“…As depicted in Figure S17, the full-survey-scan spectra illustrate the coexistence of C, N, Cd, and I elements in Cd-MOF , and the O element is newly emerged from the survey spectrum of Cd-MOF-PO . In the high-resolution spectra of Cd 3d, the double peaks at 405.17 and 411.88 eV could be assigned to 3d 5/2 and 3d 3/2 spin-orbit splits of the Cd(II) oxidation state, respectively (Figure c) . With the attack of the oxygen atom of PO to the Cd(II) center, the large electronegativity of O (χ O = 3.44) increases the electronic cloud density around Cd(II), leading to slight shifts of binding energy from 405.17 to 405.28 eV and 411.88 to 412.05 eV .…”
Section: Resultsmentioning
confidence: 99%
“…In the high-resolution spectra of Cd 3d, the double peaks at 405.17 and 411.88 eV could be assigned to 3d 5/2 and 3d 3/2 spin-orbit splits of the Cd(II) oxidation state, respectively (Figure 4c). 67 With the attack of the oxygen atom of PO to the Cd(II) center, the large electronegativity of O (χ O = 3.44) increases the electronic cloud density around Cd(II), leading to slight shifts of binding energy from 405.17 to 405.28 eV and 411.88 to 412.05 eV. 68 Meanwhile, two deconvolution peaks are recognized at 406.63 and 413.66 eV in the Cd 3d XPS spectrum of Cd-MOF-PO.…”
Due to the inherent thermodynamic
stability and kinetic inertness
of CO2, heterogeneous catalytic conversion of CO2 to cyclic carbonates often requires harsh operating conditions,
high temperature and high pressure, and the addition of cocatalysts.
Therefore, the development of efficient heterogeneous catalysts under
cocatalyst-free and mild conditions for CO2 conversion
has always been a challenge. Herein, an infrequent tetracoordinated Cd-MOF was synthesized and used to catalyze CO2 cycloaddition reactions efficiently without the addition of any
cocatalyst, and its catalytic mechanism was systematically investigated
through a series of experiments, including fluorescence analysis,
X-ray photoelectron spectroscopy, microcalorimetry, and density functional
theory (DFT) calculation. Cd-MOF features a 3D supermolecule
structure with 1D 11.6 × 7.7 Å2 channels, and
the abundant Lewis acid/base and I– sites located
in the confined channel boost efficient CO2 conversion
with a maximum yield of 98.2% and a turnover number value of 1080.11
at 60 °C and 0.5 MPa, far surpassing most pristine MOF-based
catalytic systems. A combined experimental and DFT calculation demonstrates
that the exposed Cd(II) Lewis acid sites rapidly participate in coordination
to activate the epoxides, and the resulting large steric hindrance
facilitates leaving of the coordinated iodide ions in a reversibly
dynamic fashion convenient for the rate-determining step ring-opening
as a strong nucleophile. Such a pristine MOF catalyst with self-independent
catalytic ring-opening overcomes the complicated operation limitation
of the traditional cocatalyst-free MOF systems based on encapsulating/postmodifying
cocatalysts, providing a whole new strategy for the development of
simple, green, and efficient heterogeneous catalysts for CO2 cycloaddition.
“…As depicted in Figure S17, the full-survey-scan spectra illustrate the coexistence of C, N, Cd, and I elements in Cd-MOF , and the O element is newly emerged from the survey spectrum of Cd-MOF-PO . In the high-resolution spectra of Cd 3d, the double peaks at 405.17 and 411.88 eV could be assigned to 3d 5/2 and 3d 3/2 spin-orbit splits of the Cd(II) oxidation state, respectively (Figure c) . With the attack of the oxygen atom of PO to the Cd(II) center, the large electronegativity of O (χ O = 3.44) increases the electronic cloud density around Cd(II), leading to slight shifts of binding energy from 405.17 to 405.28 eV and 411.88 to 412.05 eV .…”
Section: Resultsmentioning
confidence: 99%
“…In the high-resolution spectra of Cd 3d, the double peaks at 405.17 and 411.88 eV could be assigned to 3d 5/2 and 3d 3/2 spin-orbit splits of the Cd(II) oxidation state, respectively (Figure 4c). 67 With the attack of the oxygen atom of PO to the Cd(II) center, the large electronegativity of O (χ O = 3.44) increases the electronic cloud density around Cd(II), leading to slight shifts of binding energy from 405.17 to 405.28 eV and 411.88 to 412.05 eV. 68 Meanwhile, two deconvolution peaks are recognized at 406.63 and 413.66 eV in the Cd 3d XPS spectrum of Cd-MOF-PO.…”
Due to the inherent thermodynamic
stability and kinetic inertness
of CO2, heterogeneous catalytic conversion of CO2 to cyclic carbonates often requires harsh operating conditions,
high temperature and high pressure, and the addition of cocatalysts.
Therefore, the development of efficient heterogeneous catalysts under
cocatalyst-free and mild conditions for CO2 conversion
has always been a challenge. Herein, an infrequent tetracoordinated Cd-MOF was synthesized and used to catalyze CO2 cycloaddition reactions efficiently without the addition of any
cocatalyst, and its catalytic mechanism was systematically investigated
through a series of experiments, including fluorescence analysis,
X-ray photoelectron spectroscopy, microcalorimetry, and density functional
theory (DFT) calculation. Cd-MOF features a 3D supermolecule
structure with 1D 11.6 × 7.7 Å2 channels, and
the abundant Lewis acid/base and I– sites located
in the confined channel boost efficient CO2 conversion
with a maximum yield of 98.2% and a turnover number value of 1080.11
at 60 °C and 0.5 MPa, far surpassing most pristine MOF-based
catalytic systems. A combined experimental and DFT calculation demonstrates
that the exposed Cd(II) Lewis acid sites rapidly participate in coordination
to activate the epoxides, and the resulting large steric hindrance
facilitates leaving of the coordinated iodide ions in a reversibly
dynamic fashion convenient for the rate-determining step ring-opening
as a strong nucleophile. Such a pristine MOF catalyst with self-independent
catalytic ring-opening overcomes the complicated operation limitation
of the traditional cocatalyst-free MOF systems based on encapsulating/postmodifying
cocatalysts, providing a whole new strategy for the development of
simple, green, and efficient heterogeneous catalysts for CO2 cycloaddition.
“…The decrease in band gap when CdS deposited on ZnS and CoS could be due to strain and increase in the grain size as shown in SEM micrograph of CdS/ZnS and CdS/CoS films (Figure 2) [43,44]. In the case of CdS/CoS, the band gap decrease can also be resulted from the substitution of some of the Cd ions specially at the interface region by relatively larger atomic radius Co ions [45].…”
In this work multilayer films of CdS/ZnS and CdS/CoS were prepared using the chemical bath deposition technique. The influence of substrate materials on structural, morphological, compositional and optical properties of the films was investigated. The powder X-ray diffraction (XRD) pattern of CdS/ZnS thin film showed nearly similar structure to that of the cubic ZnS structure. The XRD pattern of CdS/CoS thin films confirmed the co-existence of hexagonal and orthorhombic CdS phases. A cubic CdS structure is observed for CdS/glass thin film. The scanning electron microscopy (SEM) micrograph of CdS/glass film revealed spherical grains of size 125 nm covering the substrate uniformly without voids and cracks. The as large grain size as 800 nm with distinct grain boundaries was observed for CdS/ZnS multilayer film with some voids on the surface. The SEM micrograph of CdS/CoS thin film showed spherical surface grains of size 450 nm on flat and compact background. The energy dispersive X-ray spectra of single and multilayer CdS films confirmed the presence of Cd and S. The optical analysis of the CdS/glass, CdS/ZnS and CdS/CoS thin films confirmed band gaps of 2.5, 2.3 and 2.27 eV respectively.
“…It has a high absorption coefficient, good transfer efficiency, reliable, and inexpensive [1]. CdS considered as interesting material because it used at different applications for instance diode sensor [2], transistor [3], photosensor [4], photodetectors [5], photodiodes [6]. CdS have been deposited by chemical bath deposition (CBD) method [7], sol-gel [8], pules laser deposition technique (PLD) [9], chemical vapour deposition (CVD) [10], RF-sputtering [11].…”
<p>The monitoring of CO2 in our life safety, industrial, and chemical laboratory<br />applications make it an inspiring task. The chemical spray pyrolysis technique<br />was used to prepare CdS/Ag thin films. The nanocrystalline cadmium sulfide<br />thin films were doped with Silver at different doping concentrations (0%, 2%,<br />and 4%). The morphologies, structures, and gas sensing properties of CdS/Ag<br />films are presented. The samples were characterized using X-ray diffraction<br />(XRD) and atomic force microscope (AFM). The XRD results show that the<br />films are a polycrystalline composition and hexagonal type with a favoured<br />orientation along (111) direction. The average grain size (nm) of AFM is<br />between 75 and 55 nm. As a result, Ag doping changes the sensitivity of the<br />samples respectively with the percentage of doping with time. The synthesis<br />samples show controlling sensitivity and the small response of sensitivity are<br />the key point in this study.</p>
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.