Correction: An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques

• Felix M. Badaczewski,
• Marc O. Loeh,
• Torben Pfaff,
• Dirk Wallacher,
• Daniel Clemens and
• Bernd M. Smarsly

Beilstein J. Nanotechnol. 2020, 11, 678–679, doi:10.3762/bjnano.11.54

• structure; small-angle neutron scattering (SANS); wide-angle X-ray scattering (WAXS); The following graph (A) should be implemented in Figure 4 of the original article, since it was part of the manuscript and was accidently removed during the revision process. No other change in the corresponding text and

• caption of Figure 4 is necessary. Figure 4 in the original article: SANS raw data (A) and CLD analysis (B) for the four resin- and pitch-based carbon materials, treated at 800 °C and 3000 °C. For all samples, SANS analysis was performed on evacuated samples (hollow symbols), as well as under a maximum

An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques

• Felix M. Badaczewski,
• Marc O. Loeh,
• Torben Pfaff,
• Dirk Wallacher,
• Daniel Clemens and
• Bernd M. Smarsly

Beilstein J. Nanotechnol. 2020, 11, 310–322, doi:10.3762/bjnano.11.23

• mesoporosity of these monolithic carbon materials was studied by the sorption behavior of a relatively large organic molecule (p-xylene) in comparison to typical gas adsorbates (Ar). In addition, to obtain a detailed view on the nanopore space small-angle neutron scattering (SANS) combined with in situ

• process is analyzed by special evaluation approaches for SANS and wide-angle X-ray scattering (WAXS). The WAXS analysis shows that the pitch-based monolithic material exhibits a more ordered microstructure consisting of larger graphene stacks and similar graphene layer sizes compared to the monolithic

• physisorption using probe gases such as Ar or N2 can provide misleading parameters if to be used to appraise the accessibility of the nanoscale pore space. Keywords: adsorption; carbon materials; mesoporosity; microporosity; microstructure; pore structure; small-angle neutron scattering (SANS); wide-angle X

Wearable, stable, highly sensitive hydrogel–graphene strain sensors

• Jian Lv,
• Chuncai Kong,
• Chao Yang,
• Lu Yin,
• Itthipon Jeerapan,
• Fangzhao Pu,
• Xiaojing Zhang,
• Sen Yang and
• Zhimao Yang

Beilstein J. Nanotechnol. 2019, 10, 475–480, doi:10.3762/bjnano.10.47

• foil using the silver epoxy. The size of the graphene/hydrogel sensor is 5 × 30 mm. Characterization of the hydrogel and graphene/hydrogel: The mechanical properties of the hydrogel were characterized in an electronic universal testing machine (CMT6503, Sans, Shenzhen, China). A field-emission scanning

Electrodeposition of reduced graphene oxide with chitosan based on the coordination deposition method

• Mingyang Liu,
• Yanjun Chen,
• Chaoran Qin,
• Zheng Zhang,
• Shuai Ma,
• Xiuru Cai,
• Xueqian Li and
• Yifeng Wang

Beilstein J. Nanotechnol. 2018, 9, 1200–1210, doi:10.3762/bjnano.9.111

• morphology of the deposited HACC-rGO/CS film were observed by a field emission scanning electron microscope (JSM-5610LV, JEOL Ltd., JP). The tensile strength and elongation at break of the deposited HACC-rGO/CS film were tested by a universal testing machine (CMT6503, Shenzhen SANS Test Machine Co., China

Solvent-mediated conductance increase of dodecanethiol-stabilized gold nanoparticle monolayers

• Patrick A. Reissner,
• Jean-Nicolas Tisserant,
• Antoni Sánchez-Ferrer,
• Raffaele Mezzenga and
• Andreas Stemmer

Beilstein J. Nanotechnol. 2016, 7, 2057–2064, doi:10.3762/bjnano.7.196

• transfer range of 0.1 nm−1 < q < 2 nm−1, where q = 4π sin θ/λCuKα, and 2θ is the scattering angle. The scattering intensity profiles were analyzed using the software SANS & USANS Analysis with IGOR Pro and OriginPro 10 [33]. Information about the measurement of nanoparticle size and distribution with SAXS

Multifunctional layered magnetic composites

• Maria Siglreitmeier,
• Baohu Wu,
• Tina Kollmann,
• Martin Neubauer,
• Gergely Nagy,
• Dietmar Schwahn,
• Vitaliy Pipich,
• Damien Faivre,
• Dirk Zahn,
• Andreas Fery and
• Helmut Cölfen

Beilstein J. Nanotechnol. 2015, 6, 134–148, doi:10.3762/bjnano.6.13

• (MNPs) are synthesized. The amount of MNPs can be controlled through the synthesis protocol therefore mineral loadings starting from 15 wt % up to 65 wt % can be realized. The demineralized organic nacre matrix is characterized by small-angle and very-small-angle neutron scattering (SANS and VSANS

• eight reaction cycles the upper limit of mineral load is reached and further repetition does not lead to an increase in the mineral content. Nacre organic matrix – SANS Nacre, an inorganic and organic composite natural material, is typically found as the inner shells of mollusks, and is referred to as

• mineralization, hierarchical structure and toughness enhancement [23][29]. Different techniques have been used to resolve the chemical and structural composition of the organic matrix. Small angle neutron scattering (SANS) is a non-destructive method to study the nacreous organic matrix without potential changes

Non-covalent and reversible functionalization of carbon nanotubes

• Antonello Di Crescenzo,
• Valeria Ettorre and
• Antonella Fontana

Beilstein J. Nanotechnol. 2014, 5, 1675–1690, doi:10.3762/bjnano.5.178

• proximity of the tube, they speculated that the individual nanotubes were essentially in a pure hydrocarbon environment. On the other hand, SANS data, performed by Yurekli et al. [65] strongly suggested that the dispersion of SWCNTs by SDS is due to the formation of a structureless, adsorbed layer of

Continuous parallel ESI-MS analysis of reactions carried out in a bespoke 3D printed device

• Jennifer S. Mathieson,
• Mali H. Rosnes,
• Victor Sans,
• Philip J. Kitson and
• Leroy Cronin

Beilstein J. Nanotechnol. 2013, 4, 285–291, doi:10.3762/bjnano.4.31

• Jennifer S. Mathieson Mali H. Rosnes Victor Sans Philip J. Kitson Leroy Cronin School of Chemistry, University of Glasgow, G12 8QQ, United Kingdom 10.3762/bjnano.4.31 Abstract Herein, we present an approach for the rapid, straightforward and economical preparation of a tailored reactor device

Distribution of functional groups in periodic mesoporous organosilica materials studied by small-angle neutron scattering with in situ adsorption of nitrogen

• Monir Sharifi,
• Dirk Wallacher and
• Michael Wark

Beilstein J. Nanotechnol. 2012, 3, 428–437, doi:10.3762/bjnano.3.49

• functionalized with SO3H or SO3− groups and investigated by small-angle neutron scattering (SANS) with in situ nitrogen adsorption at 77 K. If N2 is adsorbed in the pores the SANS measurements show a complete matching of all of the diffraction signals that are caused by the long-range ordering of the mesopores

• in the benzene-PMO, due to the fact that the benzene-PMO walls possess a neutron scattering length density (SLD) similar to that of nitrogen in the condensed state. However, signals at higher q-values (>1 1/Å) are not affected with respect to their SANS intensity, even after complete pore filling

• ; SANS; surface functionalization; Introduction Regarding functionalization with organic groups, Si-MCM-41 often suffers from pore blocking at the pore mouths and inhomogeneous distribution of the functional groups in the case of post-synthetic grafting [1][2][3] or, if the co-condensation route is

Studies towards synthesis, evolution and alignment characteristics of dense, millimeter long multiwalled carbon nanotube arrays

• Pitamber Mahanandia,
• Jörg J. Schneider,
• Martin Engel,
• Bernd Stühn,
• Somanahalli V. Subramanyam and
• Karuna Kar Nanda

Beilstein J. Nanotechnol. 2011, 2, 293–301, doi:10.3762/bjnano.2.34

• long CNTs can be detached easily from the aligned CNT bundle or mat like structure. Atomic force microscope (AFM) images of individual CNTs, synthesized at 650 °C and 1100 °C, are depicted in Figure 6. They confirm the uniform diameter as found by TEM. SAXS and small angle neutron scattering (SANS) are