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71481-64-6

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71481-64-6 Usage

Description

METHANOL WITH FORMALDEHYDE, also known as F-M, is a non-fullerene acceptor that has the ability to absorb visible light. It is a promising material for use in the development of high-performance organic solar cells.
Used in Organic Solar Cells:
METHANOL WITH FORMALDEHYDE is used as a non-fullerene acceptor in the development of tandem organic solar cells. When paired with a NIR absorbing rear cell, the resulting tandem cell has achieved a record energy conversion efficiency of 17.3%.
Tandem Cell Device Performance:
In the specific tandem cell device, METHANOL WITH FORMALDEHYDE is used in the front cell, which has the following performance metrics:
Open-circuit voltage (Voc): 1.642 V
Short-circuit current density (Jsc): 14.35 mA/cm2
Fill factor (FF): 73.7%
Power conversion efficiency (PCE): 17.3%
This high-performance tandem cell device demonstrates the potential of METHANOL WITH FORMALDEHYDE as a key component in the advancement of organic solar cell technology.

Check Digit Verification of cas no

The CAS Registry Mumber 71481-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,8 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71481-64:
(7*7)+(6*1)+(5*4)+(4*8)+(3*1)+(2*6)+(1*4)=126
126 % 10 = 6
So 71481-64-6 is a valid CAS Registry Number.

71481-64-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name METHANOL WITH FORMALDEHYDE

1.2 Other means of identification

Product number -
Other names METHYL HEMIFORMAL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:71481-64-6 SDS

71481-64-6Upstream product

71481-64-6Relevant articles and documents

The isomeric .+ Hydrogen-Bridged Radical Cations .+, .+, and .+: Theory and Experiment

Burgers, Peter C.,Holmes, John L.,Hop, Cornelis E. C. A.,Postma, Ron,Ruttink, Paul J. A.,Terlouw, Johan K.

, p. 7315 - 7321 (2007/10/02)

From combination of mass spectrometry based experiments and high-level molecular orbital theory calculations, three new, thermodinamically stable isomers of ionized ethylene glycol, .+ (1), have been identified.These are the hydrogen-bridged radical cations .+ (2), .+ (3), and .+ (4); a fifth isomer, also H-bridged, .+, has been previously reported.The ion .+ (3) was experimentally identified (via a double collision experiment) as the stable ion formed by loss of CO from ionized methyl glycolate, whereas 2 was proposed to be a long-lived, rearranged form of ionized glycol, 1.The common unimolecular dissociations of 2 and 3 into CH3OH2+ and HCO0 were associated with energy barriers attributed to their rearrangement into (energy-rich) ions of structure 4, from which the dissociation proceeds by direct bond cleavage.This study underlines the important role that -H-O- hydrogen-bridged radical cations can play in the gas-phase ion chemistry of oxigencontaining compounds and is another example of the succesful combination of theory and experiment in gas-phase ion chemistry.

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