Abstract

Self‐doped TiO2 nanotube array (DTNA) electrodes were fabricated through anodic oxidation combined with cathodic reduction. The morphology and structural features of pristine TiO2 nanotube arrays and DTNA electrodes were studied through scanning electron microscopy, X‐ray diffractometry, and X‐ray photoelectron spectroscopy. An accelerated life test was used to test the electrode service lifetime and thus the electrode's stability. The service lifetime of the DTNA electrode prepared at constant 40 V for 6 hr was approximately 338.7 hr at constant 1 mA/cm2 in a 1 M NaClO4 solution. Methyl orange (MO) was employed as the degradation probe for measuring electrochemical oxidation performance. The color removal rate of 200 mg/L MO of the DTNA electrode (85.2% at 1 mA/cm2) was greater than that of the Ti/IrO2 electrode (31.1% at 1 mA/cm2). The larger the surface area of the DTNA electrode is, the more conductive the electrode is for the degradation of organic substances. Organic degradation on the DTNA electrode occurred primarily through an indirect pathway (producing [∙OH]).

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