Porous 4H-SiC layers were fabricated by photochemical etching of n-type 4H-SiC samples with varying resistivity. An etching solution of Na 2 S 2 O 8 and HF was used while Pt deposited at the 4H-SiC surface served as catalyst for the reduction of Na 2 S 2 O 8 . The contact resistance at the Pt/4H-SiC junction was decreased by annealing and surface near phosphorous doping. This enabled the porosification of 4H-SiC with photochemical etching. © The Author(s) 2017. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. [DOI: 10.1149/2.0021603jss] All rights reserved.Manuscript submitted November 9, 2015; revised manuscript received December 14, 2015. Published December 24, 2015 Compared to porous silicon, porous silicon carbide has many outstanding properties such as an enhanced chemical inertness, high heat conductivity and a relatively large bandgap. Therefore it offers novel application scenarios as electrode material in super-capacitors, 1 membranes for biomedical devices 2 or in the manufacturing of high temperature gas sensors. Controlling the etching depth for 6H-SiC is still an unresolved issue, while the formation of a porous structure on 4H-SiC is limited to surface regions in the nanometer range. 6,7 In this letter the formation of porous 4H-SiC by MAPCE is presented for samples having different bulk resistivity by decreasing the contact resistance at the Pt/4H-SiC junction.
ExperimentalAs substrates, n-type 4H-SiC wafers with low and high resistivity (ρ = 0.02 · cm and ρ = 0.106 · cm respectively) were purchased from CREE. Square samples of these substrates with an area of 1 cm 2 were used for experiments. For cleaning, all samples were consecutively soaked for 5 minutes in acetone, isopropanol and ethanol. Then a 300 nm thin Pt layer was sputter deposited on the samples with a LS730S Von Ardenne sputter machine, while a 0.7 × 0.7 cm 2 silicon piece in the center of the sample served as shadow mask. Prior to Pt deposition, the samples were cleaned in situ using an inverse sputter etching procedure with Argon plasma for 60 s at 1000 W. Finally the samples were placed in an etching solution containing 0.04 mol/L Na 2 S 2 O 8 and 1.31 mol/L HF for 2 hours under UV irradiation. As etching chamber a porous silicon etching cell from AMMT GmbH with a total volume of 1.5 L was used. Front side illumination was z E-mail: markus.leitgeb@tuwien.ac.at done with a 250 Watt ES280LL mercury arc lamp at full spectrum. The distance from the samples to the UV source was approximately 3 cm. In this configuration the effective volume of the etching solution was 150 mL.For electrical characterization the Agilent B2911A Precision Source/Measure Unit was used. An array of circular Pt/TiN/Pt trilayered pads was sputter deposited onto 1 cm 2 square samples. The diameter of the pads was 1 mm and the dist...