Constructing a interfacial electric field for efficient reduction of nitrogen to ammonia

被引:0
|
作者
Zheng, Jiaqi [1 ]
Liu, Shihan [1 ]
Xiang, Lijuan [1 ]
Kuang, Junda [1 ]
Guo, Jing [1 ]
Wang, Lin [1 ]
Li, Nan [1 ]
机构
[1] Jilin Univ, Sch Mat Sci & Engn, Key Lab Automobile Mat, Minist Educ, 2699 Qianjin St, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROCATALYTIC N-2 REDUCTION; OXIDE; ELECTROSYNTHESIS; SELECTIVITY; ADSORPTION; SEPARATION; CATALYSTS; FACET;
D O I
10.1016/j.jcis.2024.04.102
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
Electrochemical nitrogen reduction (eNRR) is a cost-effective and environmentally sustainable approach for ammonia production. MoS2, as a typical layered transition metal compound, holds significant potential as an electrocatalyst for the eNRR. Nevertheless, it suffers from a limited number of active sites and low electron transfer efficiency. In this study, we constructed a heterostructure by depositing SnO2 (an n-type semiconductor) nanoparticles on MoS2 (a p-type semi-conductor). This unique interfacial structure not only generates abundant interfacial contacts but also facilitates the transfer of electrons from SnO2 to MoS2, leading to the formation of an interfacial electric field. Theoretical calculations demonstrate that this electric field increases the number of active electrons, facilitating N-2 adsorption and N-N bond activation. Moreover, it increases the degree of orbital overlap between N-2 and SnO2/MoS2, effectively reducing the energy barrier of the rate-determining step. Benefiting from the interfacial electric field effect, the SnO2/MoS2 catalyst exhibits significant catalytic activity and selectivity towards eNRR, with an ammonia yield of 47.1 mu g h(-1) mg(-1) and a Faraday efficiency of 19.3 %, surpassing those reported for the majority of MoS2- and SnO2-based catalysts.
引用
收藏
页码:460 / 469
页数:10
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