Merfat M Alsabban, Karthik Peramaiah, Alessandro Genovese, Rafia Ahmad, Luis Miguel Azofra, Vinoth Ramalingam, Mohamed N Hedhili, Nimer Wehbe, Luigi Cavallo, Kuo-Wei Huang
{"title":"通过掺硼实现 MoxSy 的界面工程,实现 N2 到 NH3 的电化学转化。","authors":"Merfat M Alsabban, Karthik Peramaiah, Alessandro Genovese, Rafia Ahmad, Luis Miguel Azofra, Vinoth Ramalingam, Mohamed N Hedhili, Nimer Wehbe, Luigi Cavallo, Kuo-Wei Huang","doi":"10.1002/adma.202405578","DOIUrl":null,"url":null,"abstract":"<p><p>The electrocatalytic synthesis of ammonia (NH<sub>3</sub>) through the nitrogen reduction reaction (NRR) under ambient temperature and pressure is emerging as an alternative approach to the conventional Haber-Bosch process. However, it remains a significant challenge due to poor kinetics, low nitrogen (N<sub>2</sub>) solubility in aqueous electrolytes, and the competing hydrogen evolution reaction (HER), which can significantly impact NH<sub>3</sub> production rates and Faradaic efficiency (FE). Herein, a rationally designed boron-doped molybdenum sulfide (B-Mo-Mo<sub>x</sub>S<sub>y</sub>) electrocatalyst is reported that effectively enhances N<sub>2</sub> reduction to NH<sub>3</sub> with an onset potential of -0.15 V versus RHE, achieving a FE of 78% and an NH<sub>3</sub> yield of 5.83 µg h⁻¹ cm⁻<sup>2</sup> in a 0.05 m H<sub>2</sub>SO<sub>4</sub>(aq). Theoretical studies suggest that the effectiveness of NRR originates from electron density redistribution due to boron (B) doping, which provides an ideal pathway for nitrogenous species to bind with electron-deficient B sites. This work demonstrates a significant exploration, showing that Mo-based electrocatalysts are capable of facilitating artificial N<sub>2</sub> fixation.</p>","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":null,"pages":null},"PeriodicalIF":27.4000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interfacial Engineering of Mo<sub>x</sub>S<sub>y</sub> via Boron-Doping for Electrochemical N<sub>2</sub>-to-NH<sub>3</sub> Conversion.\",\"authors\":\"Merfat M Alsabban, Karthik Peramaiah, Alessandro Genovese, Rafia Ahmad, Luis Miguel Azofra, Vinoth Ramalingam, Mohamed N Hedhili, Nimer Wehbe, Luigi Cavallo, Kuo-Wei Huang\",\"doi\":\"10.1002/adma.202405578\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The electrocatalytic synthesis of ammonia (NH<sub>3</sub>) through the nitrogen reduction reaction (NRR) under ambient temperature and pressure is emerging as an alternative approach to the conventional Haber-Bosch process. However, it remains a significant challenge due to poor kinetics, low nitrogen (N<sub>2</sub>) solubility in aqueous electrolytes, and the competing hydrogen evolution reaction (HER), which can significantly impact NH<sub>3</sub> production rates and Faradaic efficiency (FE). Herein, a rationally designed boron-doped molybdenum sulfide (B-Mo-Mo<sub>x</sub>S<sub>y</sub>) electrocatalyst is reported that effectively enhances N<sub>2</sub> reduction to NH<sub>3</sub> with an onset potential of -0.15 V versus RHE, achieving a FE of 78% and an NH<sub>3</sub> yield of 5.83 µg h⁻¹ cm⁻<sup>2</sup> in a 0.05 m H<sub>2</sub>SO<sub>4</sub>(aq). Theoretical studies suggest that the effectiveness of NRR originates from electron density redistribution due to boron (B) doping, which provides an ideal pathway for nitrogenous species to bind with electron-deficient B sites. This work demonstrates a significant exploration, showing that Mo-based electrocatalysts are capable of facilitating artificial N<sub>2</sub> fixation.</p>\",\"PeriodicalId\":114,\"journal\":{\"name\":\"Advanced Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":27.4000,\"publicationDate\":\"2024-11-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adma.202405578\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adma.202405578","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
摘要
在常温常压下通过氮还原反应(NRR)电催化合成氨(NH3)正在成为传统哈伯-博什工艺的一种替代方法。然而,由于动力学性能差、氮气(N2)在水性电解质中的溶解度低以及相互竞争的氢气进化反应(HER)会严重影响 NH3 的生产率和法拉第效率(FE),因此这仍然是一个巨大的挑战。本文报告了一种合理设计的掺硼硫化钼(B-Mo-MoxSy)电催化剂,它能有效提高 N2 还原成 NH3 的能力,与 RHE 相比,起始电位为 -0.15 V,在 0.05 m H2SO4(aq) 中的 FE 为 78%,NH3 产量为 5.83 µg h-¹ cm-2。理论研究表明,NRR 的有效性源于硼(B)掺杂导致的电子密度重新分布,这为含氮物质与电子缺乏的 B 位点结合提供了理想途径。这项工作进行了重要的探索,表明钼基电催化剂能够促进人工固定氮气。
Interfacial Engineering of MoxSy via Boron-Doping for Electrochemical N2-to-NH3 Conversion.
The electrocatalytic synthesis of ammonia (NH3) through the nitrogen reduction reaction (NRR) under ambient temperature and pressure is emerging as an alternative approach to the conventional Haber-Bosch process. However, it remains a significant challenge due to poor kinetics, low nitrogen (N2) solubility in aqueous electrolytes, and the competing hydrogen evolution reaction (HER), which can significantly impact NH3 production rates and Faradaic efficiency (FE). Herein, a rationally designed boron-doped molybdenum sulfide (B-Mo-MoxSy) electrocatalyst is reported that effectively enhances N2 reduction to NH3 with an onset potential of -0.15 V versus RHE, achieving a FE of 78% and an NH3 yield of 5.83 µg h⁻¹ cm⁻2 in a 0.05 m H2SO4(aq). Theoretical studies suggest that the effectiveness of NRR originates from electron density redistribution due to boron (B) doping, which provides an ideal pathway for nitrogenous species to bind with electron-deficient B sites. This work demonstrates a significant exploration, showing that Mo-based electrocatalysts are capable of facilitating artificial N2 fixation.
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.