{"title":"通过磷诱导的活性氢调制促进串联硝酸盐制氨电催化。","authors":"Xing Yan, Yuxiang Li, Junliang Xie, Tingyi Weng, Yanhui Liu, Wen Shen, Fang Jiang* and Huan Chen*, ","doi":"10.1021/acsami.5c11589","DOIUrl":null,"url":null,"abstract":"<p >The electrocatalytic nitrate reduction reaction (NO<sub>3</sub>RR) offers a sustainable route for ammonia synthesis while addressing nitrate pollution, yet it faces challenges such as sluggish kinetics, competing hydrogen evolution reaction (HER), and poor selectivity under high current densities. Herein, we report a phosphorus-doped Co(OH)<sub>2</sub>/Cu nanowire (P–Co(OH)<sub>2</sub>/Cu NW) tandem catalyst engineered via in situ reconstruction, which achieves exceptional NO<sub>3</sub>RR performance through synergistic dual-site mechanisms. The Cu phase promotes NO<sub>3</sub><sup>–</sup> adsorption and activation, Co(OH)<sub>2</sub> facilitates ammonia formation, while P doping induces water dissociation to generate *H for hydrogenation instead of H<sub>2</sub> evolution. In 1 M KOH + 0.1 M NO<sub>3</sub><sup>–</sup>, the catalyst delivers a record ammonia yield of 110.14 mg h<sup>–1</sup> cm<sup>–2</sup> with 95.13% Faradaic efficiency at −0.8 V vs RHE and industrially relevant current densities (−1 A cm<sup>–2</sup> at −0.55 V). In situ spectroscopic studies reveal that P doping modulates interfacial water structure, accelerating *H generation and optimizing the tandem pathway. Further, a Zn-NO<sub>3</sub><sup>–</sup> battery integrating this cathode achieves simultaneous power output (28.4 mW cm<sup>–2</sup>) and ammonia production (6.65 mg h<sup>–1</sup> cm<sup>–2</sup>, FE: 90.8%), demonstrating its practical viability.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 33","pages":"47094–47105"},"PeriodicalIF":8.2000,"publicationDate":"2025-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Boosting Tandem Nitrate-to-Ammonia Electrocatalysis via Phosphorus-Induced Active Hydrogen Modulation\",\"authors\":\"Xing Yan, Yuxiang Li, Junliang Xie, Tingyi Weng, Yanhui Liu, Wen Shen, Fang Jiang* and Huan Chen*, \",\"doi\":\"10.1021/acsami.5c11589\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The electrocatalytic nitrate reduction reaction (NO<sub>3</sub>RR) offers a sustainable route for ammonia synthesis while addressing nitrate pollution, yet it faces challenges such as sluggish kinetics, competing hydrogen evolution reaction (HER), and poor selectivity under high current densities. Herein, we report a phosphorus-doped Co(OH)<sub>2</sub>/Cu nanowire (P–Co(OH)<sub>2</sub>/Cu NW) tandem catalyst engineered via in situ reconstruction, which achieves exceptional NO<sub>3</sub>RR performance through synergistic dual-site mechanisms. The Cu phase promotes NO<sub>3</sub><sup>–</sup> adsorption and activation, Co(OH)<sub>2</sub> facilitates ammonia formation, while P doping induces water dissociation to generate *H for hydrogenation instead of H<sub>2</sub> evolution. In 1 M KOH + 0.1 M NO<sub>3</sub><sup>–</sup>, the catalyst delivers a record ammonia yield of 110.14 mg h<sup>–1</sup> cm<sup>–2</sup> with 95.13% Faradaic efficiency at −0.8 V vs RHE and industrially relevant current densities (−1 A cm<sup>–2</sup> at −0.55 V). In situ spectroscopic studies reveal that P doping modulates interfacial water structure, accelerating *H generation and optimizing the tandem pathway. Further, a Zn-NO<sub>3</sub><sup>–</sup> battery integrating this cathode achieves simultaneous power output (28.4 mW cm<sup>–2</sup>) and ammonia production (6.65 mg h<sup>–1</sup> cm<sup>–2</sup>, FE: 90.8%), demonstrating its practical viability.</p>\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"17 33\",\"pages\":\"47094–47105\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-08-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsami.5c11589\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsami.5c11589","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
电催化硝酸还原反应(NO3RR)在解决硝酸盐污染的同时为氨合成提供了一条可持续的途径,但它面临动力学缓慢、析氢反应(HER)竞争以及高电流密度下选择性差等挑战。本文报道了一种通过原位重构设计的磷掺杂Co(OH)2/Cu纳米线(P-Co(OH)2/Cu NW)串联催化剂,该催化剂通过协同双位点机制实现了卓越的NO3RR性能。Cu相促进NO3-的吸附和活化,Co(OH)2促进氨的形成,P掺杂诱导水解离生成*H进行加氢而不是析氢。在1 M KOH + 0.1 M NO3-条件下,该催化剂在-0.8 V vs RHE和工业相关电流密度(- 0.55 V时-1 a cm-2)下的氨产量为110.14 mg h-1 cm-2,具有95.13%的法拉第效率。原位光谱研究表明,P掺杂调节了界面水结构,加速了*H的生成,优化了串联途径。此外,集成该阴极的Zn-NO3-电池实现了同时输出功率(28.4 mW cm-2)和氨产量(6.65 mg h-1 cm-2, FE: 90.8%),证明了其实际可行性。
Boosting Tandem Nitrate-to-Ammonia Electrocatalysis via Phosphorus-Induced Active Hydrogen Modulation
The electrocatalytic nitrate reduction reaction (NO3RR) offers a sustainable route for ammonia synthesis while addressing nitrate pollution, yet it faces challenges such as sluggish kinetics, competing hydrogen evolution reaction (HER), and poor selectivity under high current densities. Herein, we report a phosphorus-doped Co(OH)2/Cu nanowire (P–Co(OH)2/Cu NW) tandem catalyst engineered via in situ reconstruction, which achieves exceptional NO3RR performance through synergistic dual-site mechanisms. The Cu phase promotes NO3– adsorption and activation, Co(OH)2 facilitates ammonia formation, while P doping induces water dissociation to generate *H for hydrogenation instead of H2 evolution. In 1 M KOH + 0.1 M NO3–, the catalyst delivers a record ammonia yield of 110.14 mg h–1 cm–2 with 95.13% Faradaic efficiency at −0.8 V vs RHE and industrially relevant current densities (−1 A cm–2 at −0.55 V). In situ spectroscopic studies reveal that P doping modulates interfacial water structure, accelerating *H generation and optimizing the tandem pathway. Further, a Zn-NO3– battery integrating this cathode achieves simultaneous power output (28.4 mW cm–2) and ammonia production (6.65 mg h–1 cm–2, FE: 90.8%), demonstrating its practical viability.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.