Facile synthesis of Fe-based metal–organic frameworks from Fe₂O₃ nanoparticles and their application for CO₂/N₂ separation

• Van Nhieu Le,
• Hoai Duc Tran,
• Minh Tien Nguyen,
• Hai Bang Truong,
• Toan Minh Pham and
• Jinsoo Kim

Beilstein J. Nanotechnol. 2024, 15, 897–908, doi:10.3762/bjnano.15.74

• defined for the physisorption regime [37][38], implying that a spent M-100Fe@Fe2O3#1.80 sample could be easily refreshed under soft conditions for reuse, thus, extending the material’s life cycle. To affirm this aspect, a conservative trial of five cycles for CO2 adsorption/desorption was carried out at

Humidity-dependent electrical performance of CuO nanowire networks studied by electrochemical impedance spectroscopy

• Jelena Kosmaca,
• Juris Katkevics,
• Jana Andzane,
• Raitis Sondors,
• Liga Jasulaneca,
• Raimonds Meija,
• Kiryl Niherysh,
• Yelyzaveta Rublova and
• Donats Erts

Beilstein J. Nanotechnol. 2023, 14, 683–691, doi:10.3762/bjnano.14.54

• chemisorption and physisorption at the nanowire interface, which suppress electronic transport inside the p-type semiconductor nanowire but enhance ionic transport in the water layers adsorbed on the nanowire surface. Possible physicochemical processes at the nanowire surface are discussed in line with

• contribution from resistance, capacitance, constant phase element, and Warburg element to the total impedance at various RH. Physical models describing the impact of chemisorption and physisorption processes are proposed to clarify the observed changes in the impedance spectra, discuss gas sensing mechanisms

• physisorption of the second layer, that is, H2O molecules forming hydrogen bonds with the hydroxy groups [23][29][32]. This enables the formation of H+ and H3O+ ions, for example, when a proton is transferred from a hydroxy group to a water molecule [33]. A further increase of humidity up to ca. 90% causes the

A comprehensive review on electrospun nanohybrid membranes for wastewater treatment

• Senuri Kumarage,
• Imalka Munaweera and
• Nilwala Kottegoda

Beilstein J. Nanotechnol. 2022, 13, 137–159, doi:10.3762/bjnano.13.10

• groups endow CS with metal adsorption capabilities via physisorption. Due to the poor spinnability of CS alone, it is often spun along with another polymer. For instance, a nanofibrous electrospun nonwoven sorbent from CS blended with PEO and phosphorylated nanocellulose (PNC) has been developed by

• . Adsorption membranes decontaminate wastewater by adsorbing the impurities via chemisorption or physisorption. Polymeric membranes have functional groups that can interact with the solutes. In chemisorption, an irreversible chemical bond is formed between the adsorbate and the adsorbent, whereas in

• physisorption, only a reversible physical bond due to electrostatic interactions or intermolecular interactions forms between adsorbate and the adsorbent. An ideal adsorption membrane should exhibit both high adsorption capacity and a high adsorption rate. ENH membranes have been widely used as adsorption

Unravelling the interfacial interaction in mesoporous SiO₂@nickel phyllosilicate/TiO₂ core–shell nanostructures for photocatalytic activity

• Bridget K. Mutuma,
• Xiluva Mathebula,
• Isaac Nongwe,
• Bonakele P. Mtolo,
• Boitumelo J. Matsoso,
• Rudolph Erasmus,
• Zikhona Tetana and
• Neil J. Coville

Beilstein J. Nanotechnol. 2020, 11, 1834–1846, doi:10.3762/bjnano.11.165

• . Therefore, in this study we report on the growth of mesoporous SiO2@NiPS and titania-coated mSiO2@NiPS (mSiO2@NiPS/TiO2) core–shell nanostructures using a simple deposition-precipitation method. Transmission electron microscopy (TEM), N2 physisorption analysis, diffuse reflectance UV–visible spectroscopy

• silica in mSiO2@NiPS/TiO2 (Supporting Information File 1, Figure S3). The textural properties of the core–shell nanostructures were evaluated using N2 physisorption analysis. Figure 2a shows that the nitrogen gas adsorption–desorption isotherms of mSiO2 and the mSiO2@NiPS core–shell nanostructure are of

Detecting stable adsorbates of (1S)-camphor on Cu(111) with Bayesian optimization

• Jari Järvi,
• Patrick Rinke and
• Milica Todorović

Beilstein J. Nanotechnol. 2020, 11, 1577–1589, doi:10.3762/bjnano.11.140

• resemble the HOMO and LUMO of an isolated camphor molecule and are at −1.0 and 2.9 eV, respectively, with an energy gap of 3.9 eV. This indicates physisorption between the molecule and the substrate in class Hy. Discussion With the low-dimensional studies of molecular translation (1D and 2D) and rotation

• indicates chemisorption of camphor via O to the Cu substrate. Conversely, in class Hy structures we observed the characteristics of physisorption. Class Hy structures have systematically lower adsorption energies, energy barriers, and electron transfer to the substrate, and their DOS resembles the HOMO and

• the molecule via oxygen (class Ox) and (b) physisorption via hydrogen (class Hy). (c) Adsorption site of camphor in the relaxed structures (center of the molecule) and the high-symmetry points of the Cu(111) surface. Electronic properties of different camphor adsorbates. (a) The sum of partial charges

Impact of fluorination on interface energetics and growth of pentacene on Ag(111)

• Qi Wang,
• Meng-Ting Chen,
• Antoni Franco-Cañellas,
• Bin Shen,
• Thomas Geiger,
• Holger F. Bettinger,
• Frank Schreiber,
• Ingo Salzmann,
• Alexander Gerlach and
• Steffen Duhm

Beilstein J. Nanotechnol. 2020, 11, 1361–1370, doi:10.3762/bjnano.11.120

• physisorptive [29][53]. On Cu(111), PFP shows a behavior close to physisorption [9], although the coupling strength might be slightly stronger than with Au(111) [54]. PEN on Cu(111), however, is strongly chemisorbed, involving a partial filling of the former lowest unoccupied molecular orbital (LUMO) by a

• chemisorption of PEN [28][51] and physisorption of PFP [50]. Multilayers of PEN adopt a herringbone arrangement on virtually all substrates [47][56][57][58][59], whereas PFP multilayers exhibit π-stacking [18][56]. The different multilayer packing motifs of PEN and PFP can again be explained by electrostatic

Role of redox-active axial ligands of metal porphyrins adsorbed at solid–liquid interfaces in a liquid-STM setup

• Thomas Habets,
• Sylvia Speller and
• Johannes A. A. W. Elemans

Beilstein J. Nanotechnol. 2020, 11, 1264–1271, doi:10.3762/bjnano.11.110

• Mn(II)TUP complexes are formed, they must be able to desorb and replaced by molecules of Mn(III)TUPCl from the supernatant solution so that the reduction reactions can continue. Given the fact that the molecules of MnTUPCl are adsorbed to the interface via relatively weak physisorption interactions

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

• physisorption was applied, using deuterated p-xylene (DPX) as a contrast-matching agent in the neutron scattering process. The impact of the carbon precursor on the structural order on an atomic scale in terms of size and disorder of the carbon microstructure, on the nanopore structure, and on the template

• 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

• neutron scattering (SANS) combined with in situ physisorption were the methods of choice. Deuterated p-xylene (DPX) acts as a contrast-matching agent in the neutron scattering process. In a perfect case, that is if DPX filled all pores, the scattering contrast would be zero and the SANS intensity would

Multiwalled carbon nanotube based aromatic volatile organic compound sensor: sensitivity enhancement through 1-hexadecanethiol functionalisation

• Nadra Bohli,
• Meryem Belkilani,
• Juan Casanova-Chafer,
• Eduard Llobet and
• Adnane Abdelghani

Beilstein J. Nanotechnol. 2019, 10, 2364–2373, doi:10.3762/bjnano.10.227

• they are strong covalent (chemisorption) or weak (physisorption), highly impact the sensor performance, that is, the sensitivity, response and recovery time, and detection range. Unlike metal-oxide-based gas sensors, CNT-based sensors operate at room temperature (low activation energy) and can

• concentrations measured were 2 ppm for benzene and 0.5 ppm for toluene. Physisorption is observed for toluene at concentrations below 7 ppm (below 5 ppm for benzene), indicating weak interaction forces between the vapour molecules and the Au-MWCNT active sensor layer and the signal returns to the baseline. For a

• the non-functionalised sensor. The same kinetics were also observed, where physisorption is visible for toluene below a concentration of 7 ppm (below 5 ppm for benzene). A short heating for a few seconds at 70 °C is sufficient for desaturating the sensor (desorbing the vapour molecules) and its return

Adsorption and desorption of self-assembled L-cysteine monolayers on nanoporous gold monitored by in situ resistometry

• Elisabeth Hengge,
• Eva-Maria Steyskal,
• Rupert Bachler,
• Alexander Dennig,
• Bernd Nidetzky and
• Roland Würschum

Beilstein J. Nanotechnol. 2019, 10, 2275–2279, doi:10.3762/bjnano.10.219

• ) after cysteine adding (grey arrow). This delay is attributed to a physisorption step prior to chemisorption (reported to take few minutes for planar Au [13]), which does not significantly change the electronic structure and thus the resistance of the substrate. Since SAMs are known to decrease the

The influence of porosity on nanoparticle formation in hierarchical aluminophosphates

• Matthew E. Potter,
• Lauren N. Riley,
• Alice E. Oakley,
• Panashe M. Mhembere,
• June Callison and
• Robert Raja

Beilstein J. Nanotechnol. 2019, 10, 1952–1957, doi:10.3762/bjnano.10.191

• hydrothermal gel (HP-SAPO-5) preserved the phase purity, as only AlPO-5 features are present (Figure S1, Supporting Information File 1). Nitrogen physisorption measurements show that while the type-I isotherm of MP-SAPO-5 strongly indicates microporosity, HP-SAPO-5 has a type-IV isotherm, indicating the

• of microporous MP-SAPO-5 (A) and hierarchical HP-SAPO-5 (B). Nitrogen physisorption isotherms of gold-deposited microporous (A) and hierarchical (B) SAPO-5 systems showing that porosity is maintained in hierarchical HP-SAPO-5, but not in microporous MP-SAPO-5. The magnitude and imaginary component of

The impact of crystal size and temperature on the adsorption-induced flexibility of the Zr-based metal–organic framework DUT-98

• Simon Krause,
• Volodymyr Bon,
• Hongchu Du,
• Rafal E. Dunin-Borkowski,
• Ulrich Stoeck,
• Irena Senkovska and
• Stefan Kaskel

Beilstein J. Nanotechnol. 2019, 10, 1737–1744, doi:10.3762/bjnano.10.169

• supercritical solvent removal. Water physisorption experiments at 298 K on: a) DUT-98(1)–(4) and c) DUT-98(3) after cycling and after thermal treatment. (Filled symbols: adsorption, open symbols: desorption). In situ temperature-variable PXRD of: b) DUT-98(2) and d) DUt-98(2) cycled at lower temperature

Upcycling of polyurethane waste by mechanochemistry: synthesis of N-doped porous carbon materials for supercapacitor applications

• Christina Schneidermann,
• Pascal Otto,
• Desirée Leistenschneider,
• Sven Grätz,
• Claudia Eßbach and
• Lars Borchardt

Beilstein J. Nanotechnol. 2019, 10, 1618–1627, doi:10.3762/bjnano.10.157

• -derived carbon materials were investigated by N2 physisorption at −196 °C (Figure 2A), and the calculation of the pore size distributions was carried out under the assumption of slit and cylindrical pore geometry using quenched solid density functional theory (QSDFT; Figure 2B). The sample PU-BM-800 (i.e

• . Characterization Nitrogen physisorption measurements were performed with a Quadrasorb EVO/SI from Quantachrome Instruments at −196 °C. The samples were degassed before all measurements under vacuum at 150 °C for at least 24 h. The multi-point BET method was used to calculate the specific surface areas of the

• data of different N-doped carbon samples after milling and carbonization. Physisorption data derived from N2 isotherms measured at −196 °C. Element concentrations derived from elemental analysis. Electrochemical characterization data of PUPC-800-3, PUUPC-800-1 and PUUPC-800-2 measured in aqueous (1 M

Playing with covalent triazine framework tiles for improved CO₂ adsorption properties and catalytic performance

• Giulia Tuci,
• Andree Iemhoff,
• Housseinou Ba,
• Lapo Luconi,
• Andrea Rossin,
• Vasiliki Papaefthimiou,
• Regina Palkovits,
• Jens Artz,
• Cuong Pham-Huu and
• Giuliano Giambastiani

Beilstein J. Nanotechnol. 2019, 10, 1217–1227, doi:10.3762/bjnano.10.121

• focussed on 4,5-dicyanoimidazole (DCI, III) as a novel and highly N-rich monomer to be used for CTF synthesis as such (III→CTF3), or in equimolar mixture with one of the two other building blocks (IV→CTF4; V→CTF5). N2 physisorption isotherms recorded on CTF3–5 present classical type-I(b) profiles [46] that

• measurements. In a similar manner as described before [22], nitrogen physisorption experiments were conducted on a Micromeritics ASAP 2010 instrument. Samples were degassed for at least 15 h at 150 °C using a FloVacDegasser. Static volumetric measurements were carried out at 77 K. The empty volume of the cell

Mo-doped boron nitride monolayer as a promising single-atom electrocatalyst for CO₂ conversion

• Qianyi Cui,
• Gangqiang Qin,
• Weihua Wang,
• Lixiang Sun,
• Aijun Du and
• Qiao Sun

Beilstein J. Nanotechnol. 2019, 10, 540–548, doi:10.3762/bjnano.10.55

• . Meanwhile, the CO2 angle is also determined by the strength of the interaction of CO2 with different TMs that anchor on the BN monolayer. The configuration of captured CO2 is significantly distorted by strong chemisorption as illustrated in Figure 1a–c. Regarding the electronic properties, physisorption of

Improving control of carbide-derived carbon microstructure by immobilization of a transition-metal catalyst within the shell of carbide/carbon core–shell structures

• Teguh Ariyanto,
• Jan Glaesel,
• Andreas Kern,
• Gui-Rong Zhang and
• Bastian J. M. Etzold

Beilstein J. Nanotechnol. 2019, 10, 419–427, doi:10.3762/bjnano.10.41

• influence on the final material properties was characterized by using physisorption analysis with nitrogen as well as carbon dioxide, X-ray diffraction, temperature-programmed oxidation (TPO), Raman spectroscopy, SEM and TEM. The results showed that this improved route allows one to greatly vary the

• of the carbon material is characterized by X-ray diffraction (XRD), temperature-programmed oxidation (TPO) and physisorption analysis. Results and Discussion Properties of CDC-shell/carbide core starting material First of all, the properties of the hybrid starting material (Figure 1, left) were

Biocompatible organic–inorganic hybrid materials based on nucleobases and titanium developed by molecular layer deposition

• Leva Momtazi,
• Henrik H. Sønsteby and
• Ola Nilsen

Beilstein J. Nanotechnol. 2019, 10, 399–411, doi:10.3762/bjnano.10.39

• prolonged pulse times of TTIP, although at a significantly lower rate. A purge time of 2 s is required after TTIP for the thymine case, indicating that most of the mass increase after the first 0.25 s of TTIP pulse is due to physisorption. Any similar effects of purge time after TTIP for the uracil and

One-step nonhydrolytic sol–gel synthesis of mesoporous TiO₂ phosphonate hybrid materials

• Yanhui Wang,
• P. Hubert Mutin and
• Johan G. Alauzun

Beilstein J. Nanotechnol. 2019, 10, 356–362, doi:10.3762/bjnano.10.35

• infrared spectroscopy, Raman spectroscopy, X-ray diffraction, and nitrogen physisorption. For P/Ti ratios up to 0.1, the hybrid materials can be described as aggregated, roughly spherical, crystalline anatase nanoparticles grafted by octylphosphonate groups via Ti–O–P bonds. The crystallite size decreases

• materials and TiO2. N2 physisorption isotherms at 77 K (left) and Barrett–Joyner–Halenda (BJH) mesopore size distribution (desorption branch, right) of TiO2–octylphosphonate hybrid materials and TiO2. Open and filled symbols in the isotherms refer to adsorption and desorption, respectively. Ideal reaction

Hydrothermal-derived carbon as a stabilizing matrix for improved cycling performance of silicon-based anodes for lithium-ion full cells

• Mirco Ruttert,
• Florian Holtstiege,
• Jessica Hüsker,
• Markus Börner,
• Martin Winter and
• Tobias Placke

Beilstein J. Nanotechnol. 2018, 9, 2381–2395, doi:10.3762/bjnano.9.223

• -sections were prepared by a focused ion beam (FIB) milling process using gallium ions extracted from a high brightness liquid metal ion source. Nitrogen adsorption experiments were performed on a 3Flex Physisorption device (Micromeritics GmbH) at the temperature of liquid nitrogen (−196 °C). Before the

SO₂ gas adsorption on carbon nanomaterials: a comparative study

• Deepu J. Babu,
• Divya Puthusseri,
• Frank G. Kühl,
• Sherif Okeil,
• Michael Bruns,
• Manfred Hampe and
• Jörg J. Schneider

Beilstein J. Nanotechnol. 2018, 9, 1782–1792, doi:10.3762/bjnano.9.169

• found to dominate the adsorption behavior in activated carbon, SO2 adsorption on carbon nanomaterials occurs by a physisorption mechanism. Keywords: adsorption; carbon nanohorns; carbon nanotubes; heat of adsorption; sulfur dioxide; vertically aligned carbon nanotubes; Introduction Compared to the

• physisorption was theoretically studied by Furmaniak and co-workers [42]. Using the hyper-parallel tempering Monte Carlo method, they found that the influence of the oxygen functionalities is more pronounced at lower relative pressures (P/P0 < 0.3) and attributed it to the increase in the adsorption energy

• . Physisorption alone cannot account for such a high value of the heat of adsorption. In activated carbons, it is known that the presence of oxygen functional groups and micropores in the 0.7 nm range can promote SO2 chemisorption [52][53]. The extensive microporous structure and the presence of oxygen functional

Response under low-energy electron irradiation of a thin film of a potential copper precursor for focused electron beam induced deposition (FEBID)

• Leo Sala,
• Iwona B. Szymańska,
• Céline Dablemont,
• Anne Lafosse and
• Lionel Amiaud

Beilstein J. Nanotechnol. 2018, 9, 57–65, doi:10.3762/bjnano.9.8

• –5 eV, considerably enhancing the probability of DEA. Moreover, the ESD experiments presented here were done at 300 K and are more susceptible to detect light species. At this temperature, heavier fragments can remain trapped by physisorption on the surface, but lighter neutral species would desorb

Adsorption of iron tetraphenylporphyrin on (111) surfaces of coinage metals: a density functional theory study

• Hao Tang,
• Nathalie Tarrat,
• Véronique Langlais and
• Yongfeng Wang

Beilstein J. Nanotechnol. 2017, 8, 2484–2491, doi:10.3762/bjnano.8.248

• reference configuration (HS, fcc), the adsorption energy is calculated to be −1.86 eV while the vdW contribution is found to be −1.70 eV. This small energy difference confirms the physisorption of FeTPP on Au(111). The molecule–surface distance of 3.63 ± 0.06 Å is consistent with the presence of the four

• , has an adsorption energy of −1.83 ± 0.02 eV with a contribution of vdW interactions of −1.70 eV, and the central porphyrin macrocyle is at a distance of 3.63 ± 0.06 Å above the surface. These physisorption characteristics were confirmed by a small charge transfer (0.24e) from the molecule to the

• interactions in self-assembled monolayers on Au(111), Ag(111) and Cu(111) surfaces. In spite of the presence of two stable magnetic states in the free molecule, only the high-spin (S = 2) state is stable when adsorbed on metal. These results show that the physisorption of FeTPP on coinage metal surfaces is

Modelling focused electron beam induced deposition beyond Langmuir adsorption

• Dédalo Sanz-Hernández and
• Amalio Fernández-Pacheco

Beilstein J. Nanotechnol. 2017, 8, 2151–2161, doi:10.3762/bjnano.8.214

• adsorption processes. Two types of adsorption energies, describing both physisorption and spontaneous chemisorption, are included. Steady state solutions under no diffusion are investigated and compared under a wide range of conditions. The different growth regimes observed are fully explained by relative

• various growth regimes when considering a single adsorbate, and has been restricted to physisorption processes, except for a few exceptions [28][29]. Relevant effects present in common FEBID precursors, such as autocatalytic effects [15][16][30][31][32] cannot be described either. Moreover, current

• employed in FEBID for physisorption [1]. The ML model presented here assumes several simplifications. First, chemisorption processes considered are spontaneous; energy barriers for activated chemisorption, which can be modelled via the inclusion of Arrhenius terms in the sticking coefficient [29], are not

Bi-layer sandwich film for antibacterial catheters

• Gerhard Franz,
• Florian Schamberger,
• Hamideh Heidari Zare,
• Sara Felicitas Bröskamp and
• Dieter Jocham

Beilstein J. Nanotechnol. 2017, 8, 1982–2001, doi:10.3762/bjnano.8.199

• of the depositing molecules decreases exponentially with penetration depth not only by diffusion but also by deposition losses, which causes a steeply dropping layer thickness. The reaction can occur in the gas phase as well as during or after the process of condensation (physisorption). By diluting

Fabrication of carbon nanospheres by the pyrolysis of polyacrylonitrile–poly(methyl methacrylate) core–shell composite nanoparticles

• Dafu Wei,
• Youwei Zhang and
• Jinping Fu

Beilstein J. Nanotechnol. 2017, 8, 1897–1908, doi:10.3762/bjnano.8.190

• /IG of CP6 suggests the extent of graphitization of the obtained carbon nanospheres is still very low. This is due to the fairly low carbonization temperature. The pore structure of the carbonized sample CP6 was characterized by nitrogen physisorption. As shown in Figure 8a, CP6 displayed a IV-type