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High-efficient electrooxidation of ethylene glycol and ethanol on PdSn alloy loaded by versatile poly(3,4-ethylenedioxythiophene).
Yu, Xiuqing; Yue, Ruirui; Yang, Shiyao; Fu, Changqing; Shu, Jinbing; Shen, Liang.
Afiliación
  • Yu X; College of Chemistry and Chemical Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, PR China.
  • Yue R; College of Life Science, Jiangxi Science and Technology Normal University, Nanchang 330013, PR China.
  • Yang S; College of Chemistry and Chemical Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, PR China.
  • Fu C; Institute of Organic Functional Molecules, Jiangxi Science and Technology Normal University, Nanchang 330013, PR China.
  • Shu J; College of Chemistry and Chemical Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, PR China. Electronic address: jinbingshu@jxstnu.com.cn.
  • Shen L; College of Chemistry and Chemical Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, PR China. Electronic address: liangshen@jxstnu.com.cn.
J Colloid Interface Sci ; 670: 473-485, 2024 Sep 15.
Article en En | MEDLINE | ID: mdl-38772263
ABSTRACT
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 Pd4Sn6/PEDOT catalyst exhibits the highest mass activity (7125/4166 mA mgPd-1) and specific activity (26/15 mA cm-2) towards EGOR/EOR. The mass activity of Pd4Sn6/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 Pd4Sn6/PEDOT catalyst were superior to Pd4Sn6, 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.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Colloid Interface Sci Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Colloid Interface Sci Año: 2024 Tipo del documento: Article