Accelerating electrochemically catalyzed nitrogen reductions using metalloporphyrin-mediated metal-nitrogen-doped carbon (M-N-C) catalysts

被引:6
|
作者
Dong, Xinyi [1 ]
Zhu, Weihua [1 ]
Liang, Xu [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
SINGLE-ATOM CATALYSTS; AMMONIA-SYNTHESIS; ATMOSPHERIC-PRESSURE; AMBIENT CONDITIONS; N-2; IDENTIFICATION; NANOPARTICLES; TEMPERATURE; SITES; WATER;
D O I
10.1039/d2dt01258h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Herein, a series of transition metal coordinated metalloporphyrin-mediated M-N-C catalysts with single and dual metal atoms were prepared and characterized. Interestingly, these M-N-C catalysts exhibit accelerated N-2 reduction behaviors through electrochemical catalysis. At the potential of E = -0.4V (vs. RHE), the optimum catalyst Fe0.95Ni0.05TPP@rGO-800 shows excellent catalytic activity, and the NH3 yield is 22.5 mu g mg(cat)(-1) h(-1), which is much higher than that of its single metal counterparts alone, and the faradaic efficiency is as high as 50.7%, which is better than those of most reported catalysts. These results provide an opportunity to further explore the efficient electrochemical synthesis of NH3 from M-N-C materials in the future.
引用
收藏
页码:12240 / 12249
页数:10
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