4.6 Article

Hydrogen Treated Niobium Oxide Nanotube Arrays for Photoelectrochemical Water Oxidation

期刊

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
卷 163, 期 14, 页码 H1165-H1170

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ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.1091614jes

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资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT and future Planning [2014R1A2A2A04004950]
  2. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2015R1D1A3A01016158]

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Self-aligned Nb2O5 nanotube (NT) arrays are grown by facile electrochemical anodization at 180 degrees C with an applied bias of 10 V for 10 min in anhydrous glycerol electrolyte. Amorphous Nb2O5 NT arrays can be transformed into pseudo-hexagonal Nb2O5 NT arrays by annealing at 440 degrees C for 20 min in ambient air. Hydrogen treatment of this film was conducted at 440 degrees C for 20 min with flowing 4% H-2/96% Ar mixed gas. Hydrogen treatment causes no modification of crystalline properties and hydrogen-treated Nb2O5 (denoted as H-2-Nb2O5) NT arrays exhibit no apparent change in the optical bandgap, indicating negligible visible light absorbance. Only small changes in structural properties, such as pore diameter, wall thickness, and chemical state, are observed in the surface region of H-2-Nb2O5 NT arrays. However, H-2-Nb2O5 NT arrays exhibit a significant increase in electron concentration by the formation of oxygen vacancies, leading to significantly enhanced electronic conductivity. As a result, charge recombination reactions in the interfacial region between H-2-Nb2O5 NT arrays and electrolyte are efficiently hindered, resulting in remarkably enhanced photocurrent density in the photoelectrochemical cell. The air-Nb2O5 NT arrays exhibit a photocurrent density of only 0.11 mA/cm(2) at 1.0 VNHE, while H-2-Nb2O5 NT arrays show a significantly increased photocurrent density up to 0.69 mA/cm(2) at 1.0 V-NHE, a more than six-fold improvement in photoelectrochemical performance. (C) 2016 The Electrochemical Society. All rights reserved.

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