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在氮掺杂碳上使用协同钌基纳米合金实现高效中性硝酸盐到氨的电合成

Efficient Neutral Nitrate-to-Ammonia Electrosynthesis Using Synergistic Ru-Based Nanoalloys on Nitrogen-Doped Carbon.

作者信息

Huang Lisi, Zhang Pingzhi, Ge Xin, Wang Bingyu, Yuan Jili, Li Wei, Zhang Jian, Zhang Baohua, Hanay Ozge, Wang Liang

机构信息

Department of Polymer Materials and Engineering, College of Materials & Metallurgy, Guizhou University, Huaxi District, Guiyang, 550025, People's Republic of China.

State Key Laboratory of Green Pesticide, Center for R&D of Fine Chemicals of Guizhou University, Guiyang, 550025, People's Republic of China.

出版信息

Nanomicro Lett. 2025 Sep 15;18(1):66. doi: 10.1007/s40820-025-01896-w.

Abstract

Electrocatalytic nitrate reduction reaction (NORR) represents a sustainable and environmentally benign route for ammonia (NH) synthesis. However, NORR is still limited by the competition from hydrogen evolution reaction (HER) and the high energy barrier in the hydrogenation step of nitrogen-containing intermediates. Here, we report a selective etching strategy to construct RuM nanoalloys (M = Fe, Co, Ni, Cu) uniformly dispersed on porous nitrogen-doped carbon substrates for efficient neutral NH electrosynthesis. Density functional theory calculations confirm that the synergic effect between Ru and transition metal M modulates the electronic structure of the alloy, significantly lowering the energy barrier for the conversion of *NO to *HNO. Experimentally, the optimized RuFe-NC catalyst achieves 100% Faraday efficiency with a high yield rate of 0.83 mg h mg at a low potential of - 0.1 V vs. RHE, outperforming most reported catalysts. In situ spectroscopic analyses further demonstrate that the RuM-NC effectively promotes the hydrogenation of nitrogen intermediates while inhibiting the formation of hydrogen radicals, thereby reducing HER competition. The RuFe-NC assembled Zn-NO battery achieved a high open-circuit voltage and an outstanding power density and capacity, which drive selective NO conversion to NH. This work provides a powerful synergistic design strategy for efficient NH electrosynthesis and a general framework for the development of advanced multi-component catalysts for sustainable nitrogen conversion.

摘要

电催化硝酸盐还原反应(NORR)是一种可持续且环境友好的合成氨(NH₃)途径。然而,NORR仍受到析氢反应(HER)竞争以及含氮中间体氢化步骤中高能量壁垒的限制。在此,我们报道了一种选择性蚀刻策略,用于构建均匀分散在多孔氮掺杂碳基底上的RuM纳米合金(M = Fe、Co、Ni、Cu),以实现高效的中性NH₃电合成。密度泛函理论计算证实,Ru与过渡金属M之间的协同效应调节了合金的电子结构,显著降低了NO转化为HNO的能量壁垒。实验上,优化后的RuFe-NC催化剂在相对于可逆氢电极(RHE)为 -0.1 V的低电位下,实现了100%的法拉第效率,产率高达0.83 mg h⁻¹ mgcat⁻¹,性能优于大多数已报道的催化剂。原位光谱分析进一步表明,RuM-NC有效地促进了氮中间体的氢化,同时抑制了氢自由基的形成,从而减少了HER的竞争。RuFe-NC组装的Zn-NO电池实现了高开路电压、出色的功率密度和容量,可驱动NO选择性转化为NH₃。这项工作为高效NH₃电合成提供了一种强大的协同设计策略,并为开发用于可持续氮转化的先进多组分催化剂提供了一个通用框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eff/12436672/c5d2b2a5029c/40820_2025_1896_Fig1_HTML.jpg

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