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用于合成氨的基于石墨炔的金属原子催化剂。

Graphdiyne-based metal atomic catalysts for synthesizing ammonia.

作者信息

Yu Huidi, Xue Yurui, Hui Lan, Zhang Chao, Fang Yan, Liu Yuxin, Chen Xi, Zhang Danyan, Huang Bolong, Li Yuliang

机构信息

Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, China.

出版信息

Natl Sci Rev. 2020 Aug 28;8(8):nwaa213. doi: 10.1093/nsr/nwaa213. eCollection 2021 Aug.

Abstract

Development of novel catalysts for nitrogen reduction at ambient pressures and temperatures with ultrahigh ammonia (NH) yield and selectivity is challenging. In this work, an atomic catalyst with separated Pd atoms on graphdiyne (Pd-GDY) was synthesized, which shows fascinating electrocatalytic properties for nitrogen reduction. The catalyst has the highest average NH yield of 4.45 ± 0.30 mg mg h, almost tens of orders larger than for previously reported catalysts, and 100% reaction selectivity in neutral media. Pd-GDY exhibits almost no decreases in NH yield and Faradaic efficiency. Density functional theory calculations show that the reaction pathway prefers to perform at the (Pd, C1, C2) active area because of the strongly coupled (Pd, C1, C2), which elevates the selectivity via enhanced electron transfer. By adjusting the coupling accurately, reduction of self-activated nitrogen is promoted by anchoring atom selection, and side effects are minimized.

摘要

开发在环境压力和温度下具有超高氨(NH₃)产率和选择性的新型氮还原催化剂具有挑战性。在这项工作中,合成了一种在石墨炔(Pd-GDY)上具有分离钯原子的原子催化剂,该催化剂对氮还原显示出迷人的电催化性能。该催化剂的平均NH₃产率最高可达4.45±0.30 mg mg⁻¹ h⁻¹,几乎比先前报道的催化剂高出数十个数量级,并且在中性介质中具有100%的反应选择性。Pd-GDY的NH₃产率和法拉第效率几乎没有下降。密度泛函理论计算表明,由于(Pd, C1, C2)的强耦合,反应途径更倾向于在(Pd, C1, C2)活性区域进行,这通过增强电子转移提高了选择性。通过精确调整耦合,通过锚定原子选择促进了自活化氮的还原,并将副作用降至最低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1458/8363333/0a772653db92/nwaa213fig1.jpg

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