Bombyx mori silk/titania/gold hybrid materials for photocatalytic water splitting: combining renewable raw materials with clean fuels

• Stefanie Krüger,
• Michael Schwarze,
• Otto Baumann,
• Christina Günter,
• Michael Bruns,
• Christian Kübel,
• Dorothée Vinga Szabó,
• Rafael Meinusch,
• Verónica de Zea Bermudez and
• Andreas Taubert

Beilstein J. Nanotechnol. 2018, 9, 187–204, doi:10.3762/bjnano.9.21

• authors also showed that methanol is the most efficient sacrificial agent when compared to isopropanol, glycerol, and glucose [25]. A further study by Jose et al. focused on the effect of TiO2 modification (anatase and/or rutile). These authors observed that TiO2 P25/Au mixed systems performed best in the

• , ethanol, ethylacetoacetate (EtAcAc), and possibly isopropanol from unreacted TiO2 precursors [82]. The PEO-containing hybrid materials TPS and TPS_Au2.5 essentially exhibit an identical thermal stability. The first weight loss of 9% below 120 °C can be assigned to water and ethanol evaporation. The second

Hydrothermal synthesis of ZnO quantum dot/KNb₃O₈ nanosheet photocatalysts for reducing carbon dioxide to methanol

• Xiao Shao,
• Weiyue Xin and
• Xiaohong Yin

Beilstein J. Nanotechnol. 2017, 8, 2264–2270, doi:10.3762/bjnano.8.226

• , East China University of Science and Technology, Shanghai 200237, China 10.3762/bjnano.8.226 Abstract ZnO quantum dots and KNb3O8 nanosheets were synthesized by a two-step hydrothermal method for the photocatalytic reduction of CO2 to methanol where isopropanol is simultaneously oxidized to acetone

• by reducing CO2 in isopropanol to methanol under UV-light irradiation. Experimental Catalyst synthesis Niobium oxide (Nb2O5, 99.99 wt %) was purchased from Aladdin Industrial Corporation. Potassium hydroxide (KOH, 96 wt %), isopropanol (C3H8O, 99.9 wt %), hydrochloric acid (HCl, 36.5 wt %), zinc

• Raman system using a 325 nm laser. Photocatalytic reaction The photocatalytic reduction of CO2 to methanol was carried out at ambient conditions in a quartz container and batch operated slurry reactor with cooling jacket. 20 mg of the catalyst was added to 20 mL of isopropanol under magnetic stirring

Three-in-one approach towards efficient organic dye-sensitized solar cells: aggregation suppression, panchromatic absorption and resonance energy transfer

• Jayita Patwari,
• Samim Sardar,
• Bo Liu,
• Peter Lemmens and
• Samir Kumar Pal

Beilstein J. Nanotechnol. 2017, 8, 1705–1713, doi:10.3762/bjnano.8.171

• substrates via thermal decomposition of 5 mM platinum chloride (in isopropanol) at 385 °C for 30 min. 60 μm thick Surlyn was used as a spacer between the active and counter electrodes. The I−/I3− redox couple, which was prepared by mixing iodine crystal (I2), lithium iodide (LiI), and 4-tert-butylpyridine

A top-down approach for fabricating three-dimensional closed hollow nanostructures with permeable thin metal walls

• Carlos Angulo Barrios and
• Víctor Canalejas-Tejero

Beilstein J. Nanotechnol. 2017, 8, 1231–1237, doi:10.3762/bjnano.8.124

• , acetone, isopropanol, tetrahydrofuran and deionized water. The maximum peak wavelength red-shifts, approximately linearly, with the refractive index of the top cladding liquid, with a slope of 327 nm/refractive index unit (RIU), as depicted in Figure 5b. Although bulk sensitivity of refractometric sensors

• for different superstrate media: air, methanol (MeOH), acetone, isopropanol (IPA), tetrahydrofuran (THF) and deionized water (DIW). b) Spectral position of the reflectance maximum peak as a function of the liquid refractive index. Cross-section of the modelled hollow nanopillar array unit cell. White

Nano-engineered skin mesenchymal stem cells: potential vehicles for tumour-targeted quantum-dot delivery

• Liga Saulite,
• Dominyka Dapkute,
• Karlis Pleiko,
• Ineta Popena,
• Simona Steponkiene,
• Ricardas Rotomskis and
• Una Riekstina

Beilstein J. Nanotechnol. 2017, 8, 1218–1230, doi:10.3762/bjnano.8.123

• evaluated using Oil Red O staining. Cells were washed with PBS and fixed with 4% formaldehyde for 30 min at room temperature. After fixation, cells were washed with distilled water. Prior to staining, cells were incubated for 5 min at room temperature with 60% isopropanol and subsequently stained with 180

• mg/L Oil Red O solution in isopropanol/water (3:2, v/v) for 15 min at room temperature. After staining, the cells were washed four to five times with distilled water and imaged. Chondrogenic differentiation was evaluated using Alcian Blue staining. Cells were washed once with PBS and fixed with 4

Growth, structure and stability of sputter-deposited MoS₂ thin films

• Reinhard Kaindl,
• Bernhard C. Bayer,
• Roland Resel,
• Thomas Müller,
• Viera Skakalova,
• Gerlinde Habler,
• Rainer Abart,
• Alexey S. Cherevan,
• Dominik Eder,
• Maxime Blatter,
• Fabian Fischer,
• Jannik C. Meyer,
• Dmitry K. Polyushkin and
• Wolfgang Waldhauser

Beilstein J. Nanotechnol. 2017, 8, 1115–1126, doi:10.3762/bjnano.8.113

• ). As substrates silicon wafers (100) with ≈100 nm thermal SiO2 layer were used, which were cleaned with isopropanol and dried with nitrogen prior to deposition. The substrates were fixed on a static, floating potential substrate holding device kept at approximately ten centimetres away from the

Study of the correlation between sensing performance and surface morphology of inkjet-printed aqueous graphene-based chemiresistors for NO₂ detection

• F. Villani,
• C. Schiattarella,
• T. Polichetti,
• R. Di Capua,
• F. Loffredo,
• B. Alfano,
• M. L. Miglietta,
• E. Massera,
• L. Verdoliva and
• G. Di Francia

Beilstein J. Nanotechnol. 2017, 8, 1023–1031, doi:10.3762/bjnano.8.103

• deposition of small ink volumes and the versatility of the exploitable inks and substrates. Herein we present a feasibility study of chemiresistive gas sensors inkjet-printed onto paper substrates, in which a LPE graphene suspension dispersed in a water/isopropanol (H2O/IPA) mixture is used as sensing ink

• printing a LPE graphene suspension dispersed in a water/isopropanol (H2O/IPA) mixture as sensing ink onto paper substrates. Analogous paper-based graphene sensors, relying on different fabrication processes, such as CVD (chemical vapour deposition) grown transferred graphene [13] or inkjet-printed GO

• sonication-assisted liquid phase exfoliation of graphite in a mixture of water and isopropanol as described in details in the Experimental section and fully investigated in [8]. As already reported, the dispersed material consists of exfoliated flakes having less than five layers and a lateral size around

3D Nanoprinting via laser-assisted electron beam induced deposition: growth kinetics, enhanced purity, and electrical resistivity

• Brett B. Lewis,
• Robert Winkler,
• Xiahan Sang,
• Pushpa R. Pudasaini,
• Michael G. Stanford,
• Harald Plank,
• Raymond R. Unocic,
• Jason D. Fowlkes and
• Philip D. Rack

Beilstein J. Nanotechnol. 2017, 8, 801–812, doi:10.3762/bjnano.8.83

• using an FEI NOVA 600 dual-beam system equipped with multiple gas injection systems (GIS). Before loading the Si substrate, it was cleaned via sonication in acetone for 5 minutes and rinsed in isopropanol before drying. The precursor gas was injected using a FEI GIS and the temperature was held at 45 °C

Nanostructured carbon materials decorated with organophosphorus moieties: synthesis and application

• Giacomo Biagiotti,
• Vittoria Langè,
• Cristina Ligi,
• Stefano Caporali,
• Maurizio Muniz-Miranda,
• Anna Flis,
• K. Michał Pietrusiewicz,
• Giacomo Ghini,
• Alberto Brandi and
• Stefano Cicchi

Beilstein J. Nanotechnol. 2017, 8, 485–493, doi:10.3762/bjnano.8.52

• 8 was more easily isolated by filtration and repeated washing for complete removal of the excess reagents while GPs-Nit-PO derivative 9 was recovered using cycles of centrifugation and re-dispersion of the carbon material in a 1:1 isopropyl ether-isopropanol solution. The decoration of the

• , entries 5 and 6). X-ray photoelectron spectroscopy analysis showed the presence of the P(V) atoms in all the samples considered. The samples for the analysis where prepared by dispersion of 1 mg of substance in 1 mL of isopropanol and the dispersion was drop casted on a cleaned glass support. The spectra

• DMF. The mixture was kept in an ultrasound bath for 10 min, under inert atmosphere, and 19.3 mg (0.165 mmol) of isopentyl nitrite were added. The mixture was stirred at 80 °C under nitrogen for 16 h. The dispersion was diluted a 1:1 solution of isopropanol/diisopropyl ether and centrifuged for 15 min

The longstanding challenge of the nanocrystallization of 1,3,5-trinitroperhydro-1,3,5-triazine (RDX)

• Florent Pessina and
• Denis Spitzer

Beilstein J. Nanotechnol. 2017, 8, 452–466, doi:10.3762/bjnano.8.49

• as the yield of about 25% and the importance of the residence time and the drying step. Liu et al. [34][35] studied the effect of drying n-RDX and HMX samples under various conditions. They first obtained n-RDX in solution from a mixture of water, ethanol, isopropanol and RDX. The suspension was put

Functionalized TiO₂ nanoparticles by single-step hydrothermal synthesis: the role of the silane coupling agents

• Antoine R. M. Dalod,
• Lars Henriksen,
• Tor Grande and
• Mari-Ann Einarsrud

Beilstein J. Nanotechnol. 2017, 8, 304–312, doi:10.3762/bjnano.8.33

• background was collected under medium vacuum, without sample. Between each analysis, the ATR diamond was cleaned with isopropanol, for which vacuum provides fast evaporation and no specific adsorption bands of isopropanol were observed. A total of 128 scans were acquired for each sample at a resolution of 1

• -functionalized TiO2 nanoparticles are shown in Figure 5b (see Table S1 of Supporting Information File 1 for the assignments of the absorption bands). No specific bands from isopropanol were observed indicating full reaction of the TIP precursor and high purity of the nanoparticles. In the case of in situ surface

Colorimetric gas detection by the varying thickness of a thin film of ultrasmall PTSA-coated TiO₂ nanoparticles on a Si substrate

• Urmas Joost,
• Andris Šutka,
• Meeri Visnapuu,
• Aile Tamm,
• Meeri Lembinen,
• Mikk Antsov,
• Kathriin Utt,
• Krisjanis Smits,
• Ergo Nõmmiste and
• Vambola Kisand

Beilstein J. Nanotechnol. 2017, 8, 229–236, doi:10.3762/bjnano.8.25

• shift of interference maxima and minima) to isopropanol. In the present work results obtained using one typical thin film are presented. However, experiments were repeated with several thin films all showing similar behavior. Experimental Titania NPs were synthesised using a method described by Scolan

• film-based sensor element is more responsive to isopropanol and toluene, and the response to hexane is much smaller. Toluene probably interacts strongly with the aromatic ring in PTSA, and isopropanol is probably more compatible with the polar part of the molecule, due to the ability to form hydrogen

Nanocrystalline TiO₂/SnO₂ heterostructures for gas sensing

• Barbara Lyson-Sypien,
• Anna Kusior,
• Mieczylaw Rekas,
• Jan Zukrowski,
• Marta Gajewska,
• Katarzyna Michalow-Mauke,
• Thomas Graule,
• Marta Radecka and
• Katarzyna Zakrzewska

Beilstein J. Nanotechnol. 2017, 8, 108–122, doi:10.3762/bjnano.8.12

• heterostructures of 90 mol % SnO2/10 mol % TiO2 and 10 mol % SnO2/90 mol % TiO2 were synthesized as well. Titanium diisopropoxide bis(acetylacetonate) (TiC16H28O, 75 wt % in isopropanol, ABCR, CAS: 17927-72-9) and tetramethyltin (CAS: 594-27-4), dissolved in absolute ethanol (C2H5OH, 99%, Sigma Aldrich) were used

Effect of Anderson localization on light emission from gold nanoparticle aggregates

• Mohamed H. Abdellatif,
• Marco Salerno,
• Gaser N. Abdelrasoul,
• Ioannis Liakos,
• Alice Scarpellini,
• Sergio Marras and
• Alberto Diaspro

Beilstein J. Nanotechnol. 2016, 7, 2013–2022, doi:10.3762/bjnano.7.192

• commercial optical microscope slides (Menzel-Gläser, Germany) and pure fused silica (Heraeus, Germany), called quartz in the following. Before use, the substrates were cleaned by successive sonication (5 min at each step) in warm acetone, then isopropanol, then water, and finally blown dry under a nitrogen

Organoclay hybrid materials as precursors of porous ZnO/silica-clay heterostructures for photocatalytic applications

• Marwa Akkari,
• Pilar Aranda,
• Abdessalem Ben Haj Amara and
• Eduardo Ruiz-Hitzky

Beilstein J. Nanotechnol. 2016, 7, 1971–1982, doi:10.3762/bjnano.7.188

• ). This suspension was stirred at 50 °C to homogenize the system and then stoichiometric amounts of water and isopropanol (H2O/isopropanol/TMOS 4:2:1 molar ratio) is added to start the hydrolysis of TMOS. After the sol–gel transition the system was dried overnight at 50 °C. The final ZnO/SiO2-clay

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

• . The mixture was stirred for 30 min, ultrasonically treated for at least 2 h and then deposited onto glass sheets (20 × 30 cm2), which had been cleaned with 10% KOH, isopropanol and acetone and dried at 100 °C. The deposited films were exposed to ambient humidity at room temperature for 24 h (for

Nanostructured TiO₂-based gas sensors with enhanced sensitivity to reducing gases

• Wojciech Maziarz,
• Anna Kusior and
• Anita Trenczek-Zajac

Beilstein J. Nanotechnol. 2016, 7, 1718–1726, doi:10.3762/bjnano.7.164

• × 20 mm squares and degreased in the ultrasonic cleaner with the use of acetone and isopropanol. The following samples were prepared: (A) T30 – prior to thermal treatment, the Ti foils were etched in concentrated hydrochloric acid HCl (35–38%, Avantor Performance Materials, Poland) at 55 °C for 30 min

Graphene-enhanced plasmonic nanohole arrays for environmental sensing in aqueous samples

• Christa Genslein,
• Peter Hausler,
• Eva-Maria Kirchner,
• Rudolf Bierl,
• Antje J. Baeumner and
• Thomas Hirsch

Beilstein J. Nanotechnol. 2016, 7, 1564–1573, doi:10.3762/bjnano.7.150

• graphite following a modified Hummers method and a subsequent chemical reduction [55]. To cover the substrates with a uniform layer of reduced graphene oxide 200 μL of a 0.25 μg·mL solution containing 1:1 (v/v) water and isopropanol was deposited in the middle on the surface and allowed to settle for 5 min

Mesoporous hollow carbon spheres for lithium–sulfur batteries: distribution of sulfur and electrochemical performance

• Anika C. Juhl,
• Artur Schneider,
• Boris Ufer,
• Torsten Brezesinski,
• Jürgen Janek and
• Michael Fröba

Beilstein J. Nanotechnol. 2016, 7, 1229–1240, doi:10.3762/bjnano.7.114

• electrochemical testing A mixture of the carbon/sulfur composite powder (83 wt %), Super C65 (Timcal, 6 wt %), Printex XE2 (Orion, 6 wt %) and poly(vinyl alcohol) Selvol 425 (Sekisui, 5 wt %) in water, isopropanol and 1-methoxy-2-propanol (65:30:5 weight ratio) was prepared to form a homogeneous slurry. The

Role of solvents in the electronic transport properties of single-molecule junctions

• Katharina Luka-Guth,
• Sebastian Hambsch,
• Andreas Bloch,
• Philipp Ehrenreich,
• Bernd Michael Briechle,
• Filip Kilibarda,
• Torsten Sendler,
• Dmytro Sysoiev,
• Thomas Huhn,
• Artur Erbe and
• Elke Scheer

Beilstein J. Nanotechnol. 2016, 7, 1055–1067, doi:10.3762/bjnano.7.99

• solvents that are commonly used in the field of molecular electronics (ethanol, toluene, mesitylene, 1,2,4-trichlorobenzene, isopropanol, toluene/tetrahydrofuran mixtures) for the study of single-molecule contacts of functional molecules. We present measurements of the conductance as a function of gap

• -designed MCBJ system equipped with a pipette containing the solvent mesitylene (Mes), 1,2,4-trichlorobenzene (TCB), toluene (Tol), ethanol (EtOH), a mixture of 50% tetrahydrofuran and 50% toluene (Tol/THF) or isopropanol (IPA), see Figure 2c. The mixture Tol/THF has been chosen because with pure THF the

Selective photocatalytic reduction of CO₂ to methanol in CuO-loaded NaTaO₃ nanocubes in isopropanol

• Tianyu Xiang,
• Feng Xin,
• Jingshuai Chen,
• Yuwen Wang,
• Xiaohong Yin and
• Xiao Shao

Beilstein J. Nanotechnol. 2016, 7, 776–783, doi:10.3762/bjnano.7.69

• photocatalysts were characterized by XRD, SEM, UV–vis, EDS and XPS and used to photocatalytically reduce CO2 in isopropanol. This worked to both absorb CO2 and as a sacrificial reagent to harvest CO2 and donate electrons. Methanol and acetone were generated as the reduction product of CO2 and the oxidation

• product of isopropanol, respectively. NaTaO3 nanocubes loaded with 2 wt % CuO and synthesized in 2 mol/L NaOH solution showed the best activity. The methanol and acetone yields were 137.48 μmol/(g·h) and 335.93 μmol/(g·h), respectively, after 6 h of irradiation. Such high activity could be attributed to

• the good crystallinity, morphology and proper amount of CuO loading, which functioned as reductive sites for selective formation of methanol. The reaction mechanism was also proposed and explained by band theory. Keywords: CO2 reduction; CuO loading; isopropanol; NaTaO3 nanocubes; photocatalysis

Charge injection and transport properties of an organic light-emitting diode

• Peter Juhasz,
• Juraj Nevrela,
• Michal Micjan,
• Miroslav Novota,
• Jan Uhrik,
• Lubica Stuchlikova,
• Jan Jakabovic,
• Ladislav Harmatha and
• Martin Weis

Beilstein J. Nanotechnol. 2016, 7, 47–52, doi:10.3762/bjnano.7.5

• transport properties of OLED devices has been done on the organic double-layer sandwiched between two electrodes ITO/α-NPD/Alq3/Al. The devices were grown on glass slides precoated with ITO with sheet resistance lower than 10 Ω/sq. The substrates were cleaned sequentially in ultrasonic bath by isopropanol

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

Electrospray deposition of organic molecules on bulk insulator surfaces

• Antoine Hinaut,
• Rémy Pawlak,
• Ernst Meyer and
• Thilo Glatzel

Beilstein J. Nanotechnol. 2015, 6, 1927–1934, doi:10.3762/bjnano.6.195

• performed a deposition of the solvent solution only, i.e., toluene/isopropanol in the ratio 2:1 on a clean KBr(001) surface. Figure 2a shows a topography image acquired by nc-AFM at room temperature on a KBr(001) surface after a total time of 30 min of UHV-ESI deposition of the pure solvent. This is a long

• -cyanophenyl groups are known to enhance the binding to ionic substrates by electrostatic interaction [37][38]. For the UHV-ESI deposition, molecules were diluted at 1 μL/mL in a mixture of toluene and isopropanol with a 2:1 ratio. Deposition was performed for 5 min at a constant rate of injected solution of 5

• min at controlled flux, by the use of a syringe pump, of 2–10 μL/min. The molecules were diluted in a solution of toluene/isopropanol made from high purity solvents (Sigma-Aldrich) with a ratio of 2:1. Molecule concentration in solution was 1 μg/mL. Molecules, see Figure 3, are based on a triply fused

A facile method for the preparation of bifunctional Mn:ZnS/ZnS/Fe₃O₄ magnetic and fluorescent nanocrystals

• Houcine Labiadh,
• Tahar Ben Chaabane,
• Romain Sibille,
• Lavinia Balan and
• Raphaël Schneider

Beilstein J. Nanotechnol. 2015, 6, 1743–1751, doi:10.3762/bjnano.6.178

• (Mn(OAc)2·4H2O, 99%), iron(III) chloride hexahydrate (FeCl3·6H2O, 99%), sodium sulfide nonahydrate (Na2S·9H2O, 98+%), 3-mercaptopropionic acid (MPA, 99%) and isopropanol (HPLC grade) were used as received without additional purification. All solutions were prepared using Milli-Q® water (18.2 MΩ·cm

• QDs was labelled as solution A. The Mn:ZnS/ZnS QDs were precipitated by adding isopropanol, collected by centrifugation, and washed three times with isopropanol, then dried in vacuum. The obtained nanocrystals could be dispersed in water to form a stable and clear colloidal solution. Preparation of

• temperature. A black powder was recovered by centrifugation after adding isopropanol. Synthesis of bifunctional core/shell/shell Mn:ZnS/ZnS/Fe3O4 nanocrystals The bifunctional Mn:ZnS/ZnS/Fe3O4 QDs were prepared from the Mn:ZnS/ZnS colloidal solution A. 5.5 mL of solution A was added to 94.5 mL of ultrapure