JP2008016383A5 - Photoelectric conversion material and semiconductor electrode - Google Patents

Photoelectric conversion material and semiconductor electrode Download PDF

Info

Publication number
JP2008016383A5
JP2008016383A5 JP2006188203A JP2006188203A JP2008016383A5 JP 2008016383 A5 JP2008016383 A5 JP 2008016383A5 JP 2006188203 A JP2006188203 A JP 2006188203A JP 2006188203 A JP2006188203 A JP 2006188203A JP 2008016383 A5 JP2008016383 A5 JP 2008016383A5
Authority
JP
Japan
Prior art keywords
group
ring
represent
nitrogen
pka
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2006188203A
Other languages
Japanese (ja)
Other versions
JP5166708B2 (en
JP2008016383A (en
Filing date
Publication date
Application filed filed Critical
Priority to JP2006188203A priority Critical patent/JP5166708B2/en
Priority claimed from JP2006188203A external-priority patent/JP5166708B2/en
Publication of JP2008016383A publication Critical patent/JP2008016383A/en
Publication of JP2008016383A5 publication Critical patent/JP2008016383A5/en
Application granted granted Critical
Publication of JP5166708B2 publication Critical patent/JP5166708B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Claims (2)

下記一般式(1)、(2)、(3)で示される化合物の少なくとも1種を用いることを特徴とする光電変換材料。
Figure 2008016383
式中、R〜R10は脂肪族基、芳香族基、複素環基を表す。なおR、R、R、Rは、それぞれ窒素原子が結合しているベンゼン環と連結して環を形成していても良い。Z〜Zは、それぞれ5または6員の含窒素複素環を形成するのに必要な原子群を表す。mは0または1を表す。L、Lは共役メチン基ユニットを表す。Lは2価の連結基を表す。但し(1)の分子中には少なくとも2個のpKa6未満の酸性基を有しているものとする。
Figure 2008016383
式中、R11〜R20は脂肪族基、芳香族基、複素環基を表す。なおR11、R12、R16、R17は、それぞれ窒素原子が結合しているベンゼン環と連結して環を形成していても良い。Z〜Z12は、それぞれ5または6員の含窒素複素環を形成するのに必要な原子群を表す。nは0または1を表す。L、Lは共役メチン基ユニットを表す。Lは2価の連結基を表す。但し(2)の分子中には少なくとも2個のpKa6未満の酸性基を有しているものとする。
Figure 2008016383
式中、R21〜R30は脂肪族基、芳香族基、複素環基を表す。なおR21、R22、R26、R27は、それぞれ窒素原子が結合しているベンゼン環と連結して環を形成していても良い。Z13〜Z18は、それぞれ5または6員の含窒素複素環を形成するのに必要な原子群を表す。L、Lは共役メチン基ユニットを表す。Lは2価の連結基を表す。但し(3)の分子中には少なくとも2個のpKa6未満の酸性基を有しているものとする。
The photoelectric conversion material characterized by using at least 1 sort (s) of the compound shown by following General formula (1), (2), (3).
Figure 2008016383
Wherein, R 1 to R 10 represents an aliphatic group, an aromatic group, a heterocyclic group. R 1 , R 2 , R 6 and R 7 may each be linked to a benzene ring to which a nitrogen atom is bonded to form a ring. Z 1 to Z 6 each represent an atomic group necessary to form a 5- or 6-membered nitrogen-containing heterocyclic ring. m represents 0 or 1; L 1 and L 2 each represent a conjugated methine group unit. L 3 represents a divalent linking group. However, the molecule of (1) is assumed to have at least two acidic groups having a pKa of less than 6.
Figure 2008016383
Wherein, R 11 to R 20 represents an aliphatic group, an aromatic group, a heterocyclic group. R 11 , R 12 , R 16 and R 17 may each be linked to a benzene ring to which a nitrogen atom is bonded to form a ring. Z 7 to Z 12 represents an atomic group necessary for forming a nitrogen-containing heterocyclic ring, respectively 5 or 6 membered. n represents 0 or 1; L 4 and L 5 each represent a conjugated methine group unit. L 6 represents a divalent linking group. However, the molecule of (2) is assumed to have at least two acidic groups having a pKa of less than 6.
Figure 2008016383
Wherein, R 21 to R 30 represents an aliphatic group, an aromatic group, a heterocyclic group. R 21 , R 22 , R 26 and R 27 may each be linked to a benzene ring to which a nitrogen atom is bonded to form a ring. Z 13 to Z 18 represents an atomic group necessary for forming a nitrogen-containing heterocyclic ring, respectively 5 or 6 membered. L 7 and L 8 each represent a conjugated methine group unit. L 9 represents a divalent linking group. However, in the molecule of (3), it is assumed that it has at least two acidic groups having a pKa of less than 6.
表面に導電性を有する基板と、その導電性表面上に被覆された半導体層と、その半導体層の表面に吸着した色素からなる半導体電極において、色素として前記一般式(1)、(2)、(3)で示される化合物を少なくとも1種以上用いることを特徴とする半導体電極。   In the semiconductor electrode comprising a substrate having conductivity on the surface, a semiconductor layer coated on the conductive surface, and a dye adsorbed on the surface of the semiconductor layer, the dyes represented by the general formulas (1), (2), A semiconductor electrode characterized by using at least one or more compounds represented by (3).
JP2006188203A 2006-07-07 2006-07-07 Photoelectric conversion material and semiconductor electrode Expired - Fee Related JP5166708B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006188203A JP5166708B2 (en) 2006-07-07 2006-07-07 Photoelectric conversion material and semiconductor electrode

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2006188203A JP5166708B2 (en) 2006-07-07 2006-07-07 Photoelectric conversion material and semiconductor electrode

Publications (3)

Publication Number Publication Date
JP2008016383A JP2008016383A (en) 2008-01-24
JP2008016383A5 true JP2008016383A5 (en) 2008-12-04
JP5166708B2 JP5166708B2 (en) 2013-03-21

Family

ID=39073188

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006188203A Expired - Fee Related JP5166708B2 (en) 2006-07-07 2006-07-07 Photoelectric conversion material and semiconductor electrode

Country Status (1)

Country Link
JP (1) JP5166708B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5416118B2 (en) 2008-08-06 2014-02-12 三菱製紙株式会社 Dye for dye-sensitized solar cell, semiconductor electrode, and dye-sensitized solar cell
JP2010182467A (en) * 2009-02-04 2010-08-19 Dainippon Printing Co Ltd Manufacturing method of dye-sensitized photoelectric conversion element and dye-sensitized solar cell
JP6239338B2 (en) * 2013-10-11 2017-11-29 三菱製紙株式会社 Organic dye

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000106224A (en) * 1998-09-29 2000-04-11 Fuji Photo Film Co Ltd Photoelectric conversion element and photo electrochemical cell
JP4180841B2 (en) * 2002-05-24 2008-11-12 三菱製紙株式会社 Photoelectric conversion element
JP4326272B2 (en) * 2003-06-26 2009-09-02 三菱製紙株式会社 Dye-sensitized solar cell dye

Similar Documents

Publication Publication Date Title
Mutolo et al. Enhanced open-circuit voltage in subphthalocyanine/C60 organic photovoltaic cells
Bässler et al. Site-selective fluorescence spectroscopy of conjugated polymers and oligomers
Jadhav et al. Singlet exciton fission in nanostructured organic solar cells
Wang et al. Synthesis, characterization, and non‐volatile memory device application of an N‐substituted heteroacene
JP2008244465A5 (en) Light emitting element and light emitting device
JP2008524869A5 (en)
JP2007234580A5 (en)
Oyamada et al. Electroluminescence of 2, 4-bis (4-(2′-thiophene-yl) phenyl) thiophene in organic light-emitting field-effect transistors
Hirade et al. Formation of organic crystalline nanopillar arrays and their application to organic photovoltaic cells
JP2009231515A5 (en)
JP2011513530A5 (en)
JP2005310733A5 (en)
JP2012508227A5 (en)
JP2009135422A5 (en)
JP2006073992A5 (en)
JP2007314506A5 (en)
TW200613409A (en) Optical recording material and optical recording medium
JP2006124373A5 (en)
JP2008270736A5 (en)
JP2005203340A5 (en)
JP2007039431A5 (en) Substance, material for light emitting element, light emitting element, light emitting device and electronic device
JP2010533981A5 (en)
JP2006156562A5 (en)
JP2008521811A5 (en)
TW201242929A (en) Organic electro-luminescence device