Electrochemical Deposition of Nanocatalysts on an Oxide Scaffold Enhances the Activity of Oxygen Reduction

Seongwoo Nam, Jinwook Kim, Hyunseung Kim, SungHyun Jeon, Sejong Ahn, Yoonseok Choi, Beom-Kyeong Park, WooChul Jung
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Abstract

Solid oxide fuel cells (SOFCs) are devices that directly convert the chemical energy of hydrogen and oxygen into electrical energy, and are attracting attention for their high efficiency and eco-friendliness. Since the recent research trend is to lower the operating temperature of the device, there is a considerable demand for a way to effectively introduce a catalyst to overcome the poor electrochemical activity of the most commercially available lanthanum strontium manganite–yttria-stabilized zirconia (LSM-YSZ) composite electrode. Praseodymium oxide (PrO x ) is an excellent catalyst for the ORR and has also been applied to LSM-YSZ electrodes via infiltration, the most widely used catalyst fabrication method. However, this previously well-established method still experiences time-consuming and energy-intensive limitations; therefore, other catalyst fabrication approaches are required. Cathodic electrochemical deposition (CELD) is chosen as a central strategy to decorate the PrO x catalyst which strongly empowers the exclusive ORR activity of the LSM-YSZ electrode. CELD is an excellent catalyst fabrication method that combines electroplating and chemical precipitation, and is simple, fast, cost-effective, and capable of deposition at room temperature and ambient pressure. Herein, we present an electrochemical deposition method that fabricating a PrO x overlayer significantly improves the catalytic activity of composite electrodes with only a short process of less than 4 min, even in an ambient environment. Moreover, it does not require additional processes such as heat treatment. The PrO x -coated electrode exhibits a decrease in initial polarization resistance compared to the bare, and maintained an oxygen reduction reaction characteristic by more than 10 times even after about 400 hours of operation at 650 °C. Transmission line model analysis with impedance spectra describes how PrO x improves the reactivity of the oxygen reduction reaction of composite electrodes. Finally, we demonstrate that a two-element material, (Pr, Ce)O x , was electrochemically deposited. Electrochemical deposition considerably improves the catalytic properties of the cathode via a concise and straightforward process.
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纳米催化剂在氧化物支架上的电化学沉积提高了氧还原活性
固体氧化物燃料电池(SOFCs)是将氢和氧的化学能直接转化为电能的装置,因其高效率和环保性而备受关注。由于最近的研究趋势是降低器件的工作温度,因此迫切需要一种有效引入催化剂的方法来克服市面上最常见的镧锶锰钇稳定氧化锆(LSM-YSZ)复合电极电化学活性差的问题。氧化镨(PrO x)是一种优良的ORR催化剂,也被应用于LSM-YSZ电极上,这是最广泛使用的催化剂制造方法。然而,这种先前建立的方法仍然存在耗时和能量密集的局限性;因此,需要其他的催化剂制造方法。选择阴极电化学沉积(CELD)作为装饰PrO x催化剂的核心策略,这有力地增强了LSM-YSZ电极的排他ORR活性。CELD是一种优秀的催化剂制造方法,结合了电镀和化学沉淀,简单,快速,成本效益高,能够在室温和常压下沉积。在此,我们提出了一种电化学沉积方法,即使在环境中,也只需不到4分钟的短过程,就可以显著提高复合电极的催化活性。此外,它不需要额外的工艺,如热处理。与裸电极相比,PrO x涂层电极的初始极化电阻降低,即使在650℃下工作约400小时后,其氧还原反应特性仍保持在10倍以上。阻抗谱传输线模型分析描述了PrO x如何提高复合电极的氧还原反应活性。最后,我们证明了电化学沉积了一种双元素材料(Pr, Ce)O x。电化学沉积通过一个简洁直接的过程大大提高了阴极的催化性能。
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