Chang Rui, Li Hongdong, Tian Xiaofeng, Yang Yu, Dong Tian, Wang Zhenhui, Lai Jianping, Feng Shouhua, Wang Lei
Key Laboratory of Eco-Chemical Engineering, International Science and Technology Cooperation Base of Eco-Chemical Engineering and Green Manufacturing, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, 266042, P. R. China.
Shandong Engineering Research Center for Marine Environment Corrosion and Safety Protection, College of Environment and Safety Engineering, Qingdao University of Science and Technology, Qingdao, 266042, P. R. China.
Small. 2024 Jun;20(24):e2309937. doi: 10.1002/smll.202309937. Epub 2024 Jan 4.
High entropy materials offer almost unlimited catalytic possibilities due to their variable composition, unique structure, and excellent electrocatalytic performance. However, due to the strong tendency of nanoparticles to coarsen and agglomerate, it is still a challenge to synthesize nanoparticles using simple methods to precisely control the morphology and size of the nanoparticles in large quantities, and their large-scale application is limited by high costs and low yields. Herein, a series of high-entropy oxides (HEOs) nanoparticles with high-density and ultrasmall size (<5 nm) loaded on carbon nanosheets with large quantities are prepared by Joule-heating treatment of gel precursors in a short period of time (≈60 s). Among them, the prepared (FeCoNiRuMn)O catalyst shows the best electrocatalytic activity for oxygen evolution reaction, with low overpotentials (230 mV @10 mA cm, 270 mV @100 mA cm), small Tafel slope (39.4 mV dec), and excellent stability without significant decay at 100 mA cm after 100 h. The excellent performance of (FeCoNiRuMn)O can be attributed to the synergistic effect of multiple elements and the inherent structural stability of high entropy systems. This study provides a more comprehensive design idea for the preparation of efficient and stable high entropy catalysts.
高熵材料因其可变的组成、独特的结构和优异的电催化性能而提供了几乎无限的催化可能性。然而,由于纳米颗粒强烈的粗化和团聚趋势,使用简单方法大量精确控制纳米颗粒的形态和尺寸来合成纳米颗粒仍然是一个挑战,并且它们的大规模应用受到高成本和低产率的限制。在此,通过在短时间内(≈60秒)对凝胶前驱体进行焦耳热处理,制备了一系列大量负载在碳纳米片上的高密度且超小尺寸(<5nm)的高熵氧化物(HEOs)纳米颗粒。其中,所制备的(FeCoNiRuMn)O催化剂对析氧反应表现出最佳的电催化活性,具有低过电位(10 mA cm时为230 mV,100 mA cm时为270 mV)、小塔菲尔斜率(39.4 mV dec)以及优异的稳定性,在100 mA cm下100小时后无明显衰减。(FeCoNiRuMn)O的优异性能可归因于多种元素的协同效应以及高熵体系固有的结构稳定性。本研究为制备高效稳定的高熵催化剂提供了更全面的设计思路。