4.8 Article

Efficient Electrochemical Nitrate Reduction to Ammonia with Copper-Supported Rhodium Cluster and Single-Atom Catalysts

期刊

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202202556

关键词

Ammonia Synthesis; Copper Nanowires; Electrochemical Nitrate Reduction; Hydrogen Transfer Mechanism; Single-Atom Catalysts

资金

  1. Chinese Thousand Talents Program for Young Professionals
  2. Nankai University
  3. 111 project [B16027]
  4. Spanish Ministry of Science AMP
  5. Innovation for the Ramon y Cajal Program [RYC- RYC2018-023888-I]
  6. Singapore Ministry of Education AcRF Tier 2 [2016-T2-2-153, 2016-T2-1-131]
  7. Swiss National Science Foundation [P2ELP2_199800]
  8. Singapore Ministry of Education AcRF Tier 1 [RG7/18, RG161/19]
  9. Swiss National Science Foundation (SNF) [P2ELP2_199800] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

This study demonstrates a novel electrocatalyst for the electrochemical nitrate reduction reaction (NITRR), which can efficiently produce ammonia with high efficiency. The synergistic catalytic cooperation between Rh and Cu sites enables high activity and high yield of ammonia production.
The electrochemical nitrate reduction reaction (NITRR) provides a promising solution for restoring the imbalance in the global nitrogen cycle while enabling a sustainable and decentralized route to source ammonia. Here, we demonstrate a novel electrocatalyst for NITRR consisting of Rh clusters and single-atoms dispersed onto Cu nanowires (NWs), which delivers a partial current density of 162 mA cm(-2) for NH3 production and a Faradaic efficiency (FE) of 93 % at -0.2 V vs. RHE. The highest ammonia yield rate reached a record value of 1.27 mmol h(-1) cm(-2). Detailed investigations by electron paramagnetic resonance, in situ infrared spectroscopy, differential electrochemical mass spectrometry and density functional theory modeling suggest that the high activity originates from the synergistic catalytic cooperation between Rh and Cu sites, whereby adsorbed hydrogen on Rh site transfers to vicinal *NO intermediate species adsorbed on Cu promoting the hydrogenation and ammonia formation.

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