催化作用
氧化钇稳定氧化锆
电催化剂
材料科学
法拉第效率
氧化物
电子结构
化学工程
氧化还原
过渡金属
密度泛函理论
纳米技术
无机化学
化学
工程类
电极
冶金
电化学
计算化学
物理化学
陶瓷
复合材料
生物化学
立方氧化锆
作者
Nidu Wang,Jianghua Huang,Li Chen,Yujie Wang,Dongguang Wang,Shuying Gao,Zhouhao Zhu,Baoying Guo,Hengcong Tao
标识
DOI:10.1016/j.cej.2024.150273
摘要
Constructing 2D geometric structure and optimize electronic structure of transition metal oxide have been demonstrated to be effective strategy to reinforce its electrochemical dinitrogen reduction reaction (NRR) performances. But combining these two advantages into metal oxide based electrocatalyst simultaneously to achieve synergic effects remains one technological challenge but very significant. Here, a self-sacrificing template coupling with Fe doped strategy were proposed to optimize the geometric and electronic structure of Zr-based electrocatalyst. Experimental results revealed that the optimal sample 2Fe-YSZ was endowed with uniform 2D heterostructures, rich oxygen vacancy and increased electronic density, which induced by the framework Fe element. These traits thus confer the 2Fe-YSZ produced through extensive exposure to extra active sites, significantly boosting the absorption and activation of N2 molecules. And the DFT calculation further validates the promotive effect of framework Fe. As expected, in the electrocatalytic NRR test, 2Fe-YSZ demonstrated high Faradaic efficiency (38.89 %) and NH3 yield rate (19.58 μg h−1 mg−1) at − 0.5 V in 0.1 M HCl, comparable to most Zr-based electrocatalytic materials for ambient NRR. This geometric/electronic structure engineering strategy could provide an idea the rational design of efficient NRR catalysts.
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