Synthesis of Polystyrene Microsphere-Supported Ag–Ni-Alloyed Catalysts with Core–Shell Structures for Electrocatalytic Performance

Yue Yu, D. Luan, Changlong Bi, Yu Ma, Yongheng Chen, Dongyu Zhao
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引用次数: 8

Abstract

ABSTRACT Rationally designed synthesis strategy for well-defined morphology which can endow the catalysts with unexpectedly enhanced catalytic properties remains a significant challenge in heterogeneous catalytic reactions. Hence, here we report a facile and controllable synthesis of polystyrene microsphere-supported Ag–Ni-alloyed catalysts (PS@Ag–Ni) with uniform core–shell structures through sulfonated treatment coupled with the subsequent liquid-phase reduction strategy. In this typical synthesis, sulfuric acid acts as the bifunctional roles in directing the core–shell morphology and the linker between the polystyrene microspheres and Ag–Ni alloy. The as-obtained PS@Ag–Ni optimized by tuning in a mass ratio of 1:1 shows superior oxygen reduction reaction activity and electrocatalytic performance toward the degradation of p-nitrophenol in comparison with other range of polystyrene microspheres and Ag–Ni alloy feeding ratios. The superior electrocatalytic and oxygen reduction reaction activity are attributed to its highly uniform core–shell morphology and exposure of much more active sites. Moreover, our as-prepared core–shell electrocatalysts will enable further investigation in other catalytic reactions. GRAPHICAL ABSTRACT
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聚苯乙烯微球负载银镍合金核壳结构催化剂的合成及其电催化性能
合理设计合成策略,使催化剂具有良好的形态,使催化剂的催化性能得到意想不到的提高,这是多相催化反应的一个重大挑战。因此,本文报道了一种简单可控的聚苯乙烯微球负载ag -Ni合金催化剂(PS@Ag -Ni)的合成方法,该催化剂具有均匀的核壳结构,通过磺化处理和随后的液相还原策略。在这种典型的合成中,硫酸在指导聚苯乙烯微球和银镍合金之间的核壳形态和连接方面起着双重功能作用。以质量比为1:1优化得到的PS@Ag -Ni与其他范围的聚苯乙烯微球和Ag-Ni合金投料比相比,表现出更好的氧还原反应活性和电催化降解对硝基苯酚的性能。优异的电催化和氧还原反应活性归因于其高度均匀的核壳形态和暴露更多的活性位点。此外,我们所制备的核壳电催化剂将为其他催化反应的进一步研究提供基础。图形抽象
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来源期刊
Polymer-Plastics Technology and Engineering
Polymer-Plastics Technology and Engineering 工程技术-高分子科学
CiteScore
1.71
自引率
0.00%
发文量
0
审稿时长
4 months
期刊最新文献
Fundamentals Index Plastics Technology Recommendations for Writing a Bachelor's/Master's Thesis at the IKT Plastics Materials Engineering
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