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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >A novel in situ preparation method for nanostructured alpha-Fe2O3 films from electrodeposited Fe films for efficient photoelectrocatalytic water splitting and the degradation of organic pollutants
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A novel in situ preparation method for nanostructured alpha-Fe2O3 films from electrodeposited Fe films for efficient photoelectrocatalytic water splitting and the degradation of organic pollutants

机译:一种由电沉积铁薄膜制备纳米结构α-Fe2O3薄膜的新颖原位制备方法,用于有效的光电催化水分解和有机污染物的降解

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摘要

A novel method has been developed for the preparation of nanostructured haematite (alpha-Fe2O3) films for use in photoelectrocatalytic (PEC) water splitting and the degradation of organic pollutants. The method has two stages, the electrodeposition of Fe films in alkalescent aqueous electrolyte with ferrous sulphate and ammonia, and the in situ thermal oxidation of the Fe films to alpha-Fe2O3. The thickness and crystallinity of the alpha-Fe2O3 films can be precisely controlled by adjusting the duration and the annealing conditions of the electrodeposition, respectively, avoiding the microstructural defects arising from the traditional electrodeposition of FeOOH films and the unwanted phases of FeO and Fe3O4 produced by thermal oxidation of Fe foils. This facilitates the generation, transportation and collection of photogenerated charges on the alpha-Fe2O3 film. The optimized alpha-Fe2O3 film, obtained from a Fe film deposited for 30 s and then annealed at 500 degrees C for 2 h, showed a stable PEC water oxidation current around 1.35 mA cm(-2) at 1.23 V vs. a reversible hydrogen electrode (RHE) under AM 1.5 irradiation. This was the highest current so far obtained using undoped alpha-Fe2O3 films produced by electrodeposition. When further coated with a cobalt phosphate (Co-Pi) co-catalyst, the optimized Co-Pi/alpha-Fe2O3 photoanode showed an incident photon-to-current conversion efficiency (IPCE) above 18% at 400 nm and a stable photocurrent of 1.89 mA cm(-2). The alpha-Fe2O3 film also showed excellent stability and degradation efficiency (rate constant 0.9372 h(-1)) in the PEC degradation of methylene blue (MB) in neutral aqueous solution under a positive bias potential.
机译:已开发出一种用于制备纳米结构赤铁矿(α-Fe2O3)膜的新方法,该膜可用于光催化(PEC)水分解和有机污染物的降解。该方法具有两个阶段,即在碱性水溶液中用硫酸亚铁和氨水电沉积Fe膜,以及将Fe膜原位热氧化为α-Fe2O3。通过分别调节电沉积的持续时间和退火条件,可以精确控制α-Fe2O3膜的厚度和结晶度,避免了传统的FeOOH膜电沉积以及由FeOOH膜产生的有害相FeO和Fe3O4产生的微观结构缺陷。铁箔的热氧化。这有助于在α-Fe2O3薄膜上产生,运输和收集光生电荷。从沉积30 s的Fe膜中获得的优化的α-Fe2O3膜,然后在500摄氏度下退火2小时,在1.23 V电压下,相对于可逆氢,PEC水氧化电流稳定在1.35 mA cm(-2)左右电极(RHE)在AM 1.5辐射下。这是迄今为止通过电沉积生产的未掺杂α-Fe2O3薄膜获得的最高电流。当进一步用磷酸钴(Co-Pi)助催化剂涂覆时,优化的Co-Pi / alpha-Fe2O3光电阳极在400 nm处的入射光子-电流转换效率(IPCE)高于18%,并且稳定的光电流为1.89 mA厘米(-2)。 α-Fe2O3薄膜在正偏压电势下在中性水溶液中亚甲基蓝(MB)的PEC降解中也显示出优异的稳定性和降解效率(速率常数0.9372 h(-1))。

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