纳米反应器
氨
硝酸盐
碳纤维
级联
介孔材料
材料科学
纳米技术
无机化学
化学工程
化学
催化作用
有机化学
复合数
纳米颗粒
工程类
复合材料
作者
Minghao Li,Chunhong Qi,Jingsan Xu,Rujia Zou,Lianjun Wang,Wan Jiang,Yuchi Fan,Pengpeng Qiu,Wei Luo
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-03-11
卷期号:19 (11): 11309-11322
被引量:3
标识
DOI:10.1021/acsnano.5c00187
摘要
The electrochemical reduction of nitrate (NO3-) offers a promising waste-to-value strategy for synthesizing ammonia (NH3), yet it involves a complex multi-interface system with several stages such as mass transport, species enrichment, and interfacial transformation. This complexity necessitates catalysts with diverse structural characteristics across multiple temporal and spatial scales. Herein, a three-in-one nanoreactor system is designed with 1D geometry, open mesochannels, and synergistic active sites for optimized NH3 synthesis. Guided by finite element simulations, a 1D mesoporous carbon carrier is engineered to create a distinctive microenvironment that enhances NO3- transfer and adsorption while confining reaction intermediates. Meanwhile, iron single atomic sites (Fe-N4 SAs) and iron nanoclusters (Fe4 NCs) are embedded in situ into the carbon carrier, yielding an efficient cascade nanoreactor. This design demonstrates large Faraday efficiencies, rapid NO3- removal rates, and impressive NH3 yield rates under both neutral and alkaline conditions. Detailed in situ experimental results and theoretical analysis reveal that Fe-N4 SAs and Fe4 NCs can adapt their electronic structures in tandem, allowing the Fe-N4 SAs to effectively reduce NO3- and Fe4 NCs to oxidize H2O. As a demonstration, the assembled Zn-NO3- battery achieves a power density of 20.12 mW cm-2 coupled with excellent rechargeability.
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