Flexible Linker-Based Triazine-Functionalized 2D Covalent Organic Frameworks for Supercapacitor and Gas Sorption Applications.

Covalent organic frameworks (COFs) having a large surface area, porosity, and substantial amounts of heteroatom content are recognized as the ideal class of materials for energy storage and gas sorption applications. In this work, we have synthesized four different porous COF materials by the polycondensation of a heteroatom-rich flexible triazine-based trialdehyde linker, namely 2,4,6-tris(4-formylphenoxy)-1,3,5-triazine (TPT-CHO), with four different triamine linkers. Triamine linkers were chosen based on differences in size, symmetry, planarity, and heteroatom content, leading to the synthesis of four different COF materials named IITR-COF-1, IITR-COF-2, IITR-COF-3, and IITR-COF-4.

A sustainable management of polycyclic aromatic hydrocarbons to synthesize microporous organic polymers for adsorptive desulphurization of fuels.

A sustainable management of carcinogenic polycyclic aromatic hydrocarbons (PAHs) to synthesize a series of high surface area (SA of 563-1553 m g) microporous polymeric adsorbents is reported. The products with high yield (>90%) were obtained within only 30 min at a low temperature of 50 °C using a microwave-assisted approach with 400 W microwave power followed by 30 min of ageing by raising the temperature to 80 °C. The synthesized adsorbents are used for removing another category of carcinogenic pollutants i.

Machine learning implemented exploration of the adsorption mechanism of carbon dioxide onto porous carbons.

Adsorption of CO on porous carbons has been identified as one of the promising methods for carbon capture, which is essential for meeting the sustainable developmental goal (SDG) with respect to climate action, i.e., SDG 13.

Photo- and Electrocatalytic Reduction of CO over Metal-Organic Frameworks and Their Derived Oxides: A Correlation of the Reaction Mechanism with the Electronic Structure.

A Ce/Ti-based bimetallic 2-aminoterephthalate metal-organic framework (MOF) was synthesized and evaluated for photocatalytic reduction of CO in comparison with an isoreticular pristine monometallic Ce-terephthalate MOF. Owing to highly selective CO adsorption capability, optimized band gaps, higher flux of photogenerated electron-hole pairs, and a lower rate of recombination, this material exhibited better photocatalytic reduction of CO and lower hydrogen evolution compared to Ce-terephthalate. Thorough probing of the surface and electronic structure inferred that the reducibility of Ce to Ce was due to the introduction of an amine functional group into the linker, and low-lying Ti(3) orbitals in Ce/Ti-2-aminoterephthalate facilitated the photoreduction reaction.

Tuning the morphology of CeO nanostructures using a template-free solvothermal process and their oxygen reduction reaction activity.

In fuel cells, the oxygen reduction reaction (ORR) at the cathode plays a crucial role in their performance. High cost, low abundance, catalyst poisoning, and poor durability of the pioneering ORR catalyst Pt make it less desirable for commercial fuel cells. Herein, we demonstrate a greener process to synthesize CeO2 nanostructures by varying reaction parameters in a single-step solvothermal route and provide a detailed mechanism for the formation of CeO2 nanostructures with different shapes.

Plant-based nanocellulose: A review of routine and recent preparation methods with current progress in its applications as rheology modifier and 3D bioprinting.

"Nanocellulose" have captivated the topical sphere of sturdily escalating market for sustainable materials. The review focuses on the comprehensive understanding of the distinct surface chemistry and functionalities pertaining to the renovation of macro-cellulose at nanodimensional scale to provide an intuition of their processing-structure-function prospective. The abundant availability, cost effectiveness and diverse properties associated with plant-based resources have great economical perspective for developing sustainable cellulose nanomaterials.

Correction: Citrate combustion synthesized Al-doped CaCuTiO quadruple perovskite: synthesis, characterization and multifunctional properties.

Correction for 'Citrate combustion synthesized Al-doped CaCu3Ti4O12 quadruple perovskite: synthesis, characterization and multifunctional properties' by Kamalesh Pal et al., Phys. Chem.

Citrate combustion synthesized Al-doped CaCuTiO quadruple perovskite: synthesis, characterization and multifunctional properties.

The facile synthesis of the Al-doped CaCuTiO quadruple perovskite, a well-known and vastly studied material for various technological applications, using the modified citrate combustion route along with structural, microstructural, and X-ray photoelectron spectroscopic (XPS) characterization and magnetic, dielectric and electrical properties has been investigated and reported here. The possible applications of the material as a Schottky barrier diode (SBD) in optoelectronic devices and as a catalyst in methanol steam reforming (MSR) reaction for hydrogen generation, hitherto unreported in the open literature, have also been explored. The compound is crystallized in the cubic body centered Im3[combining macron] space group and the particle size is found to be in nanodimension with rather narrow size distribution.

Enhancing photocatalytic degradation of quinoline by ZnO:TiO mixed oxide: Optimization of operating parameters and mechanistic study.

This study focuses on the photocatalytic degradation of quinoline, a recalcitrant heterocyclic nitrogenous aromatic organic compound, using the mixed oxide ZnO-TiO photo-catalyst. Photo-catalysts were synthesized by the solid-state reaction method at different calcination temperatures of 400 °C, 600 °C, and 800 °C. Different analytical methods, including Field emission scanning electron microscope, Brunauer-Emmett-Teller surface area, X-ray diffraction, UV-vis diffuse reflectance spectroscopy, Fourier-transform infrared spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy analysis were used for the catalyst characterization.

A multifunctional triazine-based nanoporous polymer as a versatile organocatalyst for CO utilization and C-C bond formation.

A triazine-based nanoporous multifunctional polymer with a SABET of 304 m2 g-1 has shown versatile catalytic activity in the conversion of CO2 to cyclic carbonates at 4 bar with almost 100% yield and selectivity, and in the conversion of CO2 to methanol and methane electrochemically. Additionally, it also catalyzes C-C bond formation via the Knoevenagel reaction.

Nitrogen Amelioration-Driven Carbon Dioxide Capture by Nanoporous Polytriazine.

Nitrogen-enriched nanoporous polytriazines (NENPs) have been synthesized by ultrafast microwave-assisted condensation of melamine and cyanuric chloride. The experimental conditions have been optimized to tune the textural properties by synthesizing materials at different times, temperatures, microwave powers, and solvent contents. The maximum specific surface area (SA) of 840 m g was estimated in the sample (NENP-1) synthesized at 140 °C with a microwave power of 400 W and reaction time of 30 min.

Cyclophosphazene-Based Hybrid Nanoporous Materials as Superior Metal-Free Adsorbents for Gas Sorption Applications.

Cyclophosphazene-based inorganic-organic hybrid nanoporous materials (CHNMs) have been synthesized by a facile solvothermal method. The condensation of pyrrole with the reaction product of phosphonitrilic chloride trimer and 4-hydroxybenzaldehyde resulted in the formation of high-surface-area CHNMs. The maximum specific surface area (SA) of 1328 m g with hierarchical pore structures having micropores centered at 1.

Mixed titanium, silicon, and aluminum oxide nanostructures as novel adsorbent for removal of rhodamine 6G and methylene blue as cationic dyes from aqueous solution.

Mixed oxide nanoparticles containing Ti, Si, and Al of 8-15 nm size range were synthesized using a combined sol-gel - hydrothermal method. Effects of composition on the structure, morphology, and optical properties of the nanoparticles were studied using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), microRaman spectroscopy, and diffuse reflectance spectroscopy (DRS). Dye removal abilities of the nanoparticles from aqueous solutions were tested for different cationic dyes.

Iron phthalocyanine modified mesoporous titania nanoparticles for photocatalytic activity and CO2 capture applications.

An iron(II)phthalocyanine (Fepc) modified mesoporous titania (Fepc-TiO2) nanocatalyst with a specific surface area of 215 m(2) g(-1) has been synthesized by a hydrothermal method. Fepc-TiO2 degrades one of the highly toxic chemical warfare agents, sulfur mustard (SM), photocatalytically under sunlight with an exposure time of as low as 70 min. Furthermore, the mesoporous Fepc-TiO2 also captured 2.

ZnO-modified cellulose fiber sheets for antibody immobilization.

Cellulose fiber sheets impregnated with saccharide capped-ZnO nanoparticles were used as bioactive materials for antibody immobilization. First, ZnO nanoparticles were synthesized in the presence of glucose (monosaccharide), sucrose (disaccharide) as well as alginic acid and starch (polysaccharides). The pine cellulose fibers were then modified by the obtained saccharide capped nanoparticles and further incorporated into the sheets.

Porous covalent electron-rich organonitridic frameworks as highly selective sorbents for methane and carbon dioxide.

Carbon dioxide capture from point sources like coal-fired power plants is considered to be a solution for stabilizing the CO(2) level in the atmosphere to avoid global warming. Methane is an important energy source that is often highly diluted by nitrogen in natural gas. For the separation of CO(2) and CH(4) from N(2) in flue gas and natural gas, respectively, sorbents with high and reversible gas uptake, high gas selectivity, good chemical and thermal stability, and low cost are desired.

Synthesis of coesite nanocrystals from ethane bridged periodic mesoporous organosilica at low temperature and extreme pressure.

Coesite nanocrystals have been synthesized from periodic mesoporous organosilica (PMO) with (CH(2))(2) bridges heated at 300 °C for 150 min and 12 GPa. The crystals are not sintered, single crystalline, and have diameters of ca. 100-300 nm.

Catalyst-free synthesis of transparent, mesoporous diamond monoliths from periodic mesoporous carbon CMK-8.

We report on the synthesis of optically transparent, mesoporous, monolithic diamond from periodic mesoporous carbon CMK-8 at a pressure of 21 GPa. The phase transformation is already complete at a mild synthesis temperature of 1,300 degrees C without the need of a catalyst. Surprisingly, the diamond is obtained as a mesoporous material despite the extreme pressure.

Discoid Bicelles as Efficient Templates for Pillared Lamellar Periodic Mesoporous Silicas at pH 7 and Ultrafast Reaction Times.

We report the first synthesis of periodic mesoporous silicas templated by bicelles. The obtained materials form novel pillared lamellar structures with a high degree of periodic order, narrow pore size distributions, and exceptionally high surface areas.

Ultrafast sonochemical synthesis of methane and ethane bridged periodic mesoporous organosilicas.

Periodic mesoporous organosilicas (PMOs) with methane and ethane bridging groups were synthesized by the condensation of bis(triethoxysilyl)methane and bis(triethoxysilyl)ethane, respectively, in an ultrafast sonochemical method with a short reaction time of 30 min using a cationic template (1-hexadecyl)trimethylammonium bromide (HTABr). Subsequently, the template HTABr was extracted by another 30 min of sonication in an acetone/HCl mixture. The whole experimental process for the synthesis and extraction of the PMOs took about 1 h, which is much shorter than any other reported methods.

Synthesis of periodic mesoporous coesite.

Periodic mesoporous coesite was obtained by a modified nanocasting process from a periodic mesoporous silica SBA-16/C composite at a pressure of 12 GPa and 350 degrees C.

Synthesis of stishovite nanocrystals from periodic mesoporous silica.

Faceted stishovite nanocrystals with sizes of 200-400 nm were synthesized at a pressure of 12 GPa and a temperature of 400 degrees C in a multianvil apparatus using mesoporous silica SBA-16 as the precursor.

Simple systematic synthesis of periodic mesoporous organosilica nanoparticles with adjustable aspect ratios.

One-dimensional periodic mesoporous organosilica (PMO) nanoparticles with tunable aspect ratios are obtained from a chain-type molecular precursor octaethoxy-1,3,5-trisilapentane. The aspect ratio can be tuned from 2:1 to >20:1 simply by variation in the precursor concentration in acidic aqueous solutions containing constant amounts of triblock copolymer Pluronic P123. The mesochannels are highly ordered and are oriented parallel to the longitudinal axis of the PMO particles.