CN103977821A - Cu3SnS4-graphene composite visible-light-driven photocatalyst and preparation method thereof - Google Patents

Cu3SnS4-graphene composite visible-light-driven photocatalyst and preparation method thereof Download PDF

Info

Publication number
CN103977821A
CN103977821A CN201410068296.0A CN201410068296A CN103977821A CN 103977821 A CN103977821 A CN 103977821A CN 201410068296 A CN201410068296 A CN 201410068296A CN 103977821 A CN103977821 A CN 103977821A
Authority
CN
China
Prior art keywords
graphene
sns
preparation
graphene composite
light
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201410068296.0A
Other languages
Chinese (zh)
Inventor
刘红
靳智通
苏芸
陈振
徐征征
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
University of Shanghai for Science and Technology
Original Assignee
University of Shanghai for Science and Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by University of Shanghai for Science and Technology filed Critical University of Shanghai for Science and Technology
Priority to CN201410068296.0A priority Critical patent/CN103977821A/en
Publication of CN103977821A publication Critical patent/CN103977821A/en
Pending legal-status Critical Current

Links

Landscapes

  • Catalysts (AREA)

Abstract

The invention relates to a Cu3SnS4-graphene composite visible-light-driven photocatalyst and a preparation method thereof. The preparation method comprises: adding 0.060 g of CuAc2.H2O, 0.030 g of thioacetamide (TAA) and 0.035 g of SnCl4.5H2O into 45 mL of N,N-dimethylformamide (DMF), stirring at room temperature to complete dissolved; ultrasonically dispersing 0.015 g of graphite oxide into 10 mL of anhydrous ethanol, so as to obtain a suspension of graphene oxide; slowly dropwise adding the graphene oxide suspension into the above solution, and continuing to stirring for 1 h; transferring the obtained mixture into a high-pressure reaction vessel with a teflon liner, and performing a crystallization reaction at 180-200 DEG C for 12 h; and performing filtering, washing and drying on the obtained solid product, so as to obtain the Cu3SnS4-graphene composite visible-light-driven photocatalyst. The preparation method is environment-friendly and simple in technology. The prepared composite catalyst has extremely high visible-light catalytic activity, and has potential application value to technologies for photocatalytically decomposing organic pollutants by utilizing solar energy.

Description

A kind of Cu 3snS 4/ Graphene composite visible light catalyst and preparation method thereof
Technical field
The present invention relates to a kind of Cu 3snS 4/ Graphene composite visible light catalyst and preparation method thereof, belongs to photocatalysis and environmental technology field.
Background technology
Current environment problem and energy crisis become two large bottlenecks of restriction human development.Photocatalysis technology is expected to become the effective means that solves environment and energy problem; because will thoroughly solve the crisis of fossil energy exhaustion by converting solar energy into the photodissociation water technology of clean Hydrogen Energy, and photocatalytic degradation is removed the approach that cheapness is feasible that toxic organic pollutant will become solution environmental problem.Traditional TiO 2photochemical catalyst forbidden band wider (Eg=3.2 eV), only can be by the ultraviolet excitation in sunshine (accounting for 3.8 % of solar energy), can not utilize visible ray in sunshine (account for solar energy 45%), make its solar energy utilization ratio low, seriously hindered the large-scale commercial of photocatalysis technology and promoted.Therefore, the novel photocatalysis material of exploitation high-performance visible light response has become one of the most popular current research direction, is also inexorable trend and developing direction that photocatalysis technology further moves towards industrialization.
Cu 3snS 4belonging to I-IV-VI family ternary compound, is a kind of important semiconductor and nonlinear optical material, has outstanding optics, calorifics and mechanical performance.Cu 3snS 4in fields such as solar cell, photocatalysis, there is potential using value.Recently, the discoveries such as Chen, Cu 3snS 4in sunlight catalytic hydrolytic hydrogen production, there is good photocatalytic activity (F. K. Chen, J. T. Zai, M. Xu, X. F. Qian, J. Mater. Chem. A, 2013, Isosorbide-5-Nitrae 316 – 4323), in addition, there is not yet Cu 3snS 4report for other light-catalyzed reactions.Pure Cu 3snS 4absorption wavestrip narrower, quantum efficiency is lower, in order to be better suitable for practical application, is necessary further to improve its photocatalysis performance.
Graphene is by sp 2the material with carbon element tightly packed one-tenth of hydridization carbon atom, that have monoatomic layer thickness, basic structural unit is benzene hexatomic ring the most stable in organic material.As catalyst carrier, Graphene stability is high, specific area is large, light transmission is good, not only can meet the requirement of chemical absorption of surface, also for condition has been created in fixing, separated, the recovery of catalyst.As electron acceptor, graphene nanometer sheet has good electron mobility, can improve the transfer of interface charge and the combination again of inhibition electron-hole pair.Therefore, by Graphene and Cu 3snS 4carry out compound its photocatalysis performance of further raising being had to positive effect.Up to now, there is not yet Cu 3snS 4the report of/graphene complex.
Summary of the invention
Object of the present invention aims to provide a kind of Cu 3snS 4/ Graphene composite visible light catalyst and preparation method thereof.
A kind of Cu of the present invention 3snS 4/ Graphene composite visible light catalyst, is characterized in that having following composition: Cu 3snS 475.0 wt. %, Graphene 25.0 wt.%.
A kind of Cu for preparing of the present invention 3snS 4the method of/graphene composite photocatalyst, is characterized in that, has following preparation process and step:
A. by 0.060 g CuAc 2h 2the SnCl of the thioacetamide of O, 0.030 g (TAA), 0.035 g 45H 2o is added to 45 ml n, nin-dimethyl formamide (DMF), be at room temperature stirred to completely and dissolve;
B. be dispersed in 10 ml absolute ethyl alcohols 0.015 g graphite oxide is ultrasonic, obtain the suspension of graphene oxide;
C. graphene oxide suspension is slowly added drop-wise in step (a) gained solution, and continues to stir 1 h;
D. step (c) gained mixture is transferred in the autoclave of teflon gasket to crystallization 12 h at 180-200 ℃;
E. the solid product obtaining after filtration, washs, and after being dried, obtaining Graphene content is the Cu of 25.0 % 3snS 4/ Graphene composite visible light catalyst.
Cu provided by the invention 3snS 4/ Graphene composite visible light catalyst, by Cu 3snS 4form with Graphene, wherein, Cu 3snS 4in the form of sheets, be evenly distributed on graphene platelet, the mass percent of Graphene is 25.0 %.
The present invention compared with prior art, has following remarkable advantage:
1, in one-step method solvent heat building-up process, the reduction of graphene oxide and Cu 3snS 4the formation of crystal completes simultaneously, and preparation technology is simple;
2, do not need to use other chemical reducing agents, the economic environmental protection of preparation process;
3, in the composite of preparation, Cu 3snS 4sheet is evenly dispersed on graphene platelet, and both contact closely, is conducive to the transmission of light induced electron;
4, the Cu of preparation 3snS 4/ graphen catalyst has very high visible light catalysis activity, in utilizing solar energy photocatalytic decomposing organic pollutant treatment technology, has potential using value.
Accompanying drawing explanation
Fig. 1 is X-ray diffraction (XRD) figure of embodiment and comparative example.
Fig. 2 is transmission electron microscope (TEM) figure of embodiment and ESEM (SEM) figure of comparative example.
Fig. 3 is the uv-visible absorption spectra of embodiment and comparative example.
Fig. 4 is the photocatalysis performance curve of embodiment and comparative example.
The specific embodiment
Now specific embodiments of the invention are described in detail in rear.
Embodiment
A. by 0.060 g CuAc 2h 2the SnCl of the thioacetamide of O, 0.030 g (TAA), 0.035 g 45H 2o is added to 45 ml n, nin-dimethyl formamide (DMF), be at room temperature stirred to completely and dissolve;
B. be dispersed in 10 ml absolute ethyl alcohols 0.015 g graphite oxide is ultrasonic, obtain the suspension of graphene oxide;
C. graphene oxide suspension is slowly added drop-wise in step (a) gained solution, and continues to stir 1 h;
D. step (c) gained mixture is transferred in the autoclave of teflon gasket to crystallization 12 h at 180-200 ℃;
E. the solid product obtaining after filtration, washs, and after being dried, obtaining Graphene content is the Cu of 25.0 % 3snS 4/ Graphene composite visible light catalyst.
XRD analysis result (Fig. 1) shows, sample Cu 3snS 428.3,47.2 and 56.0 othere is diffraction maximum in place, with the Cu of tetragonal phase structure 3snS 4characteristic diffraction peak (the JCPDS card number: 33-0501), do not occur other dephasign peaks in figure, show in product containing CuS, Cu that matches 2s, SnS, SnS 2deng impurity, purity is very high.At Cu 3snS 4in/Graphene, do not find 2q=10.7 othe diffraction maximum of the graphite oxide at place, illustrates that, in solvent heat process, graphene oxide has been reduced into Graphene.The TEM result of Fig. 2 shows, uniform Cu 3snS 4sheet is evenly dispersed on ultra-thin graphene film, and both contact closely.The uv-visible absorption spectra of sample (Fig. 3) result shows, Cu 3snS 4after compound with Graphene, not only widen the absorption region of visible ray, and increased the absorption intensity of visible ray.The Cu of preparation 3snS 4/ graphene composite photocatalyst has very high catalytic activity, under 150 min radiation of visible light, can methyl orange is degradable, can rhodamine B is degradable in 125 min, in 200 min, Pyrogentisinic Acid's Visible Light Induced Photocatalytic rate reaches 88.0 %, and its catalytic activity is higher than pure Cu 3snS 4(Fig. 4).
comparative example
In preparation process except not adding graphite oxide, the same embodiment of all the other operating process.
Finally make the not pure Cu of graphene-containing 3snS 4photochemical catalyst.
The XRD result of sample is referring to Fig. 1.The SEM result (Fig. 2) of sample shows, pure Cu 3snS 4for floriform appearance.The uv-visible absorption spectra result of sample is referring to Fig. 3, and photocatalysis performance is referring to Fig. 4.

Claims (2)

1. a Cu 3snS 4/ Graphene composite visible light catalyst, is characterized in that having following composition: Cu 3snS 4mass percent be 75.0 %, the mass percent of Graphene is 25.0 %.
2. a Cu 3snS 4the preparation method of/Graphene composite visible light catalyst, is characterized in that, has following preparation process and step:
A. by 0.060 g CuAc 2h 2the SnCl of the thioacetamide of O, 0.030 g (TAA), 0.035 g 45H 2o is added to 45 ml n, nin-dimethyl formamide (DMF), be at room temperature stirred to completely and dissolve;
B. be dispersed in 10 ml absolute ethyl alcohols 0.015 g graphite oxide is ultrasonic, obtain the suspension of graphene oxide;
C. graphene oxide suspension is slowly added drop-wise in step (a) gained solution, and continues to stir 1 h;
D. step (c) gained mixture is transferred in the autoclave of teflon gasket to crystallization 12 h at 180-200 ℃;
E. the solid product obtaining after filtration, washs, and after being dried, obtaining Graphene content is the Cu of 25.0 % 3snS 4/ Graphene composite visible light catalyst.
CN201410068296.0A 2014-02-27 2014-02-27 Cu3SnS4-graphene composite visible-light-driven photocatalyst and preparation method thereof Pending CN103977821A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410068296.0A CN103977821A (en) 2014-02-27 2014-02-27 Cu3SnS4-graphene composite visible-light-driven photocatalyst and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410068296.0A CN103977821A (en) 2014-02-27 2014-02-27 Cu3SnS4-graphene composite visible-light-driven photocatalyst and preparation method thereof

Publications (1)

Publication Number Publication Date
CN103977821A true CN103977821A (en) 2014-08-13

Family

ID=51270132

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410068296.0A Pending CN103977821A (en) 2014-02-27 2014-02-27 Cu3SnS4-graphene composite visible-light-driven photocatalyst and preparation method thereof

Country Status (1)

Country Link
CN (1) CN103977821A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105709780A (en) * 2016-01-22 2016-06-29 中南大学 Sn1-0.5xCuxS2 nanoflower and preparation method and application thereof
CN107364882A (en) * 2017-07-25 2017-11-21 东北大学 The method of plant phenolic acid assisted hydrothermal synthesis CTS ternary compounds
CN108010733A (en) * 2017-12-25 2018-05-08 电子科技大学 A kind of flower-shaped Cu2SnS3The preparation method of flexible super capacitor electrode material

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103182315A (en) * 2013-01-12 2013-07-03 上海大学 BiOBr0.2I0.8/graphene composite visible-light-induced photocatalyst and preparation method thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103182315A (en) * 2013-01-12 2013-07-03 上海大学 BiOBr0.2I0.8/graphene composite visible-light-induced photocatalyst and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
FUKUN CHEN ET AL: "3D-hierarchical Cu3SnS4 flowerlike microspheres: controlled synthesis, formation mechanism and photocatalytic activity for H2 evolution from water", 《JOURNAL OF MATERIALS CHEMISTRY A》 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105709780A (en) * 2016-01-22 2016-06-29 中南大学 Sn1-0.5xCuxS2 nanoflower and preparation method and application thereof
CN105709780B (en) * 2016-01-22 2018-07-31 中南大学 A kind of Sn1-0.5xCuxS2Nano flower and its preparation and application
CN107364882A (en) * 2017-07-25 2017-11-21 东北大学 The method of plant phenolic acid assisted hydrothermal synthesis CTS ternary compounds
CN108010733A (en) * 2017-12-25 2018-05-08 电子科技大学 A kind of flower-shaped Cu2SnS3The preparation method of flexible super capacitor electrode material

Similar Documents

Publication Publication Date Title
Liu et al. Two-dimensional/two-dimensional Z-scheme photocatalyst of graphitic carbon nitride/bismuth vanadate for visible-light-driven photocatalytic synthesis of imines
CN103638922B (en) Preparation method of mesoporous tungsten trioxide/reduction-oxidation graphene composite photocatalyst
CN104591301B (en) Porous nano CoFe2O4Preparation method of (1)
CN103861621B (en) A kind of Bi 7o 9i 3/ Graphene composite visible light catalyst and preparation method thereof
CN106000431B (en) Sheet CdS/BiOCl composite nano materials and preparation method thereof
CN103182315B (en) BiOBr0.2I0.8/graphene composite visible-light-induced photocatalyst and preparation method thereof
CN110252346B (en) MoS2/SnS2Preparation method and application of/r-GO composite photocatalyst
CN102698775A (en) BiOI-graphene visible light catalyst and preparation method thereof
CN108262054A (en) A kind of preparation method of silver vanadate/nitride porous carbon heterojunction composite photocatalyst
CN105521789B (en) A kind of porous nano BiFeO3Preparation method
CN105502286B (en) A kind of porous nano NiFe2O4Preparation method
CN105289689A (en) Synthesis and application of nitrogen-doped graphene quantum dot/similar-graphene phase carbon nitride composite material
CN107983387B (en) Preparation method and application of carbon nitride/bismuth selenate composite material
CN107638886B (en) Method for preparing bismuth oxychloride/bismuth oxyiodide composite ultrathin nanosheet by ion exchange method
CN105664950B (en) A kind of porous nano ZnFe2O4Preparation method
CN107552072B (en) graphene-CuInS2Nano composite photocatalyst
CN110624583A (en) Preparation method of composite graphite phase carbon nitride heterojunction photocatalyst
CN110624563A (en) Preparation method of silver ion doped zinc thioindate heterojunction photocatalyst
CN102085482A (en) Preparation method of p-CoO/n-CdS/TiO2 composite semiconductor photocatalyst
CN105600828A (en) Preparation method of porous nano CuFe2O4
CN108686681B (en) graphene/ZnS-MoS with visible light catalytic activity2Nano solid solution photocatalyst
Liu et al. S-scheme heterojunction ZnO/g-C3N4 shielding polyester fiber composites for the degradation of MB
CN111705419A (en) Metal-loaded carbon nitride-doped graphene-based flexible non-woven fabric and preparation method and application thereof
CN116020496A (en) BiOI/Zn with discrete structure 2 TiO 4 Heterojunction nanofiber photocatalyst and preparation method and application thereof
CN103977821A (en) Cu3SnS4-graphene composite visible-light-driven photocatalyst and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20140813