Yu Xiuqing, Yue Ruirui, Yang Shiyao, Fu Changqing, Shu Jinbing, Shen Liang
College of Chemistry and Chemical Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, PR China.
College of Life Science, Jiangxi Science and Technology Normal University, Nanchang 330013, PR China.
J Colloid Interface Sci. 2024 Sep 15;670:473-485. doi: 10.1016/j.jcis.2024.05.100. Epub 2024 May 18.
Developing a novel catalyst with lower noble-metal loading and higher catalytic efficiency is significant for promoting the widespread application of direct alcohol fuel cells (DAFCs). In this work, poly(3,4-ethylenedioxythiophene) (PEDOT) supported the PdSn alloy (PdSn/PEDOT) were simply synthesized and their electrocatalytic performance toward the oxidation of ethylene glycol and ethanol (EGOR and EOR) were investigated in alkaline media, respectively. In comparison with other control catalysts, the optimized PdSn/PEDOT catalyst exhibits the highest mass activity (7125/4166 mA mg) and specific activity (26/15 mA cm) towards EGOR/EOR. The mass activity of PdSn/PEDOT for EGOR and EOR are 11.9 and 10.9 times higher than commercial Pd/C, respectively. Moreover, chronoamperometry (CA) and successive cyclic voltammetry (CV) tests show that the CO resistance ability and durability of the PdSn/PEDOT catalyst were superior to PdSn, Pd/PEDOT and commercial Pd/C catalysts, which can be attributed to the d-band center of Pd can be effectively downshifted and the interface strain effect between electrons caused by the conjugated structure between PEDOT groups. This work provides an effective strategy for the development of highly efficient anode catalysts of DAFCs.
开发一种具有更低贵金属负载量和更高催化效率的新型催化剂对于推动直接醇类燃料电池(DAFCs)的广泛应用具有重要意义。在这项工作中,简单合成了聚(3,4-乙撑二氧噻吩)(PEDOT)负载的PdSn合金(PdSn/PEDOT),并分别研究了它们在碱性介质中对乙二醇和乙醇氧化(EGOR和EOR)的电催化性能。与其他对照催化剂相比,优化后的PdSn/PEDOT催化剂对EGOR/EOR表现出最高的质量活性(7125/4166 mA mg)和比活性(26/15 mA cm)。PdSn/PEDOT对EGOR和EOR的质量活性分别比商业Pd/C高11.9倍和10.9倍。此外,计时电流法(CA)和连续循环伏安法(CV)测试表明,PdSn/PEDOT催化剂的抗CO能力和耐久性优于PdSn、Pd/PEDOT和商业Pd/C催化剂,这可归因于Pd的d带中心可以有效地向下移动以及PEDOT基团之间的共轭结构引起的电子间界面应变效应。这项工作为开发高效的DAFCs阳极催化剂提供了一种有效策略。