4.8 Article

Extensive Penetration of Evaporated Electrode Metals into Fullerene Films: Intercalated Metal Nanostructures and Influence on Device Architecture

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 7, 期 45, 页码 25247-25258

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b06944

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资金

  1. National Science Foundation [CHE-1510353, CHE-1112569]
  2. NSF IGERT: Materials Creation Training Program (MCTP) [DGE-0654431]
  3. California NanoSystems Institute
  4. NSF [CMMI-1200547, 0840531]
  5. NIH [1S10RR23057]
  6. CNSI at UCLA
  7. Direct For Mathematical & Physical Scien [0840531] Funding Source: National Science Foundation
  8. Directorate For Engineering
  9. Div Of Chem, Bioeng, Env, & Transp Sys [1510353] Funding Source: National Science Foundation
  10. Division Of Chemistry [0840531] Funding Source: National Science Foundation
  11. Division Of Chemistry
  12. Direct For Mathematical & Physical Scien [1112569] Funding Source: National Science Foundation

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Although it is known that evaporated metals can penetrate into films of various organic molecules that are a few nanometers thick, there has been little work aimed at exploring the interaction of the common electrode metals used in devices with fullerene derivatives, such as organic photovoltaics (OPVs) or perovskite solar cells that use fullerenes as electron transport layers. In this paper, we show that when commonly used electrode metals (e.g., Au, Ag, Al, Ca, etc.) are evaporated onto films of fullerene derivatives (such as [6-6]-phenyl-C-61-butyric acid methyl ester (PCBM)), the metal penetrates many tens of nanometers into the fullerene layer. This penetration decreases the effective electrical thickness of fullerene-based sandwich structure devices, as measured by the device's geometric capacitance, and thus significantly alters the device physics. For the case of Au/PCBM, the metal penetrates a remarkable 70 nm into the fullerene, and we see penetration of similar magnitude in a wide variety of fullerene derivative/evaporated metal combinations. Moreover, using transmission electron microscopy to observed cross-sections of the films, we show that when gold is evaporated onto poly(3-hexylthiophene) (P3HT)/PCBM sequentially processed OPV quasi-bilayers, Au nanoparticles with diameters of similar to 3-20 nm are formed and are dispersed entirely throughout the fullerene-rich overlayer. The plasmonic absorption and scattering from these nanoparticles are readily evident in the optical transmission spectrum, demonstrating that the interpenetrated metal significantly alters the optical properties of fullerene-rich active layers. This opens a number of possibilities in terms of contact engineering and light management so that metal penetration in devices that use fullerene derivatives could be used to advantage, making it critical that researchers are aware of the electronic and optical consequences of exposing fullerene-derivative films to evaporated electrode metals.

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