NL2031042A - Ternary visible light photocatalytic nanocomposite and preparation method thereof - Google Patents
Ternary visible light photocatalytic nanocomposite and preparation method thereof Download PDFInfo
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- NL2031042A NL2031042A NL2031042A NL2031042A NL2031042A NL 2031042 A NL2031042 A NL 2031042A NL 2031042 A NL2031042 A NL 2031042A NL 2031042 A NL2031042 A NL 2031042A NL 2031042 A NL2031042 A NL 2031042A
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- visible light
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- phosphorus
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- 239000002114 nanocomposite Substances 0.000 title claims abstract description 27
- 230000001699 photocatalysis Effects 0.000 title claims abstract description 27
- 238000002360 preparation method Methods 0.000 title claims abstract description 14
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 42
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 claims abstract description 30
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 21
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000007864 aqueous solution Substances 0.000 claims abstract description 17
- NFEURUSKIHJCRP-UHFFFAOYSA-N 1,2,3-trinitropyrene Chemical compound C1=CC=C2C=CC3=C([N+]([O-])=O)C([N+](=O)[O-])=C([N+]([O-])=O)C4=CC=C1C2=C43 NFEURUSKIHJCRP-UHFFFAOYSA-N 0.000 claims abstract description 14
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000002105 nanoparticle Substances 0.000 claims abstract description 13
- 238000001914 filtration Methods 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 10
- 229910001961 silver nitrate Inorganic materials 0.000 claims abstract description 10
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000011574 phosphorus Substances 0.000 claims abstract description 9
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 9
- 238000001035 drying Methods 0.000 claims abstract description 8
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims abstract description 7
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000001027 hydrothermal synthesis Methods 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 7
- 229910017604 nitric acid Inorganic materials 0.000 claims abstract description 7
- 238000002156 mixing Methods 0.000 claims abstract description 3
- 239000000463 material Substances 0.000 claims description 24
- 239000000243 solution Substances 0.000 claims description 13
- 238000003756 stirring Methods 0.000 claims description 7
- 238000000502 dialysis Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910021389 graphene Inorganic materials 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 7
- 229940061607 dibasic sodium phosphate Drugs 0.000 claims 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims 1
- 238000010992 reflux Methods 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 abstract description 8
- 239000002086 nanomaterial Substances 0.000 abstract description 5
- STZCRXQWRGQSJD-UHFFFAOYSA-M sodium;4-[[4-(dimethylamino)phenyl]diazenyl]benzenesulfonate Chemical compound [Na+].C1=CC(N(C)C)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-UHFFFAOYSA-M 0.000 abstract description 3
- 239000008204 material by function Substances 0.000 abstract description 2
- 229910021612 Silver iodide Inorganic materials 0.000 description 19
- 229960005196 titanium dioxide Drugs 0.000 description 17
- 235000010215 titanium dioxide Nutrition 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 11
- 238000010586 diagram Methods 0.000 description 11
- 239000011259 mixed solution Substances 0.000 description 8
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 7
- 229940045105 silver iodide Drugs 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 229960004839 potassium iodide Drugs 0.000 description 6
- 235000007715 potassium iodide Nutrition 0.000 description 6
- 238000001816 cooling Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- 239000002131 composite material Substances 0.000 description 3
- DGLRDKLJZLEJCY-UHFFFAOYSA-L disodium hydrogenphosphate dodecahydrate Chemical group O.O.O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].OP([O-])([O-])=O DGLRDKLJZLEJCY-UHFFFAOYSA-L 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 238000000026 X-ray photoelectron spectrum Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000003344 environmental pollutant Substances 0.000 description 2
- 238000000445 field-emission scanning electron microscopy Methods 0.000 description 2
- 238000002173 high-resolution transmission electron microscopy Methods 0.000 description 2
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 2
- 229940012189 methyl orange Drugs 0.000 description 2
- 238000007146 photocatalysis Methods 0.000 description 2
- 231100000719 pollutant Toxicity 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003917 TEM image Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000349 field-emission scanning electron micrograph Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002957 persistent organic pollutant Substances 0.000 description 1
- 239000011941 photocatalyst Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000003911 water pollution Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/16—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr
- B01J27/18—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr with metals other than Al or Zr
- B01J27/1802—Salts or mixtures of anhydrides with compounds of other metals than V, Nb, Ta, Cr, Mo, W, Mn, Tc, Re, e.g. phosphates, thiophosphates
- B01J27/1817—Salts or mixtures of anhydrides with compounds of other metals than V, Nb, Ta, Cr, Mo, W, Mn, Tc, Re, e.g. phosphates, thiophosphates with copper, silver or gold
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/72—Treatment of water, waste water, or sewage by oxidation
- C02F1/725—Treatment of water, waste water, or sewage by oxidation by catalytic oxidation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- B01J21/063—Titanium; Oxides or hydroxides thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/18—Carbon
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/48—Silver or gold
- B01J23/50—Silver
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
- B01J35/39—Photocatalytic properties
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
- B01J37/0207—Pretreatment of the support
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
- B01J37/0217—Pretreatment of the substrate before coating
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/30—Treatment of water, waste water, or sewage by irradiation
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Abstract
The disclosure discloses a ternary visible light photocatalytic nanocomposite and a preparation method thereof, and belongs to the technical field, of functional materials. The preparation. method comprises the following steps: Sl, preparing phosphorus—doped graphene quantum dots: preparing trinitro—pyrene from pyrene and nitric acid; and adding water into the trinitro—pyrene, adding a phosphorus source, adjusting pH to 10—11, and performing a hydrothermal reaction at 180 degrees Celsius to prepare the phosphorus—doped graphene quantum dots; and SZ, preparing an aqueous solution of the phosphorus—doped graphene quantum dots in Sl, mixing the aqueous solution with titanium dioxide nanoparticles, silver nitrate and potassium iodide, and filtering and drying the mixture to prepare the ternary visible light photocatalytic nanocomposite. The catalytic efficiency in 10 min can reach 99.35% when the prepared nanomaterial is put in a methyl orange solution. under visible light irradiation, and the nanomaterial shows excellent catalytic performance.
Description
TECHNICAL FIELD The disclosure belongs to the technical field of functional materials, and particularly relates to a ternary visible light photocatalytic nanocomposite and a preparation method thereof.
BACKGROUND ART Organic dyestuff water pollution brings huge hidden danger to health and safety of people, and has become a major challenge in the world. Semiconductor photocatalysis is a prospective method for solving this problem. In semiconductor multielement photoca- talysis, multiple refractory pollutants from the environment are decomposed under ultraviolet/visible light irradiation, and tita- nium dioxide is the most potential in several known researched photocatalytic semiconductor materials, has the characteristics of being stable in performance, free of toxicity, low in cost, etc., and has been widely applied to multiple fields when it was applied to water decomposition for the first time in 1972. However, its photocatalytic efficiency is limited due to the defects such as broad band gap and high carrier recombination rate. A currently- prepared photocatalytic composite with the titanium dioxide as a main component can catalytically degrade organic dyestuff pollu- tants in water only under ultraviolet light, but is poor in cata- lytic effect in a visible light wavelength area, is extremely low in solar energy utilization rate and is hardly used commercially on a large scale.
SUMMARY In order to solve the above technical problems, the disclo- sure provides a ternary visible light photocatalytic nanocomposite and a preparation method thereof, titanium dioxide nanoparticles and phosphorus-doped graphene duantum dots are bonded with silver iodide through a simple and convenient method to form the nanocom- posite, the phosphorus-doped graphene quantum dots are introduced to the surface of titanium dioxide so as to improve photosensiti-
zation of the titanium dioxide, form P/N junctions with the tita- nium dioxide, remarkably improve carrier transport and reduce re- combination with photo-induced electrons, the silver iodide and the titanium dioxide are coupled to establish heterojunctions to form interface energy deviation between surfaces of semiconduc- tors, the charge hole separation efficiency can be improved, and the silver iodide has high absorption capacity for visible light radiation absorption; and the composite of the disclosure can ef- ficiently utilize sclar energy for decomposing different organic pollutants in water.
The disclosure is specifically achieved through the following technical solution.
The first objective of the disclosure is to provide a prepa- ration method of a ternary visible light photocatalytic nanocompo- site, comprising the following steps: Sl, preparing phosphorus-doped graphene quantum dots: preparing trinitro-pyrene from pyrene and nitric acid; and adding water into the trinitro-pyrene, adding a phosphorus source, adjusting pH to 10-11, and performing a hydrothermal reaction at 180 degrees Celsius to prepare the phosphorus-doped graphene quan- tum dots; and S2,; preparing an aqueous solution of the phosphorus-doped graphene quantum dots in S1, mixing the aqueous solution with ti- tanium dioxide nanoparticles, silver nitrate and potassium iodide, and filtering and drying the mixture to prepare the ternary visi- ble light photocatalytic nanocomposite.
Optionally, in S1, a usage ratio of the pyrene to the nitric acid is 1 g: 100 mL.
Optionally, in S1, the trinitro-pyrene is prepared by heating in a water bath at 80 degrees Celsius, flowing back and stirring for 12 h.
Optionally, in S81, the phosphorus source is sodium phosphate dibasic dodecahydrate.
Optionally, in S1, a usage ratio of the trinitro-pyrene to the water to the phosphorus source is 1 mg: 1 mL: 0.03 g.
Optionally, in Sl, time of the hydrothermal reaction is 6 h.
Optionally, in S1, a solution is dialyzed through a dialysis bag with the molecular weight cut-off of 3500 Da for 24-36 h after the hydrothermal reaction and then dried.
Optionally, in S2, the raw material adding sequence is as follows: the titanium dioxide nano-particles are dispersed in the aqueous solution of the phosphorus-doped graphene quantum dots, the silver nitrate is added, and after the materials are uniformly mixed, a potassium iodide aqueous solution is added dropwise in the stirring process.
Optionally, in S2, the concentration of the aqueous solution of the phosphorus-doped graphene quantum dots is 0.2 mg/mL, and the usage ratio of the titanium dioxide nanoparticles to the aque- ous solution of the phosphorus-doped graphene quantum dots to the silver nitrate to the potassium iodide is 0.5 g : 500 mL : 0.097 g : 0.092 g.
The second objective of the disclosure is to provide the ter- nary visible light photocatalytic nanocomposite prepared through the above preparation method.
Compared with the prior art, the disclosure has the following beneficial effects: (1) in the disclosure, the titanium dioxide nanoparticles and the phosphorus-doped graphene quantum dots are bonded with the silver iodide to form the nanocomposite, the titanium dioxide, the phosphorus-doped graphene quantum dots and the silver iodide are successfully recombined into the ternary nanomaterial through a simple manner of dissolving in water, stirring and suspension ad- sorption when the nanocomposite is synthesized, manners such as heating are not used, the cost is low, and the operation is con- venient.
{2) the catalytic efficiency in 10 min can reach 99.35% when the prepared nanomaterial is put in the methyl orange solution un- der visible light irradiation, and the nanomaterial shows excel- lent catalytic performance.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a TEM diagram of a P25/PCDs/AgI material prepared in an embodiment 1; FIG. 2 is a HRTEM diagram of a P25/PCDs/AgI material prepared in an embodiment 1;
FIG. 3 is an FESEM diagram of a P25/PCDs/AgI material pre- pared in an embodiment 1; FIG. 4 is an EDS diagram of a P25/PCDs/AgI material prepared in an embodiment 1; FIG. 5 is an XPS spectrum diagram of a P25/PCDs/AgI material prepared in an embodiment 1; and FIG. 6 is a catalytic performance diagram of materials in an embodiment 1 and comparative examples 1-4 to methyl orange.
DETAILED DESCRIPTION OF THE EMBODIMENTS In order to make those skilled in the art better understand the technical solutions of the disclosure for implementation, the disclosure is further illustrated below with reference to specific embodiments and accompanying drawings, but the listed embodiments do not limit the disclosure.
Experimental methods and detection methods in the embodiments below are all conventional methods unless otherwise specified; and reagents and materials can be purchased on the market unless oth- erwise specified.
Embodiment 1 A preparation method of a ternary visible light photocatalyt- ic nanocomposite, comprises the following steps: (1) after 1 g of pyrene and 100 ml of nitric acid are mixed, the mixture is heated in a water bath at 80 degrees Celsius, flows back, and is stirred for 12 h, the reactant is added into 500 ml of purified water for filtering, a yellow solid, namely trinitro- pyrene is obtained, 40 mg of trinitro-pyrene is put in 40 ml of water, 1.2 g of sodium phosphate dibasic dodecahydrate is added as a phosphorus source, sodium hydroxide is added to enable the PH value of the mixed liquid to reach 10, and the mixed liquid is put in a 100 ml reaction still to be heated at 180 degrees Celsius for 6 h. Filtering is performed after cooling to obtain a solution, the solution is dialyzed through a dialysis bag at 3500 Da for 24 h, and then the dialyzed solution is dried by cooling to obtain phosphorus-doped graphene quantum dots (PCDs).
(2) 0.5 g of commercial-level titanium dioxide nanoparticles (P25) are taken and dispersed in 500 ml of aqueous solution of the phosphorus-doped graphene quantum dots (0.2 mg/ml) to be rapidly magnetically stirred for 0.5 h, 0.097 g of silver nitrate is put in the mixed solution to be rapidly magnetically stirred for 1 h, then 0.092 g of potassium iodide is dissolved in 20 ml of water, the mixture is added dropwise into the mixed solution, the mixture 5 is added dropwise into the mixed solution under stirring, it is found that the color obviously turns into yellow green, then fil- tering is performed and drying is performed at 60 degrees Celsius to obtain the novel ternary excellent visible light photocatalytic nanocomposite (P25/PCDs/AgI) with the titanium dioxide, phospho- rus-doped graphene quantum dots and silver iodide.
Embodiment 2 After 1 g of pyrene and 100 ml of nitric acid are mixed, the mixture is heated in a water bath at 80 degrees Celsius, flows back, and is stirred for 12 h, the reactant is added into 500 ml of purified water for filtering, a yellow solid, namely trinitro- pyrene is obtained, 40 mg of trinitro-pyrene is put in 40 ml of water, 1.2 g of sodium phosphate dibasic dodecahydrate is added as a phosphorus source, sodium hydroxide is added to enable the PH value of the mixed liquid to reach 11, and the mixed liquid is put in a 100 ml reaction still to be heated at 180 degrees Celsius for 6 h. Filtering is performed after cooling to obtain a solution, the solution is dialyzed through a dialysis bag at 3500 Da for 36 h, and then the dialyzed solution is dried by cooling to obtain phosphorus-doped graphene quantum dots.
0.5 g of commercial-level titanium dioxide nanoparticles (P25) are taken and dispersed in 500 ml of aqueous solution of the phosphorus-doped graphene quantum dots (0.2 mg/ml) to be rapidly magnetically stirred for 0.5 h, 0.097 g of silver nitrate is put in the mixed solution to be rapidly magnetically stirred for 1 h, then 0.092 g of potassium iodide is dissolved in 20 ml of water, the mixture is added dropwise into the mixed solution, the mixture is added dropwise into the mixed solution under stirring, it is found that the color obviously turns into yellow green, and then filtering is performed and drying is performed at 60 degrees Cel- sius to obtain the novel ternary excellent visible light photo- catalytic nanocomposite with the titanium dioxide, phosphorus- doped graphene quantum dots and silver iodide.
Comparative Example 1 Titanium dioxide nanoparticles (P25) are dispersed in 500 ml of aqueous solution of the phosphorus-doped graphene quantum dots (0.2 mg/ml) prepared in step (1) of the embodiment 1 to be rapidly magnetically stirred for 0.5 h, and then filtering is performed and drying is performed at 60 degrees Celsius to prepare a P25/PCDs material. Comparative Example 2 P25 is dispersed in 500 ml of aqusous solution of pure gra- phene quantum dots (0.2 mg/ml) to be rapidly magnetically stirred for 0.5 h, and then filtering is performed and drying is performed at 60 degrees Celsius to prepare a P25/CDs material. Comparative Example 3 P25 is dispersed in 500 ml of aqueous solution of pure gra- phene quantum dots {0.2 mg/ml) to be rapidly magnetically stirred for 0.5 h, 0.097 g of silver nitrate is put in the mixed solution to be rapidly magnetically stirred for 1 h, then 0.092 g of potas- sium iodide is dissolved in 20 ml of water, the mixture is added dropwise into the mixed solution, and then filtering is performed and drying is performed at 60 degrees Celsius to prepare a P25/CDs/AgI material. Comparative Example 4 Titanium dioxide nanoparticles (P25) The materials prepared in the embodiment 1 and the embodiment 2 have similar performance, the above material prepared in the em- bodiment 1 is taken as an example below, firstly, the material is represented, FIG. 1 is a TEM diagram of a P25/PCDs/AgI material, FIG. 2 is an HRTEM diagram of a P25/PCDs/AgI material, it can be seen from FIG. 2 that in three lattice distances, the plane lat- tice distance 0.35 nm corresponds to P25, the plane lattice dis- tance 0.231 nm corresponds to AgI, the plane lattice distance
0.243 nm corresponds to PCDs, and thus it proves that the compo- site is successfully synthesized; and FIG. 3 is an FESEM diagram of a material, it can be seen from FIG. 1 and FIG. 3 that TEM and FESEM images of the material are highly matched, they show that the nanocomposite is almost formed by spherical particles, and particle aggregation is observed due to the fact that the nanocom-
posite highly grows. FIG. 4 is an EDS diagram of a material, FIG. is an XPS spectrum diagram of a material, it can be clearly seen from FIG. 4 and FIG. 5 that a ternary catalyst sample contains C, FP, Ag, I, TI and O, and it shows that a ternary photocatalyst with 5 a stable structure is established through PCDs, AgI and TIOZ in a physical adsorption manner.
The comparative examples 1-4 are taken as controls below to represent the performance of P25/PCDs/AgI prepared in the embodi- ment 1, and the specific operation is as follows:
0.1 g of catalyst in the embodiment 1, 0.1 g of catalyst in the comparative example 1, 0.1 g of catalyst in the comparative example 2, 0.1 g of catalyst in the comparative example 3 and 0.1 g of catalyst in the comparative example 4 are taken and put in 10 mg/L of methyl orange solution respectively for ultrasonic treat- ment for 1 h in the dark to achieve adsorption equilibrium. Under 300 w visible light lamp irradiation, 5 ml of sample solution is filtered out every 5 min, and the methyl orange concentration in the solution is tested. The specific result is shown in FIG. 6, and it can be seen from the result in FIG. 6 that compared with the comparative examples 1-4, the catalytic efficiency in 10 min of the material prepared in the embodiment 1 can reach 99.35% un- der visible light irradiation, and the material shows excellent catalytic performance.
Obviously, those skilled in the art can make various modifi- cations and variations on the disclosure without departing from the spirit and the scope of the disclosure. Thus, if these modifi- cations and variations of the disclosure belong to the scope of the claims of the disclosure and equivalent technologies thereof, the disclosure also intends to include these modifications and variations.
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