General and scalable strategy for synthesis of Pt-rare earth alloys as highly durable oxygen reduction electrocatalysts

催化作用 材料科学 铂金 质子交换膜燃料电池 层状结构 化学工程 氧还原反应 微观结构 氧还原 纳米技术 化学 物理化学 复合材料 电极 电化学 工程类 生物化学
作者
Fangren Qian,Chengsi Hu,Wei Jiang,Jiawei Zhang,Lishan Peng,Li Song,Qingjun Chen
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:468: 143665-143665 被引量:24
标识
DOI:10.1016/j.cej.2023.143665
摘要

Platinum-rare earth (Pt-RE) alloys are effective oxygen reduction reaction (ORR) catalysts, which are promising to show robust durability in proton-exchange membrane fuel cells (PEMFCs). Whereas, the large difference in reduction potentials between the two kinds of metals and the very oxophilicity of RE elements bring big challenges in the controllable synthesis of Pt-RE alloys. Herein we propose a general and scalable strategy to synthesize Pt-RE catalysts with tunable compositions and microstructures. The as-obtained catalysts possess a lamellar structure with hierarchical pore sizes ranging from 4 to 8 nm and a typical face-centered cubic (FCC) crystalline structure, and the Pt and RE are homogeneously distributed in the alloys. The electronic structures of Pt are well modulated by incorporating RE atoms, resulting in the adjusted d band center for these Pt-RE alloys compare with Pt, which facilitates OH* adsorption behavior and accelerate the ORR kinetics. Furthermore, the energy barrier for Pt demetallation is enhanced by incorporating of RE into the Pt lattice, which significantly enhances ORR durability. Notably, the optimal Pt3Y catalyst exhibits a greatly improved catalytic activity, including a large half-wave potential (0.89 V, at an ultralow Pt loading of 7.8 μg cm−2), high mass activity (0.53 A mg−1 at 0.9 ViR-free) and robust stability (0.01 V decay after 60,000 cycles) exceeding the commercial Pt/C (0.06 V decay after 30,000 cycles). This study provides a new facile strategy for the controllable preparation of Pt-RE alloys, which might pave the way for the large-scale applications of PEMFCs.
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