Affiliation:
1. School of Mechatronics Engineering Harbin Institute of Technology Harbin 150001 China
2. Department of Mechanical and Energy Engineering Southern University of Science and Technology Shenzhen 518055 China
Abstract
AbstractNanoporous single‐crystal silicon carbide (SiC) is widely used in various applications such as protein dialysis, as a catalyst support, and in photoanodes for photoelectrochemical water splitting. However, the fabrication of nano‐structured SiC is challenging owing to its extreme chemical and mechanical stability. This study demonstrates a highly‐efficient, open‐circuit electrolytic plasma‐assisted chemical etching (EPACE) method without aggressive fluorine‐containing reactants. The EPACE method enables the nano‐structuring of SiC via a plasma‐enveloped microtool traversing over the target material in an electrolyte bath. Through process design, EPACE readily produces a uniform nanoporous layer on a 4H‐SiC wafer in KOH aqueous solution, with adjustable pore diameters in the range 40–130 nm. Plasma diagnosis by optical emission spectrometry (OES) and surface microanalysis reveal that EPACE realizes a nanoporous structure by electrolytic plasma‐assisted oxidation and subsequent thermochemical reduction of an oxide. An increase in voltage or a decrease in etch gap intensifies the plasma and improves the etching efficiency. The maximum etch rate and depth reach 540 nm min−1 and 10 µm, respectively, demonstrating the significant potential of the approach as a time‐saving and sustainable nanofabrication method for industrial applications. Further, the effectiveness of the fabricated SiC nanoporous structure for application in photoelectrochemical water splitting is demonstrated.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
Science, Technology and Innovation Commission of Shenzhen Municipality
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献