Using solar energy to convert CO into valuable fuels or chemicals offers a powerful solution to urgent energy and environmental problems. However, the development of efficient and selective catalysts remains a considerable scientific challenge. To address this, catalytically active Co centers can be anchored into the porous matrix of metal-organic frameworks (MOFs) by utilizing a robust Zr-based MOF (Zr-DMBD) functionalized with freestanding thiol groups to enable efficient post-synthetic metal insertion. The thus-prepared Zr-DMBD-Co MOF solids are modified by well-defined Co-thiolate units and have the capability of photocatalytically converting CO into CO with high efficiency and selectivity under visible-light irradiation in a water-containing system. The turnover number and CO selectivity reach as high as 97 941 and 98 %, respectively.
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http://dx.doi.org/10.1002/cssc.201900338 | DOI Listing |
Nanoscale
January 2025
Department of Chemistry, Indian Institute of Technology Patna, Patna 801106, Bihar, India.
Covalent organic frameworks (COFs) are crystalline porous materials bearing well-ordered two- or three-dimensional molecular tectons in their polymeric skeletal framework. COFs are structurally robust as well as physiochemically stable. Currently, these are being developed for their use as "heterogeneous catalysts" for various organic transformations.
View Article and Find Full Text PDFBiosensors (Basel)
January 2025
Furong Labratory, Changsha 410083, China.
A fluorescence probe for "switch-on" detection of alkaline phosphatase (ALP) was developed based on Au nanoclusters anchored MnO nanosheets (Au NCs-MnO NSs), which were synthesized using bovine serum albumin (BSA) as template through a simple one-pot approach. In the sensing system, MnO NSs function as both energy acceptors and target identifiers, effectively quenches the fluorescence of Au NCs via fluorescence resonance energy transfer (FRET). The presence of ALP catalyzes the hydrolysis of L-ascorbic acid-2-phosphate (AAP) to ascorbic acid (AA), reducing MnO NSs to Mn and facilitate the fluorescence recovery of Au NCs.
View Article and Find Full Text PDFLangmuir
January 2025
College of Textile Science and Engineering, Jiangnan University, 1800 Lihu Road, 214122 Wuxi, P. R. China.
In the realm of zinc-air batteries, high bifunctional catalytic efficacy is intimately tied to the evaluation of catalysts. Consequently, the pursuit of proficient bifunctional catalysts that can efficiently catalyze both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) remains a paramount objective in this research area. In this study, the spiny cobalt tetroxide (CoO) encapsulated hollow carbon spheres (HCSs) are constructed by anchoring CoO onto HCS via hydrothermal or annealing treatment.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
National Energy Metal Resources and New Materials Key Laboratory, Engineering Research Center of the Ministry of Education for Advanced Battery Materials, Hunan Provincial Key Laboratory of Nonferrous Value-Added Metallurgy, School of Metallurgy and Environment, Central South University, Changsha 410083, P. R. China.
Rechargeable Zn-air batteries (RZABs) are poised for industrial application, yet they require low-cost, high-performance catalysts that efficiently facilitate both the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER). The pivotal challenge lies in designing multimetal active sites and optimizing the carbon skeleton structure to modulate catalyst activity. In this study, we introduce a novel hierarchical porous carbon-supported FeCoNi bifunctional catalyst, synthesized via a spray combustion method.
View Article and Find Full Text PDFNat Commun
January 2025
Department of Civil and Environmental Engineering, Rice University, Houston, TX, USA.
Gypsum (CaSO·2HO) plays a critical role in numerous natural and industrial processes. Nevertheless, the underlying mechanisms governing the formation of gypsum crystals on surfaces with diverse chemical properties remain poorly understood due to a lack of sufficient temporal-spatial resolution. Herein, we use in situ microscopy to investigate the real-time gypsum nucleation on self-assembled monolayers (SAMs) terminated with -CH, -hybrid (a combination of NH and COOH), -COOH, -SO, -NH, and -OH functional groups.
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