期刊
ACS APPLIED MATERIALS & INTERFACES
卷 12, 期 6, 页码 7038-7046出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b17170
关键词
nanoporous silicon carbide; Ni-FeOOH nanorods; water oxidation cocatalyst; photoelectrochemical water splitting; zero-onset potential
资金
- Swedish Research Council (Vetenskapsradet) [621-2014-5461, 2018-04670]
- Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning (FORMAS) [2016-00559]
- Swedish Foundation for International Cooperation in Research and Higher Education (STINT) [CH2016-6722]
- AForsk foundation [16-399]
- Stiftelsen Olle Engkvist Byggmastare [189-0243]
- China Scholarship Council [201706400041]
A surface-nanostructured semiconductor photoelectrode is highly desirable for photo-electrochemical (PEC) solar-to-fuel production due to its large active surface area, efficient light absorption, and significantly reduced distance for charge transport. Here, we demonstrate a facile approach to fabricate a nanoporous 6H-silicon carbide (6H-SiC) photoanode with a conformal coating of Ni-FeOOH nanorods as a water oxidation cocatalyst. Such a nanoporous photoanode shows significantly enhanced photocurrent density (j(ph)) with a zero-onset potential. A dendritic porous 6H-SiC with densely arranged holes with a size of similar to 40 nm on the surface is fabricated by an anodization method, followed by the hydrothermal deposition of FeOOH nanorods and electrodeposition of NiOOH. Under an illumination of AM1.5G 100 mW/cm(2), the Ni-FeOOH-coated nanoporous 6H-SiC photoanode exhibits an onset potential of 0 V versus the reversible hydrogen electrode (V-RHE) and a high j(ph) of 0.684 mA/cm(2) at 1 V-RHE, which is 342 times higher than that of the Ni-FeOOH-coated planar 6H-SiC photoanode. Moreover, the nanoporous photoanode shows a maximum applied-bias-photon-to-current efficiency (ABPE) of 0.58% at a very low bias of 0.36 V-RHE, distinctly outperforming the planar counterpart. The impedance measurements demonstrate that the nanoporous photoanode possesses a significantly reduced charge-transfer resistance, which explains the dramatically enhanced PEC water-splitting performance. The reported approach here can be widely used to fabricate other nanoporous semiconductors for solar energy conversion.
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