Mohamed A. Ghanem, Abdullah M. Al-Mayouf, Khalaf A. Alfudhayli, Mohamed O. Abdelkader
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Using the CsNiVF6 catalyst, the electrochemical analysis, conducted through cyclic voltammetry, demonstrates a current mass activity of ~1500 mA mg−1, recorded at 1.8 V vs. RHE, along with low-resistance (3.25 ohm) charge transfer and good long-term stability for 0.33 M urea oxidation in an alkaline solution. Moreover, the volumetric hydrogen production rate at the cathode (bare nickel foam) is increased from 12.25 to 39.15 µmol/min upon the addition of 0.33 M urea to a 1.0 KOH solution and at a bias potential of 2.0 V. The addition of urea to the electrolyte solution enhances hydrogen production at the cathode, especially at lower voltages, surpassing the volumes produced in pure 1.0 M KOH solution. This utilization of a CsNiVF6 pyrochlore nano-sheet catalyst and renewable urea as a feedstock contributes to the development of a green and sustainable hydrogen economy. 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引用次数: 0
摘要
本研究介绍了通过固相合成法成功合成的氟化铯镍钒(CsNiVF6)热核纳米片催化剂及其在碱性介质中通过尿素电解进行绿色制氢的电化学性能。理化表征结果表明,CsNiVF6呈现出由无序立方角共享(Ni, V)F6八面体结构和纳米片状形态组成的热核型结构,厚度在10至20纳米之间。利用 CsNiVF6 催化剂,通过循环伏安法进行的电化学分析表明,在 1.8 V 对 RHE 的电压下记录到的当前质量活性约为 1500 mA mg-1,同时还具有低电阻(3.25 欧姆)电荷转移和良好的长期稳定性,可用于 0.33 M 尿素在碱性溶液中的氧化。此外,在 1.0 KOH 溶液中加入 0.33 M 尿素,偏置电位为 2.0 V 时,阴极(泡沫裸镍)的体积产氢率从 12.25 µmol/min 提高到 39.15 µmol/min。在电解质溶液中加入尿素可提高阴极的氢气产量,尤其是在较低的电压下,超过了纯 1.0 M KOH 溶液的产量。利用 CsNiVF6 烧结矿纳米片催化剂和可再生尿素作为原料,有助于发展绿色和可持续的氢经济。总之,这项研究强调了 CsNiVF6 作为一种具有成本效益的镍基烧绿核电催化剂在推动可再生和可持续尿素电解工艺实现绿色制氢方面的潜在用途。
Nano-Sheets of CsNiVF6 Pyrochlore Electrocatalyst for Enhanced Urea Oxidation and Hydrogen Green Production Reactions
This study presents the successful synthesis of a cesium–nickel–vanadium fluoride (CsNiVF6) pyrochlore nano-sheet catalyst via solid-phase synthesis and its electrochemical performance in green hydrogen production through urea electrolysis in alkaline media. The physicochemical characterizations revealed that the CsNiVF6 exhibits a pyrochlore-type structure consisting of a disordered cubic corner-shared (Ni, V)F6 octahedra structure and nano-sheet morphology with a thickness ranging from 10 to 20 nm. Using the CsNiVF6 catalyst, the electrochemical analysis, conducted through cyclic voltammetry, demonstrates a current mass activity of ~1500 mA mg−1, recorded at 1.8 V vs. RHE, along with low-resistance (3.25 ohm) charge transfer and good long-term stability for 0.33 M urea oxidation in an alkaline solution. Moreover, the volumetric hydrogen production rate at the cathode (bare nickel foam) is increased from 12.25 to 39.15 µmol/min upon the addition of 0.33 M urea to a 1.0 KOH solution and at a bias potential of 2.0 V. The addition of urea to the electrolyte solution enhances hydrogen production at the cathode, especially at lower voltages, surpassing the volumes produced in pure 1.0 M KOH solution. This utilization of a CsNiVF6 pyrochlore nano-sheet catalyst and renewable urea as a feedstock contributes to the development of a green and sustainable hydrogen economy. Overall, this research underscores the potential use of CsNiVF6 as a cost-effective nickel-based pyrochlore electrocatalyst for advancing renewable and sustainable urea electrolysis processes toward green hydrogen production.