电催化剂
材料科学
兴奋剂
多孔性
碳纤维
无机化学
纳米技术
化学工程
电化学
金属
电极
物理化学
化学
光电子学
复合材料
复合数
工程类
冶金
作者
Yan Liu,Qiuyao Li,Xu Guo,Xiangdong Kong,Jingwen Ke,Mingfang Chi,Qunxiang Li,Zhigang Geng,Jie Zeng
标识
DOI:10.1002/adma.201907690
摘要
Abstract N 2 electroreduction into NH 3 represents an attractive prospect for N 2 utilization. Nevertheless, this process suffers from low Faraday efficiency (FE) and yield rate for NH 3 . In this work, a highly efficient metal‐free catalyst is developed by introducing F atoms into a 3D porous carbon framework (F‐doped carbon) toward N 2 electroreduction. At −0.2 V versus reversible hydrogen electrode (RHE), the F‐doped carbon achieves the highest FE of 54.8% for NH 3 , which is 3.0 times as high as that (18.3%) of pristine carbon frameworks. Notably, at −0.3 V versus RHE, the yield rate of F‐doped carbon for NH 3 reaches 197.7 µg NH3 mg −1 cat. h −1 . Such a value is more than one order of magnitude higher than those of other metal‐free electrocatalysts under the near‐ambient conditions for NH 3 product to date. Mechanistic studies reveal that the improved performance in N 2 electroreduction for F‐doped carbon originates from the enhanced binding strength of N 2 and the facilitated dissociation of N 2 into *N 2 H. F bonding to C atom creates a Lewis acid site due to the different electronegativity between the F and C atoms. As such, the repulsive interaction between the Lewis acid site and proton H suppresses the activity of H 2 evolution reaction, thus enhancing the selectivity of N 2 electroreduction into NH 3 .
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