohol system. The formation mechanism of these intriguing nanocomposites investigated by transmission electron microscopy and Raman and ultraviolet−visible absorption spectroscopy is proposed as intercalation and adsorption of manganese ions onto the GO sheets, followed by the nucleation and growth of the crystal species in a double solvent system via dissolution−crystallization and oriented attachment mechanisms, which in turn results in the exfoliation of GO sheets. Interestingly, it was found that the electrochemical performance of as-prepared nanocomposites could be enhanced by the chemical interaction between GO and MnO2. This method provides a facile and straightforward approach to deposit MnO2 nanoparticles onto the graphene oxide sheets (single layer of graphite oxide) and may be readily extended to the preparation of othe...

1,953 citations


Journal ArticleDOI
Liangbing Hu1, Han Sun Kim, Jung-Yong Lee1, Peter Peumans1, Yi Cui 
28 Apr 2010-ACS Nano
TL;DR: In this paper, a comprehensive study of transparent and conductive silver nanowire (Ag NW) electrodes, including a scalable fabrication process, morphologies, and optical, mechanical adhesion, and flexibility properties, and various routes to improve the performance.
Abstract: We report a comprehensive study of transparent and conductive silver nanowire (Ag NW) electrodes, including a scalable fabrication process, morphologies, and optical, mechanical adhesion, and flexibility properties, and various routes to improve the performance. We utilized a synthesis specifically designed for long and thin wires for improved performance in terms of sheet resistance and optical transmittance. Twenty Ω/sq and ∼80% specular transmittance, and 8 ohms/sq and 80% diffusive transmittance in the visible range are achieved, which fall in the same range as the best indium tin oxide (ITO) samples on plastic substrates for flexible electronics and solar cells. The Ag NW electrodes show optical transparencies superior to ITO for near-infrared wavelengths (2-fold higher transmission). Owing to light scattering effects, the Ag NW network has the largest difference between diffusive transmittance and specular transmittance when compared with ITO and carbon nanotube electrodes, a property which could gr...

Journal ArticleDOI
22 Jun 2010-ACS Nano
TL;DR: The present review critically investigates to what extent self-assembly can be directed, enhanced, or controlled by either changing the energy or entropy landscapes, using templates or applying external fields.
Abstract: Within the field of nanotechnology, nanoparticles are one of the most prominent and promising candidates for technological applications. Self-assembly of nanoparticles has been identified as an important process where the building blocks spontaneously organize into ordered structures by thermodynamic and other constraints. However, in order to successfully exploit nanoparticle self-assembly in technological applications and to ensure efficient scale-up, a high level of direction and control is required. The present review critically investigates to what extent self-assembly can be directed, enhanced, or controlled by either changing the energy or entropy landscapes, using templates or applying external fields.

Journal ArticleDOI
07 Apr 2010-ACS Nano
TL;DR: A facile strategy to prepare N-doped graphene by using nitrogen plasma treatment of graphene synthesized via a chemical method is reported, which has displayed high electrocatalytic activity for reduction of hydrogen peroxide and fast direct electron transfer kinetics for glucose oxidase.
Abstract: Chemical doping with foreign atoms is an effective method to intrinsically modify the properties of host materials. Among them, nitrogen doping plays a critical role in regulating the electronic properties of carbon materials. Recently, graphene, as a true two-dimensional carbon material, has shown fascinating applications in bioelectronics and biosensors. In this paper, we report a facile strategy to prepare N-doped graphene by using nitrogen plasma treatment of graphene synthesized via a chemical method. Meanwhile, a possible schematic diagram has been proposed to detail the structure of N-doped graphene. By controlling the exposure time, the N percentage in host graphene can be regulated, ranging from 0.11 to 1.35%. Moreover, the as-prepared N-doped graphene has displayed high electrocatalytic activity for reduction of hydrogen peroxide and fast direct electron transfer kinetics for glucose oxidase. The N-doped graphene has further been used for glucose biosensing with concentrations as low as 0.01 mM ...

Journal ArticleDOI
25 Jan 2010-ACS Nano
TL;DR: The optoelectronic properties of graphene are exploited to realize an ultrafast laser and pave the way to graphene-based photonics.
Abstract: Graphene is at the center of a significant research effort Near-ballistic transport at room temperature and high mobility make it a potential material for nanoelectronics Its electronic and mechanical properties are also ideal for micro- and nanomechanical systems, thin-film transistors, and transparent and conductive composites and electrodes Here we exploit the optoelectronic properties of graphene to realize an ultrafast laser A graphene-polymer composite is fabricated using wet-chemistry techniques Pauli blocking following intense illumination results in saturable absorption, independent of wavelength This is used to passively mode-lock an erbium-doped fiber laser working at 1559 nm, with a 524 nm spectral bandwidth and approximately 460 fs pulse duration, paving the way to graphene-based photonics

Journal ArticleDOI
16 Jun 2010-ACS Nano
TL;DR: The magnetite-graphene hybrids show a high binding capacity for As(III) and As(V), whose presence in the drinking water in wide areas of South Asia has been a huge problem.
Abstract: Magnetite−graphene hybrids have been synthesized via a chemical reaction with a magnetite particle size of ∼10 nm. The composites are superparamagnetic at room temperature and can be separated by an external magnetic field. As compared to bare magnetite particles, the hybrids show a high binding capacity for As(III) and As(V), whose presence in the drinking water in wide areas of South Asia has been a huge problem. Their high binding capacity is due to the increased adsorption sites in the M−RGO composite which occurs by reducing the aggregation of bare magnetite. Since the composites show near complete (over 99.9%) arsenic removal within 1 ppb, they are practically usable for arsenic separation from water.

Journal ArticleDOI
01 Jul 2010-ACS Nano
TL;DR: Graphene-based nanomaterials can effectively inhibit the growth of E. coli bacteria while showing minimal cytotoxicity and it is demonstrated that macroscopic freestanding GO and rGO paper can be conveniently fabricated from their suspension via simple vacuum filtration.
Abstract: Graphene is a monolayer of tightly packed carbon atoms that possesses many interesting properties and has numerous exciting applications. In this work, we report the antibacterial activity of two water-dispersible graphene derivatives, graphene oxide (GO) and reduced graphene oxide (rGO) nanosheets. Such graphene-based nanomaterials can effectively inhibit the growth of E. coli bacteria while showing minimal cytotoxicity. We have also demonstrated that macroscopic freestanding GO and rGO paper can be conveniently fabricated from their suspension via simple vacuum filtration. Given the superior antibacterial effect of GO and the fact that GO can be mass-produced and easily processed to make freestanding and flexible paper with low cost, we expect this new carbon nanomaterial may find important environmental and clinical applications.

Journal ArticleDOI
30 Nov 2010-ACS Nano
TL;DR: It is proposed that TiO (2)-GR cannot provide truly new insights into the fabrication of TiO(2)-carbon composite as high-performance photocatalysts, hence offering a valuable source of reference on fabricating TiO(*(2))-carbon composites for their application as a photocatalyst in the environment cleanup.
Abstract: The nanocomposites of TiO2−graphene (TiO2−GR) have been prepared via a facile hydrothermal reaction of graphene oxide and TiO2 in an ethanol−water solvent. We show that such a TiO2−GR nanocomposite exhibits much higher photocatalytic activity and stability than bare TiO2 toward the gas-phase degradation of benzene, a volatile aromatic pollutant in air. By investigating the effect of different addition ratios of graphene on the photocatalytic activity of TiO2−GR systematically, we find that the higher weight ratio in TiO2−GR will decrease the photocatalytic activity. Analogous phenomenon is also observed for the liquid-phase degradation of dyes over TiO2−GR. In addition, the key features for TiO2−GR including enhancement of adsorptivity of pollutants, light absorption intensity, electron−hole pairs lifetime, and extended light absorption range have also been found in the composite of TiO2 and carbon nanotubes (TiO2−CNT). These strongly manifest that TiO2−GR is in essence the same as other TiO2−carbon (carb...

Journal ArticleDOI
08 Oct 2010-ACS Nano
TL;DR: A controlled growth of nitrogen-doped graphene layers by liquid precursor based chemical vapor deposition (CVD) technique is demonstrated, making this a feasible and efficient process for integration into current battery manufacture technology.
Abstract: We demonstrate a controlled growth of nitrogen-doped graphene layers by liquid precursor based chemical vapor deposition (CVD) technique. Nitrogen-doped graphene was grown directly on Cu current collectors and studied for its reversible Li-ion intercalation properties. Reversible discharge capacity of N-doped graphene is almost double compared to pristine graphene due to the large number of surface defects induced due to N-doping. All the graphene films were characterized by Raman spectroscopy, transmission electron microscopy, and X-ray photoemission spectroscopy. Direct growth of active electrode material on current collector substrates makes this a feasible and efficient process for integration into current battery manufacture technology.

Journal ArticleDOI
21 Sep 2010-ACS Nano
TL;DR: A high-voltage asymmetric electrochemical capacitor based on graphene as negative electrode and a MnO(2) nanowire/graphene composite (MGC) as positive electrode in a neutral aqueous Na( 2)SO(4) solution as electrolyte opens up the possibility of graphene-based composites for applications in safe aqueously electrolyte-based high- voltage asymmetric ECs with high energy and power densities.
Abstract: In order to achieve high energy and power densities, we developed a high-voltage asymmetric electrochemical capacitor (EC) based on graphene as negative electrode and a MnO2 nanowire/graphene composite (MGC) as positive electrode in a neutral aqueous Na2SO4 solution as electrolyte. MGC was prepared by solution-phase assembly of graphene sheets and α-MnO2 nanowires. Such aqueous electrolyte-based asymmetric ECs can be cycled reversibly in the high-voltage region of 0−2.0 V and exhibit a superior energy density of 30.4 Wh kg−1, which is much higher than those of symmetric ECs based on graphene//graphene (2.8 Wh kg−1) and MGC//MGC (5.2 Wh kg−1). Moreover, they present a high power density (5000 W kg−1 at 7.0 Wh kg−1) and acceptable cycling performance of ∼79% retention after 1000 cycles. These findings open up the possibility of graphene-based composites for applications in safe aqueous electrolyte-based high-voltage asymmetric ECs with high energy and power densities.

Journal ArticleDOI
08 Feb 2010-ACS Nano
TL;DR: A solar energy based technology to recycle carbon dioxide into readily transportable hydrocarbon fuel (i.e., a solar fuel) would help reduce atmospheric CO2 levels and partly fulfill energy demands within the present hydrocarbon based fuel infrastructure.
Abstract: The past several decades have seen a significant rise in atmospheric carbon dioxide levels resulting from the combustion of hydrocarbon fuels. A solar energy based technology to recycle carbon dioxide into readily transportable hydrocarbon fuel (i.e., a solar fuel) would help reduce atmospheric CO2 levels and partly fulfill energy demands within the present hydrocarbon based fuel infrastructure. We review the present status of carbon dioxide conversion techniques, with particular attention to a recently developed photocatalytic process to convert carbon dioxide and water vapor into hydrocarbon fuels using sunlight.

Journal ArticleDOI
01 Apr 2010-ACS Nano
TL;DR: It is found that GNS-based materials could be of great value for applications in various fields, such as good electrocatalytic activity toward catecholamines (dopamine, epinephrine, and norepinephrine).
Abstract: In this paper, we developed a green and facile approach to the synthesis of chemically converted graphene nanosheets (GNS) based on reducing sugars, such as glucose, fructose and sucrose using exfoliated graphite oxide (GO) as precursor. The obtained GNS is characterized with atomic force microscopy, UV−visible absorption spectroscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and so on. The merit of this method is that both the reducing agents themselves and the oxidized products are environmentally friendly. It should be noted that, besides the mild reduction capability to GO, the oxidized products of reducing sugars could also play an important role as a capping reagent in stabilizing as-prepared GNS simultaneously, which exhibited good stability in water. This approach can open up the new possibility for preparing GNS in large-scale production alternatively. Moreover, it is found that GNS-based materials could be of great value for applications in various fields, such as good...

Journal ArticleDOI
26 Aug 2010-ACS Nano
TL;DR: The hierarchical nanocomposite possessed higher electrochemical capacitance and better stability than each individual component as supercapacitor electrode materials, showing a synergistic effect of PANI and GO.
Abstract: We introduced a facile method to construct hierarchical nanocomposites by combining one-dimensional (1D) conducting polyaniline (PANI) nanowires with 2D graphene oxide (GO) nanosheets. PANI nanowire arrays are aligned vertically on GO substrate. The morphologies of PANI nanowires can be controlled by adjusting the ratios of aniline to GO, which are attributed to different nucleation processes. The hierarchical nanocomposite structures of PANI−GO were further proved by UV−vis, FTIR, and XRD measurements. The hierarchical nanocomposite possessed higher electrochemical capacitance and better stability than each individual component as supercapacitor electrode materials, showing a synergistic effect of PANI and GO. This study will further guide the preparation of functional nanocomposites by combining different dimensional nanomaterials.

Journal ArticleDOI
04 May 2010-ACS Nano
TL;DR: A novel nanothermometer, capable of accurately determining the temperature of solutions as well as biological systems such as HeLa cancer cells, is devised based on the temperature-sensitive fluorescence of NaYF(4):Er(3+),Yb(3+) nanoparticles.
Abstract: Acquiring the temperature of a single living cell is not a trivial task. In this paper, we devise a novel nanothermometer, capable of accurately determining the temperature of solutions as well as biological systems such as HeLa cancer cells. The nanothermometer is based on the temperature-sensitive fluorescence of NaYF4:Er3+,Yb3+ nanoparticles, where the intensity ratio of the green fluorescence bands of the Er3+ dopant ions (2H11/2 → 4I15/2 and 4S3/2 → 4I15/2) changes with temperature. The nanothermometers were first used to obtain thermal profiles created when heating a colloidal solution of NaYF4:Er3+,Yb3+ nanoparticles in water using a pump−probe experiment. Following incubation of the nanoparticles with HeLa cervical cancer cells and their subsequent uptake, the fluorescent nanothermometers measured the internal temperature of the living cell from 25 °C to its thermally induced death at 45 °C.

Journal ArticleDOI
15 Apr 2010-ACS Nano
TL;DR: CVD graphene solar cells demonstrated outstanding capability to operate under bending conditions up to 138 degrees, whereas the ITO-based devices displayed cracks and irreversible failure under bending of 60 degrees, indicating the great potential of CVD graphene films for flexible photovoltaic applications.
Abstract: We report the implementation of continuous, highly flexible, and transparent graphene films obtained by chemical vapor deposition (CVD) as transparent conductive electrodes (TCE) in organic photovoltaic cells. Graphene films were synthesized by CVD, transferred to transparent substrates, and evaluated in organic solar cell heterojunctions (TCE/poly-3,4-ethylenedioxythiophene:poly styrenesulfonate (PEDOT:PSS)/copper phthalocyanine/fullerene/bathocuproine/aluminum). Key to our success is the continuous nature of the CVD graphene films, which led to minimal surface roughness (∼0.9 nm) and offered sheet resistance down to 230 Ω/sq (at 72% transparency), much lower than stacked graphene flakes at similar transparency. In addition, solar cells with CVD graphene and indium tin oxide (ITO) electrodes were fabricated side-by-side on flexible polyethylene terephthalate (PET) substrates and were confirmed to offer comparable performance, with power conversion efficiencies (η) of 1.18 and 1.27%, respectively. Further...

Journal ArticleDOI
26 Jan 2010-ACS Nano
TL;DR: The electrochemical data indicate that the as-prepared graphene/bimetallic nanodendrite hybrids exhibited much higher electrocatalytic activity toward methanol oxidation reaction than the platinum black (PB) and commercial E-TEK Pt/C catalysts.
Abstract: Graphene nanosheet, the hottest material in physics and materials science, has been studied extensively because of its unique electronic, thermal, mechanical, and chemical properties arising from its strictly 2D structure and because of its potential technical applications. Particularly, these remarkable characteristics enable it to be a promising candidate as a new 2D support to load metal nanoparticles (NPs) for application in fuel cells. However, constructing high-quality graphene/bimetallic NP hybrids with high electrochemical surface area (ECSA) remains a great challenge to date. In this paper, we demonstrate for the first time a wet-chemical approach for the synthesis of high-quality three-dimensional (3D) Pt-on-Pd bimetallic nanodendrites supported on graphene nanosheets (TP-BNGN), which represents a new type of graphene/metal heterostructure. The resulting hybrids were characterized by atomic force microscopy (AFM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), energy-disper...

Journal ArticleDOI
16 Jun 2010-ACS Nano
TL;DR: An evolution from a loosely attached toward an irreversible attached protein corona over time was observed and mass spectrometry of the digested protein coronia revealed albumin as the most abundant component which suggests an improved biocompatibility.
Abstract: In this work, we explore the formation of the protein corona after exposure of metallic Au nanoparticles (NPs), with sizes ranging from 4 to 40 nm, to cell culture media containing 10% of fetal bovine serum. Under in vitro cell culture conditions, zeta potential measurements, UV-vis spectroscopy, dynamic light scattering and transmission electron microscope analysis were used to monitor the time evolution of the inorganic NP-protein corona formation and to characterize the stability of the NPs and their surface state at every stage of the experiment. As expected, the red-shift of the surface plasmon resonance peak, as well as the drop of surface charge and the increase of the hydrodynamic diameter indicated the conjugation of proteins to NPs. Remarkably, an evolution from a loosely attached toward an irreversible attached protein corona over time was observed. Mass spectrometry of the digested protein corona revealed albumin as the most abundant component which suggests an improved biocompatibility.

Journal ArticleDOI
12 Oct 2010-ACS Nano
TL;DR: It is demonstrated that a functionalized graphene sheet based ink can serve as a catalytic, flexible, electrically conductive counter electrode material and a new electrochemical impedance spectroscopy equivalent circuit is proposed that matches the observed spectra features to the appropriate phenomena.
Abstract: When applied on the counter electrode of a dye-sensitized solar cell, functionalized graphene sheets with oxygen-containing sites perform comparably to platinum (conversion efficiencies of 5.0 and 5.5%, respectively, at 100 mW cm−2 AM1.5G simulated light). To interpret the catalytic activity of functionalized graphene sheets toward the reduction of triiodide, we propose a new electrochemical impedance spectroscopy equivalent circuit that matches the observed spectra features to the appropriate phenomena. Using cyclic voltammetry, we also show that tuning our material by increasing the amount of oxygen-containing functional groups can improve its apparent catalytic activity. Furthermore, we demonstrate that a functionalized graphene sheet based ink can serve as a catalytic, flexible, electrically conductive counter electrode material.

Journal ArticleDOI
09 Nov 2010-ACS Nano
TL;DR: Factors contributing to droplet retraction, pinning and freezing are addressed by combining classical nucleation theory with heat transfer and wetting dynamics, forming the foundation for the development of rationally designed ice-preventive materials.
Abstract: Materials that control ice accumulation are important to aircraft efficiency, highway and powerline maintenance, and building construction. Most current deicing systems include either physical or chemical removal of ice, both energy and resource-intensive. A more desirable approach would be to prevent ice formation rather than to fight its build-up. Much attention has been given recently to freezing of static water droplets resting on supercooled surfaces. Ice accretion, however, begins with the droplet/substrate collision followed by freezing. Here we focus on the behavior of dynamic droplets impacting supercooled nano- and microstructured surfaces. Detailed experimental analysis of the temperature-dependent droplet/surface interaction shows that highly ordered superhydrophobic materials can be designed to remain entirely ice-free down to ca. -25 to -30 °C, due to their ability to repel impacting water before ice nucleation occurs. Ice accumulated below these temperatures can be easily removed. Factors contributing to droplet retraction, pinning and freezing are addressed by combining classical nucleation theory with heat transfer and wetting dynamics, forming the foundation for the development of rationally designed ice-preventive materials. In particular, we emphasize the potential of hydrophobic polymeric coatings bearing closed-cell surface microstructures for their improved mechanical and pressure stability, amenability to facile replication and large-scale fabrication, and opportunities for greater tuning of their material and chemical properties.

Journal ArticleDOI
18 May 2010-ACS Nano
TL;DR: It is shown that the shape of these materials is directly related to their induced cellular toxicity, and both G and SWCNT induce cytotoxic effects, and these effects are concentration- and shape-dependent.
Abstract: Graphitic nanomaterials such as graphene layers (G) and single-wall carbon nanotubes (SWCNT) are potential candidates in a large number of biomedical applications. However, little is known about the effects of these nanomaterials on biological systems. Here we show that the shape of these materials is directly related to their induced cellular toxicity. Both G and SWCNT induce cytotoxic effects, and these effects are concentration- and shape-dependent. Interestingly, at low concentrations, G induced stronger metabolic activity than SWCNT, a trend that reversed at higher concentrations. Lactate dehydrogenase levels were found to be significantly higher for SWCNT as compared to the G samples. Moreover, reactive oxygen species were generated in a concentration- and time-dependent manner after exposure to G, indicating an oxidative stress mechanism. Furthermore, time-dependent caspase 3 activation after exposure to G (10 μg/mL) shows evidence of apoptosis. Altogether these studies suggest different biological...

Journal ArticleDOI
22 Oct 2010-ACS Nano
TL;DR: In this paper, the authors apply elements of the drug delivery paradigm to nanosilver dissolution and present a systematic study of chemical concepts for controlled release, where the particle contains a concentrated inventory of an active species, the ion, which is transported to and released near biological target sites.
Abstract: Major pathways in the antibacterial activity and eukaryotic toxicity of nanosilver involve the silver cation and its soluble complexes, which are well established thiol toxicants. Through these pathways, nanosilver behaves in analogy to a drug delivery system, in which the particle contains a concentrated inventory of an active species, the ion, which is transported to and released near biological target sites. Although the importance of silver ion in the biological response to nanosilver is widely recognized, the drug delivery paradigm has not been well developed for this system, and there is significant potential to improve nanosilver technologies through controlled release formulations. This article applies elements of the drug delivery paradigm to nanosilver dissolution and presents a systematic study of chemical concepts for controlled release. After presenting thermodynamic calculations of silver species partitioning in biological media, the rates of oxidative silver dissolution are measured for nan...