Enhancing electrocatalytic nitrogen reduction to ammonia with rare earths (La, Y, and Sc) on high-index faceted platinum alloy concave nanocubes

被引:31
|
作者
Mao, Yu-Jie [1 ]
Liu, Feng [1 ]
Chen, You-Hu [2 ]
Jiang, Xin [1 ]
Zhao, Xin-Sheng [1 ]
Sheng, Tian [3 ]
Ye, Jin-Yu [2 ]
Liao, Hong-Gang [2 ]
Wei, Lu [1 ]
Sun, Shi-Gang [2 ]
机构
[1] Jiangsu Normal Univ, Sch Phys & Elect Engn, Xuzhou 221116, Jiangsu, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab PCOSS, Xiamen 361005, Peoples R China
[3] Anhui Normal Univ, Coll Chem & Mat Sci, Wuhu 241000, Peoples R China
基金
中国国家自然科学基金;
关键词
SHAPE EVOLUTION; N-2; REDUCTION; CATALYSTS; NANOCRYSTALS; GOLD; PD; NANOPARTICLES; CHEMISTRY; SURFACES; CARBON;
D O I
10.1039/d1ta05515a
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
Surface structure effect is the key subject in electrocatalysis, and consists of the structure dependence of interaction between reaction molecules and the catalyst surface in specifying the surface atomic arrangement, chemical composition and electronic structure. Herein, we develop a controllable synthesis of Pt-RE (RE = La, Y, Sc) alloy concave nanocubes (PtRENCs) with {410} high-index facets (HIFs) by an electrochemical method in a choline chloride-urea based deep eutectic solvent. The PtRENCs are used as an efficient catalyst in electrocatalytic nitrogen reduction to ammonia (NH<INF>3</INF>). Owing to the high density of low-coordinated Pt step sites (HIF structure) and the unique electronic effect of Pt-RE, the as-prepared PtRENCs exhibit an excellent electrocatalytic performance for the nitrogen reduction reaction (NRR) under ambient conditions. The NH<INF>3</INF> yield rate and faradaic efficiency (FE) share the same trend of Pt-La (r<INF>NH<INF>3</INF></INF>: 71.4 mu g h-1 mu g<INF>cat</INF>-1, FE: 35.6%) > Pt-Y (r<INF>NH<INF>3</INF></INF>: 65.2 mu g h-1 mu g<INF>cat</INF>-1, FE: 26.7%) > Pt-Sc (r<INF>NH<INF>3</INF></INF>: 48.5 mu g h-1 mu g<INF>cat</INF>-1, FE: 19%) > Pt (r<INF>NH<INF>3</INF></INF>: 25.8 mu g h-1 mu g<INF>cat</INF>-1, FE: 10.7%). Moreover, the PtRENCs demonstrate high selectivity for N<INF>2</INF> reduction to NH<INF>3</INF> and high stability retaining 90% of the NH<INF>3</INF> yield rate and FE values after 12 h continuous NRR tests. Density functional theory (DFT) calculations indicate that the rate determining step of the NRR process is the formation of N<INF>2</INF>H<INF>2</INF>* from N<INF>2</INF> with the transfer of two proton-coupled electrons, and the upshift of the d-band center boosts the NRR activity by enhancing the bonding strength of reaction intermediates on the high-index faceted Pt-RE (RE = La, Y, Sc) alloying surface. In addition, the introduction of RE (RE = La, Y, Sc) on the Pt step surface can effectively suppress the HER process and provide appropriate sites for the NRR.
引用
收藏
页码:26277 / 26285
页数:9
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