Peng Lu, Jurca Bogdan, Garcia-Baldovi Alberto, Tian Liang, Sastre German, Primo Ana, Parvulescu Vasile, Dhakshinamoorthy Amarajothi, Garcia Hermenegildo
Instituto de Tecnología Química, Consejo Superior de Investigaciones Científicas-Universitat Politecnica de Valencia, Av. De los Naranjos s/n, 46022 Valencia, Spain.
Department of Organic Chemistry, Biochemistry and Catalysis, University of Bucharest, B-dul Regina Elisabeta 4-12, 030016 Bucharest, Romania.
Nanomaterials (Basel). 2024 Mar 6;14(5):476. doi: 10.3390/nano14050476.
The quest for efficient catalysts based on abundant elements that can promote the selective CO hydrogenation to green methanol still continues. Most of the reported catalysts are based on Cu/ZnO supported in inorganic oxides, with not much progress with respect to the benchmark Cu/ZnO/AlO catalyst. The use of carbon supports for Cu/ZnO particles is much less explored in spite of the favorable strong metal support interaction that these doped carbons can establish. This manuscript reports the preparation of a series of Cu-ZnO@(N)C samples consisting of Cu/ZnO particles embedded within a N-doped graphitic carbon with a wide range of Cu/Zn atomic ratio. The preparation procedure relies on the transformation of chitosan, a biomass waste, into N-doped graphitic carbon by pyrolysis, which establishes a strong interaction with Cu nanoparticles (NPs) formed simultaneously by Cu salt reduction during the graphitization. Zn ions are subsequently added to the Cu-graphene material by impregnation. All the Cu/ZnO@(N)C samples promote methanol formation in the CO hydrogenation at temperatures from 200 to 300 °C, with the temperature increasing CO conversion and decreasing methanol selectivity. The best performing Cu-ZnO@(N)C sample achieves at 300 °C a CO conversion of 23% and a methanol selectivity of 21% that is among the highest reported, particularly for a carbon-based support. DFT calculations indicate the role of pyridinic N doping atoms stabilizing the Cu/ZnO NPs and supporting the formate pathway as the most likely reaction mechanism.
寻找基于丰富元素的高效催化剂以促进一氧化碳选择性加氢制绿色甲醇的工作仍在继续。大多数已报道的催化剂是基于负载在无机氧化物上的铜/氧化锌,相对于基准的铜/氧化锌/氧化铝催化剂而言进展不大。尽管这些掺杂碳能够建立有利的强金属-载体相互作用,但对于铜/氧化锌颗粒使用碳载体的研究却少得多。本文报道了一系列Cu-ZnO@(N)C样品的制备,该样品由嵌入在氮掺杂石墨碳中的铜/氧化锌颗粒组成,具有广泛的铜/锌原子比。制备过程依赖于将生物质废料壳聚糖通过热解转化为氮掺杂石墨碳,这与石墨化过程中通过铜盐还原同时形成的铜纳米颗粒建立了强相互作用。随后通过浸渍将锌离子添加到铜-石墨烯材料中。所有的Cu/ZnO@(N)C样品在200至300°C的温度下的一氧化碳加氢反应中都能促进甲醇生成,随着温度升高,一氧化碳转化率增加,甲醇选择性降低。性能最佳的Cu-ZnO@(N)C样品在300°C时实现了23%的一氧化碳转化率和21%的甲醇选择性,这是已报道的最高值之一,特别是对于基于碳的载体而言。密度泛函理论计算表明吡啶型氮掺杂原子在稳定铜/氧化锌纳米颗粒以及支持甲酸途径作为最可能的反应机理方面所起的作用。