Jan Witte, Vinzent Olszok, Alfred P. Weber, Thomas Turek
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引用次数: 0
摘要
本文系统地研究了阴离子交换膜电解(AEMWE)用NiFe2O4催化剂的结晶度和合成方法的影响。催化剂的制备采用气溶胶辅助喷雾热解法,有或没有煅烧后处理和共沉淀法。喷雾热解法产生非晶态颗粒,而共沉淀法和焙烧法导致颗粒部分结晶。值得注意的是,煅烧后的催化剂结晶度最高,相应的催化活性和稳定性降低。采用非晶NiFe2O4催化剂,在1 A cm−2下,无irhf电池电压为1.565 V,具有最高的活性。通过使用Nafion而不是PiperION离子单体,无irhf的电池电压进一步降低了37 mV。此外,在这种结构下,电池性能保持稳定,降解率仅为91 μV h−1,在3 a cm−2和80°C下,电池电压仅为1.8 V,超过200小时。这些发现突出了非晶阳极催化剂在AEMWE应用中实现高性能和持久稳定性的关键作用,为未来催化剂的优化提供了途径。
Efficient Anion Exchange Membrane Water Electrolysis on Amorphous Spray-Pyrolyzed NiFe2O4
In the present study, the influence of crystallinity and synthesis method of a NiFe2O4 catalyst for anion exchange membrane water electrolysis (AEMWE) is systematically investigated. Catalysts are prepared using an aerosol-assisted spray-pyrolysis approach, both with and without post-calcination treatment, and a co-precipitation method. The spray-pyrolysis approach produces amorphous particles, whereas the co-precipitation and post-calcination result in partial crystallization of the particles. Notably, the post-calcinated catalyst demonstrated the highest degree of crystallinity, corresponding to reduced catalytic activity and stability. Employing the amorphous NiFe2O4 catalyst provides the highest activity with an iRHF-free cell voltage of 1.565 V at 1 A cm−2. By utilizing a Nafion instead of a PiperION ionomer the iRHF-free cell voltage is further lowered by 37 mV. Moreover, in this configuration the cell performance remained stable, with a degradation rate of only 91 μV h−1, over 200 h at 3 A cm−2 and 80 °C with a cell voltage of just 1.8 V. These findings highlight the critical role of amorphous anode catalysts in achieving both high performance and enduring stability in AEMWE applications, suggesting pathways for future catalyst optimization.
期刊介绍:
ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.