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掺硫石墨烯用于高效电催化 N 到 NH 的固定。

Sulfur-doped graphene for efficient electrocatalytic N-to-NH fixation.

机构信息

College of Chemistry and Materials Science, Sichuan Normal University, Chengdu 610068, Sichuan, China.

出版信息

Chem Commun (Camb). 2019 Mar 14;55(23):3371-3374. doi: 10.1039/c9cc00602h.

Abstract

Industrial NH3 synthesis mainly relies on the carbon-emitting Haber-Bosch process operating under severe conditions. Electrocatalytic N2-to-NH3 fixation under ambient conditions is an attractive approach to reduce energy consumption and avoid direct carbon emission. In this communication, sulfur-doped graphene (S-G) is proposed as an efficient and stable electrocatalyst to drive the nitrogen reduction reaction (NRR) under ambient conditions. In 0.1 M HCl, this S-G attains a remarkably large NH3 yield of 27.3 μg h-1 mgcat.-1 and a high Faradaic efficiency of 11.5% at -0.6 and -0.5 V vs. a reversible hydrogen electrode, respectively, much higher than those of undoped G (6.25 μg h-1 mgcat.-1; 0.52%). Density functional theory calculations reveal that carbon atoms close to substituted sulfur atoms are the underlying catalytic active sites for the NRR on S-G, and the related NRR mechanism is also explored.

摘要

工业氨合成主要依赖于在恶劣条件下运行的碳排放 Haber-Bosch 工艺。在环境条件下电催化 N2 到 NH3 的固定是一种很有吸引力的方法,可以降低能耗并避免直接碳排放。在本通讯中,提出了掺硫石墨烯 (S-G) 作为一种高效稳定的电催化剂,可在环境条件下驱动氮气还原反应 (NRR)。在 0.1 M HCl 中,与未掺杂的 G(6.25 μg h-1 mgcat.-1;0.52%)相比,S-G 在-0.6 和-0.5 V 相对于可逆氢电极时分别获得了高达 27.3 μg h-1 mgcat.-1 和 11.5%的高法拉第效率的显著大的 NH3 产率。密度泛函理论计算表明,取代硫原子附近的碳原子是 S-G 上 NRR 的潜在催化活性位,还探索了相关的 NRR 机制。

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