Abstract:In
this work, CdS quantum dots (QDs)-sensitized self-doped Bi
2
MoO
6
has been
synthesized using glucose as reducing agent by hydrothermal method,
followed by in situ deposition of the QDs. The synthesized catalyst
has been employed to reduce toxic Cr(VI) and degrade phenol from the
aqueous solution. The structural, optical,
and electrochemical characterizations are performed using X-ray diffraction,
UV–vis diffuse reflection, photoluminescence (PL), scanning
elect… Show more
“…The HRTEM images further confirmed the anchoring of Co 3 O 4 QDs on CNNS nanosheets and demonstrated the formation of Co 3 O 4 /CNNS heterojunction, in which the particle size of Co 3 O 4 QDs was centered at ≈2.2–3.2 nm, matching well with the statistical particle size distribution diagram (Figure F–H). That is, the particle size of Co 3 O 4 QDs is small enough to exhibit the quantum confinement effect . Moreover, the distances of ≈0.200 and ≈0.243 nm correspond to the (400) and (311) planes in the spinel Co 3 O 4 lattice, respectively (Figure H) .…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, the distances of ≈0.200 and ≈0.243 nm correspond to the (400) and (311) planes in the spinel Co 3 O 4 lattice, respectively (Figure H) . Obviously, high crystallinity and ultrasmall particle size will accelerate photogenerated carrier to diffuse toward the surface, thus enhances its photocatalytic activity . Furthermore, both Co 3 O 4 QDs and CNNS are in tight contact with each other to form heterojunction in the interfacial area, which can efficiently retard the photogenerated electron/hole recombination and enhance the possibility of photogenerated charge participating in AOPs.…”
Section: Resultsmentioning
confidence: 99%
“…That is, the particle size of Co 3 O 4 QDs is small enough to exhibit the quantum confinement effect. [55,62] Moreover, the distances of ≈0.200 and ≈0.243 nm correspond to the (400) and (311) planes in the spinel Co 3 O 4 lattice, respectively ( Figure 5H). [54] Obviously, high crystallinity and ultrasmall particle size will accelerate photogenerated carrier to diffuse toward the surface, thus enhances its photocatalytic activity.…”
The development of effective approaches for the preparation of 0D quantum dots (QDs)/2D nanosheets (NSs) heterostructures, which have been proven to be favorable for heterogeneous catalysis, is highly desirable but remains a great challenge. Herein, 0D metal oxide nanocrystals-2D ultrathin g-C N nanosheets (Co O /CNNS) heterostructures are synthesized via a facile chemical reaction, followed by annealing in air. Ultrafine Co O QDs (≈2.2-3.2 nm) are uniformly and tightly attached on the surface of g-C N nanosheets. Detailed characterization reveals that the specially designed unique 0D/2D structure is critical to the high photocatalytic performance for the degradation of tetracycline (TC) via peroxymonosulfate (PMS) activation. The optimal catalyst, namely, Co O /CNNS-1100, exhibits excellent performance and ≈98.7% TC can be degraded under visible light irradiation. Moreover, TC degradation is almost completely insusceptible to several real water samples. Meanwhile, other dye pollutants can also be efficiently degraded by the Co O /CNNS-1100/PMS/vis system. The quenching tests display that that the h , ∙OH, O , and SO are responsible for TC removal. The improved photocatalytic performance can be attributed to the synergistic effect of the photocatalytic- and chemical-processes in the PMS activation. This work gives an insight into the development of multifunctional 0D/2D nanocomposites for further potential applications which are not limited to environmental purification.
“…The HRTEM images further confirmed the anchoring of Co 3 O 4 QDs on CNNS nanosheets and demonstrated the formation of Co 3 O 4 /CNNS heterojunction, in which the particle size of Co 3 O 4 QDs was centered at ≈2.2–3.2 nm, matching well with the statistical particle size distribution diagram (Figure F–H). That is, the particle size of Co 3 O 4 QDs is small enough to exhibit the quantum confinement effect . Moreover, the distances of ≈0.200 and ≈0.243 nm correspond to the (400) and (311) planes in the spinel Co 3 O 4 lattice, respectively (Figure H) .…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, the distances of ≈0.200 and ≈0.243 nm correspond to the (400) and (311) planes in the spinel Co 3 O 4 lattice, respectively (Figure H) . Obviously, high crystallinity and ultrasmall particle size will accelerate photogenerated carrier to diffuse toward the surface, thus enhances its photocatalytic activity . Furthermore, both Co 3 O 4 QDs and CNNS are in tight contact with each other to form heterojunction in the interfacial area, which can efficiently retard the photogenerated electron/hole recombination and enhance the possibility of photogenerated charge participating in AOPs.…”
Section: Resultsmentioning
confidence: 99%
“…That is, the particle size of Co 3 O 4 QDs is small enough to exhibit the quantum confinement effect. [55,62] Moreover, the distances of ≈0.200 and ≈0.243 nm correspond to the (400) and (311) planes in the spinel Co 3 O 4 lattice, respectively ( Figure 5H). [54] Obviously, high crystallinity and ultrasmall particle size will accelerate photogenerated carrier to diffuse toward the surface, thus enhances its photocatalytic activity.…”
The development of effective approaches for the preparation of 0D quantum dots (QDs)/2D nanosheets (NSs) heterostructures, which have been proven to be favorable for heterogeneous catalysis, is highly desirable but remains a great challenge. Herein, 0D metal oxide nanocrystals-2D ultrathin g-C N nanosheets (Co O /CNNS) heterostructures are synthesized via a facile chemical reaction, followed by annealing in air. Ultrafine Co O QDs (≈2.2-3.2 nm) are uniformly and tightly attached on the surface of g-C N nanosheets. Detailed characterization reveals that the specially designed unique 0D/2D structure is critical to the high photocatalytic performance for the degradation of tetracycline (TC) via peroxymonosulfate (PMS) activation. The optimal catalyst, namely, Co O /CNNS-1100, exhibits excellent performance and ≈98.7% TC can be degraded under visible light irradiation. Moreover, TC degradation is almost completely insusceptible to several real water samples. Meanwhile, other dye pollutants can also be efficiently degraded by the Co O /CNNS-1100/PMS/vis system. The quenching tests display that that the h , ∙OH, O , and SO are responsible for TC removal. The improved photocatalytic performance can be attributed to the synergistic effect of the photocatalytic- and chemical-processes in the PMS activation. This work gives an insight into the development of multifunctional 0D/2D nanocomposites for further potential applications which are not limited to environmental purification.
“…[15] They demonstrated that incorporation of CdS QDs into BiOI microplates (up to 4wt%)c ould improve the photocatalytic efficiencies to al arge extent. The enhanced performance was attributed to increased visible absorption and the significant separation of electron-hole pairs over CdS/BiOI type-II heterostructures.P arida and co-workers [16] designed CdS QD decorated self-doped Bi 2 MoO 6 nanocomposites and demonstrated their superior photocatalytic performance toward the degradation of phenol and fast reduction of toxic Cr VI .T he 3% CdS QD sensitized self-doped Bi 2 MoO 6 sample displayed Am agnetically separable Fe 3 O 4 @CdS type-II core-shell nanohybrid (NH) photocatalyst, with excellent antibacterial properties and photocatalytic activity,w as synthesized and characterized by means of structural, elemental, and morphological analyses. Steady-state and time-resolved emission and absorption spectroscopyw ere also exploited to realize the location of chargecarrier wave functions in the NHs.…”
Section: Introductionmentioning
confidence: 98%
“…The enhanced performance was attributed to increased visible absorption and the significant separation of electron–hole pairs over CdS/BiOI type‐II heterostructures. Parida and co‐workers designed CdS QD decorated self‐doped Bi 2 MoO 6 nanocomposites and demonstrated their superior photocatalytic performance toward the degradation of phenol and fast reduction of toxic Cr VI . The 3 % CdS QD sensitized self‐doped Bi 2 MoO 6 sample displayed the highest efficiency, namely, 47.5 and 97 %, toward the degradation of phenol and reduction of Cr VI , respectively, under solar light.…”
A magnetically separable Fe3O4@CdS type‐II core–shell nanohybrid (NH) photocatalyst, with excellent antibacterial properties and photocatalytic activity, was synthesized and characterized by means of structural, elemental, and morphological analyses. Steady‐state and time‐resolved emission and absorption spectroscopy were also exploited to realize the location of charge‐carrier wave functions in the NHs. The antibacterial activity of NHs was then evaluated against Escherichia coli (1.4×108 CFU mL−1; CFU=colony forming units) and Staphylococcus saprophyticus (1.2×108 CFU mL−1) as model strains of Gram‐negative and ‐positive microbes. Compared with CdS and Fe3O4, the as‐synthesized Fe3O4@CdS composite exhibited highly improved bactericidal activity and recyclability. Concentration values of 5.0 and 4.0 mg mL−1 were required for Fe3O4@CdS NHs to inhibit the growth of E. coli and S. saprophyticus, respectively. The contribution of OH. radicals to photocatalysis at the Fe3O4@CdS surface was also considered. Moreover, thiobarbituric acid reactive substances and protein carbonyl assay protocols have been exploited to monitor levels of oxidative damage to lipids and proteins in cells. Additionally, the photocatalytic activity of Fe3O4@CdS NHs was monitored for the degradation of xylenol orange dye. Compared with CdS and Fe3O4, as‐synthesized Fe3O4@CdS displayed superior performances in the photodegradation of xylenol orange. Possible mechanisms involved in the degradation of xylenol orange are also discussed.
photocatalyst. In this context, there are several reported works on Z-scheme-based semiconductors such as CdS/BiVO 4 , [2] BiVO 4 /CdS quantum dots (QDs), [3] CdS-WO 3 , [4] TiO 2 /CdS, [5] etc. Yet, the typical charge transfer process competes with the binary Z-scheme charge transfer and the photocatalytic performance is still unable to triumph the practical application, i.e., to conquer the concerns of sustainable energy and environment-related issues. Understandably then, scientists started focusing on the construction of ternary semiconductors with dual Z-scheme pathway for more effective charge separation. Many research groups have reported their findings in designing unidirectional double Z-scheme-based photocatalysts for water redox reactions and degradation of harmful pollutants. [6][7][8][9][10][11] Moreover, our group has reported photocatalytic reduction of Cr 6+ → Cr 3+ and water → H 2 over Cu-MoO 3 /g-C 3 N 4 hybrid nanocomposite. [6] Ternary Ag 2 CO 3 /CeO 2 /AgBr photocatalyst has been reported by Wen et al. with double Z-scheme configuration performing photodegradation of levofloxacin. [7] GO/Ag 2 CrO 4 /g-C 3 N 4 nanocomposite has been reported with superior photocatalytic performance toward refractory pollutant degradation [8] and AgBr@Bi 2 WO 6 /WO 3 for degrading rhodamine B. [9] A similar double Z-scheme photocatalytic system (Bi 2 S 3 /SnS 2 /Bi 2 O 3 ) has also been reported by Yu et al. for dye removal under sunlight irradiation. [10] ZnO/ZnS/g-C 3 N 4 ternary double Z-scheme heterojunction has been synthesized by Dong et al. for photocatalytic H 2 generation. [11] Despite accomplishments of certain stimulating achievements by these double Z-scheme photocatalysts, still improvements can be attained to scale up the practical application in the photocatalytic field. We report here a prototype novel confronting bidirectional double Z-schemebased UV-vis active photocatalyst with two single Z-scheme systems acting in opposite direction toward enhanced photocatalytic water oxidation reaction (WOR) and organic pollutants, i.e., tetracycline (TC) and methyl orange (MO). It consists of an oxygen evolution catalyst, i.e., BiVO 4 abbreviated as "B" (monoclinic clinobisvanite phase) composed of tetrahedron and octahedron of VO 4 and BiO 8 , respectively, with threefold coordinated O, fourfold coordinated V, and eightfold coordinated Bi. This phase of B collects distinct attention in WORs Fabricating competent nanoarchitecture photocatalytic systems with desired band edge potential is crucial for effective charge separation that manifolds photocatalytic action. Here, a prototype pristine rational design of allsolid-state coupled confronting Z-scheme (CCZ) system is synthesized by coprecipitation and hydrothermal method. This proof of concept comprises BiVO 4 (B) and MgAl layered double hydroxide (L) as photosystem II (PS-II) whereas CdS quantum dots (QDs, C) as photosystem I (PS-I). CdS QDs trigger H 2 production that subsequently boosts O 2 production at PS-II. Furthermore, this rare CCZ system shows ...
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.