Photoelectric conversion device and imaging device having decreased dark current

1. A photoelectric conversion device comprising a transparent electrically conductive film, a photoelectric conversion film, and an electrically conductive film, wherein said photoelectric conversion film contains a compound represented by the following formula (i):

wherein R 1 represents an alkyl group, an aryl group or a heterocyclic group, each of R 2 to R 9 independently represents a hydrogen atom or a substituent, provided that each of at least two out of R 3 , R 4 , R 7 and R 8 independently represents an aryl group, a heterocyclic group or —N(Ra)(Rb), each of Ra and Rb independently represents a hydrogen atom or a substituent, and at least either Ra or Rb represents an aryl group or a heterocyclic group,

wherein in formula (i), each of R 3 and R 8 is independently a carbazolyl group substituted with an alkyl group having a carbon number of 1 to 12 and said alkyl group may be bonded through a heterocyclic group as the linking group.

2. The photoelectric conversion device as claimed in claim 1 , wherein said photoelectric conversion film further contains a material having an electron affinity (Ea) of 4.0 eV or more and in said photoelectric conversion film, said compound represented by formula (i) is put into contact with said material having an electron affinity (Ea) of 4.0 eV or more.

3. The photoelectric conversion device as claimed in claim 1 , wherein said compound represented by formula (i) does not contain a condensed ring structure composed of 5 or more rings.

4. The photoelectric conversion device as claimed in claim 1 , wherein in formula (i), R 1 is an aryl group.

5. The photoelectric conversion device as claimed in claim 1 , wherein in formula (i), each of at least two out of R 3 , R 4 , R 7 and R 8 is independently —N(Ra)(Rb), an azepinyl group or a carbazolyl group and at least either Ra or Rb is a fluorenyl group.

6. The photoelectric conversion device as claimed in claim 1 , wherein in formula (i), each of at least two out of R 3 , R 4 , R 7 and R 8 is independently —N(Ra)(Rb) and at least either Ra or Rb is a fluorenyl group.

7. The photoelectric conversion device as claimed in claim 1 , wherein in formula (i), each of R 2 , R 5 , R 6 and R 9 is a hydrogen atom.

8. The photoelectric conversion device as claimed in claim 1 , wherein in formula (i), each of R 4 and R 7 is a hydrogen atom.

9. The photoelectric conversion device as claimed in claim 1 , wherein the ionization potential (Ip) of said compound represented by formula (i) is less than 5.7 eV.

10. The photoelectric conversion device as claimed in claim 1 , wherein the ionization potential (Ip) of said compound represented by formula (i) is 4.9 eV or more.

11. The photoelectric conversion device as claimed in claim 1 , wherein the molecular weight of said compound represented by formula (i) is from 500 to 2,000.

12. The photoelectric conversion device as claimed in claim 1 , wherein the mobility of said compound represented by formula (i) as measured by a Time of Flight (TOF) method is 1×10 −5 cm 2 /Vs or more.

13. The photoelectric conversion device as claimed in claim 1 , wherein said photoelectric conversion film contains a photoelectric conversion layer and an electron blocking layer and said electron blocking layer contains said compound represented by formula (i).

14. The photoelectric conversion device as claimed in claim 1 , wherein said electrically conductive film, said photoelectric conversion film and said transparent electrically conductive film are stacked in this order.

15. An imaging device comprising the photoelectric conversion device claimed in claim 1 .

16. The photoelectric conversion device as claimed in claim 2 , wherein said material having an electron affinity (Ea) of 4.0 eV or more is a fullerene or a fullerene derivative.