{"title":"A Cu-Cu2O/Ni2P Heterostructure for Efficient Tandem Catalysis of Electrosynthesis of Ammonia from Nitrate Reduction Reaction in Neutral Medium","authors":"Huilin Zhao, Pengfei Liu, Xuetao Cheng, Chao Fan, Jian Liu, Dongxiao Kan, Yan-Qin Wang","doi":"10.1002/adfm.202425459","DOIUrl":null,"url":null,"abstract":"<p>Electrochemical nitrate reduction to ammonia (eNO<sub>3</sub>RR) in neutral conditions is an effective and sustainable method for ammonia production while treating nitrate pollution. Nevertheless, it still faces a great challenge due to the complicated multiple proton-coupled-electron process in eNO<sub>3</sub>RR. Herein, an efficient heterostructure electrocatalyst Cu-Cu<sub>2</sub>O/Ni<sub>2</sub>P has been successfully fabricated for neutral ammonia electrosynthesis from nitrate reduction. Cu-Cu<sub>2</sub>O/Ni<sub>2</sub>P exhibits outstanding eNO<sub>3</sub>RR performance with a Faradaic efficiency (FE) as high as 96.4% and ammonia yield rate of 14636 µg·h<sup>−1</sup>·cm<sup>−2</sup> at −1.0 V (vs RHE) in 0.1 <span>m</span> PBS solution, which outperforms most of the reported eNO<sub>3</sub>RR electrocatalysts in neutral media. More importantly, the catalyst demonstrates an exceptional stability for 30 consecutive electrolysis cycles and outstanding durability even at large current density of 440 mA cm<sup>−2</sup> in a flow cell. The tandem catalysis mechanism of NO<sub>3</sub><sup>−</sup> → NO<sub>2</sub><sup>−</sup> → NH<sub>3</sub> by the synergism of two components of Cu-Cu<sub>2</sub>O and Ni<sub>2</sub>P in Cu-Cu<sub>2</sub>O/Ni<sub>2</sub>P is verified by the experimental and theoretical calculations. Cu-Cu<sub>2</sub>O has strong adsorption capacity for NO<sub>3</sub><sup>−</sup> and which can be reduced into NO<sub>2</sub><sup>−</sup>, while Ni<sub>2</sub>P can facilitate the water splitting, which promotes the abundant *H production, thus boosting the subsequent hydrogenation process during eNO<sub>3</sub>RR process whilst inhibiting the competitive hydrogen evolution reaction (HER).</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"35 27","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/adfm.202425459","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Electrochemical nitrate reduction to ammonia (eNO3RR) in neutral conditions is an effective and sustainable method for ammonia production while treating nitrate pollution. Nevertheless, it still faces a great challenge due to the complicated multiple proton-coupled-electron process in eNO3RR. Herein, an efficient heterostructure electrocatalyst Cu-Cu2O/Ni2P has been successfully fabricated for neutral ammonia electrosynthesis from nitrate reduction. Cu-Cu2O/Ni2P exhibits outstanding eNO3RR performance with a Faradaic efficiency (FE) as high as 96.4% and ammonia yield rate of 14636 µg·h−1·cm−2 at −1.0 V (vs RHE) in 0.1 m PBS solution, which outperforms most of the reported eNO3RR electrocatalysts in neutral media. More importantly, the catalyst demonstrates an exceptional stability for 30 consecutive electrolysis cycles and outstanding durability even at large current density of 440 mA cm−2 in a flow cell. The tandem catalysis mechanism of NO3− → NO2− → NH3 by the synergism of two components of Cu-Cu2O and Ni2P in Cu-Cu2O/Ni2P is verified by the experimental and theoretical calculations. Cu-Cu2O has strong adsorption capacity for NO3− and which can be reduced into NO2−, while Ni2P can facilitate the water splitting, which promotes the abundant *H production, thus boosting the subsequent hydrogenation process during eNO3RR process whilst inhibiting the competitive hydrogen evolution reaction (HER).
中性条件下电化学硝酸还原制氨(eNO3RR)是一种有效且可持续的制氨处理硝酸盐污染的方法。然而,由于en3rr中复杂的多质子-电子耦合过程,它仍然面临着很大的挑战。本文成功制备了一种高效的异质结构电催化剂Cu-Cu2O/Ni2P,用于硝酸还原电合成中性氨。Cu-Cu2O/Ni2P表现出优异的en3rr性能,在- 1.0 V (vs RHE)条件下,在0.1 m PBS溶液中,Faradaic效率(FE)高达96.4%,氨收率为14636µg·h−1·cm−2,优于大多数已报道的中性介质中的en3rr电催化剂。更重要的是,该催化剂在连续30次电解循环中表现出优异的稳定性,即使在440 mA cm−2的大电流密度下,也表现出出色的耐久性。通过实验和理论计算验证了Cu-Cu2O/Ni2P中Cu-Cu2O和Ni2P两组分协同作用NO3−→NO2−→NH3的串联催化机理。Cu-Cu2O对NO3−具有较强的吸附能力,可以还原为NO2−,而Ni2P有利于水的裂解,促进了丰富的*H生成,从而促进了eNO3RR过程的后续加氢过程,同时抑制了竞争性析氢反应(HER)。
期刊介绍:
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