We have analyzed the role of the bond densities of a-SiNx:H films on the passivation properties at the SiNx:H/Si interface. The films are deposited onto silicon wafers by plasma enhanced chemical vapor deposition using a 13.56 MHz direct plasma system and a SiH4/N2/H2 gas mixture. Fourier transform infrared spectroscopy measurements are performed in order to obtain the bonding concentration of Si–Si, Si–H, Si–N and N–H. The passivation properties are deduced by lifetime measurements using a microwave-detected photoconductance decay technique. Carrier lifetimes of the SiNx:H-passivated silicon wafers of up to 1200 μs correlate to surface recombination velocities, Seff, as low as 4–6 cm/s. This means that the films provide excellent passivation of silicon surfaces, which is necessary for high-efficiency solar cells. The Si–H bond density and the total bond density are considered as measures of the passivation quality. Models for the formation of K+ centers and for the passivation pathways during the plasma deposition are proposed. The addition of a further hydrogen source to the plasma gas (H2) leads to a better defect passivation of Si dangling bonds during the deposition.
Charge-carrier mobility is a fundamental material parameter, which plays an important role in determining solar-cell efficiency. The higher the mobility, the less time a charge carrier will spend in a device and the less likely it is that it will be lost to recombination. Despite the importance of this physical property, it is notoriously difficult to measure accurately in disordered thin-film solar cells under operating conditions. We, therefore, investigate a method previously proposed in the literature for the determination of mobility as a function of current density. The method is based on a simple analytical model that relates the mobility to carrier density and transport resistance. By revising the theoretical background of the method, we clearly demonstrate what type of mobility can be extracted (constant mobility or effective mobility of electrons and holes). We generalize the method to any combination of measurements that is able to determine the mean electron and hole carrier density, and the transport resistance at a given current density. We explore the robustness of the method by simulating typical organic solar-cell structures with a variety of physical properties, including unbalanced mobilities, unbalanced carrier densities, and for high or low carrier trapping rates. The simulations reveal that near V OC and J SC , the method fails due to the limitation of determining the transport resistance. However, away from these regions (and, importantly, around the maximum power point), the method can accurately determine charge-carrier mobility. In the presence of strong carrier trapping, the method overestimates the effective mobility due to an underestimation of the carrier density.
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