欢迎访问《电化学(中英文)》期刊官方网站,今天是

电化学(中英文)

• 研究论文 •    

微波合成Pd@PdPtCuFe凹面截角八面体纳米晶体及其多功能电催化

胡德忠a, 姜文丹a, 黄伟杰a, 杨俊b,*, 康雄武a,*   

  1. a. 华南理工大学, 环境与能源学院, 新能源研究所, 广东省广州市番禺区大学城外环东路382号, 510006; b. 广东石油化工学院, 茂名市茂南区官渡二路139号, 525000.
  • 发布日期:2026-06-10
  • 通讯作者: 杨俊, 康雄武 E-mail:yangjun@gdupt.edu.cn; esxkang@scut.edu.cn

Microwave-Assisted Synthesis of Core–Shell Structured Pd@PdPtCuFe Recessed Truncated Octahedral Nanocrystals for Multifunctional Electrocatalysis

Dezhong Hua, Wendan Jianga, Wei Keat Nga, Jun Yangb,*, Xiongwu Kanga,*   

  1. a. New Energy Research Institute, School of Environment and Energy, South China University of Technology, 382 East Waihuan Road, 510006, China; b. School of Chemical Engineering, Guangdong University of Petrochemical Technology, 139 Guandu Er Road, 525000, China.
  • Online:2026-06-10
  • Contact: Jun Yang, Xiongwu Kang E-mail:yangjun@gdupt.edu.cn; esxkang@scut.edu.cn

摘要: 开发兼具低成本与高稳定性的电解水析氢(HER)、氧还原反应(ORR)和析氧反应(OER)等多功能电催化剂,可以显著提升电解水析氢及可充电锌空气电池(ZABs)的能量转换效率。具有明确晶面的多面体纳米晶是一类典型的模型催化剂,可为构效关系研究提供理想平台。然而,由于多种金属间存在复杂的氧化还原电位与混合焓差异,制备多组元合金纳米晶仍极具挑战性。本文采用快速微波辅助还原法成功合成出八面体及凹面截角八面体 Pd@PdPtCuFe 纳米晶。由于钯前驱体具有极快的还原与成核速率,反应优先形成钯内核;其余金属前驱体随后同步还原并高效扩散,最终形成 PdPtCu 或 PdPtCuM(M = Ni、Co、Fe、Zn)合金壳层。铁元素诱导晶体形貌从八面体向凹面截角八面体演变。得益于多金属组分间的协同电子耦合效应,以及应变调控的表面构型,Pd@PdPtCuFe/C 表现出优异的多功能电催化性能:在 10 mA⋅cm-2电流密度下,HER 过电位仅为 18 mV,塔菲尔斜率为 27 mV⋅dec-1;在 10 mA⋅cm-2电流密度下,OER 过电位为 360 mV,塔菲尔斜率为 75.9 mV⋅dec-1,与商业催化剂IrO2相当。所有催化剂均展现出一定的 ORR 活性,其中 Pd@PdPtCuFe/C 在碱性电解液中的 ORR 半波电位为 0.792 V。其作为锌空气电池阴极催化剂时,实现了81.2 mW⋅cm-2的峰值功率密度,并可稳定循环超过 50 小时。本工作为多金属纳米晶的超快形貌可控合成提供了一种普适性策略,为高性能合金催化剂的理性设计奠定了基础。

关键词: 合金, 核壳结构, 八面体, 截角八面体, 多功能

Abstract: Developing cost-efficient and durable multifunctional electrocatalysts of hydrogen evolution reaction (HER), oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is crucial for improving energy conversion efficiency in electrolytic water splitting electrolyzer and advancing rechargeable zinc–air batteries (ZABs). Polyhedral shaped nanocrystals with well-defined crystal facets represent a type of model catalysts that enables the exploration of structure-activity. However, it is still very challenging to prepare alloy nanocrystals with multiple metal components due to their complicated redox potentials and mixing enthalpy. Herein, we report a rapid microwave-assisted polyol reduction method for synthesis of core–shell Pd@PdPtCu, Pd@PdPtCuNi, Pd@PdPtCuCo and Pd@PdPtCuZn octahedra nanocrystals and recessed truncated-octahedra Pd@PdPtCuFe nanocrystals. Ascribing to the fast reduction and nucleation rate of Pd precursors, Pd core was first formed. Further concurrent reduction and efficient diffusion of the rest metal precursors result in the PdPtCu or PdPtCuM (M = Ni, Co, Fe and Zn) alloy shell. It is observed that Fe plays a decisive role in driving the morphological evolution from octahedral to recessed truncated-octahedra nanocrystals. The Fe³⁺–Br⁻ coordination modulates crystal growth kinetics by altering surface adsorption dynamics, resulting in a mixed exposure of {111} and {100} facets rich in edge and vertex sites. Structural analyses confirm a well-defined Pd core and homogeneous PdPtCuFe alloy shell with a face-centered-cubic phase. Owing to the synergistic electronic coupling between Fe and noble-metal components and the strain-regulated surface configuration, Pd@PdPtCuFe/C exhibits superior multifunctional activity with a HER overpotential of 18 mV at 10 mA⋅cm-2 and Tafel slope of 27 mV⋅dec-1, the most active HER catalysts among the five prepared core@shell catalysts and superior to that of commercial Pt/C. In addition, it delivers an OER overpotential of 360 mV at 10 mA⋅cm-2 and a Tafel slope of 75.9 mV⋅dec-1, comparable to that of the benchmark IrO2 catalysts. All the prepared catalysts exhibit certain ORR activity, together with an ORR half-wave potential of 0.792 V in alkaline electrolyte. When applied as a cathode catalyst in ZABs, Pd@PdPtCuFe/C delivers a peak power density of 81.2 mW⋅cm-2 and maintains stable cycling for over 50 h. This work provides a generalizable route for ultrafast morphology-controlled synthesis of multimetallic nanocrystals, paving the way for the rational design of high-performance, low-PGM bifunctional catalysts for next-generation energy conversion and storage systems.

Key words: octahedra, recessed truncated-octahedra, microwave-assisted, core–shell, multifunctional electrocatalysis