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Ossila/P3HT Polymer | CAS 104934-50-1/M107 Mw=24480 (1g)/M107-1g
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Ossila/P3HT Polymer | CAS 104934-50-1/M107 Mw=24480 (1g)/M107-1g
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M107-1g
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Ossila provides a range of Regioregular poly(3-hexylthiophene-2,5-diyl), commonly known as P3HT, with different molecular weights and regioregularities for a variety of research purposes. Produced by Merck KGaA under the Lisicon® brand this high quality P3HT collection allows a wider range of science and engineering to be undertaken than by using a single P3HT.

The highest regioregularity P3HT (M104, RR = 96.3%) produces highly crystalline films and is recommended for OFETs, nanofibril formation and fast drying OPVs at the thin interference peak (90 nm). However, the exceptionally high regioregularity of this P3HT means that gelling and surface roughness can be an issue for slow-drying thick-film OPVs (>200 nm). Lower molecular weight and regioregularity P3HT is recommended for inkjet and other large area or slow drying deposition techniques where gelling/aggregation and surface roughness need to be avoided.

A fabrication report with mobility measurements of 0.12 cm2/Vs for M104 can be found below.

All the P3HT below is highly soluble (50 mg/ml) in chlorinated solvents such as chloroform, chlorobenzene, dichlorobenzene and trichlorobenzene. The intermediate and lower molecular weight P3HT materials are recommended for use with non-chlorinated solvents such as xylene, toluene and THF due to their increased solubility.

General Information

Full namePoly(3-hexylthiophene-2,5-diyl)
SynonymsP3HT
CAS number104934-50-1
Chemical formula(C4H2S)n
Molecular weightSee Batch Details table at bottom of the page for information
HOMO / LUMOHOMO = -5.2 eV, LUMO = -3.2 eV
SolubilityChloroform, chlorobenzene
Classification / FamilyPolythiophenes, Organic semiconducting materials, Low band gap polymers, Polymer donors, Organic photovoltaics, Polymer solar cells, OLEDs, OFETs

OFET Fabrication Routine

This procedure details the fabrication and charge mobility measurements for OFETs made from the M104 batch of P3HT. A full fabrication report can be downloaded here.

Field effect mobilities in excess of 0.12 cm2/Vs are recorded using M104 when the active layer is dispensed on OTS-treated silicon oxide dielectric by static spin coating from an optimized high/low boiling point solvent mix.

High hole mobility in conjunction with good solubility and partial air stability make regioregular P3HT a reference material of choice for both fundamental and applied research in organic electronic, physics and chemistry. As one of the most well-studied organic semiconductor, P3HT is often acknowledge to be one of the benchmark against which any new p-type or donor conjugate molecule should be compared and evaluated.

Mobility has previously been found to be positively correlated with increasing region-regularity, slow drying time (achieved using high boiling point solvent), lowering of the surface energy, and molecular weight in excess of 50 kD. These conditions favour p-p stacking parallels to the OFET substrate, which in turn results in improved charge transport across the transistor channel [1-13].

Substrate size20 x 15 mm
Gate conductivity1-30 O·cm (Boron doped)
Silicon oxide thickness300 nm
Device per substratesFive, common gate
Channel length30 µm
Channel width1000 µm

The active layer solution preparation, spin coating, substrate annealing and measurements are performed in a glove box under a nitrogen atmosphere (H2O <0.1 PPM; O2 < 5/8 PPM).

For generic details on the fabrication of OPV devices, please see our written guide and video demonstration.

Active Layer Preparation

High-Regioregular and high molecular weight RR-P3HT (M104) (RR = 96.3%, Mw = 77,500, Mn = 38,700) is dissolved in a mix of high and low boiling point solvent in order to exploit the beneficial effect of long drying time and increase the wettability of low energy surface, respectively.

  • 5 mg/ml of M104 dissolved in anhydrous Chloroform:Trichlorobenzene (99:1) mix;
  • Vial is placed on hot plate (70°C) with a stirrer bar for 30 minutes;
  • Solution cooled down at room temperature and then filtered with a 0.45 µm PTFE (hydrophobic) filter;
  • Solution stored overnight on a hot plate at 30°C to prevent excessive aggregation of the P3HT molecules.

Substrate Cleaning

  • Substrates loaded on to substrate rack (to keep them in upright position);
  • Sonicated in hot Hellmanex III solution (1%) for five minutes;
  • Rinsed twice in hot water;
  • Sonicated in warm Isopropyl alcohol (70°C) for five minutes;
  • Rinsed twice in cold DI water;
  • Substrates stored in DI water.

Thermal Deposition of Electrodes and Contact Pads

  • Done on Edwards 306 Thermal coater in clean room condition;
  • Substrates are blown dry and loaded in a low density evaporation stack with a low density shadow mask to pattern the desired features;
  • Secondary mask is added to selectively evaporate the gate and drain/source pads;
  • Vacuum chamber pumped down to a vacuum pressure of 5 x 10-6 mbar;
  • Chromium adhesion layer: 5 nm, rate 0.05 nm/s;
  • Aluminium: 80 nm, rate: 0.4 nm/s;
  • Changed secondary mask to deposit electrodes (FET channels);
  • Vacuum: 2-3 x 10-6 mbar;
  • Chromium adhesion layer: 1 nm, rate 0.05 nm/s;
  • Gold: 40 nm; rate 0.05 nm/s.

PFBT Treatment for Au Electrodes (Laminar flow)

  • Oxygen plasma treatment, 30 seconds at 100 W;
  • Substrates immersed in 2.5 mMol/l solution of PFBT in isopropyl alcohol at room temperature;
  • Substrates rinsed twice in pure isopropyl alcohol;
  • Substrates are blown with nitrogen gun.

OTS Treatment for SiO2 Dielectric (Laminar flow)

  • A solution of OTS (25 microlitres) in cyclohexane (anhydrous grade, 1 ml) prepared in glove box;
  • Substrates (pre-loaded on a substrate rack) loaded into the annealing beaker, which is filled with approx. 50 ml of cyclohexane in a fume hood;
  • Previously prepared OTS solution quickly added to the cyclohexane and mixed with a pipette tip;
  • The glass lid is placed halfway onto the beaker, which is carefully filled with more cyclohexane until it is full and the lid is fully closed;
    • The final solution (60 ml) contains OTS at a concentration of 1 mMol/l;
  • Substrates kept for 20 minutes in the OTS solution;
  • Substrates removed from the OTS solution, quickly rinsed twice in clean cyclohexane, and then are blown dry with nitrogen gun.

Contact Angle Assessment

The water-drop test on the treated silicon is a quick test to qualitatively assess the effect of the OTS on the silicon substrates to ensure that the fabrication has functioned correctly. You can get a good approximation of the contact angle using your eye or a simple digital photo.

Previous quantitative assessments have shown that this routine will produce contact angles between 90 and 110°C (depending on the lab temperature, humidity and other factors). You can quantify that contact angle easily and accurately using the Ossila Contact Angle Goniometer.

P3HT (M104) spin coating (glove box)

  • 30 µl of Organic Semi-Conductor (OSC) solution delivered on the middle of the substrate and then spin coated at 1000 rpm for 10 s followed by 60 s at 2000 rpm;
  • Cotton swab soaked in chlorobenzene to thoroughly wipe clean the contact pads and the rest of the substrates with the exception of the area around the channel;
  • High precision cotton swab to clean between devices to avoid cross-talking and reduce leakage;
  • Substrates annealed at 90°C for 30 minutes;
  • Cooled down for ten minutes;
  • Five devices per substrate are characterised using OFET Test Board for Low-Density OFETs in a glove box;
  • Second annealing at 120°C for 20 minutes, slow cooling down at room temperature and measurement;
  • Annealing at 150°C for 20 minutes, slow cooling down at room temperature and measurement.

MSDS Documentation

P3HT MSDSP3HT MSDS sheet

Batch Details

The below P3HT is in stock for immediate dispatch.

BatchRRMwMnPDIPrice per 1 gramNotes

M102

95.7%

65,200

29,600

2.20

£329

Discontinued

M103

94.2%

54,200

23,600

2.30

£329

Discontinued

M105

95.5%

94,100

49,500

1.90

£329

Discontinued

M106

94.7%

34,100

19,500

1.75

£329

Discontinued

M107

93.6%

24,480

8,750

2.8

£329

In Stock

M108

94.2%

36,010

13,340

2.7

£329

In Stock

M109

95.2%

36,600

18,300

2.0

£329

In Stock

M1010

97.3%

74,000

35,240

2.1

£329

In Stock

M101197.6%60,15028,6502.1£329In Stock

To the best of our knowledge the technical information provided here is accurate. However, Ossila assume no liability for the accuracy of this information. The values provided here are typical at the time of manufacture and may vary over time and from batch to batch.

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蛋白样本先进行SDS-PAGE预分离,然后根据条带情况切成数十条进行胶内酶切,随后做傅里叶变换质谱(LC-MS),结果出来有质谱峰图基本都被几个多聚物峰图给覆盖了。

谢谢各位帮忙!
PDL1123
2017-10-01
向左转|向右转
各位大侠,小弟最近在做神经元细胞培养,为了促进细胞贴壁,准备购买多聚赖氨酸铺板,请教一下,是多聚-D赖氨酸还是多聚-L赖氨酸好啊?分子量是7-15万,还是3-7万好啊?请有这方面经验的老师给予指点,小弟在此谢过了啊!:)
有个回:最好买300辆二手奥托,再雇300个司机,让他们跟在你后面开,一会排成S,一会排成B
suzhou polymer science advanced materials co.ltd
苏州高分子科学先进材料有限公司

polymer英[ˈpɒlɪmə(r)]美[ˈpɑ:lɪmə(r)]
n.多聚物; [高分子] 聚合物;
[例句]The nature of the polymer is currently a trade secret.
这一聚合物的性质目前是个商业机密。
[其他]复数:polymers
多聚半乳糖醛酸酶酶活的测定,是检测多聚半乳糖醛酸酶对底物多聚半乳糖醛酸的水解,其活性是由生成物D-半乳糖醛酸的生成量来表示,请问D-半乳糖醛酸标准曲线怎么绘制,有具体的实验步骤吗?谢谢!
聚合物水泥防水浆料工艺配方,浆料包括液料组分和粉料组分,液料组分包括高分子乳液、分散剂、防腐剂、消泡剂、余量为水;粉料组分包括普通硅酸盐水泥、超细炉渣、超细钢渣、脱硫石膏、级配石英粉、膨润土、速溶硅酸钠、硬脂酸钠、减水剂。本发明具有优异的抗渗和粘结性能,且抗老化,耐酸碱,成本低廉,可有效利用固体废弃物,同时具有自修复功能,能够在混凝土内部形成结晶体,具有一定的二次抗渗功能。
Polymer 聚合物的释义123
Maggie銆佽彶庐2017-10-01
polymer
英 [ˈpɒlɪmə(r)]
美 [ˈpɑ:lɪmə(r)]

  n.
多聚物; [高分子] 聚合物;

  [例句]The nature of the polymer is currently a trade secret.

  这一聚合物的性质目前是个商业机密。

  [其他]
复数:polymers
  高分子化合物又称高分子(聚合物),高分子是由分子量很大的长链分子所组成,高分子的分子量从几千到几十万甚至几百万。而每个分子链都是由共价键联合的成百上千的一种或多种小分子构造而成。高分子的分类有多种,按来源可分为天然高分子、天然高分子衍生物、合成高分子三大类;根据用途则可分为合成树脂和塑料、合成橡胶、合成纤维等;按热行为可分为热塑性和热固性聚合物;按主链结构可分为碳链、杂链、和元素有机三类;另外根据工业产量和价格还可分为通用高分子、中间高分子、工程塑料以及特种高分子等等。
请教各位,做免疫组化所用的二步法,是一种多聚多聚鳌合物酶法,看见资料上讲可用三种不同的物质去制备这种多聚鳌合物,例如多聚糖、氨基酸等,现在就是不明白它是怎么和IgG、HRP连在一起制备成多聚物的,请各位高人指导,先在此谢谢!
看到一篇透皮给药系统中多聚物应用的文章,感觉写的比较好,翻译过来大家共享一下。

多聚物在透皮给药系统中的应用-2.doc(296.5k)
你好!
免疫组化多聚物法
immunohistochemistry
英[ɪmjʊnəʊhɪstəʊ'kemɪstrɪ]
美[ɪmjʊnoʊhɪstoʊ'kemɪstrɪ]
[词典]免疫组织化学;
[例句]Methods Transmission electron microscope and immunohistochemistry were used.
方法采用透射电镜和免疫组化法。
Title:PolymericReceptorsfortheRecognitionofFolicAcidandRelatedCompoundsviaSubstructureImprinting

Author:AndrewJ.Hall,MilenaQuaglia,PanagiotisManesiotis,ErsiliaDeLorenzi,andBörjeSellergren

Resource:AnalyticalChemistry,2006,78(24):8362-8367.

Abstract:
Arangeof2-acrylamidopyridines,showingsubtledifferencesinsolutionbindingtowardcarboxylicacids,hasbeeninvestigatedasfunctionalmonomersinmolecularimprinting.ImprintingofN-Z-L-glutamicacidwithonesuchmonomerisshowntobeeffectiveinthecreationofamolecularlyimprintedpolymer(MIP)withrecognitionpropertiesforitstemplateandalsoforlargermoleculescontainingglutamicacidresidues.IncomparisontoaMIPpreparedviaamore"trADItional"approach,thenewpolymericreceptorsexhibitreducednonspecificbinding.Thenewreceptorsarecomparedwithpreviouslyreportedurea-basedreceptorstargetingtheglutamicacidresidueandreceptorstargetingthepteridinesubstructureoffolicacid.

PMID:17165828