New indole-based metal-free organic dyes for dye-sensitized solar cells
Two indole-based organic dyes were conveniently prepared and well characterized. The triphenylamine or carbazole moieties were bonded to the indole group acting as a potential electron donor, which can tune the HOMO and LUMO levels of the resultant dye, and another triphenylamine or carbazole group was linked to the pyrrole ring on the nitrogen atom, which was expected to suppress the aggregation of the dye in the solid state to some degree. These two dyes were utilized as dye sensitizers in dye-sensitized solar cells and demonstrated efficient photon-to-electron conversion properties.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2009 |
---|---|
Erschienen: |
2009 |
Enthalten in: |
Zur Gesamtaufnahme - volume:113 |
---|---|
Enthalten in: |
The journal of physical chemistry. B - 113(2009), 44 vom: 05. Nov., Seite 14588-95 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Li, Qianqian [VerfasserIn] |
---|
Links: |
---|
Themen: |
---|
Anmerkungen: |
Date Completed 08.02.2010 Date Revised 29.10.2009 published: Print Citation Status PubMed-not-MEDLINE |
---|
doi: |
10.1021/jp906334w |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM191946095 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM191946095 | ||
003 | DE-627 | ||
005 | 20231223192103.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231223s2009 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1021/jp906334w |2 doi | |
028 | 5 | 2 | |a pubmed24n0640.xml |
035 | |a (DE-627)NLM191946095 | ||
035 | |a (NLM)19817476 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Li, Qianqian |e verfasserin |4 aut | |
245 | 1 | 0 | |a New indole-based metal-free organic dyes for dye-sensitized solar cells |
264 | 1 | |c 2009 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 08.02.2010 | ||
500 | |a Date Revised 29.10.2009 | ||
500 | |a published: Print | ||
500 | |a Citation Status PubMed-not-MEDLINE | ||
520 | |a Two indole-based organic dyes were conveniently prepared and well characterized. The triphenylamine or carbazole moieties were bonded to the indole group acting as a potential electron donor, which can tune the HOMO and LUMO levels of the resultant dye, and another triphenylamine or carbazole group was linked to the pyrrole ring on the nitrogen atom, which was expected to suppress the aggregation of the dye in the solid state to some degree. These two dyes were utilized as dye sensitizers in dye-sensitized solar cells and demonstrated efficient photon-to-electron conversion properties | ||
650 | 4 | |a Journal Article | |
700 | 1 | |a Lu, Lanlan |e verfasserin |4 aut | |
700 | 1 | |a Zhong, Cheng |e verfasserin |4 aut | |
700 | 1 | |a Shi, Jie |e verfasserin |4 aut | |
700 | 1 | |a Huang, Qing |e verfasserin |4 aut | |
700 | 1 | |a Jin, Xianbo |e verfasserin |4 aut | |
700 | 1 | |a Peng, Tianyou |e verfasserin |4 aut | |
700 | 1 | |a Qin, Jingui |e verfasserin |4 aut | |
700 | 1 | |a Li, Zhen |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t The journal of physical chemistry. B |d 1997 |g 113(2009), 44 vom: 05. Nov., Seite 14588-95 |w (DE-627)NLM114379831 |x 1520-5207 |7 nnns |
773 | 1 | 8 | |g volume:113 |g year:2009 |g number:44 |g day:05 |g month:11 |g pages:14588-95 |
856 | 4 | 0 | |u http://dx.doi.org/10.1021/jp906334w |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 113 |j 2009 |e 44 |b 05 |c 11 |h 14588-95 |