Wen Meicheng, Mori Kohsuke, Futamura Yuya, Kuwahara Yasutaka, Navlani-García Miriam, An Taicheng, Yamashita Hiromi
Division of Materials and Manufacturing Science, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Guangzhou Key Laboratory of Environmental Catalysis and Pollution Control, School of Environmental Science and Engineering Institute of Environmental Health and Pollution control, Guangdong University of Technology, Guangdong, 51006, China.
Sci Rep. 2019 Oct 30;9(1):15675. doi: 10.1038/s41598-019-52133-5.
Formic acid (FA; HCOOH) is one of the most promising candidates for the storage of hydrogen (H). Herein, we report a H storage/production system based on the hydrogenation of CO and dehydrogenation of FA, using a nanostructured heterogeneous catalyst. PdAg nanoparticles with an average size of 2.8 nm were encapsulated within a zeolitic imidazolate framework (ZIF-8) having a core-shell structure (ZIF-8@PdAg@ZIF-8). This composite displayed high activity and stability during both the hydrogenation of CO to produce FA and the dehydrogenation of FA into H and CO. This improved performance is attributed to the use of ultrafine PdAg nanoparticles as well as the spatial regulation of the nanoparticles within the reaction field. This study suggests a new strategy for controlling the spatial distribution of metal nanoparticles within MOFs so as to fine-tune the catalytic activity and selectivity of ZIF-8@metal nanoparticles@ZIF-8 catalysts.
甲酸(FA;HCOOH)是最有前景的氢(H)存储候选物之一。在此,我们报道了一种基于CO氢化和FA脱氢的氢存储/生产系统,该系统使用了一种纳米结构的多相催化剂。平均尺寸为2.8纳米的PdAg纳米颗粒被封装在具有核壳结构的沸石咪唑酯骨架(ZIF-8)中(ZIF-8@PdAg@ZIF-8)。这种复合材料在CO氢化为FA以及FA脱氢为H和CO的过程中均表现出高活性和稳定性。这种性能的提升归因于使用了超细微的PdAg纳米颗粒以及反应场中纳米颗粒的空间调控。这项研究提出了一种控制金属纳米颗粒在金属有机框架内空间分布的新策略,以便微调ZIF-8@金属纳米颗粒@ZIF-8催化剂的催化活性和选择性。