Improving the electrocatalytic N2 reduction activity of Pd nanoparticles through surface modification

被引:119
作者
Deng, Guorong [1 ,2 ]
Wang, Ting [3 ]
Alshehri, Abdulmohsen Ali [4 ]
Alzahrani, Khalid Ahmed [4 ]
Wang, Yan [2 ]
Ye, Hejiang [5 ]
Luo, Yonglan [3 ]
Sun, Xuping [1 ]
机构
[1] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610054, Sichuan, Peoples R China
[2] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 611731, Sichuan, Peoples R China
[3] China West Normal Univ, Chem Synth & Pollut Control Key Lab Sichuan Prov, Coll Chem & Chem Engn, Nanchong 637002, Sichuan, Peoples R China
[4] King Abdulaziz Univ, Fac Sci, Chem Dept, POB 80203, Jeddah 21589, Saudi Arabia
[5] Hosp Chengdu Univ Tradit Chinese Med, Chengdu 610072, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
FIXATION; AMMONIA; NH3; NANOSHEET;
D O I
10.1039/c9ta06523g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Industrially, NH3 production mainly relies on the energy-intensive Haber-Bosch process with the release of a large amount of CO2. Electrochemical fixation of N-2 to NH3 under ambient conditions is an environmentally friendly and sustainable alternative, but the N-2 reduction reaction (NRR) requires stable and efficient electrocatalysts. In this work, we report that the electrocatalytic NRR activity of Pd nanoparticles can be improved by surface modification with oxygen-rich tannic acid. The electrochemical test results in 0.1 M Na2SO4 suggest that such a catalyst achieves a large NH3 yield of 24.12 mu g h(-1) mg(cat.)(-1) and a high faradaic efficiency of 9.49% at -0.45 V vs. the reversible hydrogen electrode (RHE), rivaling the performances of most of the reported aqueous-based NRR electrocatalysts. In addition, it also shows strong long-term electrochemical stability.
引用
收藏
页码:21674 / 21677
页数:4
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