Carrier-selective contacts: non pn-junction Si photocathode for efficient H2 production
Dowon Bae a, Peter C.K. Vesborg a, Ib Chorkendorff a, Ole Hansen b, Thomas Pedersen b
a Technical University of Denmark, Department of Physics, Fysikvej, 312, Kongens Lyngby, Denmark
b Department of Micro- and Nanotechnology, Technical University, ¨ªrsteds Plads, 345E, DTU Nanotech, Kgs. Lyngby, 2800, Denmark
Proceedings of International Conference on Light Driven Water Splitting Using Semiconductor Based Devices (SolarFuel15)
Illetes, Spain, 2015 March 11th - 13th
Organizers: Leslie Frotscher, Sixto Gimenez Julia, Wolfram Jaegermann and Bernhard Kaiser
Oral, Dowon Bae, presentation 072
Publication date: 15th December 2014

Efficiently splitting water using photoelectrochemical (PEC) cell into H2 could become a key technology towards clean, sustainable fuels. Si has suitable Eg and band alignments for the photocathode of tandem water splitting device. And also, efficient H2 production (HER) with open circuit voltage over 0.5 V and photocurrent over 20 mA cm-2 has been shown experimentally using pn+-Si homojunction with Pt co-catalyst. However, as current performance of Si PEC cells far behinds its theoretical limit, the need for different approach increases. Above all, carrier-selective contacts design with efficient carrier transport and low recombination using metal-oxide-semiconductor (MOS) structure comes into the spotlight recently. The key feature is chemical surface passivation by tunneling oxide interlayer and selective carrier transport due to an energy barrier for majority carrier by highly doped layer. This provides favorable structure for high photovoltage, however, very little work has been done studying H2 production using PEC cell with MOS structure. Talin’s group demonstrated HER using Pt/Ti/SiO2/p-Si with Voc of 490 mV, but it has inevitable limitation in current density due to the light absorption by metallic layers. Moreover, there has been no detail report on energy band level analysis to understand how the carriers can be selectively injected. In present work we demonstrate Pt/TiO2/poly-Si:P/SiO2/p-Si (front) and p-Si/SiO2/poly-Si:B/Al (back) to both front and back contacts which provide interface passivation and selective injection of minority and majority carrier to solid/liquid interface and back contact, respectively. The samples with carrier-selective contacts showed almost 100 mV enhanced photovoltage compared with reference Si electrode with conventional pn-junction. Using poly-Si as a metallic layer of MOS structure has been employed in recent state-of-art MOS based photovoltaic cells, but combination with TiO2 for PEC hydrogen has not been shown so far. Moreover, the details working principles based on the band energy analysis are outlined to understand how the carriers can be injected selectively and transferred to solid/liquid interface in PEC system.



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