Zeolite materials with Ni and Co: synthesis and catalytic potential in the selective hydrogenation of citral

• Inocente Rodríguez-Iznaga,
• Yailen Costa Marrero,
• Tania Farias Piñeira,
• Céline Fontaine,
• Lexane Paget,
• Beatriz Concepción Rosabal,
• Arbelio Penton Madrigal,
• Vitalii Petranovskii and
• Gwendoline Lafaye

Beilstein J. Nanotechnol. 2025, 16, 520–529, doi:10.3762/bjnano.16.40

• for materials obtained by IE are higher than those of ZSA. This increase is consistent with expectations [17][18], as the ion exchange and water washing treatments effectively clean the materials’ surface, thereby enhancing the available surface area and porosity (microporosity) for adsorption. The

A review of metal-organic frameworks and polymers in mixed matrix membranes for CO₂ capture

• Charlotte Skjold Qvist Christensen,
• Nicholas Hansen,
• Mahboubeh Motadayen,
• Nina Lock,
• Martin Lahn Henriksen and
• Jonathan Quinson

Beilstein J. Nanotechnol. 2025, 16, 155–186, doi:10.3762/bjnano.16.14

Influence of conductive carbon and MnCo₂O₄ on morphological and electrical properties of hydrogels for electrochemical energy conversion

• Sylwia Pawłowska,
• Karolina Cysewska,
• Yasamin Ziai,
• Jakub Karczewski,
• Piotr Jasiński and
• Sebastian Molin

Beilstein J. Nanotechnol. 2024, 15, 57–70, doi:10.3762/bjnano.15.6

• , the results indicate that microporosity, and thus the electroactive surface area of the electrode, increases with a higher content of cCB in the hydrogel-MCO film. A slightly different trend can be observed for the charge transfer resistance Rct at the solution–film interface. The highest Rct is

A novel approach to pulsed laser deposition of platinum catalyst on carbon particles for use in polymer electrolyte membrane fuel cells

• Bogusław Budner,
• Wojciech Tokarz,
• Sławomir Dyjak,
• Andrzej Czerwiński,
• Bartosz Bartosewicz and
• Bartłomiej Jankiewicz

Beilstein J. Nanotechnol. 2023, 14, 190–204, doi:10.3762/bjnano.14.19

• for Vulcan XC-72R, while the total pore volume is 1.22 cm3/g for C-11 and 0.68 cm3/g for Vulcan XC-72R. Based on the above, Vulcan has a small fraction of micropores, although more significant than C-11, and a less developed mesoporosity than C-11. C-11 has depleted microporosity but more developed

• black materials [40]. It is important to note that the higher SBET value for Vulcan XC-72R is solely due to its enhanced microporosity, yet its mesoporosity is significantly less developed compared to C-11. Therefore, the C-11 material is a better choice for deposition using the PLD method, because Pt

• will not enter the micropores but will be deposited in the meso- and macropores. Also, in a working fuel cell, extensive mesoporosity of a catalyst layer is more desired than microporosity since micropores remain mainly inaccessible to an ionomer and a catalyst. Deposition of platinum on a carbon

Recent advances in nanoarchitectures of monocrystalline coordination polymers through confined assembly

• Lingling Xia,
• Qinyue Wang and
• Ming Hu

Beilstein J. Nanotechnol. 2022, 13, 763–777, doi:10.3762/bjnano.13.67

• selectively removed, for instance, by using appropriate solvents, forming porous textures in the monocrystalline coordination polymers. This feature can solve the intrinsic problem of microporosity in coordination polymers. The micropores of the coordination polymers offer ultrahigh specific surface areas

Tubular glassy carbon microneedles with fullerene-like tips for biomedical applications

• Sharali Malik and
• George E. Kostakis

Beilstein J. Nanotechnol. 2022, 13, 455–461, doi:10.3762/bjnano.13.38

• different allotropes depending on the hybridizations of the C–C bond, that is, sp, sp2, or sp3. Furthermore, a variety of short-range ordering effects can interact with each other and this, along with the effects of microporosity, grain boundaries, and defects, render this a fascinating material. Following

Gas sorption porosimetry for the evaluation of hard carbons as anodes for Li- and Na-ion batteries

• Yuko Matsukawa,
• Fabian Linsenmann,
• Maximilian A. Plass,
• George Hasegawa,
• Katsuro Hayashi and
• Tim-Patrick Fellinger

Beilstein J. Nanotechnol. 2020, 11, 1217–1229, doi:10.3762/bjnano.11.106

• capacity. The most common method to determine SSAs and nanoporosity in the battery community are nitrogen (N2) sorption porosimetry, as well as krypton (Kr) sorption porosimetry in case of very low surface areas. A precise quantification of microporosity (pore diameters smaller than 2 nm), however, cannot

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

• Berlin für Materialien und Energie, Hahn-Meitner-Platz 1, 14109 Berlin, Germany, Center for Materials Research (LaMa), Justus-Liebig-University, Heinrich-Buff-Ring 16, 35392 Giessen, Germany 10.3762/bjnano.11.54 Keywords: adsorption; carbon materials; mesoporosity; microporosity; microstructure; pore

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 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

• can markedly affect the nanoscale porosity [13][14][15][16][17][18][19][20][21]. Hence, a combined in-depth elucidation of meso/microporosity and the graphene-based structure upon heat treatment is pursued in this study to obtain a profound understanding of the relationship between the changes in the

• ” arrangement. These graphene stacks represent the basic structural unit (BSU) of non-graphitic carbon materials and exhibit a low packing density [21][22][23][24]. The microporosity (pores below 2 nm) results from imperfections in the packing of the graphene stacks and should thus be dependent on the degree of

Synthesis of amorphous and graphitized porous nitrogen-doped carbon spheres as oxygen reduction reaction catalysts

• Maximilian Wassner,
• Markus Eckardt,
• Andreas Reyer,
• Thomas Diemant,
• Michael S. Elsaesser,
• R. Jürgen Behm and
• Nicola Hüsing

Beilstein J. Nanotechnol. 2020, 11, 1–15, doi:10.3762/bjnano.11.1

• temperatures. The overall nitrogen content of the graphitized N-doped carbon spheres is lower than that of the amorphous carbon spheres, however, also the microporosity decreases strongly with graphitization. Comparison with the electrocatalytic behavior in the ORR shows that in addition to the N-doping, the

• microporosity of the materials is critical for an efficient ORR. Keywords: amorphous carbon; graphitized carbon; hydrothermal carbonization; nitridation; nitrogen doping; oxygen reduction reaction (ORR); porosity; Introduction Fuel cells and metal–air batteries are important renewable energy technologies

• counterparts regarding porosity and surface areas. With the onset of graphitization, however, the g-NCS-850 and g-NCS-1000 samples develop a distinct mesoporosity (type-IV isotherms and a H2 hysteresis loop, Figure 7), concomitant with a loss of microporosity of about 66%. The formation of mesopores can be

Synthesis of highly active ETS-10-based titanosilicate for heterogeneously catalyzed transesterification of triglycerides

• Muhammad A. Zaheer,
• David Poppitz,
• Khavar Feyzullayeva,
• Marianne Wenzel,
• Jörg Matysik,
• Radomir Ljupkovic,
• Aleksandra Zarubica,
• Alexander A. Karavaev,
• Andreas Pöppl,
• Roger Gläser and
• Muslim Dvoyashkin

Beilstein J. Nanotechnol. 2019, 10, 2039–2061, doi:10.3762/bjnano.10.200

• titanosilicate surface with the quadrupole momentum of N2 for P-ETS-10/60 and C-P-ETS-10/60. In such a case, the precise analysis of the microporosity by N2 is difficult and the use of Ar instead is recommended [26][40]. The calcination of P-ETS-10/60 has led to a visible decrease of the adsorbed volume in 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

Processing nanoporous organic polymers in liquid amines

• Jeehye Byun,
• Damien Thirion and
• Cafer T. Yavuz

Beilstein J. Nanotechnol. 2019, 10, 1844–1850, doi:10.3762/bjnano.10.179

• organic frameworks [6], conjugated microporous polymers [7], covalent triazine frameworks [8], porous aromatic frameworks [9], porous polymer networks [10], and polymers of intrinsic microporosity [11]. We have been working on nanoporous covalent organic polymers (COP), focusing on structural durability

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

• ) exhibits type I isotherm, reflecting the microporosity of the MOF. DUT-98(3) and (4) show type I behavior at lower relative pressures and type IV behavior at higher relative pressures, reflecting the microporous nature of the MOF and additional interparticle mesoporosity, respectively. This assumption is

• again at around a relative pressure of 0.5, however the uptake is found to be almost three times higher compared to DUT-98(2). DUT-98(4) exhibits the same steep increase but a wide hysteresis at higher pressure, indicating the dominant contribution of interparticle mesoporosity over the microporosity of

Photoactive nanoarchitectures based on clays incorporating TiO₂ and ZnO nanoparticles

• Eduardo Ruiz-Hitzky,
• Pilar Aranda,
• Marwa Akkari,
• Nithima Khaorapapong and
• Makoto Ogawa

Beilstein J. Nanotechnol. 2019, 10, 1140–1156, doi:10.3762/bjnano.10.114

• sepiolite, are characterized by a large specific surface area and microporosity, as well as the presence of external silanol groups, which can immobilize species including NPs of diverse nature [11][72]. Halloysite (Figure 1D) is a layered aluminosilicate with a silica/alumina composition similar to that of

Glucose-derived carbon materials with tailored properties as electrocatalysts for the oxygen reduction reaction

• Rafael Gomes Morais,
• Natalia Rey-Raap,
• José Luís Figueiredo and
• Manuel Fernando Ribeiro Pereira

Beilstein J. Nanotechnol. 2019, 10, 1089–1102, doi:10.3762/bjnano.10.109

• were applied to modify the textural properties, while nitrogen functionalities were incorporated via different N-doping methodologies (ball milling and conventional methods) using melamine. A direct relationship between the microporosity of the activated carbons and the limiting current density was

• found, with the increase of microporosity leading to interesting improvements of the limiting current density. Regardless of the doping method used, similar amounts of nitrogen were incorporated into the carbon structures. However, significant differences were observed in the nitrogen functionalities

• an increase in the number of electrons. Accordingly, the electrocatalyst with the highest performance was obtained from the activated sample doped with nitrogen by the conventional method, which combined the most appropriate textural and chemical properties: high microporosity and adequate proportion

On the transformation of “zincone”-like into porous ZnO thin films from sub-saturated plasma enhanced atomic layer deposition

• Alberto Perrotta,
• Julian Pilz,
• Stefan Pachmajer,
• Antonella Milella and
• Anna Maria Coclite

Beilstein J. Nanotechnol. 2019, 10, 746–759, doi:10.3762/bjnano.10.74

• refractive index at 60% and 80% relatice humidity, no or limited hysteresis was witnessed. Under these conditions, the pores are generally on the edge between microporosity and mesoporosity, that is, of the order of 1–3 nm in pore diameter. The amount of porosity measured in the layers is reported in Figure

New micro/mesoporous nanocomposite material from low-cost sources for the efficient removal of aromatic and pathogenic pollutants from water

• Emmanuel I. Unuabonah,
• Robert Nöske,
• Jens Weber,
• Christina Günter and
• Andreas Taubert

Beilstein J. Nanotechnol. 2019, 10, 119–131, doi:10.3762/bjnano.10.11

• observed at low relative pressure (p/p0), which is indicative of some microporosity. A monotonic increase in the adsorbed gas amount is observed at intermediate relative pressures, followed by a steeper volume increase at high relative pressures. The increase can be related to the condensation of N2 in the

Cyclodextrin-assisted synthesis of tailored mesoporous silica nanoparticles

• Fuat Topuz and
• Tamer Uyar

Beilstein J. Nanotechnol. 2018, 9, 693–703, doi:10.3762/bjnano.9.64

• molecules prior to silica condensation led to pores in the silica particles without the requirement of any surfactant [20]. CD assemblies lead to microporosity in the particles so that only very small molecules can pass through the pores. This inevitably induces selectivity for the molecules to be

Structural properties and thermal stability of cobalt- and chromium-doped α-MnO₂ nanorods

• Romana Cerc Korošec,
• Polona Umek,
• Alexandre Gloter,
• Jana Padežnik Gomilšek and
• Peter Bukovec

Beilstein J. Nanotechnol. 2017, 8, 1032–1042, doi:10.3762/bjnano.8.104

• octahedrons, leading to an average oxidation state of 3.9, which is common for 2 × 2 tunnel structures [6][7]. The numerous studies are based on the fact that this low-cost and environmentally friendly material possesses some excellent properties: conductivity, microporosity, and catalytic activity [1]. It

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

• without assembly of ZnO NP but submitted to a similar thermal treatment. The silica-clay (SiO2-CLO) heterostructure is a porous material the isotherm of which exhibits a comparable trend with a greater adsorption capacity but also shows the presence of microporosity. This microporosity in the ZnO/SiO2-CLO

• heterostructure is probably blocked by the ZnO NP. In the case of the ZnO/SiO2-clay heterostructure derived from TSM smectite, the isotherm type is also quite similar to that of the ZnO/SiO2-CLO heterostructure with scarce microporosity. Clearly, the related SiO2-TSM heterostructure exhibits a slightly different

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

• ·g−1. The micropores (pores smaller than 2 nm) contribute 0.13 cm3·g−1 to this volume. The microporosity of carbonaceous materials can be determined more appropriately by carbon dioxide physisorption. From carbon dioxide physisorption measurements (see Figure S3 in Supporting Information File 1 for

Cantilever bending based on humidity-actuated mesoporous silica/silicon bilayers

• Christian Ganser,
• Gerhard Fritz-Popovski,
• Roland Morak,
• Parvin Sharifi,
• Benedetta Marmiroli,
• Barbara Sartori,
• Heinz Amenitsch,
• Thomas Griesser,
• Christian Teichert and
• Oskar Paris

Beilstein J. Nanotechnol. 2016, 7, 637–644, doi:10.3762/bjnano.7.56

• discrepancy can be resolved when considering that the pore volume fraction obtained from GISAXS (Table 1) does not include any micropores (i.e., pores smaller than 2 nm) within the walls of the mesopores. It is well known that wall microporosity plays an important role in mesoporous silica prepared from P123

Selective porous gates made from colloidal silica nanoparticles

• Roberto Nisticò,
• Paola Avetta,
• Paola Calza,
• Debora Fabbri,
• Giuliana Magnacca and
• Dominique Scalarone

Beilstein J. Nanotechnol. 2015, 6, 2105–2112, doi:10.3762/bjnano.6.215

• distribution curve (Figure 3B) indicates a complex pore size distribution. In detail, pores present a bimodal distribution, with the presence of meso/macroporosity in the range 15–200 nm, probably due to interparticle voids (i.e., depth-filter porosity), together with a certain degree of microporosity in the

Nanoporous composites prepared by a combination of SBA-15 with Mg–Al mixed oxides. Water vapor sorption properties

• Amaury Pérez-Verdejo,
• Alvaro Sampieri,
• Heriberto Pfeiffer,
• Mayra Ruiz-Reyes,
• Juana-Deisy Santamaría and
• Geolar Fetter

Beilstein J. Nanotechnol. 2014, 5, 1226–1234, doi:10.3762/bjnano.5.136

• porous composite, which displays a cauliflower morphology. This is an important microporosity contribution and micro and mesoporous surfaces coexist in almost the same proportion. Furthermore, the nanostructured mesoporous composites present an extraordinary water vapor sorption capacity. Such composites

• increases from 5.3 to 7.0 nm [HT/SBA(NC)] or 6.2 nm [HT/SBA(C)]. In HT/SBA composites, both microporous and mesoporous coexistence follows a similar trend to the SBA-15, with a predominant mesoporous surface. The diminution of microporosity from 74 m2/g in SBA-15 to 37 m2/g (or 31 m2/g) may be due to the

• wall thickness (AWT) are smaller than those of SBA-15. Even though both materials are texturally different, as they were prepared by distinct methods, it is interesting to observe how the microporosity and mesoporosity are exalted in the in situ prepared composite. This remark is in agreement with the