4.8 Article

Engineering Two-Phase and Three-Phase Microstructures from Water-Based Dispersions of Nanoparticles for Eco-Friendly Polymer Solar Cell Applications

期刊

CHEMISTRY OF MATERIALS
卷 30, 期 18, 页码 6521-6531

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.8b03222

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资金

  1. Faculty of Health, Science and Engineering of Karlstad University
  2. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  3. Commonwealth of Australia through the Access to Major Research Facilities Program
  4. UK EPSRC Supersolar Hub Extension [EP/P02484X/1]
  5. EPSRC Centre for Doctoral Training in New and Sustainable [PV EP/L01351X/1]

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Nanoparticle organic photovoltaics, a subfield of organic photovoltaics (OPV), has attracted increasing interest in recent years due to the eco-friendly fabrication of solar modules afforded by colloidal ink technology. Importantly, using this approach it is now possible to engineer the microstructure of the light absorbing/charge generating layer of organic photovoltaics; decoupling film morphology from film deposition. In this study, single-component nanoparticles of poly(3-hexylthiophene) (P3HT) and phenyl-C-61 butyric acid methyl ester (PC61BM) were synthesized and used to generate a two-phase microstructure with control over domain size prior to film deposition. Scanning transmission X-ray microscopy (STXM) and electron microscopy were used to characterize the thin film morphology. Uniquely, the measured microstructure was a direct input for a nanoscopic kinetic Monte Carlo (KMC) model allowing us to assess exciton transport properties that are experimentally inaccessible in these single- component particles. Photoluminescence, UV-vis spectroscopy measurements, and KMC results of the nanoparticle thin films enabled the calculation of an experimental exciton dissociation efficiency (eta(ED)) of 37% for the two-phase microstructure. The glass transition temperature (T-g) of the materials was characterized with dynamic mechanical thermal analysis (DMTA) and thermal annealing led to an increase in eta(ED) to 64% due to an increase in donor-acceptor interfaces in the thin film from both sintering of neighboring opposite-type particles in addition to the generation of a third mixed phase from diffusion of PC61BM into amorphous P3HT domains. As such, this study demonstrates the higher level of control over donor-acceptor film morphology enabled by customizing nanoparticulate colloidal inks, where the optimal three-phase film morphology for an OPV photoactive layer can be designed and engineered.

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