Department of Chemistry, Brown University , Providence, Rhode Island 02912, United States.
Department of Chemistry, Dalhousie University , Halifax, Nova Scotia B3H 4R2, Canada.
Nano Lett. 2017 Apr 12;17(4):2727-2731. doi: 10.1021/acs.nanolett.7b00870. Epub 2017 Mar 22.
We synthesize a new type of hybrid Pd/WO structure with 5 nm Pd nanoparticles (NPs) anchored on 50 × 5 nm WO nanorods. The strong Pd/WO coupling results in the lattice expansion of Pd from 0.23 to 0.27 nm and the decrease of Pd surface electron density. As a result, the Pd/WO shows much enhanced catalysis toward electrochemical oxidation of formic acid in 0.1 M HClO; it has a mass activity of ∼1600 mA/mg in a broad potential range of 0.4-0.85 V (vs RHE) and shows no obvious activity loss after a 12 h chronoamperometry test at 0.4 V. Our work demonstrates an important strategy to enhance Pd NP catalyst efficiency for energy conversion reactions.
我们合成了一种新型的 Pd/WO 杂化结构,其中 5nm 的 Pd 纳米颗粒(NPs)锚定在 50×5nm 的 WO 纳米棒上。强烈的 Pd/WO 耦合导致 Pd 的晶格从 0.23nm 扩展到 0.27nm,同时降低了 Pd 表面的电子密度。结果,Pd/WO 对甲酸在 0.1M HClO 中的电化学氧化表现出显著增强的催化作用;在 0.4-0.85V(相对于 RHE)的宽电位范围内,其质量活性约为 1600mA/mg,在 0.4V 的 12 小时计时电流测试后没有明显的活性损失。我们的工作证明了一种提高 Pd NP 催化剂在能量转换反应中效率的重要策略。