CN102120186B - Preparation method of platinum nanoparticle loaded graphene - Google Patents

Preparation method of platinum nanoparticle loaded graphene Download PDF

Info

Publication number
CN102120186B
CN102120186B CN201010552955A CN201010552955A CN102120186B CN 102120186 B CN102120186 B CN 102120186B CN 201010552955 A CN201010552955 A CN 201010552955A CN 201010552955 A CN201010552955 A CN 201010552955A CN 102120186 B CN102120186 B CN 102120186B
Authority
CN
China
Prior art keywords
graphene
glycol solution
ethylene glycol
preparation
pyrene methylamine
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.)
Expired - Fee Related
Application number
CN201010552955A
Other languages
Chinese (zh)
Other versions
CN102120186A (en
Inventor
李文博
翟东媛
潘力佳
邱浩
庞欢
施毅
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.)
Nanjing University
Original Assignee
Nanjing University
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 Nanjing University filed Critical Nanjing University
Priority to CN201010552955A priority Critical patent/CN102120186B/en
Publication of CN102120186A publication Critical patent/CN102120186A/en
Application granted granted Critical
Publication of CN102120186B publication Critical patent/CN102120186B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Abstract

The invention relates to a preparation method of platinum nanoparticle loaded graphene, comprising the following steps: (1), ultrasonically disperse restored graphene in a glycol solution, and adding the glycol solution of 1-pyrene methylamine, wherein the ratio (mg: ml: ml) of the graphene to the glycol to the glycol solution of the 1-pyrene methylamine is 1: (8-20): (1-1.5), and the concentration of the glycol solution of the 1-pyrene methylamine is 10<-3> M; stirring for 20-120 minutes to assemble the 1-pyrene methylamine on the surface of the graphene; and (2), adding Nml of a 0.048M chloroplatinic acid glycol solution, wherein the ratio (mg: ml) of the graphene to the Nml is 1: (0.8-1.5); adjusting the pH value of the glycol solution in the step (1) to be 8-9 with 0.1 M sodium hydroxide, continuing to stir, reacting for 2 hours in the oil bath at the temperature of 160 DEG C to obtain the high-density platinum nanoparticle loaded graphene, and cleaning and performing freeze-drying.

Description

The preparation method of supported platinum nano particle on Graphene
Technical field:
The present invention be a kind of on Graphene the preparation method of high density supported platinum nano particle.
Technical background:
Graphene has just received extensive concern since 2004 are found by people such as Novoselov.This two-dimensional material has the electron mobility [1] of superelevation under the room temperature, higher mechanical strength [2], high specific area and good heat endurance [3]; Make it as the nano electron device material; Sensor material, battery material, catalysis material fields such as [4] has application prospects.Recently, use Graphene more and more to be paid close attention to, and the work of having delivered has proved that the composite of this platinum/graphen has good catalytic performance [5,6], can well be applied in the methanol fuel cell by people as the carrier of catalysis material.But inertia and the slickness surperficial because of Graphene make that the direct Pt nanoparticle that reaches than steady load at Graphene surface acquisition higher density is very difficult; So the Graphene that electronation at present obtains often is used as the carrier of nano particle; Because more not reduction group and defective, fixedly nano particle are contained in the Graphene surface that this method obtains.But the particulate load amount and the quality of the composite that the randomness of group and defect distribution of not reducing make to obtain also are restricted.The purpose of present patent application is through self-assembling method, the composite of high density supported platinum nano particle on the preparation electronation Graphene.The method not only can realize platinum high density, high load uniformly, because it is not with not reduction group and the defective platinum on surface, so can also be applied to the synthesizing of composite of the Graphene that method of reducing non-chemically obtains.
Relating to Graphene area load method of metal nanoparticles can be referring to the open CN101797502A of Chinese patent, a kind of method for making of noble metal-graphene nanometer composite.Its key step is that noble metal precursor salt and electrolytic salt are joined in the aqueous solution that contains surfactant; Add the Graphene that water disperses in proportion, regulate the pH value, adopt the method for ultrasonic electrochemical, reaction makes noble metal-graphene nanometer composite under constant current density and ultrasound intensity.The open CN101799444A of Chinese patent, graphene-Pt nano composite material synthesized by microwave method and application process thereof.Its method is that graphite oxide is dissolved in the hexylene glycol solution; Through ultrasonic Treatment, chloroplatinic acid hexylene glycol drips of solution is added in the said mixture, stir the mixed solution that the back adds NaOH/hexylene glycol; Put into microwave after stirring again and handle, obtain Graphene platinum nano composite material.These two kinds of methods all do not relate to carries out surperficial self-assembled modified load.
[1]K.I.Bolotin,K.J.Sikes,Z.Jiamg,M.Klima,G?Fudenberg,J.Hone,P.Kim?and?Stormer,Solid?State?Commun.2008,146,351.
[2]T.J.Booth,P.Blake,R.R.Nair,D.Jiang,E.W.Hill,U.Bangert,A.Bleloch,M.K.S.Novoselov,M.I.Katsnelson,A.K.Geim,Nano?Lett.2008,8,2442.
[3]H.M.A.Hassan,V.Abdelsayed,A.E.R.S.Khder,K.M.AbouZeid,J.Terner,]El-Shall,S.I.Al-Resayes,A.A.El-Azhary,J.Mater.Chem.2009,19,3832.
[4]A.K.Geim,K.S.Novoselov.Nat.Mater.2007,6,183.
[5]C.Xu,X.Wang,J.W.Zhu,J.Phys.Chem.C?2008,112,19841.
[6]Y.?J.Li,W.Gao,L.J.Ci,C.M.Wang,P.M.Ajayan,carbon?2010,48,1124.
Summary of the invention
The objective of the invention is to propose a kind of through self-assembled modified, the preparation method of the composite of high density supported platinum nano particle on the electronation Graphene
Technical scheme of the present invention is: the preparation method of supported platinum nano particle on Graphene; Obtain the Graphene of reduction through the common chemical reduction; The interaction that utilizes π-π afterwards is at the surperficial self-assembled modified one deck 1-pyrene methylamine of Graphene; Because the amino load that exists for nano particle provides nuclearing centre, so at last the Graphene of 1-pyrene methylamine modified is put into reduction of ethylene glycol chloroplatinic acid system, the composite of preparation supported platinum nano particle.
Concrete preparation method:
(1) gets ultrasonic being dispersed in the ethylene glycol solution of Graphene of reduction, add the ethylene glycol solution of 1-pyrene methylamine again, the ratio of the ethylene glycol solution of Graphene, ethylene glycol and 1-pyrene methylamine (mg: ml: be 1 ml): 8-20: 1-1.5; The concentration of the ethylene glycol solution of 1-pyrene methylamine is 10 -3M stirred 20-120 minute, made 1-pyrene methylamine self-assemble to the Graphene surface;
(2) the chloroplatinic acid ethylene glycol solution of the 0.048M of adding Nml; Graphene is than Nml (mg: be 1 ml): 0.8-1.5; Regulating (1) middle ethylene glycol solution adjusting pH value with the NaOH of 0.1M is 8-9; Continue to stir, reaction obtained high density supported platinum nano particle on the Graphene in 2 hours in 160 ℃ oil bath; Clean freeze-drying afterwards.
(3) interaction that utilizes π-π of 1-pyrene methylamine forms self-assembled film on the Graphene surface, and the lone pair electrons of nitrogen can interact with platinum in the amino, for the load of platinum provides nuclearing centre
(4) non-chemically the Graphene of reduction also can obtain the high load of platinum uniformly of high density through the method.
(5) Graphene that reduces through common chemical reduction acquisition: under 95 ℃, be equipped with graphite oxide, reacted a hour, clean freeze-drying, obtain the Graphene that reduces with hydrazine reduction Hummers legal system.
The present invention relates to the preparation of high density supported platinum nano particle on Graphene; The interaction of the π-π on 4 phenyl ring through pyrene and Graphene surface is self-assembled modified one deck 1-pyrene methylamine on the Graphene surface, then because the lone pair electrons of nitrogen and the interaction of platinum in the amino, for the Pt nanoparticle load provides nuclearing centre; Obtain the composite of supported platinum nano particle; The granular size of platinum is between 2-5nm, and height is evenly distributed on the Graphene, and high density has covered the Graphene surface.This composite can be applied in the methanol fuel cell because its good catalytic performance, and in other fields such as catalysis and SERS good prospects for application is arranged.
The invention has the beneficial effects as follows: can obtain high density, the composite of high uniform load Pt nanoparticle, course of reaction is simple, and can be applicable to non-chemically to reduce the Graphene of preparation.
Description of drawings
Fig. 1: the finishing principle schematic of platinum is again carried out in self assembly
Fig. 2: (a) electromicroscopic photograph of the Graphene of area load Pt nanoparticle, scale is 100nm; (b) Electronic Speculum enlarged photograph, scale 10nm.
Fig. 3:, carry out the characteristic element imaging for proving the self-assembled modified of certain realization 1-pyrene methylamine.Be respectively the SEM photo, the element imaging of C, the element imaging of N, the element imaging of Pt
The specific embodiment
The exemplary steps of the composite of high density supported platinum nano particle is following on the preparation electronation Graphene:
(1) hydrazine electronation graphite oxide: under 95 ℃, the graphite oxide with the preparation of hydrazine reduction Hummers method reacted one hour, cleaned freeze-drying, obtained the Graphene of reduction.
(2) self-assembled modified one deck 1-pyrene methylamine on the Graphene surface, 1-pyrene methylamine utilizes the interaction of π-π to form self-assembled film on the Graphene surface: get in the ultrasonic 80ml of the being dispersed in ethylene glycol solution of Graphene of 8mg reduction, adding 12ml concentration is 10 -3The ethylene glycol solution of the 1-pyrene methylamine of M stirs 30 minutes (room temperature gets final product).Make 1-pyrene methylamine self-assemble to the Graphene surface
(3) ethylene glycol is in the pH8-9 interval, and 160 ℃ of following reduction chloroplatinic acids prepare Pt nanoparticle.Obtain the composite of high platinum load: add the chloroplatinic acid ethylene glycol solution of the 0.048M of 0.8ml, with the NaOH of 0.1M the ethylene glycol solution of step (2) being regulated the pH value is 8-9, continues to stir, and reaction is 2 hours in 160 ℃ oil bath.Clean freeze-drying afterwards, obtain sample.
(4) interaction that utilizes π-π of 1-pyrene methylamine forms self-assembled film on the Graphene surface, and the lone pair electrons of nitrogen can interact with platinum in the amino, for the load of platinum provides nuclearing centre
(5) non-chemically the Graphene of reduction also can obtain the high load of platinum uniformly of high density through the method.

Claims (1)

1. the preparation method of supported platinum nano particle on Graphene is characterized in that the step for preparing is following:
(1) hydrazine electronation graphite oxide: under 95 ℃, the graphite oxide with the preparation of hydrazine reduction Hummers method reacted one hour, cleaned freeze-drying, obtained the Graphene of reduction;
(2) self-assembled modified one deck 1-pyrene methylamine on the Graphene surface, 1-pyrene methylamine utilizes the interaction of π-π to form self-assembled film on the Graphene surface: get in the ultrasonic 80ml of the being dispersed in ethylene glycol solution of Graphene of 8mg reduction, adding 12ml concentration is 10 -3The ethylene glycol solution of the 1-pyrene methylamine of M, stirring at room 30 minutes; Make 1-pyrene methylamine self-assemble to the Graphene surface;
(3) the chloroplatinic acid ethylene glycol solution of the 0.048M of adding 0.8ml uses the NaOH of 0.1M that ethylene glycol solution adjusting pH value is 8-9, continues to stir, and reaction is 2 hours in 160 ℃ oil bath, cleans freeze-drying afterwards, the acquisition product.
CN201010552955A 2010-11-22 2010-11-22 Preparation method of platinum nanoparticle loaded graphene Expired - Fee Related CN102120186B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201010552955A CN102120186B (en) 2010-11-22 2010-11-22 Preparation method of platinum nanoparticle loaded graphene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201010552955A CN102120186B (en) 2010-11-22 2010-11-22 Preparation method of platinum nanoparticle loaded graphene

Publications (2)

Publication Number Publication Date
CN102120186A CN102120186A (en) 2011-07-13
CN102120186B true CN102120186B (en) 2012-09-05

Family

ID=44248904

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201010552955A Expired - Fee Related CN102120186B (en) 2010-11-22 2010-11-22 Preparation method of platinum nanoparticle loaded graphene

Country Status (1)

Country Link
CN (1) CN102120186B (en)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102426868B (en) * 2011-09-05 2013-11-06 湖南大学 Water-soluble graphene-noble-metal nano-composite and preparation method and application thereof
CN102502607B (en) * 2011-11-10 2013-07-31 郑州大学 Method for preparing graphene solution based on supercritical carbon dioxide and pyrenyl polymers
CN102728398B (en) * 2012-06-18 2013-12-25 华东师范大学 Preparation method for ordered mesoporous non-noble metal-nitrogen-graphitized carbon material
CN102909005B (en) * 2012-10-24 2014-02-05 中国科学院理化技术研究所 Graphene-based composite material with surface coated by mesoporous silica and loaded with noble metal nanoparticles, as well as preparation method and application of graphene-based composite material
CN102976314B (en) * 2012-11-29 2015-05-13 中国科学院宁波材料技术与工程研究所 Novel titanium dioxide-graphene nano-composite material as well as manufacturing method and application thereof
CN103041857A (en) * 2012-12-17 2013-04-17 天津大学 Preparation method of graphite nano-plate-loaded nano-noble metal catalyst
CN104181258B (en) * 2013-05-24 2016-01-20 北京蛋白质组研究中心 Based on glycoprotein N-sugar chain single stage method enrichment-derivatization treatment and the MALDI-TOF-MS analytical approach of Graphene
CN103303905B (en) * 2013-06-26 2015-01-28 郑州大学 Synthesis method of water-soluble derivative of lanthanide series metal loaded carbon nano material and application of water-soluble derivative
CN103390507B (en) * 2013-07-04 2016-04-13 宁国市龙晟柔性储能材料科技有限公司 A kind of graphene/ platinum nano particle complex fiber electrode material and preparation method thereof
CN103341358A (en) * 2013-07-18 2013-10-09 北京林业大学 Catalyst for treating chlorine-containing organic waste water, and preparation method thereof
CN103435037A (en) * 2013-08-22 2013-12-11 东华大学 Method for preparing graphene/Pt nanocomposite material by liquid phase reduction method
CN103449500B (en) * 2013-09-24 2016-03-02 渤海大学 A kind of ultrasonic wave prepares the method for Red copper oxide carbon/graphene nano hierarchical organization hybrid material
KR20150088006A (en) * 2014-01-23 2015-07-31 삼성에스디아이 주식회사 Electrode catalyst for fuel cell, method for preparing the same, electrode for fuel cell including the electrode catalyst, and fuel cell including the same
CN104882507B (en) * 2015-04-03 2017-01-25 三峡大学 Pt-GFW/SiO2/n-Si heterojunction material and preparation method thereof
CN104865236B (en) * 2015-04-24 2017-11-03 天津理工大学 A kind of surface enhanced Raman scattering substrate of terahertz wave band semi-conducting material
CN105688763B (en) * 2016-04-08 2018-08-10 江苏大学 The method that the azepine three-dimensional grapheme aeroge of nano platinum particle load is prepared using one-step method
CN106093159B (en) * 2016-06-06 2018-06-08 大连理工大学 A kind of preparation method of the biosensor based on polypeptide-gold nanoparticle detection metal ion
CN107706431B (en) * 2017-09-26 2020-04-14 西南大学 Preparation method of graphene supported Pt nanoparticle catalyst, product and application thereof
CN111320162A (en) * 2018-12-14 2020-06-23 中国石油天然气股份有限公司 Pyrenemethylamine hydrochloride non-covalent modified graphene and preparation and application thereof
WO2021137525A1 (en) * 2019-12-31 2021-07-08 성균관대학교산학협력단 Method for producing graphene-coated metal particle and molybdenum disulfide complex, and complex produced thereby
KR102454305B1 (en) * 2019-12-31 2022-10-14 성균관대학교산학협력단 Methods of manufacturing composite of graphene-coated metal particles and molybdenum disulfide and composites manufactured by the methods
CN112374528B (en) * 2020-09-30 2023-03-17 中国科学院苏州纳米技术与纳米仿生研究所广东(佛山)研究院 Graphene surface-loaded zinc oxide nanoparticle composite material and preparation method and application thereof
CN113930236A (en) * 2021-10-11 2022-01-14 福建省海凝环保科技有限公司 Fluorescent sensor based on layered double hydroxide, pyrene-containing graphene oxide composite material, preparation method and application of pyrene-containing graphene oxide composite material

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101745384A (en) * 2009-12-14 2010-06-23 浙江大学 Platinum/graphene nano electro-catalyst and preparation method thereof
CN101780420A (en) * 2010-03-05 2010-07-21 中国科学院苏州纳米技术与纳米仿生研究所 Preparation method of metal and graphene composite catalyst
CN101799444A (en) * 2010-03-30 2010-08-11 南京邮电大学 Graphene-Pt nano composite material synthesized by microwave method and application method thereof
CN101797502A (en) * 2010-03-24 2010-08-11 南京大学 Preparation method of noble metal-graphene nanometer composite

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101745384A (en) * 2009-12-14 2010-06-23 浙江大学 Platinum/graphene nano electro-catalyst and preparation method thereof
CN101780420A (en) * 2010-03-05 2010-07-21 中国科学院苏州纳米技术与纳米仿生研究所 Preparation method of metal and graphene composite catalyst
CN101797502A (en) * 2010-03-24 2010-08-11 南京大学 Preparation method of noble metal-graphene nanometer composite
CN101799444A (en) * 2010-03-30 2010-08-11 南京邮电大学 Graphene-Pt nano composite material synthesized by microwave method and application method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Chengzhou Zhu etal.Layer-by-Layer Self-Assembly for Constructing a Graphene/Platinum Nanoparticle Three-Dimensional Hybrid Nanostructure Using Ionic Liquid as a Linker.《Langmuir》.2010,第26卷(第10期),第7614-7618页. *

Also Published As

Publication number Publication date
CN102120186A (en) 2011-07-13

Similar Documents

Publication Publication Date Title
CN102120186B (en) Preparation method of platinum nanoparticle loaded graphene
Sun et al. Recent progress with electrocatalysts for urea electrolysis in alkaline media for energy-saving hydrogen production
Xie et al. Defect‐rich MoS2 ultrathin nanosheets with additional active edge sites for enhanced electrocatalytic hydrogen evolution
Fominykh et al. Rock salt Ni/Co oxides with unusual nanoscale‐stabilized composition as water splitting electrocatalysts
Zhou et al. A facile approach to the synthesis of highly electroactive Pt nanoparticles on graphene as an anode catalyst for direct methanol fuel cells
Ranjani et al. 3D flower-like hierarchical NiCo 2 O 4 architecture on carbon cloth fibers as an anode catalyst for high-performance, durable direct urea fuel cells
Ye et al. Enhancing the catalytic activity of flowerike Pt nanocrystals using polydopamine functionalized graphene supports for methanol electrooxidation
CN108517537B (en) A kind of nitrogen-doped carbon loads double scale transition metal phosphides and its preparation method and application
CN101740785B (en) Palladium/graphene nano electro-catalyst and preparation method thereof
CN106450357B (en) A kind of graphene-supported Co-N-C supermolecule heterozygosis aerogel composite and its preparation method and application
KR20060133577A (en) Carbon nanotube pastes and methods of use
Luksirikul et al. Electron promotion by surface functional groups of single wall carbon nanotubes to overlying metal particles in a fuel‐cell catalyst
CN110479329A (en) A kind of preparation and application of phosphorus doping cobaltous telluride nano material
KR101349912B1 (en) Pt/GR nanocomposites and method for producing thesame
Li et al. CoP-anchored high N-doped carbon@ graphene sheet as bifunctional electrocatalyst for efficient overall water splitting
Gong et al. Carbon-coated Co-Mo-P nanosheets supported on carbon cloth as efficient electrocatalyst for Hydrogen Evolution Reaction
Lan et al. N, S co-doped carbon quantum dots anchoring on copper-vacancy-rich Cu nanowires/Cu foam as the cathode in microbial fuel cells: Role of CS-Cu active site
CN110433842A (en) Vertical molybdenum disulfide nano sheet and porous N doping carbon ball composite material and preparation method thereof for electrolysis water liberation of hydrogen
TWI654026B (en) Redox catalyst, electrode material, electrode, membrane electrode assembly for fuel cell, and fuel cell
Zhang et al. Enhanced piezo-catalytic H2O2 production over Bi0. 5Na0. 5TiO3 via piezoelectricity enhancement and surface engineering
Zhang et al. Facile synthesis of Co–Fe layered double hydroxide nanosheets wrapped on Ni-doped nanoporous carbon nanorods for oxygen evolution reaction
Wang et al. Controlled tuning the morphology of CoNiP catalysts with ultra-high activity for water splitting at large current densities in alkaline medium
Zhou et al. Boosting oxygen evolution reaction activity and durability of phosphate doped Ni (OH) 2/FeOOH hierarchical microtubes by morphology engineering and reconstruction strategy
Zhao et al. Electrocatalytic oxidation of methanol at 2-aminophenoxazin-3-one-functionalized multiwalled carbon nanotubes supported PtRu nanoparticles
Hu et al. l-Lysine-induced green synthesis of CoS/Co 3 O 4 nanoframes for efficient electrocatalytic oxygen evolution

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20120905

Termination date: 20141122

EXPY Termination of patent right or utility model