Two-dimensional carbon-based nanocomposites for photocatalytic energy generation and environmental remediation applications

• Suneel Kumar,
• Ashish Kumar,
• Ashish Bahuguna,
• Vipul Sharma and
• Venkata Krishnan

Beilstein J. Nanotechnol. 2017, 8, 1571–1600, doi:10.3762/bjnano.8.159

• form graphene oxide (GO) [49]. GO contains carboxyl, epoxides and hydroxyl groups covalently attached to the graphene sheet. This leads to the loss of electrical conductivity and limits the application of GO in many areas. However, the presence of polar functional groups in GO makes it hydrophilic in

• nanotubes (CNT) and g-C3N4 has been presented in Table 1. The role of graphene as a cocatalyst has been investigated by various research groups. Peng et al. [123] reported graphene oxide (GO)–CdS nanocomposites for photocatalytic hydrogen evolution by using Na2S and Na2SO3 as sacrificial agents, where GO

A biofunctionalizable ink platform composed of catechol-modified chitosan and reduced graphene oxide/platinum nanocomposite

• Peter Sobolewski,
• Agata Goszczyńska,
• Małgorzata Aleksandrzak,
• Karolina Urbaś,
• Joanna Derkowska,
• Agnieszka Bartoszewska,
• Jacek Podolski,
• Ewa Mijowska and
• Mirosława El Fray

Beilstein J. Nanotechnol. 2017, 8, 1508–1514, doi:10.3762/bjnano.8.151

• graphene oxide (rGO) functionalized with Pt nanoparticles (rGO–Pt) Graphene oxide (GO) was synthesized by oxidation of graphite flakes (Aesar, 325 mesh), using a modified Hummers method [19], as described previously [20]. Next, GO was reduced and functionalized with Pt nanoparticles (Figure 5). First, 75

Fully scalable one-pot method for the production of phosphonic graphene derivatives

• Kamila Żelechowska,
• Marta Prześniak-Welenc,
• Marcin Łapiński,
• Izabela Kondratowicz and
• Tadeusz Miruszewski

Beilstein J. Nanotechnol. 2017, 8, 1094–1103, doi:10.3762/bjnano.8.111

• energy of 0.014 eV. Keywords: functionalized graphene; graphene oxide; one-pot synthesis; phosphonic derivatives; reduced graphene oxide; Introduction Graphene oxide (GO) with its multifunctionality attracts interest in different fields of science. The chemical nature and reactivity of GO have been

CVD transfer-free graphene for sensing applications

• Chiara Schiattarella,
• Sten Vollebregt,
• Tiziana Polichetti,
• Brigida Alfano,
• Ettore Massera,
• Maria Lucia Miglietta,
• Girolamo Di Francia and
• Pasqualina Maria Sarro

Beilstein J. Nanotechnol. 2017, 8, 1015–1022, doi:10.3762/bjnano.8.102

• number of publications dedicated to graphene-based sensors [2]. The gas sensor devices presented in literature are mostly based on pristine graphene, graphene oxide (GO) and reduced graphene oxide (rGO). Many approaches for the fabrication of such materials, including CVD, mechanical, chemical and

Synthesis of graphene–transition metal oxide hybrid nanoparticles and their application in various fields

• Arpita Jana,
• Elke Scheer and
• Sebastian Polarz

Beilstein J. Nanotechnol. 2017, 8, 688–714, doi:10.3762/bjnano.8.74

• structures are particularly interesting because after hybridisation they not only display the individual properties of graphene and the NPs, but also they exhibit further synergistic properties. Reduced graphene oxide (rGO), a graphene-like material, can be easily prepared by reduction of graphene oxide (GO

In situ formation of reduced graphene oxide structures in ceria by combined sol–gel and solvothermal processing

• Jingxia Yang,
• Johannes Ofner,
• Bernhard Lendl and
• Ulrich Schubert

Beilstein J. Nanotechnol. 2016, 7, 1815–1821, doi:10.3762/bjnano.7.174

• batteries) [1][2][3][4][5][6][7] or (photo-)catalysts [8][9][10][11][12][13][14][15][16]. The property enhancements are mainly due to the charge transfer between graphene and CeO2. For the preparation of graphene–CeO2 composites external graphene oxide (GO) is usually added to the ceria precursor or pre

• ]) with the difference that varying proportions of GO were added to the precursor mixture. Graphene oxide (GO) was synthesized by the modified Hummer method [20][21]. All steps involving Ce(Ot-Bu)4 were carried out under moisture-free argon using standard Schlenk or glove box techniques. Ce(Ot-Bu)4 (5

• , varying proportions of pre-synthesized graphene oxide (GO) were introduced into the ceria gel to investigate its dispersion and its effect on structure and properties of the sol–gel ceria. Raman spectra showed that the D-bands of all rGO–CeO2 composites were shifted to lower values (Figure 1), indicating

Role of RGO support and irradiation source on the photocatalytic activity of CdS–ZnO semiconductor nanostructures

• Suneel Kumar,
• Rahul Sharma,
• Vipul Sharma,
• Gurunarayanan Harith,
• Vaidyanathan Sivakumar and
• Venkata Krishnan

Beilstein J. Nanotechnol. 2016, 7, 1684–1697, doi:10.3762/bjnano.7.161

• purchased from Sigma-Aldrich. All chemicals were used as received without further purification. Deionized water (18.2 MΩ·cm) used in synthesis was obtained from a double-stage water purifier (ELGA PURELAB Option-R7). Synthesis of graphene oxide Graphene oxide (GO) was synthesized from natural graphite

Reasons and remedies for the agglomeration of multilayered graphene and carbon nanotubes in polymers

• Rasheed Atif and
• Fawad Inam

Beilstein J. Nanotechnol. 2016, 7, 1174–1196, doi:10.3762/bjnano.7.109

• can be attributed to the higher capability of graphene to rebound advancing cracks [11][12]. The Raman and XPS spectra of graphite, graphene oxide (GO), and thermally reduced graphene oxide (RGO) are shown in Figure 1a,b. The graphene structure can be studied by using transmission electron microscopy

Development of highly faceted reduced graphene oxide-coated copper oxide and copper nanoparticles on a copper foil surface

• Rebeca Ortega-Amaya,
• Yasuhiro Matsumoto,
• Andrés M. Espinoza-Rivas,
• Manuel A. Pérez-Guzmán and
• Mauricio Ortega-López

Beilstein J. Nanotechnol. 2016, 7, 1010–1017, doi:10.3762/bjnano.7.93

• surface of a copper foil supporting graphene oxide (GO) at annealing temperatures of 200–1000 °C, under an Ar atmosphere. These hybrid nanostructures were developed from bare copper oxide nanoparticles which grew at an annealing temperature of 80 °C under nitrogen flux. The predominant phase as well as

• ; copper(II) oxide; core–shell; reduced graphene oxide; Introduction In the last years, graphene oxide (GO) and reduced graphene oxide (rGO) have emerged as suitable candidates to prepare graphene-based nanocomposites [1][2], including those based on GO/inorganic nanoparticles [3]. The opportunity to

• -supported graphene oxide (GO) under an Ar atmosphere. The predominant phase as well as the particle size and shape strongly depend on the process temperature, in the ranges of 200–600 °C and 800–1000 °C, Cu2O or Cu were obtained, respectively. It was demonstrated that rGO plays a dual role of stabilizing

Synthesis and applications of carbon nanomaterials for energy generation and storage

• Marco Notarianni,
• Jinzhang Liu,
• Kristy Vernon and
• Nunzio Motta

Beilstein J. Nanotechnol. 2016, 7, 149–196, doi:10.3762/bjnano.7.17

• thermal reduction of graphene oxide. Graphene oxide (GO) is a semiconducting material originating from graphene research and can be considered a precursor of the graphene synthesis by chemical or thermal reduction [84][85][98][99]. It has recently attracted significant interest because of its potential as

Controlled graphene oxide assembly on silver nanocube monolayers for SERS detection: dependence on nanocube packing procedure

• Martina Banchelli,
• Bruno Tiribilli,
• Roberto Pini,
• Luigi Dei,
• Paolo Matteini and
• Gabriella Caminati

Beilstein J. Nanotechnol. 2016, 7, 9–21, doi:10.3762/bjnano.7.2

• means of two procedures differing for the method used in the assembly of the silver nanocubes onto the surface: Langmuir–Blodgett (LB) transfer and direct sequential physisorption of silver nanocubes (AgNCs). Adsorption of graphene oxide (GO) flakes on the AgNC assemblies obtained with both procedures

• metal nanoparticle arrays may be further extended by a proper pairing with graphene or graphene derivatives due to their exclusive chemical, electronic and mechanical properties [18]. Graphene oxide (GO) is derived in the form of single-atom sheets of conjugated sp2 carbon atoms with abundant oxygen

Green and energy-efficient methods for the production of metallic nanoparticles

• Mitra Naghdi,
• Mehrdad Taheran,
• Satinder K. Brar,
• M. Verma,
• R. Y. Surampalli and
• J. R. Valero

Beilstein J. Nanotechnol. 2015, 6, 2354–2376, doi:10.3762/bjnano.6.243

• . They reacted AgNO3 and graphene oxide (GO) with TA simultaneously and observed that GO sheets were impregnated with many Ag NPs with diameters up to 20 nm [73]. Kasthuri et al. synthesized anisotropic Au and quasi-spherical Ag NPs using apiin to reduce AgNO3 and HAuCl4 at room temperature within 60 s

• -isoprene moieties help stabilization of NPs [8]. Li et al. produced bimetallic Pd–Ag NPs from AgNO3, K2PdCl4 using graphene oxide (GO) nanosheets as reducing agent, support and stabilizer. The synthesis process took place at 84 °C for 3 h for reduction of metallic ions and 200 °C for 24 h for reduction of

Fabrication of hybrid graphene oxide/polyelectrolyte capsules by means of layer-by-layer assembly on erythrocyte cell templates

• Joseba Irigoyen,
• Nikolaos Politakos,
• Eleftheria Diamanti,
• Elena Rojas,
• Marco Marradi,
• Raquel Ledezma,
• Layza Arizmendi,
• J. Alberto Rodríguez,
• Ronald F. Ziolo and
• Sergio E. Moya

Beilstein J. Nanotechnol. 2015, 6, 2310–2318, doi:10.3762/bjnano.6.237

• , Centro de Investigación en Química Aplicada, Blvd. Enrique Reyna Hermosillo No.140 C.P. 25294 Saltillo, Coahuila, México 10.3762/bjnano.6.237 Abstract A novel and facile method was developed to produce hybrid graphene oxide (GO)–polyelectrolyte (PE) capsules using erythrocyte cells as templates. The

• tendency to form multi-layered agglomerates, which begin to acquire the properties of graphite [9][10][11]. Because of these difficulties, most studies of graphene, whether for layered assembly or other investigations, have been performed on graphite oxide or its exfoliated form, graphene oxide (GO), which

Liquid-phase exfoliated graphene: functionalization, characterization, and applications

• Mildred Quintana,
• Jesús Iván Tapia and
• Maurizio Prato

Beilstein J. Nanotechnol. 2014, 5, 2328–2338, doi:10.3762/bjnano.5.242

• exfoliate graphite by wet chemistry techniques, it is necessary to decrease the π–π staking interactions between the graphene layers. In achieving this, the sp2 lattice is partially disrupted into layers containing sp2–sp3 carbon atoms. The most drastic example is probably graphene oxide (GO), where the

Carbon-based smart nanomaterials in biomedicine and neuroengineering

• Antonina M. Monaco and
• Michele Giugliano

Beilstein J. Nanotechnol. 2014, 5, 1849–1863, doi:10.3762/bjnano.5.196

• single-layer graphene [30], and its large surface area [31], make graphene and graphene oxide (GO) one of the most promising materials for technological and biomedical applications. Carbon-based nanomaterials in biomedical applications The peculiar ability of several nanomaterials to functionally

• treatments, but also in a high degree of purity of the recovered proteins, which can be further analysed by mass spectrometry [86]. Graphene: Graphene, graphene oxide (GO) and reduced graphene oxide (r-GO) have been investigated as new biocompatible material by virtue of their unique properties, making them

Donor–acceptor graphene-based hybrid materials facilitating photo-induced electron-transfer reactions

• Anastasios Stergiou,
• Georgia Pagona and
• Nikos Tagmatarchis

Beilstein J. Nanotechnol. 2014, 5, 1580–1589, doi:10.3762/bjnano.5.170

• applications. There are two main routes to overcome this hurdle. Namely, this can be accomplished by starting with water-soluble graphene oxide (GO), which can be reduced to the so-called reduced graphene oxide (rGO), followed by post-modification to acquire functionalized graphene [11]. However, the reduction

• hybrid materials. Tetraphenylporphyrin (TTP) condensed onto graphene oxide (GO) yielding GO–TPP hybrid material [44]. Ferrocene units anchored to graphene oxide (GO) forming a GO–Fc hybrid material [50]. Free and Pd-metallated tetraphenylporphyrin moieties as substituents of pyrrolidine rings covalently

• ) aryl diazonium addition, and (d) azide addition. Iron(II) coordinated on terpyridine (tpy) moieties covalently anchored to graphene oxide (GO) forming GO–tpy–Fe hybrids [51]. “Click” reaction for the grafting of a porphyrin onto reduced graphene oxide sheets that was pre-modified by phenylacetylene

Highly NO₂ sensitive caesium doped graphene oxide conductometric sensors

• Carlo Piloto,
• Marco Notarianni,
• Mahnaz Shafiei,
• Elena Taran,
• Dilini Galpaya,
• Cheng Yan and
• Nunzio Motta

Beilstein J. Nanotechnol. 2014, 5, 1073–1081, doi:10.3762/bjnano.5.120

• Institute for Bioengineering and Nanotechnology, Australian National Fabrication Facility - QLD Node, Brisbane, QLD 4072, Australia 10.3762/bjnano.5.120 Abstract Here we report on the synthesis of caesium doped graphene oxide (GO-Cs) and its application to the development of a novel NO2 gas sensor. The GO

• energy, i.e., the gas molecules can absorb more strongly on the doped or defective graphene than the pristine graphene resulting in an enhancement of the sensitivity or selectivity. Recently, graphene oxide (GO), a graphene layer decorated with oxygen functional groups, has been subject to extensive

• studied for the first time an NO2 sensor based on caesium-doped graphene oxide (GO-Cs). We demonstrated that caesium doping is an effective technique to reduce the GO, making it a promising material for gas sensing applications. XPS, Raman and KPFM results confirm the successful incorporation of Cs into

Enhancement of photocatalytic H₂ evolution of eosin Y-sensitized reduced graphene oxide through a simple photoreaction

• Weiying Zhang,
• Yuexiang Li,
• Shaoqin Peng and
• Xiang Cai

Beilstein J. Nanotechnol. 2014, 5, 801–811, doi:10.3762/bjnano.5.92

• Weiying Zhang Yuexiang Li Shaoqin Peng Xiang Cai Department of Chemistry, Nanchang University, Nanchang 330031, China 10.3762/bjnano.5.92 Abstract A graphene oxide (GO) solution was irradiated by a Xenon lamp to form reduced graphene oxide (RGO). After irradiation, the epoxy, the carbonyl and the

• ) sheet of sp2-hybrized carbon, has received tremendous research interests based on its extraordinary electronic, thermal, optical and excellent electron transport properties [21][22]. Graphene can be easily obtained by reducing graphene oxide (GO), which is a cheap and scalable preparation method [23][24

• with 5% HCl and water until pH 5 and dried in an oven at 60 °C. 0.5 g of graphite oxide powder was added into 1 L of distilled water, and the dispersion was treated with ultrasound (KQ-800KDB, KunShan Ultrasonic Instrument Co. Ltd) for 2 h until the solution became clear to obtain a graphene oxide (GO

Nanostructure sensitization of transition metal oxides for visible-light photocatalysis

• Hongjun Chen and
• Lianzhou Wang

Beilstein J. Nanotechnol. 2014, 5, 696–710, doi:10.3762/bjnano.5.82

• ) forming an electron–hole puddle in a g-C3N4-supported graphene monolayer [100]. Song and co-workers observed an enhancement of the photoconversion efficiency up to 15 times for a TiO2 nanotube composite electrode decorated by graphene oxide (GO) in comparison with pristine TiO2 nanotube arrays under

A visible-light-driven composite photocatalyst of TiO₂ nanotube arrays and graphene quantum dots

• Donald K. L. Chan,
• Po Ling Cheung and
• Jimmy C. Yu

Beilstein J. Nanotechnol. 2014, 5, 689–695, doi:10.3762/bjnano.5.81

• for 1 h with a temperature increasing rate of 1 °C·min−1 in air was applied to improve crystallization. Synthesis of graphene quantum dots (GQDs): GQDs were synthesized from graphene oxide (GO) by heating with a solution of hydrogen peroxide and ammonia [44]. 20 mg of GO was dispersed into 5 mL of