On the energetic dependence of charge separation in low-band-gap polymer/fullerene blends.

نویسندگان

  • Stoichko D Dimitrov
  • Artem A Bakulin
  • Christian B Nielsen
  • Bob C Schroeder
  • Junping Du
  • Hugo Bronstein
  • Iain McCulloch
  • Richard H Friend
  • James R Durrant
چکیده

The energetic driving force required to drive charge separation across donor/acceptor heterojunctions is a key consideration for organic optoelectronic devices. Herein we report a series of transient absorption and photocurrent experiments as a function of excitation wavelength and temperature for two low-band-gap polymer/fullerene blends to study the mechanism of charge separation at the donor/acceptor interface. For the blend that exhibits the smallest donor/acceptor LUMO energy level offset, the photocurrent quantum yield falls as the photon excitation energy is reduced toward the band gap, but the yield of bound, interfacial charge transfer states rises. This interplay between bound and free charge generation as a function of initial exciton energy provides key evidence for the role of excess energy in driving charge separation of direct relevance to the development of low-band-gap polymers for enhanced solar light harvesting.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Efficient two-step photogeneration of long-lived charges in ground-state charge-transfer complexes of conjugated polymer doped with fullerene.

Polarization-sensitive time-resolved visible-infrared pump-probe experiments demonstrate that one can efficiently generate long-lived charges in donor-acceptor charge transfer complex (CTC) of conjugated polymer doped with fullerene, MEH-PPV/dinitroanthraquinone/C(60). In particular, a strong enhancement of the photoinduced charge generation is observed in the red part of the spectrum, i.e. ins...

متن کامل

Transient absorption spectroscopy of charge photogeneration yields and lifetimes in a low bandgap polymer/fullerene film.

Charge photogeneration yields and energetics are determined for a low band gap co-polymer, PCPDTBT blended with PC(70)BM; the increase in charge photogeneration with dithiol is correlated with an increase in the free energy of charge separation.

متن کامل

Understanding the Impact of Hierarchical Nanostructure in Ternary Organic Solar Cells

Ternary organic solar cells (OSCs), which blend two donors and fullerene derivatives with different absorption ranges, are a promising potential strategy for high-power conversion efficiencies (PCEs). In this study, inverted ternary OSCs are fabricated by blending a highly crystalline small molecule BDT-3T-CNCOO in a low band gap polymer PBDTTT-C-T:PC71BM. As the small molecule is introduced, t...

متن کامل

بررسی خواص حرارتی و مکانیکی پلی یورتان‌های بر پایه GAP

Glycidyl Azide Polymer is one of the most important energetic binders that is used in the composite solid propellant formulation. GAP is a unique binder with a positive heat of formation (+117.2 kJ⁄mol). In addition, GAP has good thermal and physical properties such as low glass transition temperature, low viscosity and high density compared to other energetic binders. GAP can be used as a bin...

متن کامل

Polaron pair mediated triplet generation in polymer/fullerene blends

Electron spin is a key consideration for the function of organic semiconductors in light-emitting diodes and solar cells, as well as spintronic applications relying on organic magnetoresistance. A mechanism for triplet excited state generation in such systems is by recombination of electron-hole pairs. However, the exact charge recombination mechanism, whether geminate or nongeminate and whethe...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Journal of the American Chemical Society

دوره 134 44  شماره 

صفحات  -

تاریخ انتشار 2012