Tantalum-oxy-nitride nanotubes (TaOxNy NTs) ordered in 1D were successfully synthesized through controlled anodic oxidation of metallic Ta foils followed by high-temperature annealing under NH3 flow to prepare unconventional nanostructured photo-electrodes active with visible light. For the synthesis, a two-step anodization process was adopted: i) the first step in ethylene glycol with 0.33 % NH4F and 3 % H2O, ii) the second step in H2SO4 (98 %) with 1 % HF and 4 % H2O, by applying different voltages and anodization times. Scanning Electron Microscopy integrated with Energy Dispersive X-ray spectroscopy (SEM-EDX) revealed the NTs length ranging from 2 to 5 µm, and the inner tube diameter from 20 to 100 nm, in good correlation with the synthesis parameters. The N-content (from 2.7 % to 19.1 %) was dependent on the nitridation temperature (from 500° to 900°C), and the conversion of bare Ta2O5 into TaOxNy strongly influenced the absorption in the visible region with a bandgap shift from 4.0 to 2.1 eV, respectively. Photo-electrochemical and catalytic performances were evaluated with chronoamperometric measurements and tests in different photo-reactions using AM 1.5 G simulated sunlight: (i) degradation of methylene blue (MB), (ii) ethanol gas-phase photo-reforming and (iii) bias-assisted photoelectrochemical water splitting. The TaOxNy NTs film-type electrode obtained by nitriding at 800 °C showed the highest photocurrent value (0.1 mA∙cm-2), and the highest rates of MB degradation (k1 of 0.0189 min-1) and H2 photo-production.

Tantalum oxynitride nanotube film arrays for unconventional nanostructured photo-electrodes active with visible light

Francesco Tavella
Primo
;
Chiara Genovese
Secondo
;
Gabriele Centi;Siglinda Perathoner
Penultimo
;
Claudio Ampelli
Ultimo
2023-01-01

Abstract

Tantalum-oxy-nitride nanotubes (TaOxNy NTs) ordered in 1D were successfully synthesized through controlled anodic oxidation of metallic Ta foils followed by high-temperature annealing under NH3 flow to prepare unconventional nanostructured photo-electrodes active with visible light. For the synthesis, a two-step anodization process was adopted: i) the first step in ethylene glycol with 0.33 % NH4F and 3 % H2O, ii) the second step in H2SO4 (98 %) with 1 % HF and 4 % H2O, by applying different voltages and anodization times. Scanning Electron Microscopy integrated with Energy Dispersive X-ray spectroscopy (SEM-EDX) revealed the NTs length ranging from 2 to 5 µm, and the inner tube diameter from 20 to 100 nm, in good correlation with the synthesis parameters. The N-content (from 2.7 % to 19.1 %) was dependent on the nitridation temperature (from 500° to 900°C), and the conversion of bare Ta2O5 into TaOxNy strongly influenced the absorption in the visible region with a bandgap shift from 4.0 to 2.1 eV, respectively. Photo-electrochemical and catalytic performances were evaluated with chronoamperometric measurements and tests in different photo-reactions using AM 1.5 G simulated sunlight: (i) degradation of methylene blue (MB), (ii) ethanol gas-phase photo-reforming and (iii) bias-assisted photoelectrochemical water splitting. The TaOxNy NTs film-type electrode obtained by nitriding at 800 °C showed the highest photocurrent value (0.1 mA∙cm-2), and the highest rates of MB degradation (k1 of 0.0189 min-1) and H2 photo-production.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3257568
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