Plasma Electrolytic Oxidation Synthesis of Heterostructured TiO2 for Photoanode Applications

R. Levinas, V. Pakštas, A. Selskis, Tomas Murauskas, Roman Viter, A. Jagminienė, I. Stankevičienė, E. Norkus
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Abstract

: In the renewable energy field, the conversion of solar light into electrical or chemical energy is considered essential to moving towards a truly green energy economy. Solar energy can be harnessed not just through generating electricity with photovoltaic cells but also by driving photoelectrochemical (PEC) reactions such as water splitting or pollutant oxidation. In this study, TiO 2 films were synthesized electrochemically through a procedure called plasma electrolytic oxidation (PEO). Under specific conditions, as the Ti substrate dissolves and the oxide film grows, electron discharges occur across the film, and this ionizes both the oxide and some amount of electrolyte that had been in contact with it. The mixture then cools, leaving a macroporous TiO 2 structure. What is particularly interesting for PEC applications is that the films can be crystalline and doped after synthesis. XRD analysis revealed that a TiO 2 film that had been obtained at a voltage of 200 V had an anatase crystal structure. In addition, during ionization and cooling, ions from the solution can be incorporated into the film. By adding 0.1 M Cu 2 SO 4 into the synthesis electrolyte, we were able to incorporate Cu into the films, as proven EDX and XPS. The TiO 2 and heterostructured films showed good PEC water-splitting activity and stability in alkaline media when illuminated with 365 nm LED light. It was found that the photocurrent obtained depends on the synthesis voltage and that the heterostructured films would generate ~2 times larger photocurrents. In addition, further surface functionalization (e.g., with Au) was investigated. Electron–hole recombination was evaluated using an advanced non-stationary photoelectrochemical technique—intensity-modulated photocurrent spectroscopy (IMPS). Generally, films have very little recombination and only at lower overpotentials up to ~1 V. Overall, the synthesis of oxide films through PEO may provide an efficient alternative to obtaining crystalline films via annealing, and various heterostructures can be created simply by modifying synthesis conditions.
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等离子电解氧化法合成用于光阳极应用的异质结构 TiO2
:在可再生能源领域,将太阳能转化为电能或化学能被认为是实现真正绿色能源经济的关键。太阳能不仅可以通过光伏电池发电来利用,还可以通过光电化学(PEC)反应(如水分离或污染物氧化)来利用。本研究采用等离子电解氧化(PEO)工艺,通过电化学方法合成了 TiO 2 薄膜。在特定条件下,随着钛基底的溶解和氧化膜的生长,电子在氧化膜上放电,使氧化物和与之接触的一定量的电解质电离。然后,混合物冷却,形成大孔的 TiO 2 结构。对于 PEC 应用来说,特别有趣的是,合成后的薄膜可以结晶和掺杂。XRD 分析表明,在 200 V 电压下获得的氧化钛薄膜具有锐钛矿晶体结构。此外,在电离和冷却过程中,溶液中的离子也会融入薄膜中。通过在合成电解液中加入 0.1 M Cu 2 SO 4,我们能够将 Cu 加入到薄膜中,EDX 和 XPS 证实了这一点。用 365 纳米 LED 光照射 TiO 2 和异质结构薄膜时,它们在碱性介质中表现出良好的 PEC 水分离活性和稳定性。研究发现,获得的光电流取决于合成电压,而异质结构薄膜产生的光电流要大 2 倍。此外,还研究了进一步的表面功能化(如金)。使用先进的非稳态光电化学技术--强度调制光电流光谱法(IMPS)对电子-空穴重组进行了评估。一般来说,薄膜的重组极少,而且仅在较低的过电位(约 1 V)下才会发生。总之,通过 PEO 合成氧化物薄膜可能是通过退火获得晶体薄膜的一种高效替代方法,而且只需改变合成条件就能制造出各种异质结构。
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