Leng Yan, Zhang Zihao, Chen Hao, Du Shengyu, Liu Jixing, Nie Shiyang, Dong Yuming, Zhang Pengfei, Dai Sheng
The Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, Jiangsu, China.
Chem Commun (Camb). 2021 Apr 18;57(30):3676-3679. doi: 10.1039/d1cc00497b. Epub 2021 Mar 16.
High-entropy crystalline materials are attracting more attention. In principle, high-entropy metal carbides (HMCs) that contain five or more metal ions, possess more negative free energy value during catalysis. But its preparation is challenging because of the immiscibility of multi metal cations in a single carbide solid solution. Here, a rational strategy for preparing HMC is proposed via a coordination-assisted crystallization process in the presence of Br-based poly(ionic liquids). Through this method, MoWVCrNbC nanoparticles, with a single cubic phase structure, incorporated on porous carbon, are obtained (HMC@NC). By combination of well dispersed small particle size (∼4 nm), high surface area (∼270 m g), and high-entropy phase, HMC@NC can function as a promising catalyst for the dehydrogenation of ethylbenzene. Unexpected activity (EB conv.: 73%) and thermal stability (>100 h on steam) at 450 °C are observed. Such a facile synthetic strategy may inspire the fabrication of other types of HMCs for more specific tasks.
高熵晶体材料正吸引着越来越多的关注。原则上,含有五种或更多金属离子的高熵金属碳化物(HMCs)在催化过程中具有更负的自由能值。但其制备具有挑战性,因为多金属阳离子在单一碳化物固溶体中互不相溶。在此,提出了一种在溴基聚(离子液体)存在下通过配位辅助结晶过程制备HMC的合理策略。通过这种方法,获得了负载在多孔碳上的具有单一立方相结构的MoWVCrNbC纳米颗粒(HMC@NC)。通过良好分散的小粒径(约4nm)、高比表面积(约270m²/g)和高熵相的结合,HMC@NC可作为乙苯脱氢的有前景的催化剂。在450℃下观察到了意外的活性(乙苯转化率:73%)和热稳定性(在蒸汽中>100小时)。这种简便的合成策略可能会激发制备用于更特定任务的其他类型HMCs。