Ag+ doped into azo-linked conjugated microporous polymer for volatile iodine capture and detection of heavy metal ions.
Ontology highlight
ABSTRACT:
SUBMITTER: Liu M
PROVIDER: S-EPMC6145922 | biostudies-literature |
REPOSITORIES: biostudies-literature
Similar Datasets
Project description:In recent decade, conjugated microporous polymers (CMPs) were treated as one of the superior porous materials for CO2 uptake. Herein, we prepared two azo-linked CMPs namely: azo-carbazole (Azo-Cz) and azo-phenothiazine (Azo-Tz) from the reduction of the corresponding nitro monomers using sodium borohydride (NaBH4). The obtained polymers were well characterized using many spectroscopic techniques. According to TGA and BET analyses, our CMPs owned good specific surface areas (reaching 315 m2 g–1), and a significant thermal stability. It is also possessed pore sizes of 0.79 and 1.18 nm, respectively, and a reasonable char yields (max. 46 %). Based on CO2 uptake measurements, the CO2 adsorption capacities of these CMPs were very good: up to 40 and 94 mg g–1 at the experiment temperatures 298 and 273 K, respectively. The great CO2 uptake is due to high surface areas that facilitate powerful interactions with CO2 molecules. Supplementary information The online version contains supplementary material available at 10.1007/s10965-021-02803-8.
| S-EPMC8540882 | biostudies-literature
Project description:Na-ion batteries (NIBs) have attracted considerable attention in recent years owing to the high abundance and low cost of Na. It is well known that S doping can improve the electrochemical performance of carbon materials for NIBs. However, the current methods for S doping in carbons normally involve toxic precursors or rigorous conditions. In this work, we report a creative and facile strategy for preparing S-doped porous carbons (SCs) via the pyrolysis of conjugated microporous polymers (CMPs). Briefly, thiophene-based CMPs served as the precursors and doping sources simultaneously. Simple direct carbonization of CMPs produced S-doped carbon materials with highly porous structures. When used as an anode for NIBs, the SCs exhibited a high reversible capacity of 440 mAh g-1 at 50 mA g-1 after 100 cycles, superior rate capability, and excellent cycling stability (297 mAh g-1 after 1000 cycles at 500 mA g-1), outperforming most S-doped carbon materials reported thus far. The excellent performance of the SCs is attributed to the expanded lattice distance after S doping. Furthermore, we employed ex situ X-ray photoelectron spectroscopy to investigate the electrochemical reaction mechanism of the SCs during sodiation-desodiation, which can highlight the role of doped S for Na-ion storage.
| S-EPMC7770694 | biostudies-literature
Project description:A metal-free synthetic protocol for azo compound formation by the direct oxidation of hydrazine HN-NH bonds to azo group functionality catalyzed by molecular iodine is disclosed. The strengths of this reactivity include rapid reaction times, low catalyst loadings, use of ambient dioxygen as a stoichiometric oxidant, and ease of experimental set-up and azo product isolation. Mechanistic studies and density functional theory computations offering insight into this reactivity, as well as the events leading to azo group formation are presented. Collectively, this study expands the potential of main-group element iodine as an inexpensive catalyst, while delivering a useful transformation for forming azo compounds.
| S-EPMC8695051 | biostudies-literature
Project description:Conjugated microporous polymers (CMPs) are a unique class of materials that combine extended ?-conjugation with a permanently microporous skeleton. Since their discovery in 2007, CMPs have become established as an important subclass of porous materials. A wide range of synthetic building blocks and network-forming reactions offers an enormous variety of CMPs with different properties and structures. This has allowed CMPs to be developed for gas adsorption and separations, chemical adsorption and encapsulation, heterogeneous catalysis, photoredox catalysis, light emittance, sensing, energy storage, biological applications, and solar fuels production. Here we review the progress of CMP research since its beginnings and offer an outlook for where these materials might be headed in the future. We also compare the prospect for CMPs against the growing range of conjugated crystalline covalent organic frameworks (COFs).
| S-EPMC7145355 | biostudies-literature
Project description:Lignosulfonate/polyaniline (LS/PANI) nanocomposite adsorbent materials were prepared by the chemical polymerization of lignosulfonate with an aniline monomer as a dopant and structure-directing agent, and the adsorption behavior of dyes as well as heavy metal ions was investigated. LS/PANI composites were used as dye adsorbents for the removal of different cationic dyes (malachite green, methylene blue, and crystal violet). The adsorption behavior of LS/PANI composites as dye adsorbents for malachite green was investigated by examining the effects of the adsorbent dosage, solution pH, initial concentration of dye, adsorption time, and temperature on the adsorption properties of this dye. The following conclusions were obtained. The optimum adsorption conditions for the removal of malachite green dye when LS/PANI composites were used as malachite green dye adsorbents were as follows: an adsorbent dosage of 20 mg, an initial concentration of the dye of 250 mg/L, an adsorption time of 300 min, and a temperature of 358 K. The LS/PANI composite adsorbed malachite green dye in accordance with the Langmuir adsorption model and pseudo-second-order kinetic model, which belongs to chemisorption-based monomolecular adsorption, and the equilibrium adsorption amount was 245.75 mg/g. In particular, the adsorption of heavy metal ion Pb2+ was investigated, and the removal performance was also favorable for Pb2+.
| S-EPMC10779345 | biostudies-literature
Project description:Benefiting from the additional active sites for sodium-ion (Na+) adsorption and porous architecture for electrolyte accessibility, nitrogen-doped porous carbon has been considered the alternative anode material for Na+-storage applications. In this study, nitrogen-doped and zinc-confined microporous carbon (N,Z-MPC) powders are successfully prepared by thermally pyrolyzing the polyhedral ZIF-8 nanoparticles under an argon atmosphere. Following the electrochemical measurements, the N,Z-MPC not only delivers good reversible capacity (423 mAh/g at 0.02 A/g) and comparable rate capability (104 mAh/g at 1.0 A/g) but also achieves a remarkable cyclability (capacity retention: 96.6% after 3000 cycles at 1.0 A/g). Those can be attributed to its intrinsic characteristics: (a) 67% of the disordered structure, (b) 0.38 nm of interplanar distance, (c) a great proportion of sp2-type carbon, (d) abundant microporosity, (e) 16.1% of nitrogen doping, and (f) existence of sodiophilic Zn species, synergistically enhancing the electrochemical performances. Accordingly, the findings observed here support the N,Z-MPC to be a potential anode material enabling exceptional Na+-storage abilities.
| S-EPMC10218166 | biostudies-literature
Project description:Understanding the interactions among dopant species and the role of the host lattice is of fundamental importance for the chemical formulation of optically active glasses. Here, we consider the archetypal dopant pair of Ag-Ce in complex fluorophosphate (PF) and sulfophosphate (PS) matrices, in which variable bonding environments and ligand selectivity exert distinct effects on dopant properties. The addition of Ag+ to PF glasses blue-shifts the ultraviolet (UV) cutoff wavelength of Ce3+ and enhances its photoluminescence (PL) intensity. In PS matrices, the exact opposite effect is observed: red-shifting the UV cutoff and lowering the PL intensity. No Ag-Ag pairs or cluster species were found in either matrix material; however, in PS, such clustering could be triggered by secondary broad-band UV-visible irradiation. The optical properties of Ag-Ce-codoped glasses are a result of the ionocovalent character of the Ag+-O-Ce3+ bond, the cross-relaxation process between Ag+ and Ce3+, and the redox ratio of Ce3+/Ce4+. In the PF glasses, the enhancement of the Ce3+ PL intensity is due to energy transfer from Ag+ to Ce3+ and a redox shift from Ce4+ to Ce3+. The more covalent Ag+-O-Ce3+ interactions in the PS series decrease the Ce3+/Ce4+ ratio. Moreover, photoinduced Ag clustering is facilitated in the more covalent environment, which indicates that glasses commonly used for Ag nanoparticle formation, such as silicate glasses, also possess more covalent Ag+-O bonding.
| S-EPMC8582266 | biostudies-literature
Project description:The synthesis of three conjugated copolymers TPP1-3 was carried out using a palladium-catalyzed [3+2] cycloaddition polymerization of 1,6-dibromopyrene with various dialkynyl thiophene derivatives 3a-c. The target copolymers were obtained in excellent yields and high purity, as confirmed by instrumental analyses. TPP1-3 were found to divulge a conspicuous iodine adsorption capacity up to 3900 mg g-1, whereas the adsorption mechanism studies revealed a pseudo-second-order kinetic model. Furthermore, recyclability tests of TPP3, the copolymer which revealed the maximum iodine uptake, disclosed its efficient regeneration even after numerous adsorption-desorption cycles. Interestingly, the target copolymers proved promising nickel ions capture efficiencies from water with a maximum equilibrium adsorption capacity (qe) of 48.5 mg g-1.
| S-EPMC10611155 | biostudies-literature
Project description:Free-form factor optoelectronics is becoming more important for various applications. Specifically, flexible and transparent optoelectronics offers the potential to be adopted in wearable devices in displays, solar cells, or biomedical applications. However, current transparent electrodes are limited in conductivity and flexibility. This study aims to address these challenges and explore potential solutions. For the next-generation transparent conductive electrode, Al-doped zinc oxide (AZO) and silver (AZO/Ag/AZO) deposited by in-line magnetron sputtering without thermal treatment was investigated, and this transparent electrode was used as a transparent organic light-emitting diode (OLED) anode to maximize the transparency characteristics. The experiment and simulation involved adjusting the thickness of Ag and AZO and OLED structure to enhance the transmittance and device performance. The AZO/Ag/AZO with Ag of 12 nm and AZO of 32 nm thickness achieved the results of the highest figure of merit (FOM) (Φ550 = 4.65 mΩ-1) and lowest roughness. The full structure of transparent OLED (TrOLED) with AZO/Ag/AZO anode and Mg:Ag cathode reached 64.84% transmittance at 550 nm, and 300 cd/m2 at about 4 V. The results demonstrate the feasibility of adopting flexible substrates, such as PET, without the need for thermal treatment. This research provides valuable insights into the development of transparent and flexible electronic devices.
| S-EPMC10818506 | biostudies-literature
Project description:The reactions of the cyclo-As5 complex [Cp*Fe(η5 -As5 )] (B) with the AgI and CuI salts of the weakly coordinating anion (WCA) [FAl{OC6 F10 (C6 F5 )}3 ]- ([FAl]- ) are studied. These reactions allow the synthesis of the mononuclear complexes [M(η5 : η2 -B)2 ][FAl] (M=Ag (1), Cu (2)) when a ratio of B/M(FAl) 2 : 1 is used. Compound 1 shows an unusual disorder of the central AgI cation between two π-coordinating cyclo-As5 ligands, which is absent in 2 pointing to a weak interaction of the Ag center towards the cyclo-As5 ligands in B. When the ratio of B/Ag(FAl) is changed to 3 : 1 or 1 : 1, the respective coordination compounds [Ag(η2 -B)3 ][FAl] (3) and [Ag2 (η2 : η2 -B)2 ][FAl]2 (4) are accessible. The coordination modes of the cyclo-As5 units in 1, 3 and 4 are all different, reflecting the adaptive coordination behavior of B towards AgI ions. The optimized geometries in the gas phase of 1-4 are determined by DFT calculations to support the bonding situation observed in their solid-state structures.
| S-EPMC8361777 | biostudies-literature