Department of Chemistry, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Fuel Cell Laboratory, Korea Institute of Energy Research, 152 Gajeong-ro, Yuseong-gu, Daejeon 34129, Republic of Korea.
Ultrason Sonochem. 2019 Nov;58:104673. doi: 10.1016/j.ultsonch.2019.104673. Epub 2019 Jul 4.
In this work, we introduce composition-tunable core-shell-like PdM@Pt (M = Mn and Fe) nanoparticles (NPs) on carbon support (PdM@Pt/C) synthesized by one-pot sonochemical reactions using high-intensity ultrasonic probe (150 W, 20 kHz, with 13 mm solid probe) and investigate their electrocatalytic performance for oxygen reduction reaction (ORR). The core-shell-like structure of the NPs are evidenced by the elemental distribution maps obtained by energy dispersive X-ray spectroscopy equipped on scanning transmission electron microscopy. Based on the characterization data, PdM@Pt NPs were synthesized with variable elemental compositions (PdFe@Pt, PdFe@Pt, PdMn@Pt and PdMn@Pt). All PdM@Pt samples are composed of large (10 nm) and small (3 nm) NPs, the large ones appear to be aggregates of the smaller ones, and the proportion of the larger NPs increases with the Pd content, which can be explained with the known mechanisms of sonochemical reactions of related systems. Electrochemical analyses on samples show that the ORR mass activity of PdM@Pt/C is 3-fold (normalized by Pt) and 1.7-fold (normalized by platinum group metal (PGM)) higher than those of Pt/C (commercial). All PdM@Pt/C sample show superior durability with the electrochemical surface area (ECSA) change of -4.4-+12.0% and half-wave potential change (ΔE) of 8-14 mV after 10 k cycles accelerated stress test (AST) to Pt/C with ECSA change of -25.6% and ΔE of 19 mV.
在这项工作中,我们通过使用高强度超声探针(150 W,20 kHz,带有 13mm 固体探针)的一锅超声化学反应,在碳载体上合成了组成可调的核壳状 PdM@Pt(M=Mn 和 Fe)纳米粒子(NPs)PdM@Pt/C,并研究了它们对氧还原反应(ORR)的电催化性能。通过配备在扫描透射电子显微镜上的能量色散 X 射线光谱法获得的元素分布图谱,证明了 NPs 的核壳结构。基于表征数据,用可变元素组成(PdFe@Pt、PdFe@Pt、PdMn@Pt 和 PdMn@Pt)合成了 PdM@Pt NPs。所有 PdM@Pt 样品均由大(10nm)和小(3nm)纳米颗粒组成,大颗粒似乎是小颗粒的聚集体,大颗粒的比例随着 Pd 含量的增加而增加,这可以用相关体系的已知声化学反应机制来解释。对样品进行的电化学分析表明,PdM@Pt/C 的 ORR 质量活性是 Pt/C(商业)的 3 倍(按 Pt 归一化)和 1.7 倍(按铂族金属(PGM)归一化)。所有 PdM@Pt/C 样品在 10k 次加速应力试验(AST)后,电化学表面积(ECSA)的变化为-4.4%至+12.0%,半波电势的变化(ΔE)为 8 至 14 mV,显示出优异的耐久性,而 Pt/C 的 ECSA 变化为-25.6%,ΔE 为 19 mV。