2019
DOI: 10.1016/j.apcatb.2019.01.091
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Powerful combination of MOFs and C3N4 for enhanced photocatalytic performance

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Cited by 322 publications
(108 citation statements)
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“…It could be used to effectively load drugs and is beneficial to package various compounds and therapeutic drugs [6,7]. The complexes formed with Cu 2+ have thousands of applications; for example as nucleic acid cleavage enzymes because of their cleavage activity to DNA, and some complexes have certain anticancer activities [8,9]. As a new type of ligand, 6-oxo-2-phenyl-1,6-dihydropyrimidine-4-carboxylate coordinate with Cu 2+ to form the title complex.…”
Section: Commentmentioning
confidence: 99%
“…It could be used to effectively load drugs and is beneficial to package various compounds and therapeutic drugs [6,7]. The complexes formed with Cu 2+ have thousands of applications; for example as nucleic acid cleavage enzymes because of their cleavage activity to DNA, and some complexes have certain anticancer activities [8,9]. As a new type of ligand, 6-oxo-2-phenyl-1,6-dihydropyrimidine-4-carboxylate coordinate with Cu 2+ to form the title complex.…”
Section: Commentmentioning
confidence: 99%
“…Another valid approach to reduce charge recombination rate and improve MOFs photocatalytic performance is based on their coupling with semiconductor nanoparticles, such as TiO 2 , ZnO, CdS, C 3 N 4 [255]. Cu(II)-porphyrin and TiO 2 nanoparticles into MOF structure (PCN-224(Cu)) leads to a marked improvement of light-harvesting features and promotes separation of photogenerated charges, reaching superior photocatalytic performance for CO 2 reduction [219,256].…”
Section: Encapsulation Of Photocatalytic Active Species (Mof Compositmentioning
confidence: 99%
“…[ 24,25 ] Constructing a C 3 N 4 /MOF heterojunction has been proved to be an effective strategy to overcome the drawbacks of both MOFs and CN, for enhancing photocatalytic performance. [ 26,27 ] For example, CN/ZIF‐8, [ 28 ] CN/MIL‐53(Al), [ 29 ] CN/MIL‐53(Fe), [ 30 ] and CN/MIL‐125(Ti) [ 31 ] have been developed for improving catalytic activity in CO 2 reduction, H 2 production, and Cr(VI) reduction, respectively. Unfortunately, the interfacial resistance restricts the interface transfer of the changer, [ 32,33 ] and the photogenerated electrons travel from the CB of CN to the surface reaction sites (metal cluster) via linker to cluster, which lengthens the distances for further proton reduction, increasing the probability of photoexcited electrons being undesirably trapped and reducing the photocatalytic efficiency.…”
Section: Introductionmentioning
confidence: 99%