In Situ Preparation of Polyamine-Derived Ru Cluster@N-Doped Porous Carbon Nanoplates for Hydrogen Evolution over Wide pH Ranges

被引:2
|
作者
Sun, Tiantian [1 ]
Wang, Xinlin [1 ]
Duan, Zhiyao [1 ]
Zhang, Qiong [1 ]
Zhao, Yingxiu [1 ]
Xu, Guang-Rui [1 ,2 ]
Wang, Wei [1 ]
Wang, Lei [1 ,3 ]
机构
[1] Qingdao Univ Sci & Technol, Key Lab Opt Elect Sensing & Analyt Chem Life Sci, Taishan Scholar Advantage & Characterist Disciplin, Coll Chem & Mol Engn,Key Lab Ecochem Engn,Sch Mat, Qingdao 266042, Peoples R China
[2] Nankai Univ, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
[3] Qingdao Univ Sci & Technol, Coll Environm & Safety Engn, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
PERFORMANCE; DESIGN; ATOMS;
D O I
10.1021/acs.inorgchem.3c02807
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Efficient and low-cost electrocatalysts for the hydrogen evolution reaction (HER) are required for producing hydrogen energy through water splitting. Carbon materials as HER catalyst supports are explored widely since the strong metal-support interactions are generally believed to be active and stable toward HER. Herein, we report N-doped porous carbon materials as novel substrates to stabilize the cluster metal sites through the Ru(III) polyamine complexes, which play an important role not only in efficient electron transfer but also in the increasing utilization of metallic active sites. Meanwhile, due to the strong metal-support interactions driven by Ru(III) polyamine complexes, the obtained Ru cluster with a mass loading of 3% on N-doped porous carbon nanoplates (Ru cluster@NCs) exhibits robust stability for HER at a constant voltage, proving to be a promising candidate catalyst for HER. Density functional theory calculations further indicate that the Gibbs free energy (Delta G) of adsorbed H* of Ru cluster@NCs is much closer to zero compared to Ru@(10%)NCs and Pt/C(20%), thus Ru cluster@NCs facilitate the HER process.
引用
收藏
页码:17012 / 17021
页数:10
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