The use of ZnO nanowires has become a widespread topic of interest in optoelectronics. In order to correctly assess the
quality, functionality, and possible applications of such nanostructures it is important to accurately understand their
electrical and optical properties. Aluminum- and gallium-doped crystalline ZnO nanowires were synthesized using a
low-temperature solution-based process, achieving dopant densities of the order of 1020 cm-3. A non-contact optical
technique, photothermal deflection spectroscopy, is used to characterize ensembles of ZnO nanowires. By modeling the
free charge carrier absorption as a Drude metal, we are able to calculate the free carrier density and mobility.
Determining the location of the dopant atoms in the ZnO lattice is important to determine the doping mechanisms of the
ZnO nanowires. Solid-state NMR is used to distinguish between coordination environments of the dopant atoms.
Optical absorption phenomena and in particular sub band gap absorption features are of great importance in the understanding of processes of charge generation and transport in organic pure and composite semiconductor films. To come towards this objective, an alternative and high sensitive spectroscopic approach is introduced to examine the absorption of light in pure and compound organic semiconductors. Because sub band gap absorption features are typically characterized by very low absorption coefficients, it is not possible to resolve them using common transmission and reflection measurements and high sensitive alternatives are needed. Therefore, a combination of photocurrent (Constant Photocurrent Method CPM/Fourier Transform Photocurrent Spectroscopy FT-PS) and photothermal techniques (Photothermal Deflection Spectroscopy PDS) has been used, increasing sensitivity by a factor of thousand, reaching detectable absorption coefficients ((E) down to 0.1 cm-1. In this way, the dynamic range of measurable absorption coefficients is increased by several orders of magnitude compared to transmission/reflection measurements. These techniques have been used here to characterize ground state absorption of thin films of MDMO-PPV, PCBM and a mixture of both materials in a 1:4 ratio, as typically used in a standard active layer in a fully organic solar cell. The spectra reveal defect related absorption phenomena and significant indication of existing interaction in the ground state between both materials, contrary to the widely spread conviction that this is not the case. Experimental details of the techniques and measurement procedures are explained.
The microstructure of MDMO-PPV:PCBM blends as used in bulk hetero-junction organic solar cells was studied by Atomic Force Microscopy (AFM) and Kelvin Force Microscopy (KFM) to image the surface morphology and by means of Transmission Electron Microscopy (TEM) to reveal images of the film's interior.
By introducing KFM, it was possible to demonstrate that phase separated domains have different local electrical properties than the surrounding matrix. Since blend morphology clearly influences global electrical properties and photovoltaic performance, an attempt to control the morphology by means of casting conditions was undertaken. By using AFM, it has been proven that not only the choice of solvent, but also drying conditions dramatically influence the blend structure. Therefore, the possibility of discovering the blend morphology by AFM, KFM and TEM makes them powerful tools for understanding today's organic photovoltaic performances and for screening new sets of materials.
Current state-of-the-art bulk hetero-junction organic photovoltaic devices will be discussed based on poly(2-methoxy-5-(3',7'-dimethyl-octyloxy))-p-phenylene vinylene, (MDMO-PPV), as an electron donor and (6,6)-phenyl-C61-butric-acid (PCBM)(a soluble C60 derivative) as electron acceptor. A brief review will be provided summarizing recent results on efficiency enhancement on morphological investigations. A significant increase in power conversion efficiency has been demonstrated for devices based on so-called 'sulphinyl' synthesized MDMO-PPV (ηAM1.5 = 2.9%) in comparison with devices based on 'Gilch' synthesized MDMO-PPV (ηAM1.5 = 2.5%). In order to understand the higher efficiency values obtained using a different solvent or a different MDMO-PPV-material, electrical and morphological investigations are being performed. Concerning the latter, it has been shown with various analytical techniques that the morphology of the blended photoactive films and also the power conversion efficiency of the corresponding photovoltaic devices are both simultaneously influenced by preparation conditions such as choice of the solvent and drying conditions.
Access to the requested content is limited to institutions that have purchased or subscribe to SPIE eBooks.
You are receiving this notice because your organization may not have SPIE eBooks access.*
*Shibboleth/Open Athens users─please
sign in
to access your institution's subscriptions.
To obtain this item, you may purchase the complete book in print or electronic format on
SPIE.org.
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.