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通过电偶置换介导合成具有强金属-载体相互作用的镍负载钯纳米颗粒用于甲醇电氧化

Galvanic Replacement-Mediated Synthesis of Ni-Supported Pd Nanoparticles with Strong Metal-Support Interaction for Methanol Electro-oxidation.

作者信息

Lei Hao, Li Xiaotong, Sun Changbin, Zeng Junrong, Siwal Samarjeet Singh, Zhang Qibo

机构信息

Department of Metallurgy, Key Laboratory of Ionic Liquids Metallurgy, Faculty of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming, 650093, P.R. China.

State Key Laboratory of Complex Nonferrous Metal Resources Cleaning Utilization in Yunnan Province, Kunming University of Science and Technology, Kunming, 650093, P.R. China.

出版信息

Small. 2019 Mar;15(11):e1804722. doi: 10.1002/smll.201804722. Epub 2019 Feb 8.

Abstract

Herein, well-defined Pd nanoparticles (NPs) developed on Ni substrate (Pd NPs/Ni) are synthesized via a facile galvanic replacement reaction (GRR) route performed in ethaline-based deep eutectic solvent (DES). For comparison, a Pd NPs/Ni composite is also prepared by the GRR method conducted in an aqueous solution. The Pd NPs/Ni obtained from the ethaline-DES is catalytically more active and durable for the methanol electro-oxidation reaction (MOR) than those of the counterpart derived from conventional aqueous solution and commercial Pd/C under alkaline media. Detailed kinetic analysis indicates that the unique solvent environment offered by ethaline plays vital roles in adjusting the reactivity of the active species and their mass transport properties to control over the genesis of the Pd NPs/Ni nanocomposite. The resulting Pd NPs/Ni catalyst possesses a homogeneous dispersion of Pd NPs with a strong Pd (metal)-Ni (support) interaction. This structure enhances the charge transfer between the support and the active phases, and optimizes the adsorption energy of OH and CO on the surface, leading to superior electrocatalytic performance. This work provides a novel GRR strategy performed in ethaline-DES to the rational design and construction of advanced metal/support catalysts with strong interaction for improving the activity and durability for MOR.

摘要

在此,通过在基于乙酰胺的深共熔溶剂(DES)中进行的简便的电置换反应(GRR)路线,合成了在镍基底上形成的明确的钯纳米颗粒(NPs)(Pd NPs/Ni)。为了进行比较,还通过在水溶液中进行的GRR方法制备了Pd NPs/Ni复合材料。在碱性介质中,从乙酰胺-DES获得的Pd NPs/Ni对甲醇电氧化反应(MOR)的催化活性和耐久性比从传统水溶液和商业Pd/C衍生的对应物更高。详细的动力学分析表明,乙酰胺提供的独特溶剂环境在调节活性物种的反应性及其传质特性以控制Pd NPs/Ni纳米复合材料的形成方面起着至关重要的作用。所得的Pd NPs/Ni催化剂具有均匀分散的Pd NPs,具有很强的Pd(金属)-Ni(载体)相互作用。这种结构增强了载体与活性相之间的电荷转移,并优化了OH和CO在表面上的吸附能,从而导致优异的电催化性能。这项工作为在乙酰胺-DES中进行的新型GRR策略提供了合理设计和构建具有强相互作用的先进金属/载体催化剂的方法,以提高MOR的活性和耐久性。

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