Boosting electrocatalytic glycerol oxidation reaction to formate based on Mn-doped Ni7P3

IF 6.3 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Journal of Alloys and Compounds Pub Date : 2025-04-10 Epub Date: 2025-03-20 DOI:10.1016/j.jallcom.2025.179867
Qin Yin, Xin Xie, Lixiong Xu, Shuo Geng
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Abstract

Replacing the oxygen evolution reaction (OER) with the thermodynamically favorable glycerol oxidation reaction (GOR) offers a promising approach for producing high-value chemicals. However, this process remains limited by slow kinetics and low selectivity. In this study, a novel manganese-doped Ni7P3 catalyst (Mn-Ni7P3/NF-1) was synthesized via a two-step method. The Mn-Ni7P3/NF-1 catalyst achieved a current density of 10 mA cm−2 at 1.306 V vs. RHE and demonstrated a high formic acid Faradaic efficiency of 95.26 % at 1.35 V vs. RHE. This enhanced GOR performance is attributed to the porous nanostructure, which increases exposure of active sites, and the electronic structure modulation resulting from Mn doping. This study presents an effective approach for the reasonable design of highly active and stable electrocatalysts for designing highly active and stable electrocatalysts applicable to GOR and other processes relevant to biodiesel byproducts.
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基于mn掺杂Ni7P3的电催化甘油氧化反应生成甲酸酯
用热力学有利的甘油氧化反应(GOR)取代析氧反应(OER)为生产高价值化学品提供了一条有前途的途径。然而,这一过程仍然受到慢动力学和低选择性的限制。本研究采用两步法合成了一种新型锰掺杂Ni7P3催化剂(Mn-Ni7P3/NF-1)。Mn-Ni7P3/NF-1催化剂在1.306 V / RHE下的电流密度为10 mA cm-2,在1.35 V / RHE下的甲酸法拉第效率高达95.26%。这种增强的GOR性能归因于多孔纳米结构,它增加了活性位点的暴露,以及Mn掺杂导致的电子结构调制。本研究为合理设计高活性稳定的电催化剂提供了有效途径,为设计适用于GOR及生物柴油副产物相关工艺的高活性稳定电催化剂提供了依据。
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来源期刊
Journal of Alloys and Compounds
Journal of Alloys and Compounds 工程技术-材料科学:综合
CiteScore
11.10
自引率
14.50%
发文量
5146
审稿时长
67 days
期刊介绍: The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.
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