4.2 Article

Atomically Precise Integration of Multiple Functional Motifs in Catalytic Metal-Organic Frameworks for Highly Efficient Nitrate Electroreduction

期刊

JACS AU
卷 -, 期 -, 页码 -

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacsau.2c00502

关键词

metal-organic frameworks; dynamic ligand dissociation; proton conductivity; electrical conductivity; nitrate electroreduction reaction

资金

  1. National Natural Science Foundation of China [22172075, 92156024, 21631006, 21875099, 21873045, 22033004]
  2. Fundamental Research Funds for the Central Universities in China [020514380195]
  3. National Natural Science Foundation for the Youth of China [2210050143]
  4. Beijing National Laboratory for Molecular Sciences [BNLMS202107]
  5. National Basic Research Program of China [2018YFA0306004]
  6. National Key Research and Development Program of China [2019YFC0408303]

向作者/读者索取更多资源

This study reports a catalytic metal-organic framework catalyst with multiple functional motifs, which can efficiently convert nitrate to ammonia. The catalyst has high-density reactive sites, selective reaction pathways, efficient multielectron transfer, and multiproton transport processes, leading to high yield rate, efficiency, and selectivity for ammonia production.
Ammonia production plays a central role in modern industry and agriculture with a continuous surge in its demand, yet the current industrial Haber-Bosch process suffers from low energy efficiency and accounts for high carbon emissions. Direct electrochemical conversion of nitrate to ammonia therefore emerges as an appealing approach with satisfactory sustainability while reducing the environmental impact from nitrate pollution. To this end, electrocatalysts for efficient conversion of eight-electron nitrate to ammonia require collective contributions at least from high-density reactive sites, selective reaction pathways, efficient multielectron transfer, and multiproton transport processes. Here, we report a catalytic metal-organic framework (two-dimensional (2D) In-MOF In8) catalyst integrated with multiple functional motifs with atomic precision, including uniformly dispersed, highdensity, single-atom catalytic sites, high proton conductivity (efficient proton transport channel), high electron conductivity (promoted by the redox-active ligands), and confined microporous environments. These eventually lead to a direct and efficient electrochemical reduction of nitrate to ammonia and record high yield rate, FE, and selectivity for NH3 production. A novel dynamic ligand dissociation mechanism provides an unprecedented working principle that allows for the use of a high-quality MOF crystalline structure to function as highly ordered, high-density, single-atom catalyst (SAC)-like catalytic systems and ensures the maximum utilization of the metal centers within the MOF structure. Further, the atomically precise assembly of multiple functional motifs within a MOF catalyst offers an effective and facile strategy for the future development of framework-based enzyme-mimic systems.

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