{"title":"超薄氮掺杂碳包覆镍纳米颗粒用于高效电化学CO2还原和含水Zn-CO2电池","authors":"Fangyuan Wang, Guan Wang, Peilin Deng, Yao Chen, Jing Li, Daoxiong Wu, Zhitong Wang, Chongtai Wang, Yingjie Hua, Xinlong Tian","doi":"10.1002/smll.202301128","DOIUrl":null,"url":null,"abstract":"<p>Electrochemical CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR), powered by renewable electricity, has attracted great attention for producing high value-added fuels and chemicals, as well as feasibly mitigating CO<sub>2</sub> emission problem. Here, this work reports a facile hard template strategy to prepare the Ni@N-C catalyst with core–shell structure, where nickel nanoparticles (Ni NPs) are encapsulated by thin nitrogen-doped carbon shells (N-C shells). The Ni@N-C catalyst has demonstrated a promising industrial current density of 236.7 mA cm<sup>−2</sup> with the superb FE<sub>CO</sub> of 97% at −1.1 V versus RHE. Moreover, Ni@N-C can drive the reversible Zn-CO<sub>2</sub> battery with the largest power density of 1.64 mW cm<sup>−2</sup>, and endure a tough cycling durability. These excellent performances are ascribed to the synergistic effect of Ni@N-C that Ni NPs can regulate the electronic microenvironment of N-doped carbon shells, which favor to enhance the CO<sub>2</sub> adsorption capacity and the electron transfer capacity. Density functional theory calculations prove that the binding configuration of N-C located on the top of Ni slabs (Top-Ni@N-C) is the most thermodynamically stable and possess a lowest thermodynamic barrier for the formation of COOH<sup>*</sup> and the desorption of CO. This work may pioneer a new method on seeking high-efficiency and worthwhile electrocatalysts for CO<sub>2</sub>RR and Zn-CO<sub>2</sub> battery.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"19 25","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2023-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":"{\"title\":\"Ultrathin Nitrogen-Doped Carbon Encapsulated Ni Nanoparticles for Highly Efficient Electrochemical CO2 Reduction and Aqueous Zn-CO2 Batteries\",\"authors\":\"Fangyuan Wang, Guan Wang, Peilin Deng, Yao Chen, Jing Li, Daoxiong Wu, Zhitong Wang, Chongtai Wang, Yingjie Hua, Xinlong Tian\",\"doi\":\"10.1002/smll.202301128\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Electrochemical CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR), powered by renewable electricity, has attracted great attention for producing high value-added fuels and chemicals, as well as feasibly mitigating CO<sub>2</sub> emission problem. Here, this work reports a facile hard template strategy to prepare the Ni@N-C catalyst with core–shell structure, where nickel nanoparticles (Ni NPs) are encapsulated by thin nitrogen-doped carbon shells (N-C shells). The Ni@N-C catalyst has demonstrated a promising industrial current density of 236.7 mA cm<sup>−2</sup> with the superb FE<sub>CO</sub> of 97% at −1.1 V versus RHE. Moreover, Ni@N-C can drive the reversible Zn-CO<sub>2</sub> battery with the largest power density of 1.64 mW cm<sup>−2</sup>, and endure a tough cycling durability. These excellent performances are ascribed to the synergistic effect of Ni@N-C that Ni NPs can regulate the electronic microenvironment of N-doped carbon shells, which favor to enhance the CO<sub>2</sub> adsorption capacity and the electron transfer capacity. Density functional theory calculations prove that the binding configuration of N-C located on the top of Ni slabs (Top-Ni@N-C) is the most thermodynamically stable and possess a lowest thermodynamic barrier for the formation of COOH<sup>*</sup> and the desorption of CO. This work may pioneer a new method on seeking high-efficiency and worthwhile electrocatalysts for CO<sub>2</sub>RR and Zn-CO<sub>2</sub> battery.</p>\",\"PeriodicalId\":228,\"journal\":{\"name\":\"Small\",\"volume\":\"19 25\",\"pages\":\"\"},\"PeriodicalIF\":12.1000,\"publicationDate\":\"2023-03-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/smll.202301128\",\"RegionNum\":2,\"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":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202301128","RegionNum":2,"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: 8
摘要
以可再生电力为动力的电化学CO2还原反应(CO2RR)在生产高附加值燃料和化学品以及切实缓解CO2排放问题方面受到了广泛关注。在这里,本研究报告了一种简单的硬模板策略来制备具有核壳结构的Ni@N-C催化剂,其中镍纳米颗粒(Ni NPs)被薄的氮掺杂碳壳(N-C壳)包裹。Ni@N-C催化剂在- 1.1 V时的工业电流密度为236.7 mA cm - 2, FECO为97%。此外,Ni@N-C可以驱动最大功率密度为1.64 mW cm - 2的可逆Zn-CO2电池,并具有很强的循环耐久性。这些优异的性能归因于Ni@N-C的协同效应,Ni NPs可以调节n掺杂碳壳的电子微环境,有利于提高CO2吸附能力和电子转移能力。密度功能理论计算证明,位于Ni板顶部的N-C结合构型(Top-Ni@N-C)是最稳定的热力学构型,对COOH*的形成和CO的解吸具有最低的热力学势垒。本研究为寻找高效、有价值的CO2RR和Zn-CO2电池电催化剂开辟了新途径。
Ultrathin Nitrogen-Doped Carbon Encapsulated Ni Nanoparticles for Highly Efficient Electrochemical CO2 Reduction and Aqueous Zn-CO2 Batteries
Electrochemical CO2 reduction reaction (CO2RR), powered by renewable electricity, has attracted great attention for producing high value-added fuels and chemicals, as well as feasibly mitigating CO2 emission problem. Here, this work reports a facile hard template strategy to prepare the Ni@N-C catalyst with core–shell structure, where nickel nanoparticles (Ni NPs) are encapsulated by thin nitrogen-doped carbon shells (N-C shells). The Ni@N-C catalyst has demonstrated a promising industrial current density of 236.7 mA cm−2 with the superb FECO of 97% at −1.1 V versus RHE. Moreover, Ni@N-C can drive the reversible Zn-CO2 battery with the largest power density of 1.64 mW cm−2, and endure a tough cycling durability. These excellent performances are ascribed to the synergistic effect of Ni@N-C that Ni NPs can regulate the electronic microenvironment of N-doped carbon shells, which favor to enhance the CO2 adsorption capacity and the electron transfer capacity. Density functional theory calculations prove that the binding configuration of N-C located on the top of Ni slabs (Top-Ni@N-C) is the most thermodynamically stable and possess a lowest thermodynamic barrier for the formation of COOH* and the desorption of CO. This work may pioneer a new method on seeking high-efficiency and worthwhile electrocatalysts for CO2RR and Zn-CO2 battery.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
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