Qiao Haiyu, Saray Mahmoud Tamadoni, Wang Xizheng, Xu Shaomao, Chen Gang, Huang Zhennan, Chen Chaoji, Zhong Geng, Dong Qi, Hong Min, Xie Hua, Shahbazian-Yassar Reza, Hu Liangbing
Department of Materials Science and Engineering, University of Maryland, College Park, Maryland 20742, United States.
Department of Mechanical and Industrial Engineering, University of Illinois at Chicago (UIC), Chicago, Illinois 60607, United States.
ACS Nano. 2021 Sep 28;15(9):14928-14937. doi: 10.1021/acsnano.1c05113. Epub 2021 Aug 23.
High entropy alloy nanoparticles (HEA-NPs) are reported to have superior performance in catalysis, energy storage, and conversion due to the broad range of elements that can be incorporated in these materials, enabling tunable activity, excellent thermal and chemical stability, and a synergistic catalytic effect. However, scaling the manufacturing of HEA-NPs with uniform particle size and homogeneous elemental distribution efficiently is still a challenge due to the required critical synthetic conditions where high temperature is typically involved. In this work, we demonstrate an efficient and scalable microwave heating method using carbon-based materials as substrates to fabricate HEA-NPs with uniform particle size. Due to the abundant functional group defects that can absorb microwave efficiently, reduced graphene oxide is employed as a model substrate to produce an average temperature reaching as high as ∼1850 K within seconds. As a proof-of-concept, we utilize this rapid, high-temperature heating process to synthesize PtPdFeCoNi HEA-NPs, which exhibit an average particle size of ∼12 nm and uniform elemental mixing resulting from decomposition nearly at the same time and liquid metal solidification without diffusion. Various carbon-based materials can also be employed as substrates, including one-dimensional carbon nanofibers and three-dimensional carbonized wood, which can achieve temperatures of >1400 K. This facile and efficient microwave heating method is also compatible with the roll-to-roll process, providing a feasible route for scalable HEA-NPs manufacturing.
据报道,高熵合金纳米颗粒(HEA-NPs)在催化、能量存储和转换方面具有卓越性能,这归因于可纳入这些材料中的元素种类广泛,从而实现了可调活性、出色的热稳定性和化学稳定性以及协同催化效应。然而,由于所需的关键合成条件通常涉及高温,高效规模化制造具有均匀粒径和均匀元素分布的HEA-NPs仍然是一项挑战。在这项工作中,我们展示了一种高效且可扩展的微波加热方法,该方法使用碳基材料作为基底来制造具有均匀粒径的HEA-NPs。由于存在能有效吸收微波的丰富官能团缺陷,还原氧化石墨烯被用作模型基底,在数秒内产生高达约1850 K的平均温度。作为概念验证,我们利用这种快速的高温加热过程来合成PtPdFeCoNi HEA-NPs,其平均粒径约为12 nm,并且由于几乎同时分解和液态金属凝固而无扩散,实现了均匀的元素混合。各种碳基材料也可作为基底使用,包括一维碳纳米纤维和三维碳化木材,它们能达到>1400 K的温度。这种简便高效的微波加热方法还与卷对卷工艺兼容,为规模化制造HEA-NPs提供了一条可行途径。