Fu Xin-Pu, Peres Laurent, Esvan Jérôme, Amiens Catherine, Philippot Karine, Yan Ning
Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore, 117585, Singapore.
CNRS, LCC (Laboratoire de Chimie de Coordination), 205 route de Narbonne, BP44099, F-31077 Toulouse Cedex 4, France.
Nanoscale. 2021 May 20;13(19):8931-8939. doi: 10.1039/d1nr01054a.
Production of formate via CO2/bicarbonate hydrogenation using cheap metal-based heterogeneous catalysts is attractive. Herein, we report the organometallic synthesis of a foam-like Ni@Ni(OH)2 composite nanomaterial which exhibited remarkable air stability and over 2 times higher catalytic activity than commercial RANEY® Ni catalyst in formate synthesis. Formate generation was achieved with an optimal rate of 6.0 mmol gcat-1 h-1 at 100 °C, a significantly lower operation temperature compared to the 200-260 °C reported in the literature. Deep characterization evidenced that this nanomaterial was made of an amorphous Ni(OH)2 phase covering metallic Ni sites; a core-shell structure which is crucial for the stability of the catalyst. The adsorption of bicarbonates onto the Ni@Ni(OH)2 catalyst was found to be a kinetically relevant step in the reaction, and the Ni-Ni(OH)2 interface was found to be beneficial for both CO2 and H2 activation thanks to a cooperative effect. Our findings emphasize the underestimated potential of Ni-based catalysts in CO2 hydrogenation to formate, indicating a viable strategy to develop stable, cheap metal catalysts for greener catalytic applications.
使用廉价的金属基多相催化剂通过二氧化碳/碳酸氢盐加氢生产甲酸盐很有吸引力。在此,我们报道了一种泡沫状Ni@Ni(OH)₂复合纳米材料的有机金属合成方法,该材料表现出显著的空气稳定性,在甲酸盐合成中催化活性比商业阮内镍催化剂高2倍以上。在100℃下甲酸盐生成的最佳速率为6.0 mmol gcat⁻¹ h⁻¹,与文献报道的200-260℃相比,操作温度显著更低。深入表征表明,这种纳米材料由覆盖金属镍位点的非晶态Ni(OH)₂相组成;这种核壳结构对催化剂的稳定性至关重要。发现碳酸氢盐在Ni@Ni(OH)₂催化剂上的吸附是反应中的一个动力学相关步骤,并且由于协同效应,发现Ni-Ni(OH)₂界面有利于二氧化碳和氢气的活化。我们的研究结果强调了镍基催化剂在二氧化碳加氢生成甲酸盐方面被低估的潜力,表明了开发用于更绿色催化应用的稳定、廉价金属催化剂的可行策略。