首页> 外文OA文献 >Electrochemical synthesis of ammonia from wet nitrogen via a dual-chamber reactor using La0.6Sr0.4Co0.2Fe0.8O3 − δCe0.8Gd0.18Ca0.02O2 − δ composite cathode
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Electrochemical synthesis of ammonia from wet nitrogen via a dual-chamber reactor using La0.6Sr0.4Co0.2Fe0.8O3 − δCe0.8Gd0.18Ca0.02O2 − δ composite cathode

机译:使用La0.6Sr0.4Co0.2Fe0.8O3-δCe0.8Gd0.18Ca0.02O2-δ复合阴极通过双室反应器从湿氮中电化学合成氨

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摘要

A La0.6Sr0.4Co0.2Fe0.8O3−δ-Ce0.8Gd0.18Ca0.02O2−δ composite cathode was used to investigate the electrochemical synthesis of ammonia from wet nitrogen. Wet nitrogen was flown through a dual chamber reactor under atmospheric pressure leading to the successful synthesis of ammonia. Ammonia was synthesised at a rate of 1.5 × 10−10 mol s−1 cm−2 at 400 °C when applying a dc voltage of 1.4 V, which is the highest reported to date. This rate is twice that of the observed ammonia formation rate (7 × 10−11 mol s−1 cm−2) when Co-free cathode, La0.6Sr0.4FeO3−δ-Ce0.8Gd0.18Ca0.02O2−δ was used as the cathode catalyst. A higher catalytic activity for ammonia synthesis may be obtained when using a catalyst with high oxygen vacancies, with the introduction of oxygen vacancies at the cathode being a good strategy to improve the catalytic activity of ammonia synthesis.
机译:利用La0.6Sr0.4Co0.2Fe0.8O3-δ-Ce0.8Gd0.18Ca0.02O2-δ复合阴极研究了湿氮气中氨的电化学合成。在大气压下将湿氮气流过双室反应器,从而成功合成氨。当施加1.4 V的直流电压时,氨在400°C时以1.5×10-10 mol s-1 cm-2的速率合成,这是迄今为止报道的最高值。该速率是使用无钴阴极La0.6Sr0.4FeO3-δ-Ce0.8Gd0.18Ca0.02O2-δ时观察到的氨形成速率(7×10-11 mol s-1 cm-2)的两倍。作为阴极催化剂。当使用具有高氧空位的催化剂时,可以获得更高的氨合成催化活性,在阴极引入氧空位是提高氨合成催化活性的良好策略。

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