TY - JOUR
T1 - Efficient Electrochemical Nitrate Reduction to Ammonia with Copper-Supported Rhodium Cluster and Single-Atom Catalysts
AU - Liu, Huimin
AU - Lang, Xiuyao
AU - Zhu, Chao
AU - Timoshenko, Janis
AU - Rüscher, Martina
AU - Bai, Lichen
AU - Guijarro, Néstor
AU - Yin, Haibo
AU - Peng, Yue
AU - Li, Junhua
AU - Liu, Zheng
AU - Wang, Weichao
AU - Cuenya, Beatriz Roldan
AU - Luo, Jingshan
N1 - Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2022/6/7
Y1 - 2022/6/7
N2 - 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.
AB - 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.
KW - Ammonia Synthesis
KW - Copper Nanowires
KW - Electrochemical Nitrate Reduction
KW - Hydrogen Transfer Mechanism
KW - Single-Atom Catalysts
UR - http://www.scopus.com/inward/record.url?scp=85127753413&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85127753413&partnerID=8YFLogxK
U2 - 10.1002/anie.202202556
DO - 10.1002/anie.202202556
M3 - Article
C2 - 35297151
AN - SCOPUS:85127753413
SN - 1433-7851
VL - 61
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 23
M1 - e202202556
ER -