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Home » Compounds » ETL

ETL

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

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

Hex-Ir(phq)3

Cas number: 1268460-37-2
Synonyms: 1,3,5-Tris(1-phenyl-1Hbenzimidazol-2-yl)benzene
Purity: Sublimed: >99.0% (HPLC)
Chemical Formula: C63H66IrN3

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

ETL – Electron Transport Layer Materials for Organic Electronics

Electron transport layer (ETL) materials form an essential component of high-performance organic electronic devices, facilitating efficient electron delivery from the cathode to the active layer. Noctiluca offers a comprehensive portfolio of ETL compounds engineered for OLED displays, perovskite solar cells, organic photovoltaics, and emerging optoelectronic applications—all manufactured to ultra-high purity standards exceeding 99.99%.

The Function of Electron Transport Layers

The electron transport layer bridges the gap between the cathode electrode and the device’s functional core, whether an emissive layer in OLEDs or an absorber in photovoltaic cells. ETL materials perform several interconnected functions:

  • Electron injection – accepting electrons from the cathode with minimal energy barrier
  • Electron transport – conducting electrons efficiently toward the recombination or collection zone
  • Hole blocking – preventing holes from reaching the cathode where they would recombine non-radiatively
  • Exciton confinement – keeping excited states within the active layer (particularly important in OLEDs)

The effectiveness of an electron transport layer directly impacts device metrics including external quantum efficiency (EQE), operating voltage, current density, and operational stability.

Critical Material Properties

Selecting optimal ETL materials requires matching electronic properties to device architecture:

PropertyRequirementImpact on Device
LUMO energy levelAligned with cathode work functionDetermines electron injection efficiency
Electron mobility>10⁻⁵ cm²/Vs (higher preferred)Controls current density and response speed
HOMO energy levelDeep (<-6.0 eV)Provides hole blocking capability
Triplet energy (ET)>2.5 eV for blue OLEDsPrevents exciton quenching
Thermal stabilityTg >80°C, Td >300°CEnsures long-term device reliability
Film morphologyAmorphous, pinhole-freeMaintains uniform charge distribution

Energy level alignment between the ETL and adjacent layers—cathode on one side, emissive or active layer on the other—proves critical for minimizing injection barriers and achieving low operating voltages.

Featured ETL Materials

Noctiluca provides established and advanced electron transport layer compounds:

MaterialCAS NumberLUMO (eV)Electron MobilityKey Applications
Alq₃2085-33-8-3.010⁻⁶ cm²/VsClassic OLED ETL, green emission
TPBi192198-85-9-2.710⁻⁵ cm²/VsUniversal ETL/HBL/Host
TmPyPB921205-03-0-2.710⁻³ cm²/VsHigh-mobility ETL/HBL
BCP4733-39-5-2.910⁻⁵ cm²/VsETL/HBL, wide bandgap
BPhen1662-01-7-3.010⁻⁴ cm²/VsETL/HBL, n-dopable
B3PyMPM1383079-95-5-3.210⁻⁴ cm²/VsDeep LUMO, efficient injection
Liq25387-93-3-2.9EIL/ETL, n-type dopant
PO-T2T1646906-26-4-3.010⁻⁴ cm²/VsTADF host/ETL

Material Classes and Molecular Design

Electron transport layer materials fall into several structural categories, each offering distinct advantages:

Phenanthroline Derivatives BCP and BPhen represent the phenanthroline family—compounds featuring nitrogen-containing heterocycles that coordinate effectively with metal cathodes. Their electron-deficient character promotes electron transport while deep HOMO levels provide hole blocking. BPhen demonstrates particular utility as an n-dopable host for enhanced conductivity.

Benzimidazole Compounds TPBi (2,2′,2″-(1,3,5-benzinetriyl)-tris(1-phenyl-1-H-benzimidazole)) exemplifies this class, offering versatile performance as ETL, hole blocking layer, and host material. Its three-dimensional molecular structure promotes amorphous film formation and resists crystallization.

Pyridine-Based Materials TmPyPB leverages pyridine groups to achieve exceptional electron mobility—approaching 10⁻³ cm²/Vs, roughly 100× higher than conventional ETL materials. The pyridine nitrogen atoms also coordinate with metal ions, providing passivation effects valuable in perovskite device interfaces.

Metal Quinolates Alq₃ (tris(8-hydroxyquinolinato)aluminum) pioneered organic electronics as both ETL and emitter in early OLEDs. While newer materials surpass its transport properties, Alq₃ remains relevant for specific architectures and fundamental studies.

Phosphine Oxide Compounds Materials like PO-T2T combine electron-withdrawing phosphine oxide groups with extended conjugation, achieving deep LUMO levels and high triplet energies suitable for TADF device architectures.

Application-Specific Selection

Different device platforms impose varying ETL requirements:

OLED Displays and Lighting OLED applications demand ETL materials balancing electron mobility, triplet energy, and morphological stability. For blue phosphorescent OLEDs, high triplet energy (>2.7 eV) prevents exciton quenching at the EML/ETL interface. TmPyPB and TPBi serve as workhorses for research devices, while commercial applications may employ proprietary optimized compounds.

Device stack positioning:

Anode | HIL | HTL | EBL | EML | HBL | ETL | EIL | Cathode

Perovskite Solar Cells (PSC) In n-i-p architecture perovskite solar cells, the ETL extracts photogenerated electrons from the perovskite absorber. TmPyPB has demonstrated particular effectiveness due to pyridine group interactions with undercoordinated Pb²⁺ ions at grain boundaries, passivating defect states while facilitating electron extraction.

Organic Photovoltaics (OPV) Organic solar cells utilize ETL materials (often called cathode interlayers) to optimize energy level alignment between the active layer and cathode. BCP and BPhen serve as exciton blocking layers preventing recombination losses at the cathode interface.

Perovskite LEDs (PeLED) Emerging perovskite light-emitting diodes benefit from mixed ETL approaches—combining materials like TmPyPB and TPBi to optimize both electron injection and interface passivation simultaneously.

N-Type Doping Strategies

Enhancing ETL conductivity through n-type doping significantly reduces device operating voltage:

  • Liq (8-Quinolinolato lithium) – widely used n-dopant compatible with most ETL hosts
  • Cs₂CO₃ (Cesium carbonate) – inorganic dopant for enhanced electron injection
  • Li metal – co-evaporated with ETL materials for maximum conductivity

Doped ETL systems like BPhen:Liq or TPBi:Liq demonstrate dramatically improved electron injection, enabling ultra-low voltage OLED operation below 3V for green emission.

Integration with Device Architecture

Electron transport layers interface with multiple functional components:

Processing Considerations

Noctiluca ETL materials accommodate various deposition methods:

Thermal Evaporation (PVD) Most small-molecule ETL materials deposit cleanly via vacuum thermal evaporation, forming dense, uniform films with controlled thickness. Our sublimation-grade materials (>99.99% purity) minimize outgassing and ensure reproducible evaporation rates.

Solution Processing Select ETL materials offer solubility in orthogonal solvents, enabling solution deposition without dissolving underlying layers. This capability proves essential for multilayer solution-processed devices and inkjet-printed electronics.

Interface Engineering Ultra-thin ETL interlayers (<5 nm) can modify electrode work functions and passivate interface defects without contributing significant series resistance.

The Noctiluca Advantage

Our electron transport layer portfolio delivers measurable performance benefits:

  • Ultra-high purity (>99.99%) – sublimation purification eliminates charge traps and quenching impurities
  • Batch-specific documentation – LUMO verification, mobility data, and thermal analysis
  • Custom synthesis – modified ETL structures and novel compounds from 1g to 1kg
  • Technical consultation – ETL selection guidance for specific device architectures
  • Dual-processing options – materials characterized for both PVD and solution methods
  • Industry validation – compounds trusted by leading display manufacturers worldwide

Whether optimizing OLED efficiency, maximizing perovskite solar cell performance, or developing next-generation optoelectronic devices, Noctiluca electron transport layer materials provide the foundation for breakthrough results.

Browse our ETL materials catalog or consult our applications team for device-specific recommendations.

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