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Ossila/Bathocuproine, >99.5% Purity Sublimed Grade BCP | 4733-39-5/5 g Unsublimed Grade (u003e98.0% purity)/B232
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Ossila/Bathocuproine, >99.5% Purity Sublimed Grade BCP | 4733-39-5/5 g Unsublimed Grade (u003e98.0% purity)/B232
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Ossila
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B232
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Bathocuproine (BCP) is a wide-band-gap material and has a high electron affinity. When it is embedded into organic electronic devices, bathocuproine acts as an exciton-blocking barrier which prohibits exciton diffusion process towards the Al electrode otherwise being quenched. One of the most commonly used buffer layer between acceptor and cathode layers is bathocuproine. The introduction of the buffer layer can greatly improve the PCE of polymer organic solar cells. BCP is one of the most popular hole-blocking layer materials that is used in organic electronics, including perovskite solar cells.

It was demonstrated that a BCP buffer layer reduces nonradiative recombination of excitons at the C60 –Al interface. Its most important function is to establish an Ohmic contact between the C60 film and the Al electrode in photovoltaic devices [4].

General Information

Full name2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline
Synonyms
  • Bathocuproine
  • BCP
CAS number4733-39-5
Molecular formulaC26H20N2
Molecular weight360.45 g/mol
HOMO / LUMOHOMO ~ 6.4 eV      LUMO ~2.9 eV
Classification / FamilyElectron-transport layer (ETL), Electron-injection layer (EIL), Hole-blocking layer, OFET, OLED, Organic Photovoltaics, Perovskite solar cells, Sublimed materials.

Product Details

Purity>99.5% (sublimed)>98.0% (unsublimed)
Melting point280-282°C (lit.)
AppearanceLight yellow powder

*Sublimation is a technique used to obtain ultra pure-grade chemicals. For more details about sublimation, please refer to the Sublimed Materials for OLED devices page.

Chemical Structure

Chemical structure of BCP
Chemical Structure of Bathocuproine (BCP)

Device Structure(s)

Device structureITO/DNTPD* (60 nm)/NPB (20 nm)/mCP (10 nm)/mCP:FIrpic (25 nm)/CBP:Ir(piq)2acac (5 nm)/BCP (5 nm)/Alq3 (20 nm)/LiF (1 nm)/Al (200 nm) [5]
ColourWhite white
EQE@500 cd/m28.2 %
Current Efficiency (@500  cd/m2)12.7 lm W1
Device structureITO/NPB (30 nm)/NPB: DCJTB: C545T* (10 nm)/NPB (4 nm)/DNA (8 nm)/BCP (9 nm)/Alq3 (30 nm)/LiF (1 nm)/Al (100 nm) [6]
ColourWhite white
Max. Luminance 13,600 cd/m2
Max. Current Efficiency12.3 cd/A
Max. Power Efficiency4.4 lm W1
Device structureITO/2T-NATA (17 nm)/TPAHQZn* (25 nm)/NPBX* (15 nm)/BCP (8 nm)/ Alq3 (35 nm)/LiF (0.5 nm)/Al (120 nm) [7]
ColourWhite   white
Max. EQE                        17.5%
Max. Luminance12,930 cd/m(12 V) 
Max. Current Efficiency2.66 cd/A (10 V)
Device structureITO/ NPB(60 nm)/Alq3:DCM(7nm)/BCP(12 nm)/ Alq3(36nm)/ MgAg(200 nm) [8]
ColourRed red
Max. Luminance1, 000 cd/m2
Max. Current Efficiency5.66 cd/A 
Device structureITO/α-NPD* (50 nm)/7%-Ir(ppy)3:CBP (20 nm)/BCP (10 nm)/Alq3 (40 nm)/Mg–Ag (100 nm)/Ag (20 nm)  [9]
ColourGreen green
Max EQE(12.0±0.6)%
Max. Powder Efficiency(45±2) lm W1

*For chemical structure information please refer to the cited references.

Characterisation

HPLC of BCP
HPLC trace of Bathocuproine (BCP).
1H NMR BCP Bathocuproine in CDCl3
1H-NMR spectrum of 2,9-Dimethyl-4,7-diphenyl-1,10-phenantroline, also known as Bathocuproine, BCP in CDCl3: Instrument AVIIIHD400 (see full version).

Pricing

Grade (Purity)Order CodeQuantityPrice
Sublimed (>99.5%)B2311 g£185.00
Sublimed (>99.5%)B2315 g£699.00
Unsublimed (>98.0%)B2325 g£326.00

MSDS Documentation

BCP MSDSBCP MSDS sheet

Literature and Reviews

  1. Detailed analysis of bathocuproine layer for organic solar cells based on copper phthalocyanine and C60, J. Huang et al., J. Appl. Phys., 105, 073105 (2009)
  2. On the Role of Bathocuproine in Organic Photovoltaic Cells, H. Gommans et al., Adv. Funct. Mater., 18, 3686-3691 (2008)
  3. A Blue Organic Light Emitting Diode, Y. Kijima et al., J. Appl. Phys., 38, 5274-5277 (1999)
  4. On the function of a bathocuproine buffer layer in organic photovoltaic cells, M. Vogel et al., Appl. Phys. Lett., 89, 163501 (2006).
  5. Improved color stability in white phosphorescent organic light-emitting diodes using charge confining structure without interlayer, S-H. Kim et al., Appl. Phys. Lett. 91, 123509 (2007); http://dx.doi.org/10.1063/1.2786853.
  6. High efficiency white organic light-emitting devices by effectively controlling exciton recombination region, F. Guo et al., Semicond. Sci. Technol. 20, 310–313 (2005).
  7. White organic light-emitting devices based on novel (E)-2-(4-(diphenylamino) styryl)quinolato zinc as a hole- transporting emitter, G. Ding et al., Semicond. Sci. Technol. 24, 025016 (2009); stacks.iop.org/SST/24/025016.
  8. High-efficiency red electroluminescence from a narrow recombination zone confined by an organic double heterostructure, Z. Xie et al., Appl. Phys. Lett., 79, 1048 (2001); doi: 10.1063/1.1390479.
  9. Efficient electrophosphorescence using a doped ambipolar conductive molecular organic thin film, C. Adachi et aL., Org. Electronics, 2(1), 37-43 (2001), doi:10.1016/S1566-1199(01)00010-6.
  10. Matching Charge Extraction Contact for Wide-Bandgap Perovskite Solar Cells, Y. Lin et al., adv. Mater., 1700607 (2017); DOI: 10.1002/adma.201700607.
  11. Role of bathocuproine as hole-blocking and electron-transporting layer in organic light emitting devices, R.Tomova et al., Phys. Status Solidi. C, 7, 3–4, 992–995 (2010); DOI: 10.1002/pssc.200982725.

To the best of our knowledge the technical information provided here is accurate. However, Ossila assume no liability for the accuracy of this information. The values provided here are typical at the time of manufacture and may vary over time and from batch to batch.

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