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用于将一氧化碳选择性还原为甲醇反应的双金属铜锌MOF-74催化剂的可扩展机械化学非晶化

Scalable Mechanochemical Amorphization of Bimetallic Cu-Zn MOF-74 Catalyst for Selective CO Reduction Reaction to Methanol.

作者信息

Stolar Tomislav, Prašnikar Anže, Martinez Valentina, Karadeniz Bahar, Bjelić Ana, Mali Gregor, Friščić Tomislav, Likozar Blaž, Užarević Krunoslav

机构信息

Ruđer Bošković Institute, Bijenička cesta 54, 10000 Zagreb, Croatia.

National Institute of Chemistry, Hajdrihova 19, SI-1001 Ljubljana, Slovenia.

出版信息

ACS Appl Mater Interfaces. 2021 Jan 20;13(2):3070-3077. doi: 10.1021/acsami.0c21265. Epub 2021 Jan 6.

Abstract

Selective catalytic reduction of CO to methanol has tremendous importance in the chemical industry. It mitigates two critical issues in the modern society, the overwhelming climate change and the dependence on fossil fuels. The most used catalysts are currently based on mixed copper and zinc phases, where the high surface of active copper species is a critical factor for the catalyst performance. Motivated by the recent breakthrough in the controllable synthesis of bimetallic MOF-74 materials by ball milling, we targeted to study the potential of ZnCu-MOF-74 for catalytic CO reduction. Here, we tested whether the nanosized channels decorated with readily accessible and homogeneously distributed Zn and Cu metal sites would be advantageous for the catalytic CO reduction. Unlike the inactive monometallic Cu-MOF-74, ZnCu-MOF-74 shows moderate catalytic activity and selectivity for the methanol synthesis. Interestingly, the postsynthetic mechanochemical treatment of desolvated ZnCu-MOF-74 resulted in amorphization and a significant increase in both the activity and selectivity of the catalyst despite the destruction of the well-ordered and porous MOF-74 architecture. The results emphasize the importance of defects for the MOF catalytic activity and the potential of amorphous MOFs to be considered as heterogeneous catalysts. Scanning electron microscopy (SEM), X-ray powder diffraction (XRD) and C magic angle-spinning nuclear magnetic resonance (MAS NMR) were applied to establish quantitative structure-reactivity relationships. The apparent activation energy of rate reaction kinetics has indicated different pathway mechanisms, primarily through reverse water-gas shift (RWGS). Prolonged time on stream productivity, stability and deactivation were assessed, analysing the robustness or degradation of metal-organic framework nanomaterials. Scalable MOF production processes are making the latter more appealing within emerging industrial decarbonisation, in particular for carbon capture and utilisation (CCU) or hydrogen carrier storage. Acknowledging scale, the costs of fabrication are paramount.

摘要

将一氧化碳选择性催化还原为甲醇在化学工业中具有极其重要的意义。它缓解了现代社会中的两个关键问题,即压倒性的气候变化和对化石燃料的依赖。目前最常用的催化剂基于铜和锌的混合相,其中活性铜物种的高比表面积是催化剂性能的关键因素。受球磨法可控合成双金属MOF-74材料的最新突破的启发,我们旨在研究ZnCu-MOF-74催化一氧化碳还原的潜力。在这里,我们测试了用易于接近且均匀分布的锌和铜金属位点修饰的纳米通道是否有利于催化一氧化碳还原。与无活性的单金属Cu-MOF-74不同,ZnCu-MOF-74对甲醇合成表现出适度的催化活性和选择性。有趣的是,脱溶剂化的ZnCu-MOF-74的合成后机械化学处理导致非晶化,并且尽管有序多孔的MOF-74结构被破坏,但催化剂的活性和选择性都显著增加。结果强调了缺陷对MOF催化活性的重要性以及非晶态MOF作为多相催化剂的潜力。应用扫描电子显微镜(SEM)、X射线粉末衍射(XRD)和碳魔角旋转核磁共振(MAS NMR)来建立定量的结构-反应性关系。速率反应动力学的表观活化能表明了不同的途径机制,主要是通过逆水煤气变换(RWGS)。评估了延长的在线生产时间、稳定性和失活情况,分析了金属有机框架纳米材料的稳定性或降解情况。可扩展的MOF生产工艺使后者在新兴的工业脱碳中更具吸引力,特别是对于碳捕获与利用(CCU)或氢载体储存。考虑到规模,制造成本至关重要。

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