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通过调节载体缺陷在Pd/g-CN上由CO增强无碱甲酸生产

Enhanced Base-Free Formic Acid Production from CO on Pd/g-C N by Tuning of the Carrier Defects.

作者信息

Mondelli Cecilia, Puértolas Begoña, Ackermann Miriam, Chen Zupeng, Pérez-Ramírez Javier

机构信息

Department of Chemistry and Applied Biosciences, Institute for Chemical and Bioengineering, ETH Zurich, Vladimir-Prelog-Weg 1, 8093, Zurich, Switzerland.

出版信息

ChemSusChem. 2018 Sep 11;11(17):2859-2869. doi: 10.1002/cssc.201801362. Epub 2018 Aug 1.

Abstract

CO hydrogenation is attracting increasing attention as a sustainable route to produce formic acid, a commodity and potential energy vector. Here, bifunctional catalysts comprising metal nanoparticles deposited on bulk graphitic carbon nitride were assessed under base-free conditions, identifying supported Pd as the best performer. The catalyst productivity was enhanced by maximizing the edge-defects of the g-C N carrier, amino groups able to activate CO , and by generating welldispersed 5 nm Pd particles, required to split H . Bottom-up synthesis methods, that is, hard-templating and carbon enrichment upon polymerization, and top-down strategies, that is, thermal exfoliation of the as-prepared solid, were explored to boost the defects, the nature and density of which were evaluated by thermal and (in situ) spectroscopic techniques. After optimization of temperature, pressure, and reaction time, a 20 times higher turnover frequency compared with the best Pd/g-C N catalyst reported producing formic acid from CO without base was attained. This activity level was retained upon recycling with intermediate catalyst regeneration at mild temperature.

摘要

作为生产甲酸(一种商品及潜在能量载体)的可持续途径,CO加氢反应正日益受到关注。在此,对负载在块状石墨相氮化碳上的金属纳米颗粒组成的双功能催化剂在无碱条件下进行了评估,确定负载型Pd是最佳催化剂。通过使g-C₃N载体的边缘缺陷最大化、使能够活化CO的氨基最大化以及生成用于分解H₂所需的分散良好的5nm Pd颗粒,提高了催化剂的生产率。研究了自下而上的合成方法(即硬模板法和聚合时的碳富集法)以及自上而下的策略(即对所制备固体进行热剥离)以增加缺陷,通过热分析和(原位)光谱技术评估了缺陷的性质和密度。在优化温度、压力和反应时间后,与报道的在无碱条件下由CO生产甲酸的最佳Pd/g-C₃N催化剂相比,周转频率提高了20倍。在温和温度下进行中间催化剂再生循环时,该活性水平得以保持。

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