Abstract

Nowadays, organic solar cells have the interest of engineers for manufacturing flexible and low cost devices. The considerable progress of this nanotechnology area presents the possibility of investigating new effects from a fundamental science point of view. In this letter we highlight the influence of the concentration of fullerene molecules on the ultrafast transport properties of charged electrons and polarons in P3HT/PCBM blended materials which are crucial for the development of organic solar cells. Especially, we report on the femtosecond dynamics of localized (P2at 1.45 eV) and delocalized (DP2at 1.76 eV) polaron states of P3HT matrix with the addition of fullerene molecules as well as the free-electron relaxation dynamics of PCBM-related states. Our study shows that as PCBM concentration increases, the amplified exciton dissociation at bulk heterojunctions leads to increased polaron lifetimes. However, the increase in PCBM concentration can be directly related to the localization of polarons, creating thus two competing trends within the material. Our methodology shows that the effect of changes in structure and/or composition can be monitored at the fundamental level toward optimization of device efficiency.

Highlights

  • Nowadays, organic solar cells have the interest of engineers for manufacturing flexible and low cost devices

  • Typical organic solar cells are based on the dissociation of photogenerated excitons by the sunlight to charged carriers and polarons at the vicinity of bulk heterojunctions formed within blends of organic semiconductors [3]

  • We have investigated the influence of phenyl-C61 butyric acid methyl ester (PCBM) concentration on the ultrafast photoinduced absorption (PA) of poly-3-hexyl thiophene (P3HT)/PCBM blends after excitation with photon energies large enough to induce excitons in both materials

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Summary

Introduction

Organic solar cells have the interest of engineers for manufacturing flexible and low cost devices.

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