2020
DOI: 10.1016/j.apcatb.2019.118311
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Composite Si-O-metal network catalysts with uneven electron distribution: Enhanced activity and electron transfer for catalytic ozonation of carbamazepine

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Cited by 48 publications
(27 citation statements)
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“…The movement of Si–O–Si bonds indicates that Co enters the SiO 2 lattice and that Si–O–Co bonds exist in the materials, which destroys the symmetry of SiO 2 and causes the move of peak position. A similar phenomenon has been reported in other literature [ 44 , 45 ]. In addition, when n Co = 0.5, an additional peak is found located at 960 cm −1 and corresponding to the Si–O–Co vibration, suggesting that cobalt enters into the silica framework and forms the Si–O–Co bonds.…”
Section: Resultssupporting
confidence: 91%
See 1 more Smart Citation
“…The movement of Si–O–Si bonds indicates that Co enters the SiO 2 lattice and that Si–O–Co bonds exist in the materials, which destroys the symmetry of SiO 2 and causes the move of peak position. A similar phenomenon has been reported in other literature [ 44 , 45 ]. In addition, when n Co = 0.5, an additional peak is found located at 960 cm −1 and corresponding to the Si–O–Co vibration, suggesting that cobalt enters into the silica framework and forms the Si–O–Co bonds.…”
Section: Resultssupporting
confidence: 91%
“…It can be observed that, with the increases of n Co , the mean pore size increases, and the micropore volume decreases; the total pore volume and BET surface area increase until n Co = 0.08, after which they begin to decrease. This is because the added cobalt atoms exist in the form of Si–O–Co bonds in the SiO 2 skeleton, and the atomic radius of the cobalt atoms is larger than that of the silicon atoms, which plays a role in expanding the pores [ 45 ]. So, with the increase of n Co , the particle size, mean pore size, total pore volume, and surface area, the distribution of pore size becomes wider and shifts gradually to the direction of the mesopores.…”
Section: Resultsmentioning
confidence: 99%
“…The bands around 292 and 479 cm −1 are attributed to the twisting vibrations and stretching vibrations of CoO bonds in amorphous CoO clusters. Notably, the unique band sited around 825 cm −1 is only observed for Co‐edta@S‐1 catalyst, which is related to the CoOSi bond vibrations 22 . In contrast, these CoO or CoOSi bands are not observed in Co/S‐1 catalyst.…”
Section: Resultsmentioning
confidence: 87%
“…Ce is less electronegative than Si and O, which invokes an electron‐rich center located around the SiO bond. [ 24 ] Electrostatic potential mapping by Li et al. [ 24 ] indicated that adding Ce to a SiOSi network can enhance electrons trapped on the oxygen vacancies, electron transfer and augment catalytic ozonation performance.…”
Section: Resultsmentioning
confidence: 99%
“…Ce is less electronegative than Si and O, which invokes an electron-rich center located around the SiO bond. [24] Electrostatic potential mapping by Li et al [24] indicated that adding Ce to a SiOSi network can enhance electrons trapped on the oxygen vacancies, electron transfer and augment catalytic ozonation performance. As a consequence of the defects in the CeOSi framework, a large amount of unpaired electrons gather around the metal atoms and free electron regions occur, particularly in the oxygen vacancy spaces.…”
Section: First Principles Calculationsmentioning
confidence: 99%