A. Basilio-Brito, M. Landa-Castro, W. Sánchez-Ortiz, S. Rivera-Hernández, M. Romero-Romo, E. Arce-Estrada, J. Aldana-González, M. Palomar-Pardavé
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引用次数: 0
摘要
本文报道了一种简单、低成本、环保的方法,在玻碳电极GCE上合成镍钴合金纳米颗粒(Ni-CoNPs),并将其用于碱性水介质中高效的尿素电氧化。从废镍氢电池阴极粉末的浸出液中,采用直线深共晶溶剂DES作为浸出剂,通过电解浴,通过一次恒电位步骤直接将Ni-CoNPs电沉积在GCE表面,GCE/Ni-CoNPs。将GCE/Ni-CoNPs浸入1 M KOH, 0.33 M尿素水溶液中,作为尿素电化学氧化的阳极。在动电位和恒电位评估期间,该电极的质量活性在ca 0.5 V vs. Ag/AgCl下的最大值为27,900 mAmg−1 cm−2,稳态质量活性为1690 mAmg−1 cm−2。在这项工作中报道的GCE/Ni-CoNPs电极的性能与使用更复杂,耗时和昂贵的方法报道的其他电极相似或更好。图形抽象
One-Step Ni-Co Alloy Nanoparticles Electrodeposition from Leach Liquor of Spent Ni-MH Batteries Using a Deep Eutectic Solvent and Its Use Towards Urea Electrooxidation
This work reports a simple, low-cost, and environmentally friendly method to synthesize Ni-Co alloy nanoparticles (Ni-CoNPs) onto a glassy carbon electrode, GCE, and its use towards the efficient urea electrooxidation in basic aqueous media. Ni-CoNPs were directly electrodeposited onto the GCE surface, GCE/Ni-CoNPs by a single potentiostatic step, from the leached liquor of the cathode powder of spent Ni-MH batteries using the reline deep eutectic solvent, DES, as leaching agent, and electrolytic bath. The GCE/Ni-CoNPs were immersed in a 1 M KOH, 0.33 M urea aqueous solution and used as anode for urea electrochemical oxidation. The mass activity of this electrode depicted a maximum value of 27,900 mAmg−1 cm−2 at ca 0.5 V vs. Ag/AgCl and a steady state mass activity of 1690 mAmg−1 cm−2 during the potentiodynamic and potentiostatic evaluation. The performance of the GCE/Ni-CoNPs electrode reported in this work is similar or better than other electrodes reported for this purpose using more sophisticated, time-consuming, and costly methods.
期刊介绍:
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