Song Tian-Wei, Chen Ming-Xi, Yin Peng, Tong Lei, Zuo Ming, Chu Sheng-Qi, Chen Ping, Liang Hai-Wei
Hefei National Research Center for Physical Sciences at the Microscale, Department of Chemistry, University of Science and Technology of China, Hefei, 230026, China.
Institute of High Energy Physics, Chinese Academy of Sciences, Beijing, 100049, China.
Small. 2022 Aug;18(31):e2202916. doi: 10.1002/smll.202202916. Epub 2022 Jul 10.
Platinum-based atomically ordered alloys (i.e., intermetallic compounds) have distinct advantages over disordered solid solution counterparts in boosting the cathodic oxygen-reduction reaction (ORR) in proton-exchange-membrane fuel cells. Nevertheless, the pivotal role of ordering degree of intermetallic catalysts in promoting ORR performance has been ignored heavily so far, probably owing to the lack of synthetic routes for controlling the ordering degree, especially for preparing highly ordered intermetallic catalysts. Herein, a family of intermetallic PtFe catalysts with similar particle size of 3-4 nm but varied ordering degree in a wide range of 10-70% are prepared. After constructing the PtFe/Pt core/shell structure with around 3 Pt-layer skin, a positive correlation between the ordering degree of the intermetallic catalysts and their ORR activity and durability is identified. Notably, the highly ordered PtFe/Pt catalyst exhibits a high mass activity of 0.92 A mg at 0.9 V as cathode catalyst in H -O fuel cell, with only 24% loss after accelerated durability tests. The ordering degree-dependent performance can be ascribed to the compressive strain effect induced by the intermetallic PtFe core with smaller lattice parameters, and the more thermodynamically stable intermetallic structure compared to disordered alloys.
在质子交换膜燃料电池中,基于铂的原子有序合金(即金属间化合物)在促进阴极氧还原反应(ORR)方面比无序固溶体合金具有明显优势。然而,到目前为止,金属间催化剂的有序度在促进ORR性能方面的关键作用一直被严重忽视,这可能是由于缺乏控制有序度的合成路线,特别是制备高度有序的金属间催化剂的路线。在此,制备了一系列金属间PtFe催化剂,其粒径相似,为3 - 4纳米,但有序度在10% - 70%的宽范围内变化。在用约3个铂层外壳构建PtFe/Pt核壳结构后,确定了金属间催化剂的有序度与其ORR活性和耐久性之间存在正相关。值得注意的是,高度有序的PtFe/Pt催化剂在氢氧燃料电池中作为阴极催化剂,在0.9 V时表现出0.92 A mg的高质量活性,经过加速耐久性测试后仅损失24%。有序度依赖的性能可归因于具有较小晶格参数的金属间PtFe核诱导的压缩应变效应,以及与无序合金相比热力学更稳定的金属间结构。