YFO photocathode fabricated via spray pyrolysis for unassisted solar water splitting for generation of hydrogen fuel†

IF 5 3区 材料科学 Q2 CHEMISTRY, PHYSICAL Sustainable Energy & Fuels Pub Date : 2024-11-26 DOI:10.1039/D4SE01276C
Bandar Y. Alfaifi, Hameed Ullah, Xin Jiang and Asif Ali Tahir
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Abstract

Efficient solar to fuel conversion technology is highly desirable to meet future global renewable energy demands as conventional energy resources are environmentally irresponsible and depleting rapidly. Photoelectrochemical (PEC) water splitting without the use of any external potential bias and/or assistance to produce hydrogen (a clean and renewable fuel) is a technology having the potential to fulfil this desire. However, the main bottleneck is the unavailability of cost-effective, efficient and stable photoelectrodes, which are used to conduct water splitting using light photons. YFeO3 (YFO) thin films with a small energy band gap (Eg), suitable band positions straddling water redox potential and high stability were fabricated using a simple, cost-effective and scalable synthesis technique i.e., spray pyrolysis. The optimum YFO film was applied, for the first time to the best of our knowledge, for generation of hydrogen fuel through water splitting without applying any external potential bias and/or assistance. Orthorhombic YFO (o-YFO) showed a maximum photocurrent of ∼0.65 mA cm−2 at 0.46 V vs. RHE, faradaic efficiency of ∼70%, and excellent stability spanning over 6 hours. UV-visible and electrochemical impedance spectroscopy (EIS) revealed the p-type characteristic, narrow Eg of 2.45 eV and suitable band positions, which encompassed the redox potential of water, of the o-YFO film. The o-YFO film generated 0.41 µmol cm−2 of hydrogen over 6 hours without any assistance in a spontaneous hydrogen evolution reaction (HER). In a subsequent cycle, it generated 0.35 µmol cm−2 of hydrogen, showing its potential as a reusable photoelectrode in the HER. Post HER characterizations did not show any visible/significant changes in the phase and morphology of the o-YFO film, indicating its stability under the applied HER conditions.

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由于传统能源对环境不负责任,而且正在迅速枯竭,因此高效的太阳能到燃料的转换技术非常适合满足未来全球可再生能源的需求。光电化学(PEC)水分裂技术无需任何外部电位偏置和/或辅助即可产生氢气(一种清洁的可再生燃料),该技术具有实现这一愿望的潜力。然而,该技术的主要瓶颈在于缺乏具有成本效益、高效且稳定的光电电极,而光电电极是利用光光子进行水分离的。我们采用一种简单、经济、可扩展的合成技术,即喷雾热解技术,制备出了能带隙(Eg)小、带位合适且横跨水氧化还原电位和稳定性高的 YFeO3(YFO)薄膜。据我们所知,这种最佳的 YFO 薄膜首次用于通过水分裂产生氢燃料,而无需施加任何外部电位偏置和/或辅助。正交 YFO(o-YFO)在 0.46 V 对 RHE 时的最大光电流为 ∼0.65 mA cm-2,远红外效率为 ∼70%,稳定性极佳,可持续 6 小时以上。紫外-可见光和电化学阻抗光谱(EIS)显示了 o-YFO 薄膜的 p 型特性、2.45 eV 的窄 Eg 和合适的带位,其中包括水的氧化还原电位。在自发氢进化反应(HER)中,o-YFO 薄膜在 6 小时内产生了 0.41 µmol cm-2 的氢气,无需任何辅助。在随后的循环中,它又产生了 0.35 µmol cm-2 的氢气,显示了它在氢转换反应中作为可重复使用光电极的潜力。HER 后的表征结果表明,o-YFO 薄膜的相位和形态没有发生任何可见或显著的变化,这表明它在应用 HER 的条件下是稳定的。
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来源期刊
Sustainable Energy & Fuels
Sustainable Energy & Fuels Energy-Energy Engineering and Power Technology
CiteScore
10.00
自引率
3.60%
发文量
394
期刊介绍: Sustainable Energy & Fuels will publish research that contributes to the development of sustainable energy technologies with a particular emphasis on new and next-generation technologies.
期刊最新文献
Back cover Back cover Interfacial engineering of a bifunctional electrocatalyst with outstanding catalytic performance, high intrinsic activity and solar-to-hydrogen conversion efficiency† Fluorine-rich Schiff base ligand derived Fe/N–C–F and Co/N–C–F catalysts for the oxygen reduction reaction: synthesis, experimental validation, and DFT insights† Electrocatalytic conversion of biomass-derived oxygenated aromatics to cycloalkanes†
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