Organic light-emitting diode with high efficiency

1. An organic light-emitting diode, comprising:

a first electrode;

a second electrode facing the first electrode; and

an electron-blocking layer and a light-emitting layer sequentially interposed between the first electrode and the second electrode,

wherein the light-emitting layer comprises at least one of the amine compounds represented by the following Chemical Formula B, and the electron-blocking layer comprises the compound represented by the following Chemical Formula C:

wherein,

A 1 , A 2 , E, and F are the same or different, and are each independently a substituted or unsubstituted aromatic hydrocarbon ring of 6 to 50 carbon atoms, or a substituted or unsubstituted heteroaromatic ring of 2 to 40 carbon atoms wherein two adjacent carbon atoms of the aromatic ring A 1 and two adjacent carbon atoms of the aromatic ring A 2 form a 5-membered fused ring together with a carbon atom to which substituents R 1 and R 2 are bonded;

linkers L 1 to L 12 are the same or different, and are each independently a direct bond or a substituted or unsubstituted arylene of 6 to 60 carbon atoms;

M is any one selected from among N—R 3 , CR 4 R 5 , O, and S;

R 1 to R 5 , and Ar 1 to Ar 8 are the same or different, and are each independently any one selected from among hydrogen, deuterium, a substituted or unsubstituted alkyl of 1 to 30 carbon atoms, a substituted or unsubstituted aryl of 6 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl of 3 to 30 carbon atoms, a substituted or unsubstituted heteroaryl of 2 to 50 carbon atoms, a substituted or unsubstituted alkylsilyl of 1 to 30 carbon atoms, a substituted or unsubstituted arylsilyl of 6 to 30 carbon atoms, a substituted or unsubstituted alkyl germanium of 1 to 30 carbon atoms, a substituted or unsubstituted aryl germanium of 6 to 30 carbon atoms, a cyano, a nitro, and a halogen, with a proviso that R 1 and R 2 together may form a mono- or polycyclic aliphatic or aromatic ring, which may be a heterocyclic ring containing a heteroatom selected from among N, O, P, Si, and S as a ring member;

p1 to p4, r1 to r4, and s1 to s4 are each independently an integer of 1 to 3, with a proviso that when any of them is 2 or greater, the corresponding linkers are the same or different,

x is 1, and y and z are the same or different and are each independently an integer of 0 or 1; and

in the alternative for Ar 1 to Ar 8 , Ar 1 forms a ring with Ar 2 , Ar 3 forms a ring with Ar 4 , Ar 5 forms a ring with Ar 6 , and Ar 7 forms a ring with Ar 8 ,

two adjacent carbon atoms of the A 2 ring moiety of Chemical Formula B occupy respective positions * of structural Formula Q 1 to form a fused ring and, two adjacent carbon atoms of the A 1 ring moiety of Chemical Formula B occupy respective positions * of structural Formula Q 2 to form a fused ring,

wherein,

Ar 21 to Ar 23 are the same or different and are each independently selected from among a substituted or unsubstituted aryl of 6 to 50 carbon atoms, a substituted or unsubstituted heteroaryl of 3 to 50 carbon atoms containing 0, N or S as a heteroatom, and a compound represented by the following Structural Formula A, with a proviso that at least one of Ar 21 to Ar 23 is the compound of Structural Formula A:

wherein,

L 21 is selected from among a single bond, a substituted or unsubstituted aryl of 6 to 50 carbon atoms, and a substituted or unsubstituted heteroaryl of 3 to 50 carbon atoms containing O, N or S as a heteroatom;

t is an integer of 1 to 3, with a proviso that when it is 2 or greater, the corresponding L 21 's is the same or different,

R 21 and R 22 are the same or different, and are each independently selected from the group consisting of hydrogen, deuterium, a substituted or unsubstituted alkyl of 1 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl of 3 to 30 carbon atoms, a substituted or unsubstituted aryl of 6 to 50 carbon atoms, a substituted or unsubstituted heteroaryl of 3 to 50 carbon atoms containing 0, N or S as a heteroatom, a nitrile, a nitro, and a halogen;

a is an integer of 0 to 3, and b is an integer of 0 to 4, with a proviso that when a and b are each 2 or greater, the corresponding R 21 's and R 22 's are the same or different,

wherein the term ‘substituted’ in the expression ‘substituted or unsubstituted’ for Chemical Formulas B and C means having at least one substituent selected from the group consisting of a deuterium, a cyano, a halogen, a nitro, an alkyl of 1 to 24 carbon atoms, a halogenated alkyl of 1 to 24 carbon atoms, an aryl of 6 to 24 carbon atoms, an arylalkyl of 7 to 24 carbon atoms, a heteroaryl of 2 to 24 carbon atoms or a heteroarylalkyl of 2 to 24 carbon atoms, an alkylsilyl of 1 to 24 carbon atoms, an arylsilyl of 6 to 24 carbon atoms.

2. The organic light-emitting diode of claim 1 , wherein the light-emitting layer comprises a host and a dopant, the amine compound of Chemical Formula B serving as the dopant.

3. The organic light-emitting diode of claim 1 , wherein A 1 , A 2 , E, and F of Chemical Formula B are identical or different, and are each independently a substituted or unsubstituted aromatic hydrocarbon ring of 6 to 50 carbon atoms.

4. The organic light-emitting diode of claim 3 , wherein the substituted or unsubstituted aromatic hydrocarbon ring of 6 to 50 carbon atoms is selected from among compounds represented by [Structural Formula 10] to [Structural Formula 21]:

wherein,

“-*” for moiety A 1 or A 2 denotes a bonding site for forming a 5-membered ring containing the carbon atom connected to both R 1 and R 2 , and “-*” for moiety E or F denotes a bonding site for forming a 5-membered ring containing M of the structural Formula Q 1 and Q 2 with moiety A 1 or A 2 ,

when one of aromatic hydrocarbon rings of [Structural Formula 10] to [Structural Formula 21] for A 1 or A 2 is bonded to Structural Formula Q 1 or Structural Formula Q 2 , two adjacent carbon atoms of the aromatic hydrocarbon ring occupy respective positions * of Structural Formula Q 1 or Q 2 to form a fused ring; and

R in Structural Formulas 10 to 21 is selected from the group consisting of a hydrogen, a deuterium, a cyano, a halogen, a nitro, an alkyl of 1 to 24 carbon atoms, an aryl of 6 to 24 carbon atoms, an arylalkyl of 7 to 24 carbon atoms, a heteroaryl of 2 to 24 carbon atoms, a heteroarylalkyl of 2 to 24 carbon atoms, an alkylsilyl of 1 to 24 carbon atoms, and an arylsilyl of 6 to 24 carbon atoms, and

m is an integer of 1 to 8, with the proviso that when m is 2 or greater or when 2 or more Rs are present, the corresponding Rs are the same or different.

5. The organic light-emitting diode of claim 1 ,

wherein

the linkers L 1 to L 12 of Chemical Formula B represent single bonds, or are each any one selected from the following [Structural Formula 22], [Structural Formula 23], [Structural Formula 25], [Structural Formula 27], [Structural Formula 28], and [Structural Formula 30],

p1 to p4, r1 to r4, and s1 to s4 are each 1 or 2, and

x is 1:

wherein hydrogen or deuterium is positioned on a carbon atom as a member in aromatic rings of the linkers.

6. The organic light-emitting diode of claim 1 , wherein linker L 21 of Chemical Formula C is a single bond or a substituted or unsubstituted arylene of 6 to 20 carbon atoms.

7. The organic light-emitting diode of claim 1 , wherein

x and y are each 1 and z is 0 or 1 in Chemical Formula B.

8. The organic light-emitting diode of claim 1 , wherein the substituents Ar 21 to Ar 23 on the compound represented by Chemical Formula C are the same or different and are each a substituted or unsubstituted aryl of 6 to 20 carbon atoms, one or two of Ar 21 to Ar 23 being the substituent represented by Structural Formula A wherein t is 1 or 2.

9. The organic light-emitting diode of claim 1 , wherein the amine compound is any one selected from among compounds represented by the following [Chemical Formula 25] to [Chemical Formula 32], [Chemical Formula 85], [Chemical Formula 91], [Chemical Formula 92], [Chemical Formula 97], [Chemical Formula 98], [Chemical Formula 102], [Chemical Formula 117], [Chemical Formula 142] to [Chemical Formula 149], [Chemical Formula 160], [Chemical Formula 162], [Chemical Formula 164], [Chemical Formula 165], [Chemical Formula 197] to [Chemical Formula 201], [Chemical Formula 210], [Chemical Formula 222] to [Chemical Formula 224], [Chemical Formula 227] to [Chemical Formula 231], and [Chemical Formula 239],

10. The organic light-emitting diode of claim 1 , wherein the compound represented by Chemical Formula C is any one selected from among the following Compounds 1 to 48:

11. The organic light-emitting diode of claim 1 , wherein the organic light-emitting diode comprises at least one of a hole injection layer, a hole transport layer, an electron transport layer, and an electron injection layer, in addition to the electron-blocking layer and the light-emitting layer.

12. The organic light-emitting diode of claim 11 , wherein at least one of the layers is formed using a deposition process or a solution process.

13. The organic light-emitting diode of claim 1 , wherein organic light-emitting diode is used for a device selected from among a flat display device, a flexible display device, a monochrome or white flat illumination device, and a monochrome or white flexible illumination device.