Bin Kui , Shuang Zhao , Yunhong Hu , Kai Zheng , Yuanhui Yao , Song Chen , Nana Wang , Peng Gao , Zhongchao Bai , Wei Ye
{"title":"强耦合Ag/Cu与MXene用于高效串联硝酸还原反应和硝酸锌电池†","authors":"Bin Kui , Shuang Zhao , Yunhong Hu , Kai Zheng , Yuanhui Yao , Song Chen , Nana Wang , Peng Gao , Zhongchao Bai , Wei Ye","doi":"10.1039/d4cy01511h","DOIUrl":null,"url":null,"abstract":"<div><div>The electrochemical conversion of nitrate ions into valuable ammonia represents a sustainable alternative to the traditional Haber–Bosch process. However, ammonia electrosynthesis from nitrate reduction is still limited by the low catalytic activity and faradaic efficiency. This work puts forward a two-step tandem strategy for nitrate reduction to ammonia by integrating charge polarized Ag nanoparticles and Cu nanoclusters on MXene to boost the electrocatalytic performance. The strongly coupled Ag nanoparticles/Cu clusters with MXene result in polarized Ag<sup><em>δ</em>+</sup>/Cu<sup><em>δ</em>+</sup>, which preferentially catalyzes NO<sub>3</sub><sup>−</sup> → NO<sub>2</sub><sup>−</sup> and NO<sub>2</sub><sup>−</sup> → NH<sub>3</sub> conversions, respectively. The synthesized Ag/Cu/MXene composite sample achieves an ammonia yield rate of 10.3 mol g<sub>cat.</sub><sup>−1</sup> h<sup>−1</sup> and a faradaic efficiency of 87.7% at −1.0 V <em>versus</em> a reversible hydrogen electrode, as well as good cycling stability. The composite was assembled into a zinc–nitrate battery as the cathode; the open-circuit voltage of the battery reaches 1.81 V, with a maximum output power density of 5.75 mW cm<sup>−2</sup>, demonstrating potential application value.</div></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":"15 5","pages":"Pages 1617-1626"},"PeriodicalIF":4.2000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Strongly coupled Ag/Cu with MXene for efficient tandem nitrate reduction reaction and zinc–nitrate batteries†\",\"authors\":\"Bin Kui , Shuang Zhao , Yunhong Hu , Kai Zheng , Yuanhui Yao , Song Chen , Nana Wang , Peng Gao , Zhongchao Bai , Wei Ye\",\"doi\":\"10.1039/d4cy01511h\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The electrochemical conversion of nitrate ions into valuable ammonia represents a sustainable alternative to the traditional Haber–Bosch process. However, ammonia electrosynthesis from nitrate reduction is still limited by the low catalytic activity and faradaic efficiency. This work puts forward a two-step tandem strategy for nitrate reduction to ammonia by integrating charge polarized Ag nanoparticles and Cu nanoclusters on MXene to boost the electrocatalytic performance. The strongly coupled Ag nanoparticles/Cu clusters with MXene result in polarized Ag<sup><em>δ</em>+</sup>/Cu<sup><em>δ</em>+</sup>, which preferentially catalyzes NO<sub>3</sub><sup>−</sup> → NO<sub>2</sub><sup>−</sup> and NO<sub>2</sub><sup>−</sup> → NH<sub>3</sub> conversions, respectively. The synthesized Ag/Cu/MXene composite sample achieves an ammonia yield rate of 10.3 mol g<sub>cat.</sub><sup>−1</sup> h<sup>−1</sup> and a faradaic efficiency of 87.7% at −1.0 V <em>versus</em> a reversible hydrogen electrode, as well as good cycling stability. The composite was assembled into a zinc–nitrate battery as the cathode; the open-circuit voltage of the battery reaches 1.81 V, with a maximum output power density of 5.75 mW cm<sup>−2</sup>, demonstrating potential application value.</div></div>\",\"PeriodicalId\":66,\"journal\":{\"name\":\"Catalysis Science & Technology\",\"volume\":\"15 5\",\"pages\":\"Pages 1617-1626\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-01-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Science & Technology\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2044475325000462\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2044475325000462","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Strongly coupled Ag/Cu with MXene for efficient tandem nitrate reduction reaction and zinc–nitrate batteries†
The electrochemical conversion of nitrate ions into valuable ammonia represents a sustainable alternative to the traditional Haber–Bosch process. However, ammonia electrosynthesis from nitrate reduction is still limited by the low catalytic activity and faradaic efficiency. This work puts forward a two-step tandem strategy for nitrate reduction to ammonia by integrating charge polarized Ag nanoparticles and Cu nanoclusters on MXene to boost the electrocatalytic performance. The strongly coupled Ag nanoparticles/Cu clusters with MXene result in polarized Agδ+/Cuδ+, which preferentially catalyzes NO3− → NO2− and NO2− → NH3 conversions, respectively. The synthesized Ag/Cu/MXene composite sample achieves an ammonia yield rate of 10.3 mol gcat.−1 h−1 and a faradaic efficiency of 87.7% at −1.0 V versus a reversible hydrogen electrode, as well as good cycling stability. The composite was assembled into a zinc–nitrate battery as the cathode; the open-circuit voltage of the battery reaches 1.81 V, with a maximum output power density of 5.75 mW cm−2, demonstrating potential application value.
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
Impact factor: 5.0
Time to first decision (peer reviewed only): 31 days