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A peanut shell-derived economical and eco-friendly biochar catalyst for electrochemical ammonia synthesis under ambient conditions: combined experimental and theoretical study

机译:花生shell-derived经济和环保生物炭催化剂电化学氨在环境条件下合成:总和实验和理论研究

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摘要

The electrochemical conversion of nitrogen (N-2) to ammonia (NH3) under ambient conditions is a highly promising alternative to the energy-intensive Haber-Bosch process. However, it suffers from poor yields and selectivity because of the lack of efficient catalysts. Herein, we prepared an economical and eco-friendly efficient biochar catalyst from peanut shells and achieved a high ammonia yield (2.32 mu mol h(-1) cm(-2)) and selectivity (faradaic efficiency of 26.97%) over 12 h of stable operation. The results of density functional theory calculations illustrate that association pathways are more likely to occur on the active sites Bio-N4, Bio-O37, and Bio-S58, while dissociation pathways always occurred on the active sites Bio-O15, Bio-O21, and Bio-O52. Furthermore, Bio-O21 is the most promising active site for the NRR following the NNH2 dissociation pathway with a lower reaction barrier. The preferable adsorption of N-2, desorption of NH3, and suppression of the HER demonstrated the peanut shell-derived material as a more promising catalyst for the NRR.
机译:电化学转换的氮(n - 2)在环境条件下氨(NH3)是一个非常有前途的替代能源密集型。哈勃-博施方法饱受贫穷因为收益率和选择性缺乏有效的催化剂。准备了一个经济、环保高效生物炭催化剂从花生壳和实现高氨产量(2.32μ摩尔h(1)厘米(2))和选择性(26.97%)的感应电流的效率在12 h的稳定运行。密度泛函理论计算说明协会途径更容易发生在活动网站Bio-N4 Bio-O37,Bio-S58,离解通道发生在活动网站Bio-O15 Bio-O21,和Bio-O52。承诺后NRR活性部位NNH2离解反应途径较低障碍。NH3的解吸,压制她证明了花生shell-derived材料一个更有前途的NRR催化剂。

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