
Methylammonium iodide (MAI), also referred to as methylamine hydroiodide, is a precursor for the synthesis of organic-inorganic hybrid perovskites for use in FETs, LEDs and PVs.
Applications
Due to the high purity of the methylammonium iodide (99.99%), it should be noted that its solubility is reduced within dimethyl formamide and dimethyl sulfoxide. This reduced solubility is due to the removal of trace amounts of residual hydroiodic acid (HI) used during the synthesis and purification of the material. This can potentially have an impact upon the performance of solar cells leading to a reduction in maximum power conversion efficiency achievable. Adding fixed concentrations of hydroiodic acid to perovskite solutions can allow for the improvement of device metrics[1-3]. Using high-purity precursor materials allows for accurate addition of amounts of hydroiodic acid giving higher reproducibility to experiments. It is recommended that between 1% and 10% hydroiodic acid is used with high-purity methylammonium iodide to achieve optimal device performance. The amount required depends on the precursors used, solution concentration, solvent used, and processing environment. Therefore, this will need to be adjusted for each individual laboratory and process.
For simpler ink fabrication, it is recommended that the lower-purity methylammonium iodide (>98%) is used.
- Hysteresis-less inverted CH3NH3PbI3 planar perovskite hybrid solar cells with 18.1% power conversion efficiency, J. H. Heo et al., Energ. Environ. Sci., 8, 602-1608 (2015); DOI: 10.1039/C5EE00120J.
- A [2,2]paracyclophane triarylamine-based hole-transporting material for high performance perovskite solar cells, S Park et al., J. Mater. Chem. A., 3, 24215-24220 (2015); DOI: 10.1039/C5TA08417B.
Enhanced optopelectronic quality of perovskite thin films with hydrophosphorous acid for planar heterojunction solar cells, W. Zhang et al., Nat. Commun., 6, 10030 (2015); doi:10.1038/ncomms10030.


Specifications
Chemical formula | CH6IN |
Synonyms | Methylamine hydroiodide |
CAS No. | 14965-49-2 |
Chemical name | Methylammonium iodide |
Physical appearance | White, crystalline solid |
Purification method | Recrystallisation (ethanol) |
Purity | >99.9% (as measured by elemental analysis) |
Molecular weight | 158.97 g/mol |
Recommended solvents for perovskite synthesis | DMF, DMSO |
NMR spectrum

Usage details
Reference devices - perovskite PVs
Reference devices were made to assess the performance of perovskite (MAI:PbCl2) based devices with the below structure. These were fabricated in air prior to spincasting the fullerene layer in a N2 glove box. Substrates were then transferred to a vacuum chamber where a composite metal cathode was thermally evaporated. Finally, substrates were encapsulated inside the glove box before measurements were taken under ambient conditions.
Glass / ITO (100 nm) / PEDOT:PSS (30 nm) / MAI:PbCl2 / PC70BM / Ca (5 nm) / Al (100 nm)
For generic details please see the fabrication guide and video. For specific details please see the below condensed fabrication report which details the optical modelling and optimisation of the multilayer stack.
The perovskite solution (MAI:PbCl2 at a molar ratio of 3:1) was made in dimethylformamide (DMF) at a concentration of 664 mg/ml. It was found to be critical that both materials were mixed dry prior to adding the solvent in order to achieve such high concentration.
For maximum efficiency, the active layer thickness was achieved from spincasting the heated solution (70°C) onto a hot PEDOT:PSS substrate (90°C) at a spin speed of 5000 rpm for 30s. The films were then placed back onto the hotplate (90°C) for 2 hrs. The data below shows the maximum performance achieved from non-optimised conditions.
Overall, the average efficiency after 5 mins light soaking was 8.89% (9.57% maximum) from MAI:PbCl2 based devices. Hysteresis was observed to be quite significant, with sweeps running from positive to negative bias presenting the best efficiencies (hereby referred to as reverse sweeps).


Fabrication
Substrates and cleaning
- Pixelated Cathode substrates (S171) or Photovoltaic (8 Pixel) Substrates
- 5 minutes sonication in hot 1% Hellmanex III
- 1x boiling DI dump rinse, 1x cold dump rinse
- 5 minutes sonication in warm IPA
- 2x DI cold dump rinse
- Stored in DI for 1hr
- 5 minutes sonication in hot 10% NaOH solution
- 2x DI dump rinse
- N2 blow dry
PEDOT:PSS
- PEDOT:PSS (Ossila M121 AI4083) filtered through a 0.45 µm PES filter (C2009S1)
- Spin on heated substrates at 6000 rpm for 30s
- Bake at 130°C after spincast
- Note that the cathode strip was not wiped clean, this is to allow a consistent perovskite layer on top
- Substrates held at a temperature of 90°C for spincasting
Active layer solution
- Old stock solution (2 weeks old) of MAI:PbCl2 (3:1 molar ratio) made at a concentration 664 mg/ml in DMF
- Heated for approx. 3 hrs at 70°C
- Old stock solution of PC70BM, 50 mg/ml in CB
- Heated for approx. 4 hrs at 70°C with stirbar
Active layers
- Devices spun onto hot substrate at 5000 rpm using 25 µl dynamic dispense for 30s
- Placed immediately onto hotplate at 90°C for 2 hrs
- Cathode wipe with dry cotton bud once all substrates were spun
- Films started with a bright yellow colour
- Changed to a dark grey colour during thermal annealing process
- Transferred to a N2 glove box
- PCBM layer was spun at 1000 rpm for 30s, 20 µl dynamic dispense
- CB cathode wipe
Evaporation
Left in vacuum chamber overnight and evaporated with the below parameters.
- 5 nm Ca at 0.2 Å/s
- 100 nm Al at 1.5 Å/s
- Deposition pressure <1e-6 mbar="" li="">
Encapsulation
- As standard using Ossila EE1, 30 mins UV in MEGA LV101
Measurements
- JV sweeps taken with Keithley 237 source-meter
- Illumination by Newport Oriel 9225-1000 solar simulator with 100 mW/cm2 AM1.5 output
- NREL certified silicon reference cell used to calibrate
- Lamp current: 7.8 A
- Solar output at start of testing: 1.00 suns at 23°C
- Solar output at end of testing: 1.00 suns at 25°C
- Air cooled substrates
- Room temperature at start of testing : 25°C
- Room temperature at end of testing: 25°C
- Calibrated aperture mask size: 0.256 mm2
We are continuously studying MAI and perovskites and expect to provide you with further information and optimised fabrication guides as we do so. Check back regularly or subscribe to our email newsletter for updates. In the meantime, please contact us if you have any further questions.
MSDS Documentation
Methylammonium iodide MSDS sheet
Pricing
Grade | Order Code | Quantity | Price |
98% purity | M272 | 10 g | £99.00 |
98% purity | M272 | 25 g | £199.00 |
98% purity | M272 | 100 g | £578.00 |
98% purity | M272 | 500 g | £1740.00 |
>99.9% purity | M271 | 5 g | £111.00 |
>99.9% purity | M271 | 10 g | £179.00 |
>99.9% purity | M271 | 25 g | £356.00 |
Note: Looking for a bulk order (100 g or above of 98% or greater purity)? Please contact us for a quote.
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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1、移液管是准确移取一定量溶液的量器(量出式量器,符号为Ex). 它是一根细长而中间膨大的玻璃管在管的上端有一环形标线,膨大部分标有它的容积和标定时的温度.常用的移液管有10 mL、25 mL、50 mL、100mL等规格。
2、吸量管的全称是"分度吸量管",又称为刻度移液管. 它是带有分度线的量出式玻璃量器。用于移取非固定量的溶液。吸量管可分为以下四类:
(1) 规定等待时间15s的吸量管
这类吸量管零位在上,完全流出式,它的任意一分度线的容量定义为:在20℃时,从零线排放到该分度线所流出20℃水的体积(m1).当液面降到该分度线以上几毫米时,应按紧管口停止排液15s,再将液面调到该分度线。在量取吸量管的全容量溶液时,排放过程中水流不应受到限制,液面降至流液口处静止后,要等待15s,再移走吸量管。
(2) 不完全流出式吸量管。
不完全流出式吸量管均为零点在上形式,最低分度线为标称容量.这类吸量管的任一分度线相应的容量定义为:20℃时,从零线排放到该分度线所流出的20C水的体积(mL) 。
(3)完全流出式吸量管。
这类吸量管有零点在上和零点在下两种形式.其任一分度线相应的容量定义为:在20℃时,从分度线排放到流液口时所流出20℃水的体积(mL),液体自由流下,直到确定弯月面已降到流液口静止后,再脱离容器(指零点在下式);或者从零线排放到该分度线或流液口所流出20℃水的体积(指零点在上式)。
(4) 吹出式吸量管。
这类吸量管流速较快,且不规定等待时间。有零点在上和零点在下两种形式,均为完全流出式。吹出式吸量管的任意一分度线的容量定义为:在20℃时,从该分度线排放到流液口(指零点在下)所流出的或从零线排放到该分度线(指零点在上)所流出的20℃水的体积(m1)。使用过程中液面降至流液口并静止时,应随即将最后一滴残留的溶液一次吹出。
目前市场上还有一种标“快”字的吸量管,其容量精度与吹出式吸量管相近似。吹出式及快流速吸量管的精度低、流速快,适于在仪器分析实验中加试剂用,最好不用其移取标准溶液。
吸量管的其它操作方法同移液管。
四字原则:吸 擦 调 放
吸:用吸耳球吸取液体,四指拿移液管,食指扣于移液管上口。
擦:吸取后用滤纸擦干管壁。
调:放松食指使液体流出,调至刻度线,按紧。
放:沿器壁放入所需容器。
垂直是为了保证最后只剩下半滴时,移液管不计算在内的体积。如果移液管上没有写“吹”字,那么最后半滴可以不要。
移液管
用来准确移取一定体积的溶液的量器。移液管是一种量出式仪器,只用来测量它所放出溶液的体积。它是一根中间有一膨大部分的细长玻璃管。其下端为尖嘴状,上端管颈处刻有一条标线,是所移取的准确体积的标志。
将用待吸液润洗过的移液管插入待吸液面下1~2cm处用吸耳球按上述操作方法吸取溶液(注意移液管插入溶液不能太深,并要边吸边往下插入,始终保持此深度)。当管内液面上升至标线以上约1~2cm处时,迅速用右手食指堵住管口(此时若溶液下落至标准线以下,应重新吸取),将移液管提出待吸液面,并使管尖端接触待吸液容器内壁片刻后提起,用滤纸擦干移液管或吸量管下端粘附的少量溶液。(在移动移液管或吸量管时,应将移液管或吸量管保持垂直,不能倾斜) 洗净移液管,放置在移液管架上。向左转|向右转
对于我们生物/医学实验ers来说,每天必用移液器;它的准确与否直接关系到实验结果的准确性及可重复性。可能在大家看来,玩“枪”就像吃饭喝水一样soeasy!但扫地僧的故事告诉我们:愈是看似简单的事物,却往往蕴藏着大道理。你真的知道吸液时该浸入液面以下多深吗?你能尽可能准确地移取Tween、高浓度蛋白溶液等粘稠、发泡的液体吗?长期使用后,你的移液器还准吗?你会自检移液器吗?
答案是No的小伙伴们,你们有任何关于移液器的问题都可以来问我,大家一起讨论共同进步哈~同时感谢丁香园交流平台和版主的支持!谢谢!
本活动技术支持来自普兰德(上海)贸易有限公司。
版主科研无止尽留言:
好帖
移液管,即带很多小刻度移液管

