电催化剂
选择性
电合成
材料科学
纳米晶
电子转移
电负性
电解质
离解(化学)
化学工程
过氧化氢
密度泛函理论
催化作用
电化学
纳米颗粒
光化学
电极
纳米技术
化学
物理化学
有机化学
计算化学
工程类
作者
Chengyong Yang,Shuxing Bai,Zhiyong Yu,Yonggang Feng,Bolong Huang,Qiuyang Lu,Tong Wu,Mingzi Sun,Ting Zhu,Chen Cheng,Liang Zhang,Qi Shao,Xiaoqing Huang
出处
期刊:Nano Energy
[Elsevier BV]
日期:2021-08-30
卷期号:89: 106480-106480
被引量:38
标识
DOI:10.1016/j.nanoen.2021.106480
摘要
For the generation of hydrogen peroxide (H2O2), a robust electrocatalyst with high activity, selectivity and stability under pH-universal conditions is a formidable challenge. Herein, Pd4Se nanoparticles (NPs) have been proposed as a highly active, selective and durable electrocatalyst for H2O2 production over a wide pH range for the first time. In particular, the Pd4Se NPs show superior H2O2 production selectivities of 93.5%, 89.7%, and 86.7% in 0.1 M HClO4, 0.1 M KCl and 0.1 M KOH electrolytes, respectively. Density functional theory (DFT) calculations reveal that Se incorporation prevents the OO early-cleavage issue by suppressing the excessive electronegativity of the Pd sites. In addition, a strong p-d repulsive correlation shifts the Pd-4d band towards the electron-depleting centre, allowing near-barrier-free electron transfer and facilitating [OOH-] stabilization. Owing to a high energy barrier of the dissociation of [OOH-], the four-electrons oxygen reduction pathway is significantly suppressed for high H2O2 selectivity. The Pd4Se NPs are also highly stable, with only a 2.4%, 9.6% and 3.4% decrease for H2O2 selectivity in 0.1 M HClO4, 0.1 M KCl and 0.1 M KOH electrolytes, respectively, after 5000 cycles, which shows that these NPs are a unique and robust Pd-based electrocatalyst for H2O2 generation under pH-universal conditions.
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