What is it about?
An efficient silicon solar cell design must compromise between two requirements: 1) defect passivation with insulating materials (to maximize photovoltage), and 2) selective extraction of positive/negative carriers via conductive materials (to maximize photocurrent). This calls for multiple materials deposited by different methods (usually at high temperatures) and with dissimilar area coverage. Hence, why not use a single semi-insulating material which can both passivate while selectively conduct charge? Moreover, what if this material is deposited by low-temperature simple processes? This paper discusses the application of thermally-evaporated transition metal oxides (V2O5, MoO3) to crystalline silicon solar cells, inquiring in the origin of their dual-functionality as passivating/hole-selective materials.
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Why is it important?
Our findings suggest that passivation of the silicon surface occurs by a SiOx ultra-thin layer which forms by spontaneous chemical reaction between silicon and the metal oxide. Additionally, this layer is poor in oxygen and allows to extract carriers (holes), performing a passivating/conducting function. Given that transition metal oxides can be deposited by low-temperature and/or solution-based processes, this offers the possibility of simplifying solar cell fabrication and reducing costs.
Perspectives
After many years of industrially-proven silicon solar cell technology, this publication contributes to recent research efforts that explore dopant-free carrier-selective materials as replacements to the standard boron/phosphorous-based layers.
Luis G. Gerling
Universitat Politecnica de Catalunya
Read the Original
This page is a summary of: Origin of passivation in hole-selective transition metal oxides for crystalline silicon heterojunction solar cells, Journal of Materials Research, December 2016, Cambridge University Press,
DOI: 10.1557/jmr.2016.453.
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