An in situ doping strategy has been developed for the generation of a novel family of hexaazatriphenylene-based conjugated triazine frameworks (CTFs) for efficient CO2 capture. The resulting task-specific materials exhibit an exceptionally high CO2 uptake capacity (up to 4.8 mmol g(-1) at 297 K and 1 bar). The synergistic effects of ultrananoporosity and rich N/O codoped CO2-philic sites bestow the framework with the highest CO2 adsorption capacity among known porous organic polymers (POPs). This innovative approach not only enables superior CO2 separation performance but also provides tunable control of surface features on POPs, thereby affording control over bulk material properties. We anticipate this novel strategy will facilitate new possibilities for the rational design and synthesis of nanoporous materials for carbon capture.
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http://dx.doi.org/10.1021/jacs.6b07644 | DOI Listing |
Langmuir
January 2025
Federal University of Itajubá, Itajubá-MG 37500-903, Brazil.
CuO/CeO and CuO/CeO-LaO catalysts, synthesized with varying CeO and LaO molar ratios (1:1, 1:2, and 2:1), were prepared via the hydrothermal method and tested in the water-gas shift reaction (150-350 °C). LaO addition altered structural properties, reducing surface area and copper dispersion. XANES and in situ XRD confirmed metallic Cu species during reduction and reaction.
View Article and Find Full Text PDFDalton Trans
January 2025
Department of Chemistry, Capital Normal University, Beijing, 100048, P. R. China.
An OER catalyst showing both high activity and stability in promoting oxygen evolution is important for its practical application in electrochemical water-splitting. Here, we report the screening of such a catalyst by optimizing the Ni(II)-doping in Co(III)-based layered double hydroxides (LDHs). Such LDH samples tailored with Ni(II)-doping are prepared by an oxidative intercalation reaction where brucite-like Ni(II)Co(II)(OH) (0 ≤ ≤ 0.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Institute of Materials Research and Engineering, Agency for Science Technology and Research, 2 Fusionopolis Way, 08-03 Innovis, Singapore 138634, Singapore.
Thermoelectric properties of conducting polymers typically suffer from molecular chain disordering, as charge transport is predominantly controlled by morphology. This is especially more problematic when counterions are introduced to tune the carrier concentration for optimal thermoelectric performance, which disturbs the morphology further. In this work, we introduce a new avenue for enhancing thermoelectric properties without needing to regulate the morphology, namely, by controlling the coulombic interaction between polarons and counterions.
View Article and Find Full Text PDFTalanta
January 2025
School of Material Science and Engineering, Shanghai University of Engineering Science, Shanghai, 201620, PR China. Electronic address:
Flexible sweat sensors play a crucial role in health monitoring and disease prevention by enabling real-time, non-invasive assessment of human physiological conditions. Sweat contains a variety of biomarkers, offering valuable insights into an individual's health status. In this study, we developed an advanced flexible electrochemical sensor featuring reduced graphene oxide (rGO)-based electrodes, modified with a composite material comprising nitrogen and sulfur co-doped holey graphene (HG) and MXene, with in-situ-grown TiO nanoparticles on the MXene.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Research Institute of Industrial Catalysis, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, PR China.
Catalytic elimination through an oxidative decomposition pathway is the most promising candidate for the purification of chlorinated volatile organic compound (CVOC) pollutants, but the complicated mechanisms and the formation pathways of hydrogenated byproducts still need to be clearly revealed. Herein, W/ZrO, as a structure-tunable catalyst, is used to catalytically oxidize dichloromethane (DCM) and clarify the formation pathway of monochloromethane (MCM). Crystal engineering of ZrO tailors surface WO species; practically, the predominant Zr-WO clusters and crystalline WO can be obtained on monoclinic (m-ZrO) and tetragonal (t-ZrO) phases.
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