4.8 Article

Supersaturated Self-Assembled Charge-Selective Interfacial Layers for Organic Solar Cells

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 136, 期 51, 页码 17762-17773

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja508453n

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资金

  1. Argonne-Northwestern Solar Energy Research (ANSER) Center, an Energy Frontier Research Center - U.S. Department of Energy, Office of Science [DE-SC0001059]
  2. Office of Basic Energy Sciences [DE-FG02-08ER46536]
  3. Northwestern Materials Research Science & Engineering Center (MRSEC) - National Science Foundation (NSF) [DMR-1121262]
  4. NSF Graduate Research Fellowship
  5. National Defense Science & Engineering Graduate Fellowship (NDSEG) Program - Department of Defense (DoD)
  6. Institute for Sustainability and Energy at Northwestern (ISEN)
  7. Northwestern University
  8. National Science Foundation (NSF) [NSF CHE-0923236, CHE-9871268]
  9. Pfizer
  10. State of Illinois
  11. U.S. Department of Energy (DOE) [DE-FG02-08ER46536] Funding Source: U.S. Department of Energy (DOE)

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To achieve densely packed charge-selective organosilane-based interfacial layers (IFLs) on the tin-doped indium oxide (ITO) anodes of organic photovoltaic (OPV) cells, a series of Ar2N-(CH2)(n)-SiCl3 precursors with Ar = 3,4-difluorophenyl, n = 3, 6, 10, and 18, was synthesized, characterized, and chemisorbed on OPV anodes to serve as IFLs. To minimize lateral nonbonded -NAr2 center dot center dot center dot Ar2N- repulsions which likely limit IFL packing densities in the resulting self-assembled monolayers (SAMs), precursor mixtures having both small and large n values are simultaneously deposited. These heterogeneous SAMs are characterized by a battery of techniques: contact angle measurements, X-ray reflectivity, X-ray photoelectron spectroscopy, ultraviolet photoelectron spectroscopy (UPS), cyclic voltammetry, and DFT computation. It is found that the headgroup densities of these supersaturated heterogeneous SAMs (SHSAMs) are enhanced by as much as 17% versus their homogeneous counterparts. Supersaturation significantly modifies the IFL properties including the work function (as much as 16%) and areal dipole moment (as much as 49%). Bulk-heterojunction OPV devices are fabricated with these SHSAMs: ITO/IFL/poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl][2-[[(2-ethylhexyl)oxy]carbonyl]-3-fluorothieno[3,4-b]thiophenediyl]]:phenyl-C-71-butyric acid methyl ester (PTB7:PC71BM)/LiF/Al. OPVs having SHSAM IFLs exhibit significantly enhanced performance (PCE by 54%; V-oc by 35%) due to enhanced charge selectivity and collection, with the PCE rivaling or exceeding that of PEDOT:PSS IFL devices -7.62%. The mechanism underlying the enhanced performance involves modified hole collection and selectivity efficiency inferred from the UPS data. The ITO/SAM/SHSAM surface potential imposed by the dipolar SAMs causes band bending and favorably alters the Schottky barrier height. Thus, interfacial charge selectivity and collection are enhanced as evident in the greater OPV V-oc.

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