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调制超薄 PdSb 基纳米片上的金属 Sb 态以实现高效甲酸电氧化。

Modulate the metallic Sb state on ultrathin PdSb-based nanosheets for efficient formic acid electrooxidation.

机构信息

School of Science, Shenyang University of Chemical Technology, Shenyang 110142, China; State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun, Jilin 130022, China.

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun, Jilin 130022, China.

出版信息

J Colloid Interface Sci. 2023 Oct 15;648:473-480. doi: 10.1016/j.jcis.2023.05.200. Epub 2023 Jun 5.

Abstract

Incorporation of oxophilic metals into Pd-based nanostructures has shown great potential in small molecule electrooxidation owing to their superior anti-poisoning capability. However, engineering the electronic structure of oxophilic dopants in Pd-based catalysts remains challenging and their impact on electrooxidation reactions is rarely demonstrated. Herein, we have developed a method for synthesizing PdSb-based nanosheets, enabling the incorporation of the Sb element in a predominantly metallic state despite its high oxophilic nature. Moreover, the PdSbW nanosheet serves as an efficient electrocatalyst for the formic acid oxidation reaction (FAOR), and the underlying promotion mechanism is investigated. Among the as-prepared PdSb-based nanosheets, the PdSbW nanosheet exhibits a remarkable 69.03% metallic state of Sb, surpassing the values observed for the PdSbW (33.01%) and PdSbW (25.41%) nanosheets. X-ray photoelectron spectroscopy (XPS) and CO stripping experiments confirm that the Sb metallic state contributes the synergistic effect of their electronic and oxophilic effect, thus leading to an effective electrooxidation removal of CO and significantly enhanced FAOR electrocatalytic activity (1.47 A mg; 2.32 mA cm) compared with the oxidated state of Sb. This work highlights the importance of modulating the chemical valence state of oxophilic metals to enhance electrocatalytic performance, offering valuable insights for the design of high-performance electrocatalysts for electrooxidation of small molecules.

摘要

将亲氧金属纳入基于钯的纳米结构中,由于其卓越的抗中毒能力,在小分子电氧化中显示出巨大的潜力。然而,工程化亲氧掺杂剂在基于钯的催化剂中的电子结构仍然具有挑战性,并且它们对电氧化反应的影响很少得到证明。在此,我们开发了一种合成 PdSb 基纳米片的方法,即使 Sb 元素具有高亲氧性,也能使其主要以金属状态存在。此外,PdSbW 纳米片作为甲酸氧化反应 (FAOR) 的高效电催化剂,并对其基础促进机制进行了研究。在所制备的 PdSb 基纳米片中,PdSbW 纳米片表现出显著的 69.03% Sb 金属态,超过了 PdSbW (33.01%)和 PdSbW (25.41%)纳米片的观察值。X 射线光电子能谱 (XPS) 和 CO 剥离实验证实,Sb 金属态有助于其电子和亲氧效应的协同作用,从而有效地去除 CO 并显著增强 FAOR 电催化活性 (1.47 A mg; 2.32 mA cm),与 Sb 的氧化态相比。这项工作强调了调节亲氧金属的化学价态以增强电催化性能的重要性,为小分子电氧化的高性能电催化剂设计提供了有价值的见解。

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