掺杂剂
法拉第效率
催化作用
离解(化学)
氮气
材料科学
密度泛函理论
石墨氮化碳
化学工程
光催化
氧化还原
吸附
化学
纳米技术
兴奋剂
无机化学
硫黄
光化学
电极
物理化学
电化学
计算化学
光电子学
有机化学
冶金
工程类
作者
Ke Chu,Qing-qing Li,Yaping Liu,Jing Wang,Yonghua Cheng
标识
DOI:10.1016/j.apcatb.2020.118693
摘要
Exploring active and durable metal-free electrocatalysts represents a promising direction for electrocatalytic N2 reduction reaction (NRR). Herein, by filling the nitrogen vacancies (NVs) with S dopants in graphitic C3N4, we showed that the resultant S-NV-C3N4 could be an efficient and robust metal-free NRR catalyst in neutral solution. S-NV-C3N4 with a high S concentration of 5.2 at.% exhibited a fascinating NRR performance with an NH3 yield of 32.7 μg h−1 mg−1 and a Faradaic efficiency of 14.1 % at −0.4 V (vs. RHE), considerably outperforming pristine C3N4 and NV-containing C3N4. S-NV-C3N4 also showed exceptional durability for at least 20 h, in stark contrast to the inferior stability of NV-containing C3N4. Density functional theory calculations disclosed that the filled S dopants could break the scaling relation to effectively stabilize *N2H and destabilize *NH2 on S-NV-C3N4, leading to more optimized adsorption of NRR intermediates and a significantly reduced energy barrier. Meanwhile, the competitive HER can be effectively suppressed on S-NV-C3N4 due to the high energy barrier for water dissociation.
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