Co-Doped Fe3S4 Nanoflowers for Boosting Electrocatalytic Nitrogen Fixation to Ammonia under Mild Conditions

被引:15
作者
Chen, Xue [1 ]
Yin, Hongfei [1 ]
Yang, Xiaoyong [3 ,4 ]
Zhang, Weining [1 ]
Xiao, Dongdong [2 ]
Lu, Zhen [2 ]
Zhang, Yongzheng [1 ]
Zhang, Ping [1 ]
机构
[1] Qufu Normal Univ, Sch Phys & Phys Engn, Qufu 273165, Peoples R China
[2] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
[3] Southwest Univ Sci & Technol, State Key Lab Environm Friendly Energy Mat, Mianyang 621010, Peoples R China
[4] KTH Royal Inst Technol, Dept Mat Sci & Engn, SE-10044 Stockholm, Sweden
基金
中国国家自然科学基金;
关键词
NANOPARTICLES; CONVERSION; CATALYSIS; CLEAVAGE;
D O I
10.1021/acs.inorgchem.2c03578
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Compared with the Haber Bosch process, the electrochemical nitrogen reduction reaction (NRR) under mild conditions provides an alternative and promising route for ammonia synthesis due to its green and sustainable features. However, the great energy barrier to break the stable N=N bond hinders the practical application of NRR. Though Fe is the only common metal element in all biological nitrogenases in nature, there is still a lack of study on developing highly efficient and lowcost Fe-based catalysts for N-2 fixation. Herein, Co-doped Fe3S4 nanoflowers were fabricated as the intended catalyst for NRR. The results indicate that 4% Co-doped Fe3S4 nanoflowers achieve a high Faradaic efficiency of 17% and a NH3 yield rate of 37.5 mu g.h(-1).mg(cat.)(-1) at -0.55 V versus RHE potential in 0.1 M HCl, which is superior to most Fe-based catalysts. The introduction of Co atoms can not only shift the partial density states of Fe3S4 toward the Fermi level but also serve as new active centers to promote N-2 absorption, lowering the energy barrier of the potential determination step to accelerate the catalytic process. This work paves a pathway of the morphology and doping engineering for Fe-based electrocatalysts to enhance ammonia synthesis.
引用
收藏
页码:20123 / 20132
页数:10
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