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5-{7-{4-[N,N-bis(4-methylphenyl)amino]phenyl}-fluorenone-2-yl}thiophene-2-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1398122-59-2

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1398122-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1398122-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,8,1,2 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1398122-59:
(9*1)+(8*3)+(7*9)+(6*8)+(5*1)+(4*2)+(3*2)+(2*5)+(1*9)=182
182 % 10 = 2
So 1398122-59-2 is a valid CAS Registry Number.

1398122-59-2Relevant academic research and scientific papers

ORGANIC DYE, DYE-SENSITIZED METAL OXIDE SEMICONDUCTOR ELECTRODE AND DYE-SENSITIZED SOLAR CELL

-

, (2013/03/26)

An object of the present invention is to provide a dye sensitizer for a solar cell having stability and an excellent conversion efficiency. There is provided a dye sensitizer represented by the following general formula, to which a donor site (D) and an acceptor site (A) are bound via linkers (L1)n and (L2)n: (φ is an aromatic ring with or without heteroatom(s); D is a triphenylamine derivative, a carbazole derivative, a coumarine derivative or an indoline derivative; A is an organic residue having an acidic group; each of L1 and L2 is an optionally substituted divalent alkenyl group, aromatic group or heterocyclic group, and n represents an integer of 0 to 3).

Incorporating a stable fluorenone unit into D-A-π-A organic dyes for dye-sensitized solar cells

Qin, Chuanjiang,Islam, Ashraful,Han, Liyuan

, p. 19236 - 19243 (2012/11/07)

Two new organic dyes based on a donor-acceptor-π-bridge-acceptor/anchor (D-A-π-A) configuration, HIQF1 and HIQF2, were synthesized, characterized, and successfully employed in dye-sensitized solar cells. The incorporation of the weakly electron-withdrawing fluorenone group as an additional acceptor enhanced the dyes' properties for solar energy conversion in several ways. First, the absorption spectra of the dyes were broadened, covering a large range of sunlight. Second, the absorption spectra observed upon dye adsorption on TiO2 were only slightly blue-shifted as compared to the spectra of the dyes in solution. Third, the orbital energy levels and electron distributions of the D-A-π-A backbone were ideal for highly efficient electron transport and injection. The incorporation of long electron-donating alkoxy groups in the donor unit of HIQF1 further increased the dye's short-circuit photocurrent density (Jsc), open-circuit voltage (Voc), and overall conversion efficiency (η), but had little negative effect on the fill factor (FF). Solar cells sensitized with HIQF1 showed excellent current-voltage characteristics; the Jsc, V oc, and FF values were 12.26 mA cm-2, 0.70 V, and 0.73, corresponding to a η value of 6.26%. The Royal Society of Chemistry.

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