Abstract

Open-pore nickel (Ni) foams are characterized using surface science and electrochemical techniques. A scanning electron microscopy analysis reveals interconnected Ni struts that generate small and large pores of ca. 50 and 500 μm in size, respectively. An X-ray photoelectron spectroscopy (XPS) analysis of the surface-chemical composition of the Ni foams shows that there are oxidized and metallic sections within their surfaces despite being prepared by sintering in an oxidizing atmosphere at a high temperature and being stored in moist air. The ratio of the areas of oxidized and metallic sections is evaluated using XPS data. Chemical etching of the Ni foams results in removal of the native surface oxide/hydroxide without altering the three-dimensional structure; it also increases the roughness (R) of the surfaces of Ni struts giving rise to an increase in the electrochemically active surface area (Aecsa). Thermal treatment of Ni foams in an H2(g) atmosphere at 500 °C reduces the native surface oxide/hydroxide but does not increase R or Aecsa. Electrochemical behavior of the Ni foams is examined in 0.5 M aqueous KOH solution using cyclic-voltammetry (CV) and electrochemical impedance spectroscopy (EIS). As-received, chemically etched, thermally reduced and electro-oxidized Ni foams generate distinct CV profiles; their features are assigned to oxidized and metallic surface states. The observations made on the basis of XPS measurements are corroborated by the results of CV analyses. The application of CV and XPS or EIS allows in situ determination of Aecsa and the specific surface area (As) of the chemically etched and thermally reduced Ni foams. The values of As determined on the basis of joint CV and XPS measurements are 227 ± 74 and 149 ± 48 cm(2) g(-1) for the etched and reduced Ni foams, respectively. The values of As determined on the basis of CV, XPS and EIS measurements are 241 ± 80 and 160 ± 23 cm g(-1) for the etched and reduced Ni foams, respectively.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.