US2023096300A1PendingUtilityA1

Photoelectric conversion element and solid-state imaging device

Assignee: SONY SEMICONDUCTOR SOLUTIONS CORPPriority: Nov 2, 2015Filed: Aug 31, 2022Published: Mar 30, 2023
Est. expiryNov 2, 2035(~9.3 yrs left)· nominal 20-yr term from priority
H10K 30/00H10F 77/00H10F 39/8033H10F 30/20H10F 39/191H10F 39/811H10F 39/192H10F 39/182H10F 39/12Y02E10/549C09B 48/00H10K 39/32C09B 15/00H10K 85/6572C09B 47/04H10K 99/00H01L 31/02H01L 27/14645H01L 27/1461H01L 27/14667H01L 27/146H01L 27/307H01L 51/00H01L 27/14636H01L 51/0072
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Claims

Abstract

A photoelectric conversion element according to an embodiment of the present disclosure includes: a first electrode 15a and a second electrode 18 facing each other; and a photoelectric conversion layer 17 provided between the first electrode 15a and the second electrode 18, and including a first quinacridone derivative represented by a formula (1).

Claims

exact text as granted — not AI-modified
1 . A photoelectric conversion element, comprising:
 a first electrode and a second electrode facing each other; and   a photoelectric conversion layer provided between the first electrode and the second electrode, and including a first quinacridone derivative represented by the following formula (1),   
       
         
           
           
               
               
           
         
       
       (where each of R1 and R2 is independently one of an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a cyano group, a nitro group, and a silyl group, each of m1 and m2 is independently 0 or an integer of 1 or more, in a case where each of m1 and m2 is 2 or more, two or more R1 are optionally bound to one another to form a ring and two or more R2 are optionally bound to one another to form a ring, and R3 is one of an alkyl group, an aryl group, and a heterocyclic group.) 
     
     
         2 . The photoelectric conversion element according to  claim 1 , wherein the photoelectric conversion layer further includes a subphthalocyanine derivative represented by the following formula (2), 
       
         
           
           
               
               
           
         
       
       (where each of R4 to R15 is independently a hydrogen atom, a halogen atom, a straight-chain, branched, or cyclic alkyl group, a thioalkyl group, a thioaryl group, an arylsulfonyl group, an alkylsulfonyl group, an amino group, an alkylamino group, an arylamino group, a hydroxy group, an alkoxy group, an acylamino group, an acyloxy group, a phenyl group, a carboxy group, a carboxyamide group, a carboalkoxy group, an acyl group, a sulfonyl group, a cyano group, and a nitro group, any adjacent ones of R4 to R15 are optionally bound to one another to form a ring, and X is an anionic group.) 
     
     
         3 . The photoelectric conversion element according to  claim 1 , wherein a content of the first quinacridone derivative included in the photoelectric conversion layer is within a range from 25% to 75% both inclusive in volume ratio. 
     
     
         4 . The photoelectric conversion element according to  claim 2 , wherein the photoelectric conversion layer includes a second quinacridone derivative represented by the following formula (3) in addition to the first quinacridone derivative and the subphthalocyanine derivative, 
       
         
           
           
               
               
           
         
       
       (where each of R16 and R17 is independently one of an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a cyano group, a nitro group, and a silyl group, each of n1 and n2 is independently 0 or an integer of 1 or more, and in a case where each of n1 and n2 is 2 or more, two or more R16 are optionally bound to one another to form a ring and two or more R17 are optionally bound to one another to form a ring.) 
     
     
         5 . The photoelectric conversion element according to  claim 4 , wherein a total content of the first quinacridone derivative and the second quinacridone derivative included in the photoelectric conversion layer is within a range from 25% to 75% both inclusive in volume ratio. 
     
     
         6 . The photoelectric conversion element according to  claim 4 , wherein a content of the first quinacridone derivative in the photoelectric conversion layer including the first quinacridone derivative and the second quinacridone derivative is within a range from 33% to 67% both inclusive in volume ratio. 
     
     
         7 . A solid-state imaging device provided with pixels each including one or a plurality of organic photoelectric converters, each of the organic photoelectric converters comprising:
 a first electrode and a second electrode facing each other; and   a photoelectric conversion layer provided between the first electrode and the second electrode, and including a first quinacridone derivative represented by the following formula (1),   
       
         
           
           
               
               
           
         
       
       (where each of R1 and R2 is independently one of an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a cyano group, a nitro group, and a silyl group, each of m1 and m2 is independently 0 or an integer of 1 or more, in a case where each of m1 and m2 is 2 or more, two or more R1 are optionally bound to one another to form a ring and two or more R2 are optionally bound to one another to form a ring, and R3 is one of an alkyl group, an aryl group, and a heterocyclic group.) 
     
     
         8 . The solid-state imaging device according to  claim 7 , wherein the one or plurality of organic photoelectric converters, and one or a plurality of inorganic photoelectric converters that performs photoelectric conversion in a wavelength region different from a wavelength region of the organic photoelectric converters are stacked in each of the pixels. 
     
     
         9 . The solid-state imaging device according to  claim 8 ,
 wherein the inorganic photoelectric converter is formed to be embedded in a semiconductor substrate, and   the organic photoelectric converter is formed on a first surface side of the semiconductor substrate.   
     
     
         10 . The solid-state imaging device according to 9, wherein
 the organic photoelectric converter performs photoelectric conversion on green light, and   an inorganic photoelectric converter that performs photoelectric conversion on blue light and an inorganic photoelectric converter that performs photoelectric conversion on red light are stacked in the semiconductor substrate.

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