We demonstrated a unique synthesis approach of graphene（GR）-wrapped AgPO/LaCOOH（APO/LCO）heterostructures by an in-situ wet chemical method. FESEM analysis reveals the formation of rhombic dodecahedrons of APO deco...We demonstrated a unique synthesis approach of graphene（GR）-wrapped AgPO/LaCOOH（APO/LCO）heterostructures by an in-situ wet chemical method. FESEM analysis reveals the formation of rhombic dodecahedrons of APO decorated with LCO and later wrapped with GR flakes. Optical studies shows two absorption edges corresponding to the band gap energies of APO（2.41 eV） and LCO（4.1 eV）. Considering the absorption edge of the heterostructures in the visible region, the photocatalytic activities of photocatalysts containing different APO/LCO mass ratios were evaluated by the degradation of MB. GR-decorated composite with 20% LCO（APO/LCO20/GR） exhibited the highest photocatalytic activity for MB degradation, with a rate constant, k of 0.541 min. The photocatalytic activity of APO/LCO20/GR more greatly enhanced than those of the individual constituents（APO, LCO, APO/LCO20）. The enhanced photocatalytic activity of the heterostructure can be attributed to the co-catalytic effect of LCO as well as intriguing physicochemical properties of GR. To understand the enhanced photocatalytic activity of the heterostructures the photocatalytic reaction mechanism is proposed in detail. The recyclability of the APO/LCO/GR composite photocatalyst is further evaluated by reusing the catalyst in replicate photocatalytic experiments which shows consistent photocatalytic activity thereby confirms the stability and reusability of heterostructure photocatalyst.展开更多
The geometry,electronic stucture and bond of L a CO,one of the rare earth carbonyl compounds,havebeen studied with SCM- DV- Xαmethod.From the resultsitiscertified thatthe L a CO isalinearmolecule,in which thebond len...The geometry,electronic stucture and bond of L a CO,one of the rare earth carbonyl compounds,havebeen studied with SCM- DV- Xαmethod.From the resultsitiscertified thatthe L a CO isalinearmolecule,in which thebond length of L a- C and C- O are 0 .2 2 73nm and 0 .1179 nm respectively,theσcoordinatebond and theπ- back bond are formed between L aand CO. Itis also showed thatthe L a- C bond hasaboutmorethan90 % covalentcharacter and the4 f orbitals play a certain role in the bonding of La CO.展开更多
Stoichiometric LaMnO3 and LaCoO3 nanoparticles were synthesized via calcination of a dried solution, containing molar ratio of La（NO3）3＋6H20/[Mn（NO3）2-4H20 or Co（NO3）2-6H20]=1 and citric acid as disperser at te...Stoichiometric LaMnO3 and LaCoO3 nanoparticles were synthesized via calcination of a dried solution, containing molar ratio of La（NO3）3＋6H20/[Mn（NO3）2-4H20 or Co（NO3）2-6H20]=1 and citric acid as disperser at temperature range of 600-900 ℃for 5 h. The role of organic additive concentration, which was 0.0, 1.0, 2.5 and 5 times of the total number of moles of the nitrate ions, was investigated on phase formation, morphology, extent of crystallization and particle size of the products. Products were characterized by X-ray diffraction （XRD）, Fourier-transform infrared spectroscopy （FT-IR）, scanning electron microscopy （SEM） and Wansmission elec- tron microscopy （TEM） analysis. The tendency of lanthanum ion toward manganese cation was observed to be more than to cobalt cation for the formation of LaBO3 （B： Mn or Co） perovskite phase. A spongy product was formed on perovskite phase formation or in the pres- ence of citric acid. A constructive or destructive effect was observed for the organic disperser on perovskite phase formation, which de- pended on mole of the citric acid.展开更多
基金Department of Electronics and Information Technology (Deit Y, New Delhi) for financial supportUGC-SAP, DST-FIST Department of Chemistry, Shivaji University Kolhapursupported by the Commercialization Promotion Agency for R&D Outcomes (COMPA) funded by the Ministry of Science, ICT and Future Planning (MISP) and NRF-2013R1A2A2A05005589
文摘We demonstrated a unique synthesis approach of graphene（GR）-wrapped AgPO/LaCOOH（APO/LCO）heterostructures by an in-situ wet chemical method. FESEM analysis reveals the formation of rhombic dodecahedrons of APO decorated with LCO and later wrapped with GR flakes. Optical studies shows two absorption edges corresponding to the band gap energies of APO（2.41 eV） and LCO（4.1 eV）. Considering the absorption edge of the heterostructures in the visible region, the photocatalytic activities of photocatalysts containing different APO/LCO mass ratios were evaluated by the degradation of MB. GR-decorated composite with 20% LCO（APO/LCO20/GR） exhibited the highest photocatalytic activity for MB degradation, with a rate constant, k of 0.541 min. The photocatalytic activity of APO/LCO20/GR more greatly enhanced than those of the individual constituents（APO, LCO, APO/LCO20）. The enhanced photocatalytic activity of the heterostructure can be attributed to the co-catalytic effect of LCO as well as intriguing physicochemical properties of GR. To understand the enhanced photocatalytic activity of the heterostructures the photocatalytic reaction mechanism is proposed in detail. The recyclability of the APO/LCO/GR composite photocatalyst is further evaluated by reusing the catalyst in replicate photocatalytic experiments which shows consistent photocatalytic activity thereby confirms the stability and reusability of heterostructure photocatalyst.
文摘The geometry,electronic stucture and bond of L a CO,one of the rare earth carbonyl compounds,havebeen studied with SCM- DV- Xαmethod.From the resultsitiscertified thatthe L a CO isalinearmolecule,in which thebond length of L a- C and C- O are 0 .2 2 73nm and 0 .1179 nm respectively,theσcoordinatebond and theπ- back bond are formed between L aand CO. Itis also showed thatthe L a- C bond hasaboutmorethan90 % covalentcharacter and the4 f orbitals play a certain role in the bonding of La CO.
文摘Stoichiometric LaMnO3 and LaCoO3 nanoparticles were synthesized via calcination of a dried solution, containing molar ratio of La（NO3）3＋6H20/[Mn（NO3）2-4H20 or Co（NO3）2-6H20]=1 and citric acid as disperser at temperature range of 600-900 ℃for 5 h. The role of organic additive concentration, which was 0.0, 1.0, 2.5 and 5 times of the total number of moles of the nitrate ions, was investigated on phase formation, morphology, extent of crystallization and particle size of the products. Products were characterized by X-ray diffraction （XRD）, Fourier-transform infrared spectroscopy （FT-IR）, scanning electron microscopy （SEM） and Wansmission elec- tron microscopy （TEM） analysis. The tendency of lanthanum ion toward manganese cation was observed to be more than to cobalt cation for the formation of LaBO3 （B： Mn or Co） perovskite phase. A spongy product was formed on perovskite phase formation or in the pres- ence of citric acid. A constructive or destructive effect was observed for the organic disperser on perovskite phase formation, which de- pended on mole of the citric acid.
