2016
DOI: 10.1016/j.apcatb.2016.01.026
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Template-free preparation of macro/mesoporous g-C 3 N 4 /TiO 2 heterojunction photocatalysts with enhanced visible light photocatalytic activity

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Cited by 584 publications
(191 citation statements)
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References 63 publications
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“…This denoted that g-C 3 N 4 could efficiently extend absorption of nanocomposities to the visible region and thus enhance the photocatalytic ability in the visible light region. These results are in good agreement with the literature report [18,36]. The absorption edge energies of prepared g-C 3 N 4 /TiO 2 photocatalyst were almost the same as pure g-C 3 N 4.…”
Section: Photocatalysts Characterizationsupporting
confidence: 92%
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“…This denoted that g-C 3 N 4 could efficiently extend absorption of nanocomposities to the visible region and thus enhance the photocatalytic ability in the visible light region. These results are in good agreement with the literature report [18,36]. The absorption edge energies of prepared g-C 3 N 4 /TiO 2 photocatalyst were almost the same as pure g-C 3 N 4.…”
Section: Photocatalysts Characterizationsupporting
confidence: 92%
“…In case of the TiO 2 /g-C 3 N 4 photocatalysts their PL intensities decreased in the order g-C 3 N 4 > TiO 2 /g-C 3 N 4 (1:6) > TiO 2 /g-C 3 N 4 (1:4) > TiO 2 /g-C 3 N 4 (1:2) > TiO 2 which agrees with observations of other authors [13,18,43,44]. This phenomenon can be explained by separation of photoinduced electrons between g-C 3 N 4 and TiO 2 structures via their heterojunctions.…”
Section: Photocatalysts Characterizationsupporting
confidence: 91%
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“…Since the CB levels of TiO 2 is more negative than the potential of O 2 /·O 2 − (−0.046 eV vs. NHE at pH = 7), as a result, the electrons in CB of TiO 2 can be trapped by dissolved oxygen to generate ·O 2 − radical species. And compared with the potential of ·OH/H 2 O (2.27 eV vs. NHE at pH = 7), the remained h + on the VB of g-C 3 N 4 can not react with H 2 O to generate ·OH radicals due to the lower VB level of g-C 3 N 4 (1.63 eV vs. NHE at pH = 7)751. Subsequently, the radical species ·O 2 − and h + can directly degrade organic pollutants.…”
Section: Resultsmentioning
confidence: 99%
“…[178] Alternatively, Hao et al directly synthesized macro/mesoporous g-C 3 N 4 /TiO 2 heterostructures by a facile calcination approach using tetrabutyl titanate and melamine as feedstocks, in which the added content of melamine greatly influenced on their photocatalytic activity. [180] In addition, ternary nanohybrids were further produced in recent years. [179] For the degradation of Rhodamine B, the reaction rate constant was up to 47.8 × 10 −3 min −1 , 7.2 and 3.1 times higher than pure TiO 2 and g-C 3 N 4 , respectively.…”
Section: Hybridization With Nanostructuresmentioning
confidence: 99%