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2019
DOI: 10.1039/c9cy00945k
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Sustainable fixation of CO2 into epoxides to form cyclic carbonates using hollow marigold CuCo2O4 spinel microspheres as a robust catalyst

Abstract: The present work demonstrates the chemical fixation of CO2 for the synthesis of organic carbonates using mesoporous hollow marigold CuCo2O4 spinel microspheres as a catalyst prepared using the solvothermal method.

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Cited by 63 publications
(50 citation statements)
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“…It is considered that the synergistic effect between crystalline and amorphous phases promotes the rapid transport of electrons and improves the electrochemical catalytic activity of the catalyst [38] . In the crystalline region of Figure 1d and 1e, the lattice fringe spacings of 0.25, 0.471 and 0.289 nm corresponds to the (311), (111), and (220) facet of the cubic phase spinel CCO, respectively [26,39–40] . Furthermore, HAADF‐STEM (Figure 1f) and EDX elemental mapping images (Figure 1g–j) indicate that Cu, Co, O, and P are uniformly distributed, which confirming that P is doped into CCO lattice.…”
Section: Resultsmentioning
confidence: 98%
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“…It is considered that the synergistic effect between crystalline and amorphous phases promotes the rapid transport of electrons and improves the electrochemical catalytic activity of the catalyst [38] . In the crystalline region of Figure 1d and 1e, the lattice fringe spacings of 0.25, 0.471 and 0.289 nm corresponds to the (311), (111), and (220) facet of the cubic phase spinel CCO, respectively [26,39–40] . Furthermore, HAADF‐STEM (Figure 1f) and EDX elemental mapping images (Figure 1g–j) indicate that Cu, Co, O, and P are uniformly distributed, which confirming that P is doped into CCO lattice.…”
Section: Resultsmentioning
confidence: 98%
“…[38] In the crystalline region of Figure 1d and 1e, the lattice fringe spacings of 0.25, 0.471 and 0.289 nm corresponds to the (311), (111), and (220) facet of the cubic phase spinel CCO, respectively. [26,[39][40] Furthermore, HAADF-STEM ( Figure 1f) and EDX elemental mapping images (Fig-Figure 1. a) and b) SEM, c) TEM, d) and e) HRTEM images of CCP 0.5 ; f) The HAADF-STEM image and g-j) corresponding EDX element mapping images of CCP 0.5 , Cu-blue, Co-yellow, O-red, P-orange.…”
Section: Resultsmentioning
confidence: 99%
“…This implies that at 343 K, the reactant (epichlorohydrin) can be able to mobilize well on the active sites of the catalysts due to the increased inhomogeneity of the catalyst in the reaction medium. As a result, more efficient collisions occurred with reactant molecules to overcome the energy barrier for ring-opening and CO 2 insertion, 25 which would in turn provide an effective conversion. Apart from that, at elevated temperatures, the conversion increases by increasing the gas–liquid mass transfer coefficient.…”
Section: Resultsmentioning
confidence: 99%
“…To date, a variety of homogeneous and heterogeneous catalytic systems have been reported for cycloaddition reactions with CO 2 and epoxide, including alkali metal salts, ionic liquids, quaternary ammonium or phosphonium salts, crown ether, organocatalysts, organometallic complexes, porphyrin, metal–salen complexes, metal oxides, zeolites, metal–organic frameworks (MOFs), porous organic framework (POFs), functional carbon nitride, functionalized silica, and so on. 21–29 Generally, homogeneous catalysts stand out as the most effective and tailor-made catalysts for cycloaddition reactions, but their intrinsic problems such as troublesome separation, purification, and regeneration restrict their commercialization. In this context, heterogeneous catalysts are gaining attention from scientists and industrialists as they are task-specific and readily separated and regenerated.…”
Section: Introductionmentioning
confidence: 99%
“…8B). 223 Numerous other materials, like Si/SiC@C hollow-nanospheres, TiPO 4 flowers, and aluminum porphyrin complexes, can also be used as a catalyst to achieve high conversion efficiency for the chemical fixation of CO 2 under milder conditions. [224][225][226] Although zeolites, 227 titanosilicates, 228 and metal oxides 229 were reported as CO 2 fixation catalyst, but they mostly required elevated temperature, pressure and extensive purification steps.…”
Section: Materials Advances Reviewmentioning
confidence: 99%