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Home » Compounds » HBL

HBL

3N-T2T

Cas number: 939430-26-9
Synonyms: TmPyTz, TmPPyTz
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C36H24N6

3P-T2T

Cas number: 352196-01-1
Synonyms: 1,3,5-Tris(1-phenyl-1Hbenzimidazol-2-yl)benzene
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C30H21N9

3TPYMB

Cas number: 929203-02-1
Synonyms: Tri[3-(3-pyridyl)mesityl]borane
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C42H42BN3

B₂PymPm

Cas number: 1266181-51-4
Synonyms: 1,3,5-Tris(1-phenyl-1Hbenzimidazol-2-yl)benzene
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C37H26N6

B3PymPm

Cas number: 925425-96-3
Synonyms: 4,6-Bis(3,5-di-3-pyridinylphenyl)-2-methylpyrimidine
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C37H26N6

B3PyPB

Cas number: 1030380-38-1
Synonyms: BmPyPB, BmPyPhB, 1,3-Bis[3,5-di(pyridin-3-yl)phenyl]benzene
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C38H26N4

B4PymPm

Cas number: 1030380-51-8
Synonyms: 4,6-Bis(3,5-di-4-pyridinylphenyl)-2-methylpyrimidine
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C37H26N6

B₄PyPPm

Cas number: 1097652-83-9
Synonyms: 4,6-Bis(3,5-di(pyridin-4-yl)phenyl)-2-phenylpyrimidine, 4,6-Bis(3,5-di-4-pyridinylphenyl)-2-phenylpyrimidine
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C42H28N6

BCP

Cas number: 4733-39-5
Synonyms: Bathocuproine
Purity: Sublimed: >99.5% (HPLC)
Chemical Formula: C26H20N2

BPBPA

Cas number: 164724-35-0
Synonyms: TBBDAz, N4,N4,N4',N4'-Tetra([1,1'-biphenyl]-4-yl)-[1,1'-biphenyl]-4,4'-diamine
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C60H44N2

BPhen

Cas number: 1662-01-07
Synonyms: Bathophenanthroline
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C24H16N2

BPPB

Cas number: 721969-94-4
Synonyms: PBPPhen, 2,2'-(1,3-Phenylene)bis[9-phenyl-1,10-phenanthroline], 2,2'-(1,3-Phenyl)bis[9-phenyl-1,10-phenanthroline]
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C42H26N4

BSB

Cas number: 18826-13-6
Synonyms: 4,4'-Bis-triphenylsilanyl-biphenyl, 4,4'-Di(triphenylsilyl)-biphenyl
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C48H38Si2

BTB

Cas number: 266349-83-1
Synonyms: 4,4'-Bis-[2-(4,6-diphenyl-1,3,5-triazinyl)]-1,10-biphenyl
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C34H28N6

C545T

Cas number: 155306-71-1
Synonyms: Coumarin 545T
Purity: Sublimed: >99%
Chemical Formula: C26H26N2O2S

CBP

Cas number: 58328-31-7
Synonyms: DCBP, 4,4′-Bis(9-carbazolyl)-1,1′-biphenyl, 4,4-N,N′-Dicarbazole-1,1′-biphenyl
Purity: Sublimed: >99.5% (HPLC)
Chemical Formula: C36H24N2

DPEPO

Cas number: 808142-23-6
Synonyms: 1,3,5-Tris(1-phenyl-1Hbenzimidazol-2-yl)benzene
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C36H28O3P2

DPPS

Cas number: 1152162-74-7
Synonyms: 3,3'-[(Diphenylsilylene)di-4,1-phenylene]bispyridine
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C34H26N2Si

FK306

Cas number: 1421058-47-0
Synonyms: Iridium(III)bis(4-(tert-butyl)-2,6-diuoro-2,3-bipyridinne)acetylacetonate
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C33H33F4IrN4O2

Liq

Cas number: 25387-93-3
Purity: >99% (sublimed)
Chemical Formula: C9H6LiNO

mSiTrz

Cas number: 2252416-90-1
Synonyms: 1,3,5-Tris(1-phenyl-1Hbenzimidazol-2-yl)benzene
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C57H43N3Si2

OXD-7

Cas number: 138372-67-5
Synonyms: 1,3-Bis[5-(4-tert-butylphenyl)-2-[1,3,4]oxadiazolyl]benzene
Purity: Sublimed: >99%
Chemical Formula: C30H30N4O2

PDIN

Cas number: 117901-97-0
Synonyms: PDI-N, DAPER, DAPER DNA precipitation reagent, 2,9-Bis[3-(dimethylamino)propyl]anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone
Purity: 98% (1H NMR)
Chemical Formula: C34H32N4O4

PO-T2T

Cas number: 1646906-26-4
Synonyms: 1,3,5-Tris(1-phenyl-1Hbenzimidazol-2-yl)benzene
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C57H42N3O3P3

HBL – Hole Blocking Layer Materials for OLED Efficiency

Hole blocking layer (HBL) materials play a decisive role in maximizing OLED device performance by confining charge carriers and excitons within the emissive zone. Noctiluca delivers high-purity HBL compounds engineered to prevent hole leakage, enhance recombination efficiency, and extend operational lifetime across fluorescent, phosphorescent, and TADF device architectures.

Understanding Hole Blocking Layers

In organic light-emitting diodes, the hole blocking layer is positioned between the emissive layer (EML) and the electron transport layer (ETL). This strategic placement serves two critical functions:

  • Hole confinement – preventing holes from escaping the emission zone into the ETL, where they would recombine non-radiatively
  • Exciton blocking – containing excited states within the EML to maximize radiative decay and light output

Without an effective hole blocking layer, excess holes penetrate into electron-transporting regions, causing efficiency losses, emission zone broadening, and accelerated device degradation. This effect becomes particularly pronounced in blue phosphorescent OLEDs where precise charge balance is essential.

Key Material Requirements

Effective HBL materials must satisfy demanding electronic and physical criteria:

PropertyRequirementFunction
Deep HOMO level<-6.0 eVCreates energy barrier blocking hole injection
Appropriate LUMOAligned with ETLEnables electron transport through HBL
High triplet energy (ET)>2.5 eV for blue devicesPrevents triplet exciton quenching
Electron mobility>10⁻⁵ cm²/VsMaintains efficient electron flow
Wide bandgap>3.0 eV typicalProvides exciton confinement
Thermal stabilityTg >80°CEnsures morphological integrity

The depth of the HOMO level directly determines hole blocking effectiveness. Materials with HOMO values below -6.0 eV create substantial energy barriers that holes cannot overcome, forcing recombination to occur within the designated emission zone.

Mechanism of Action

Hole blocking layer materials function through energy level engineering:

  1. Injection barrier formation – The deep HOMO of HBL materials creates a significant energy step relative to the EML, preventing hole injection into the blocking layer
  2. Electron transmission – Despite blocking holes, the LUMO alignment permits electrons to pass through toward the emissive layer
  3. Triplet confinement – High triplet energy prevents energy transfer from EML triplet excitons to the HBL, critical for phosphorescent devices
  4. Interface stabilization – HBL materials protect the EML from direct contact with potentially reactive ETL compounds

Featured HBL Materials

Noctiluca offers proven hole blocking compounds with verified performance:

MaterialCAS NumberHOMO (eV)ET (eV)Key Features
BCP4733-39-5-6.52.5Wide bandgap, excellent exciton blocking
BPhen1662-01-7-6.42.5Phenanthroline core, high stability
TPBi192198-85-9-6.2 to -6.72.7Dual HBL/ETL function, versatile
TmPyPB921205-03-0-6.72.8High ET, pyridine coordination sites
B3PyMPM1383079-95-5-6.82.7Excellent electron mobility
3TPYMB929203-02-1-6.82.8Ultra-deep HOMO, blue PHOLED optimized

BCP: The Industry Standard

Bathocuproine (BCP) remains the most widely used hole blocking layer material due to its combination of favorable properties:

  • Deep HOMO level (-6.5 eV) providing effective hole blocking
  • Wide bandgap ensuring exciton confinement
  • Established processing parameters for vacuum deposition
  • Compatibility with common ETL materials (Alq₃, TPBi)

However, BCP exhibits moderate thermal stability and can crystallize over extended operation periods. For demanding applications, advanced alternatives like TmPyPB or 3TPYMB offer improved stability and higher triplet energies.

Application-Specific Considerations

Different OLED technologies impose varying HBL requirements:

Blue Phosphorescent OLEDs Blue PHOLEDs demand HBL materials with triplet energies exceeding 2.7 eV to prevent quenching of high-energy blue triplet excitons. TmPyPB (ET = 2.78 eV) and 3TPYMB represent optimal choices for these challenging devices.

TADF Devices Thermally activated delayed fluorescence OLEDs benefit from HBL materials that support efficient reverse intersystem crossing without introducing additional quenching pathways. Wide-bandgap phenanthroline derivatives perform well in these architectures.

Red and Green PHOLEDs Lower triplet energy requirements for red and green emission allow broader HBL material selection. BCP and BPhen provide cost-effective solutions with proven reliability.

Tandem and Hybrid Structures Complex device architectures may employ HBL materials as charge generation layer components, requiring careful optimization of conductivity and interfacial properties.

Dual-Function Materials: HBL + ETL

Many hole blocking layer materials simultaneously serve as electron transport layers, simplifying device architecture:

  • TPBi – combines HBL function with effective electron transport and host capability
  • TmPyPB – high electron mobility enables efficient dual HBL/ETL operation
  • BPhen – frequently used as combined HBL/ETL in research devices

This dual functionality reduces layer count, simplifies fabrication, and can improve device reliability by eliminating additional interfaces.

Integration with Device Stack

Hole blocking layers work synergistically with adjacent functional layers:

Typical OLED architecture positions the HBL in this sequence:

Anode | HIL | HTL | EBL | EML (Host:Dopant) | HBL | ETL | EIL | Cathode

The Noctiluca Advantage

Our hole blocking layer materials deliver critical benefits:

  • Ultra-high purity (>99.99%) – sublimation purification eliminates trap-forming impurities
  • Batch-specific characterization – HOMO/LUMO verification and purity certificates
  • Custom synthesis capability – modified HBL structures from 1g to 1kg scale
  • Application support – guidance on HBL selection for specific device architectures
  • Processing compatibility – materials optimized for thermal evaporation and select solution processes

From fundamental OLED research to production-scale device optimization, Noctiluca HBL materials provide the performance foundation for high-efficiency organic light-emitting devices.

Explore our HBL materials or contact our device specialists for stack optimization recommendations.

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