Measurement of polarization effects in dual-phase ceria-based oxygen permeation membranes using Kelvin probe force microscopy

• Kerstin Neuhaus,
• Christina Schmidt,
• Liudmila Fischer,
• Wilhelm Albert Meulenberg,
• Ke Ran,
• Joachim Mayer and
• Stefan Baumann

Beilstein J. Nanotechnol. 2021, 12, 1380–1391, doi:10.3762/bjnano.12.102

• Forschungszentrum Jülich GmbH, Institute of Energy and Climate Research, Materials Synthesis and Processing (IEK-1), Wilhelm-Johnen-Straße, 52452 Jülich, Germany Faculty of Science and Technology, Inorganic Membranes, University of Twente, 7500 AE Enschede, Netherlands Central Facility for Electron Microscopy GFE

• interfaces between CSO and FC2O have been shown to be mainly clean with only a slight segregation of Sm. Additionally, in some areas residues of a rock salt phase have been found. This phase is prone to develop during the synthesis process of CSO-FC2O depending on the sintering parameters. The formation can

Biocompatibility and cytotoxicity in vitro of surface-functionalized drug-loaded spinel ferrite nanoparticles

• Sadaf Mushtaq,
• Khuram Shahzad,
• Tariq Saeed,
• Anwar Ul-Hamid,
• Bilal Haider Abbasi,
• Nafees Ahmad,
• Waqas Khalid,
• Muhammad Atif,
• Zulqurnain Ali and
• Rashda Abbasi

Beilstein J. Nanotechnol. 2021, 12, 1339–1364, doi:10.3762/bjnano.12.99

• M = Fe ions in all samples, as studied by energy dispersive spectroscopy (EDS), is given in Table 2. No extra impurity peaks were present in the spectrum (Figure 2b) due to the use of coprecipitation synthesis methods in which the samples were washed several times to remove any impurity. The

• ), diaminobenzidine (DAB), chromogen (DM827), and hematoxylin (K8018) ready to use were obtained from Agilent Technologies, Inc. (USA). Colloidal synthesis of MFe2O4 (M = Fe, Co, Ni, Zn) nanoparticles The two-step sonochemical method was used for the synthesis of MFe2O4 (M = Fe, Co, Zn, Ni) NPs. The coprecipitation

• method was used in the first step of the synthesis of MFe2O4 nanoparticles (0.2 M) by mixing iron nitrate [Fe(NO3)3·9H2O] and (Co/Zn/Ni) nitrates with a molar ratio of Fe/M (2:1) in 100 mL of deionized water. The solution was stirred for 15 min, heated at 70 °C, and further stirred for 1 h after the

Identifying diverse metal oxide nanomaterials with lethal effects on embryonic zebrafish using machine learning

• Richard Liam Marchese Robinson,
• Haralambos Sarimveis,
• Philip Doganis,
• Xiaodong Jia,
• Marianna Kotzabasaki,
• Christiana Gousiadou,
• Stacey Lynn Harper and
• Terry Wilkins

Beilstein J. Nanotechnol. 2021, 12, 1297–1325, doi:10.3762/bjnano.12.97

• reduced animal testing, there is considerable value in developing computational models that could reliably predict the toxic hazard of novel metal oxide ENMs, prior to experimental testing and, ideally, prior to synthesis, based upon synthesis-controlled, intrinsic characteristics of the ENMs. Indeed, the

• et al. [35] to model synthesis routes for inorganic materials. Here, the original endpoint actually being modelled was always one of the previously described binary response variables (toxic vs non-toxic) based upon whether a LOEL was identified for lethality at 24 hpf or, alternatively, excess

• suggests that the very simple, single descriptor model we identified herein could be of value in providing manufacturers of ENM-enabled products with a rapid initial hazard ranking prior to synthesis and testing. Nonetheless, we do not suggest that the toxicity of diverse ENMs towards embryonic zebrafish

Electrical, electrochemical and structural studies of a chlorine-derived ionic liquid-based polymer gel electrolyte

• Ashish Gupta,
• Amrita Jain,
• Manju Kumari and
• Santosh K. Tripathi

Beilstein J. Nanotechnol. 2021, 12, 1252–1261, doi:10.3762/bjnano.12.92

• ][23], fluoropolymers such as poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) have received much attention from the research community as potential polymer hosts for the synthesis of polymer electrolytes [10][11][24][25]. The dielectric constant value of PVdF-HFP is ≈8.4 and it comprises a

Morphology-driven gas sensing by fabricated fractals: A review

• Vishal Kamathe and
• Rupali Nagar

Beilstein J. Nanotechnol. 2021, 12, 1187–1208, doi:10.3762/bjnano.12.88

• had minimum influence. Thus, better interaction between NO2 and the sensor surface was achieved. The SnO2 DNWs were estimated to have a fractal dimension of 1.82. In 2017, Zang et al. fabricated SnO2 leaf-like hierarchical structures by hydrothermal synthesis [67]. Figure 7a–f shows SEM images of SnO2

• temperature of 260 °C, while Figure 21l and Figure 21m show the response towards 50 ppm of N2H4 at 260 °C. Other oxide-based fractals In 2020, Tran-Phu et al. demonstrated the formation of three-dimensional fractals of Au–Bi2O3, having D ≈ 1.80, on a substrate by hot-aerosol synthesis [45]. The fabricated Au

• . Stuerga, “Shape-controlled synthesis of hematite for microwave gas sensing”, pages no. 764–768, Copyright (2015), with permission from Elsevier. This content is not subject to CC BY 4.0. Dandelion-like ZnO fractals. (a–f) SEM images of the samples annealed at different temperatures. The inset in (c) shows

The effect of cobalt on morphology, structure, and ORR activity of electrospun carbon fibre mats in aqueous alkaline environments

• Markus Gehring,
• Tobias Kutsch,
• Osmane Camara,
• Alexandre Merlen,
• Hermann Tempel,
• Hans Kungl and
• Rüdiger-A. Eichel

Beilstein J. Nanotechnol. 2021, 12, 1173–1186, doi:10.3762/bjnano.12.87

• electrochemical activity using linear sweep voltammetry with a focus on the oxygen reduction reaction. Experimental Synthesis of carbon fibres and electrode preparation Polyacrylonitrile (PAN) (98%, MW = 150,000 g·mol−1; BOC sciences, USA) was dissolved in N,N-dimethyl formamide (DMF) to obtain 10 wt % solutions

Self-assembly of amino acids toward functional biomaterials

• Huan Ren,
• Lifang Wu,
• Lina Tan,
• Yanni Bao,
• Yuchen Ma,
• Yong Jin and
• Qianli Zou

Beilstein J. Nanotechnol. 2021, 12, 1140–1150, doi:10.3762/bjnano.12.85

• nanostructures at both microscopic and macroscopic scales. Amino acids, as the smallest constituent of proteins and the smallest constituent in the bottom-up approach, are the smallest building blocks that can be self-assembled. The self-assembly of single amino acids has the advantages of low synthesis cost

• ordered nanostructures through noncovalent interactions, including electrostatic, π–π stacking, van der Waals, and hydrophobic interactions. The self-assembly of single amino acids has the advantages of low synthesis cost, relatively easy modeling [27], and excellent biocompatibility and biodegradability

• biomedical science. The nanostructure of amino acids can be a good substitute for therapeutic delivery due to its good biocompatibility, functionalization, and ease of design/synthesis. Self-assembled nanostructures have become smart tools in the biomedical field, as demonstrated by the ability of self

pH-driven enhancement of anti-tubercular drug loading on iron oxide nanoparticles for drug delivery in macrophages

• Karishma Berta Cotta,
• Sarika Mehra and
• Rajdip Bandyopadhyaya

Beilstein J. Nanotechnol. 2021, 12, 1127–1139, doi:10.3762/bjnano.12.84

• permeabilization [10], in turn improving the bactericidal activity of the drug, too. For biological applications, it is essential for IONPs to be stabilized with the help of stabilizing agents [11][12]. This helps to reduce the nanoparticle toxicity and facilitates the synthesis of stable nanoparticle dispersions

• the treatment of intracellular pathogens. Experimental Reagents FeCl2·4H2O, FeCl3·6H2O and NOR used in the nanoparticle synthesis were purchased from Sigma-Aldrich, Germany. 25% ammonia solution was purchased from Merck, Germany (GR grade). RPMI-1640 and fetal bovine serum (FBS) used for the culturing

• of THP1 cells were purchased from HiMedia, India. Phorbol 12 myristate acetate (PMA) used for THP1 cell differentiation was purchased from Sigma-Aldrich, Germany. Synthesis The synthesis of IONPs and NOR@IONPs was carried out analogously to our previous study [30]. Specifically, IONPs were

Criteria ruling particle agglomeration

• Dieter Vollath

Beilstein J. Nanotechnol. 2021, 12, 1093–1100, doi:10.3762/bjnano.12.81

• Dieter Vollath NanoConsulting, Primelweg 3, 76297 Stutensee, Germany 10.3762/bjnano.12.81 Abstract Most of the technically important properties of nanomaterials, such as superparamagnetism or luminescence, depend on the particle size. During synthesis and handling of nanoparticles, agglomeration

• may occur. Agglomeration of nanoparticles may be controlled by different mechanisms. During synthesis one observes agglomeration controlled by the geometry and electrical charges of the particles. Additionally, one may find agglomeration controlled by thermodynamic interaction of the particles in the

• . Synthesis of larger particles may be carried out in the gas phase, where the probability of collision is controlled by the geometry of the particles or forces among the particles [1]. Alternatively, in case of existing particles, the agglomeration is controlled by the minimum of free enthalpy. In this case

Revealing the formation mechanism and band gap tuning of Sb₂S₃ nanoparticles

• Maximilian Joschko,
• Franck Yvan Fotue Wafo,
• Christina Malsi,
• Danilo Kisić,
• Ivana Validžić and
• Christina Graf

Beilstein J. Nanotechnol. 2021, 12, 1021–1033, doi:10.3762/bjnano.12.76

• crucial to adjust these parameters. Also, when aiming for continuous production by transferring the synthesis into a microreactor, it is necessary to know and control synthesis and particle parameters in a broader range [15]. Mainly two synthesis strategies to gain nanoparticles with uniform size and

• of 180–210 °C to facilitate the synthesis process following the hot-injection method with a sulfur–oleylamine (S-OlAm) precursor. They have found that the temperature influences the crystallinity, shape, and size of the particles [21]. These studies revealed growth processes comprising a primary

• a detailed proposal for a formation mechanism was elaborated. The mechanism involves the seeding process, growth of amorphous particles, crystallization of the particles, and the following growth of the crystals. The synthesis demonstrated that it is possible to tune the band gap of the Sb2S3

Progress and innovation of nanostructured sulfur cathodes and metal-free anodes for room-temperature Na–S batteries

• Marina Tabuyo-Martínez,
• Bernd Wicklein and
• Pilar Aranda

Beilstein J. Nanotechnol. 2021, 12, 995–1020, doi:10.3762/bjnano.12.75

• in the presence of graphene [55]. One advantage of this method over vapor impregnation routes is that it can yield very high sulfur loads of up to 90 wt % resulting in a high cathode capacity of 555 mAh·g−1 at 5C [55]. Wet chemistry synthesis routes can also produce nanostructured sulfur. Lu et al

• cycles at 167 mA·g−1 current density. While CS2 is the most efficient solvent for sulfur, it is also an extremely reactive and hazardous solvent. Therefore, more benign solution methods for the synthesis of S NPs and sols are sought. In fact, such methods have been known for more than a hundred years now

• to be highly underinvestigated despite the advantages an aqueous solution-based synthesis route can offer. Instead, commercial S NPs are increasingly employed in cathodes, for instance, by Chen et al. [58], who wrapped reduced graphene oxide sheets around such NPs (Figure 7B). In this case, the

A Au/CuNiCoS₄/p-Si photodiode: electrical and morphological characterization

• Adem Koçyiğit,
• Adem Sarılmaz,
• Teoman Öztürk,
• Faruk Ozel and
• Murat Yıldırım

Beilstein J. Nanotechnol. 2021, 12, 984–994, doi:10.3762/bjnano.12.74

• transmission electron microscopy (HR-TEM), and energy-dispersive X-ray spectroscopy (EDS). The XRD, EDS, and HR-TEM analyses confirmed the successful synthesis of CuNiCoS4. The obtained CuNiCoS4 thiospinel nanocrystals were tested for photodiode and capacitance applications as interfacial layer between Au and

• to their remarkable crystal, electric, thermoelectric, magnetic, and optical properties [6][7]. There are many studies on the usage of thiospinels in batteries, super-capacitors, and electrochemical reactions [8][9][10][11][12]. However, there are only two studies on the synthesis and application of

• quaternary CuNiCoS4 nanocrystals. The first study by Thompson is on the synthesis of CuNiCoS4 thiospinels [13]. The second is a study on the synthesis and photocatalytic hydrogen evolution, which was performed by our group [8]. In this study, the optical characterization results of the CuNiCoS4 nanocrystals

The role of deep eutectic solvents and carrageenan in synthesizing biocompatible anisotropic metal nanoparticles

• Nabojit Das,
• Akash Kumar and
• Raja Gopal Rayavarapu

Beilstein J. Nanotechnol. 2021, 12, 924–938, doi:10.3762/bjnano.12.69

• made owing to their cytotoxicity. The toxicity concern is primarily due to the conventional synthesis route that involves surfactants as a structure-directing agent and as a capping agent for nanoparticles. Wet chemical methods employ toxic auxiliary chemicals. However, the approach yields

• monodispersed nanoparticles, an essential criterion for their intended application and a limitation of the green synthesis of nanoparticles using plant extracts. Several biocompatible counterparts such as polymers, lipids, and chitosan-based nanoparticles have been successfully used in the synthesis of safe

• ]. Traditionally used stabilizing agents, such as surfactants and citrate, enable the synthesis of nanoparticles with high yield and monodispersity but also cause cytotoxicity and genotoxicity even at low concentrations [9][10]. Surfactants are known to act as a template for anisotropy in plasmonic metal

Modification of a SERS-active Ag surface to promote adsorption of charged analytes: effect of Cu²⁺ ions

• Bahdan V. Ranishenka,
• Andrei Yu. Panarin,
• Irina A. Chelnokova,
• Sergei N. Terekhov,
• Peter Mojzes and
• Vadim V. Shmanai

Beilstein J. Nanotechnol. 2021, 12, 902–912, doi:10.3762/bjnano.12.67

• detector (Princeton Instruments). Spectra were excited by a 441.6 nm of a He–Cd laser. Synthesis of silver NPs The synthetic procedure was analogous to that described in [36]. 50 mL of deionized water, 42 mg of sodium bicarbonate, 15 mg sodium citrate, and 450 mg of water-free glucose were added into a

Comprehensive review on ultrasound-responsive theranostic nanomaterials: mechanisms, structures and medical applications

• Sepand Tehrani Fateh,
• Lida Moradi,
• Elmira Kohan,
• Michael R. Hamblin and
• Amin Shiralizadeh Dezfuli

Beilstein J. Nanotechnol. 2021, 12, 808–862, doi:10.3762/bjnano.12.64

Silver nanoparticles nucleated in NaOH-treated halloysite: a potential antimicrobial material

• Yuri B. Matos,
• Rodrigo S. Romanus,
• Mattheus Torquato,
• Edgar H. de Souza,
• Rodrigo L. Villanova,
• Marlene Soares and
• Emilson R. Viana

Beilstein J. Nanotechnol. 2021, 12, 798–807, doi:10.3762/bjnano.12.63

• (Ag+) into bacterial cells [12]. However, a large-scale industrial usage of Ag-NPs is still difficult because most synthesis techniques used in labs are unsuitable for commercial use. The main issues are high procedural complexity and elevated cost, which jeopardize scalability efforts fundamental to

• the industrial mass-production of Ag-NPs. Amongst the most scalable synthesis routes for Ag-NPs, some techniques stand out by using stabilizers, such as PVP [13] or PEG [14] capping agents, to ensure that silver nucleates and stabilizes into nanosized particles, instead of dissolving back into Ag

• , and HNT-8 were recorded with TEM, while sample HNT-8 was also measured with XRD. (XRD was also performed for HNT-0 and HNT-4 but omitted from this report because it did not show any significant difference from HNT-8). Silver nanoparticle synthesis To synthesize silver nanoparticles, 10 g of HNT (from

Fate and transformation of silver nanoparticles in different biological conditions

• Barbara Pem,
• Marija Ćurlin,
• Darija Domazet Jurašin,
• Valerije Vrček,
• Rinea Barbir,
• Vedran Micek,
• Raluca M. Fratila,
• Jesus M. de la Fuente and
• Ivana Vinković Vrček

Beilstein J. Nanotechnol. 2021, 12, 665–679, doi:10.3762/bjnano.12.53

• different media and tissue extracts, but also demonstrates how different AgNPs may be affected in biological media in a short time leading to the formation of new types of materials in different tissues. The reduction and de novo synthesis of AgNPs in different biological matrices should be considered

• of AgNPs from primary particles or AgNO3 was shown in cellular fractions [52]. Also, biogenic synthesis was noted in bacterial cells and in many other organisms. It stands to reason that human intracellular or extracellular environments can provide similar conditions [53][54]. Secondary particles are

• the pH close to neutral, since the synthesis does not progress in water due to the acidic nature of GSH. The 1H NMR spectrum of 10 mM GSH in PB was recorded (Figure 8b). It showed four distinct peaks corresponding to protons bound to carbon at positions nine (overlapped with two), seven, four, and

A review of defect engineering, ion implantation, and nanofabrication using the helium ion microscope

• Frances I. Allen

Beilstein J. Nanotechnol. 2021, 12, 633–664, doi:10.3762/bjnano.12.52

High-yield synthesis of silver nanowires for transparent conducting PET films

• Gul Naz,
• Hafsa Asghar,
• Muhammad Ramzan,
• Muhammad Arshad,
• Rashid Ahmed,
• Muhammad Bilal Tahir,
• Bakhtiar Ul Haq,
• Nadeem Baig and
• Junaid Jalil

Beilstein J. Nanotechnol. 2021, 12, 624–632, doi:10.3762/bjnano.12.51

• have gained much attention in replacing ITO because of their low-cost solution-based fabrication, flexibility, and high optical transparency [14][15]. A large-scale uniform synthesis of AgNWs with high aspect ratio would be greatly preferred because of better plasmonic and optical properties [16]. An

• ]. This method involves the reduction of metallic salts in the presence of a polyol. This synthetic method was first proposed by Figlarz and co-workers for the synthesis of rod-like silver particles. They employed ethylene glycol as polyol to reduce silver salt in the presence of polyvinylpyrrolidone (PVP

• performance below that of ITO films. Hence, there is a need to modify this polyol method to produce extra-large and highly ordered silver nanowires to outperform ITO films. It is important to note that the polyol synthesis yields impurities in the form of silver nanoparticles [29]. These nanoparticles formed

Nanoporous and nonporous conjugated donor–acceptor polymer semiconductors for photocatalytic hydrogen production

• Zhao-Qi Sheng,
• Yu-Qin Xing,
• Yan Chen,
• Guang Zhang,
• Shi-Yong Liu and
• Long Chen

Beilstein J. Nanotechnol. 2021, 12, 607–623, doi:10.3762/bjnano.12.50

• (Figure 10) exhibited the highest HER of 191.82 μmol·h−1 (1.15 mg) [95]. Recently, McCulloch and co-workers discovered another D/A heterojunction (P80/P81) (Figure 10) as photocatalyst for hydrogen evolution. By stabilizing the surfactant employed during synthesis of the heterojunction, ITIC-containing

Stability and activity of platinum nanoparticles in the oxygen electroreduction reaction: is size or uniformity of primary importance?

• Kirill O. Paperzh,
• Anastasia A. Alekseenko,
• Vadim A. Volochaev,
• Ilya V. Pankov,
• Olga A. Safronenko and
• Vladimir E. Guterman

Beilstein J. Nanotechnol. 2021, 12, 593–606, doi:10.3762/bjnano.12.49

• liquid-phase synthesis. A comparative study of the structural characteristics, catalytic activity in the oxygen electroreduction reaction (ORR), and durability of the synthesized catalysts, as well as their commercial analogs, was carried out. It was shown that the uniformity of the structural and

• features of spatial distributions), and the adhesion strength of NPs to the support [10]. The latter is likely to depend on the method/conditions of the synthesis [11]. The number of publications related to the effect of the structure of Pt/C catalysts on their activity, primarily in ORR, is rather large

• regard, of particular interest are the methods for the synthesis of catalysts, which make it possible to obtain materials that combine small size of the nanoparticles, their narrow dimensional and uniform spatial distribution over the surface, and pores of support. This study was based on the hypothesis

On the stability of microwave-fabricated SERS substrates – chemical and morphological considerations

• Limin Wang,
• Aisha Adebola Womiloju,
• Christiane Höppener,
• Ulrich S. Schubert and
• Stephanie Hoeppener

Beilstein J. Nanotechnol. 2021, 12, 541–551, doi:10.3762/bjnano.12.44

• spectroscopy (SERS) substrates in different organic solvents and different buffer solutions was investigated. SERS substrates were fabricated by a microwave-assisted synthesis approach and the morphological as well as chemical changes of the SERS substrates were studied. It was demonstrated that the SERS

• of different organic solvents and buffer solutions. Keywords: chemical stability; microwave synthesis; scanning electron microscopy; silver nanoparticles; surface-enhanced Raman spectroscopy; Introduction Surface-enhanced Raman spectroscopy (SERS) has been developed into a standard analytical tool

• on the substrates [8], the synthesis of complex nanoparticle structures with tunable interparticle gap sizes [9], the utilization of micro- and nanofabricated structures obtained by lithography techniques [10][11][12] comprising nanodisk arrays [13], nanoholes [14][15], nanocups [16][17

The preparation temperature influences the physicochemical nature and activity of nanoceria

• Robert A. Yokel,
• Wendel Wohlleben,
• Johannes Georg Keller,
• Matthew L. Hancock,
• Jason M. Unrine,
• D. Allan Butterfield and
• Eric A. Grulke

Beilstein J. Nanotechnol. 2021, 12, 525–540, doi:10.3762/bjnano.12.43

• engineered nanomaterials prepared by many methods that result in products with varying physicochemical properties and applications. Those used industrially are often calcined, an example is NM-212. Other nanoceria have beneficial pharmaceutical properties and are often prepared by solvothermal synthesis

• family of metal oxide ENMs used industrially, as catalysts in diesel fuel, abrasives in chemical mechanical planarization, in integrated circuit manufacture, as structural supports for catalysts for fuel synthesis applications, in solid oxide fuel cells, and in rechargeable batteries [1][2]. Cerium oxide

• component, including cancer, radiation damage, bacterial infection, sepsis, wounds, stroke-induced ischemia, retinal degeneration, and neurodegenerative diseases [10]. Other reviews provide more information on nanoceria synthesis methods and the resulting physicochemical properties of the products as well

Surface-enhanced Raman scattering of water in aqueous dispersions of silver nanoparticles

• Paulina Filipczak,
• Krzysztof Hałagan,
• Jacek Ulański and
• Marcin Kozanecki

Beilstein J. Nanotechnol. 2021, 12, 497–506, doi:10.3762/bjnano.12.40

• synthesized via simple chemical reduction of silver nitrate with sodium borohydride [36]. The volume added of potassium bromide during the synthesis was crucial for the size control of AgNPs. The sample without added KBr turned blue and the ample with 40 µL of the added KBr turned yellow. The synthesized

Boosting of photocatalytic hydrogen evolution via chlorine doping of polymeric carbon nitride

• Malgorzata Aleksandrzak,
• Michalina Kijaczko,
• Wojciech Kukulka,
• Daria Baranowska,
• Martyna Baca,
• Beata Zielinska and
• Ewa Mijowska

Beilstein J. Nanotechnol. 2021, 12, 473–484, doi:10.3762/bjnano.12.38

• semiconductor polymer, as a metal-free and visible-light-responsive photocatalyst, has attracted dramatically growing attention in the field of visible-light-induced hydrogen evolution reaction (HER). It is characterized by facile synthesis, easy functionalization, attractive electronic band structure, and

• other hand, the amount of C–C/C=C/N3C significantly decreases. The XPS analysis indicates a successful incorporation of chlorine into the polymeric carbon nitride network. Without the doping agent melamine, thermal polycondensation leads to the formation of melon. We suppose that the presented synthesis

• PCN is a suitable strategy towards boosting photocatalytic hydrogen evolution. Experimental Materials All purchased reagents employed for catalyst preparation were analytical grade and used without further purification. Synthesis of polymeric carbon nitride Polymeric carbon nitride was synthesized by