Zhichao Xue, Yingyi Ru, Qiang Li, Xiaolong Liang, Ying Ma, Hong Sun and Ying Lv
{"title":"用于高能量密度光助二氧化硫锂电池的 Z 型 g-C3N4/TiO2 异质结†。","authors":"Zhichao Xue, Yingyi Ru, Qiang Li, Xiaolong Liang, Ying Ma, Hong Sun and Ying Lv","doi":"10.1039/D4TC01832J","DOIUrl":null,"url":null,"abstract":"<p >A lithium–oxygen battery based on the formation of lithium oxide (Li<small><sub>2</sub></small>O) can theoretically achieve a high energy density through a four-electron reaction. This is more challenging to accomplish than the one- and two-electron reactions that produce lithium superoxide (LiO<small><sub>2</sub></small>) and lithium peroxide (Li<small><sub>2</sub></small>O<small><sub>2</sub></small>), respectively. A stable cathode with a sufficient supply of electrons and Li cations to form Li<small><sub>2</sub></small>O must be developed to achieve a four-electron reaction for a lithium–oxygen battery. Herein, by utilizing a composite 3D-printed cathode composed of a g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>/TiO<small><sub>2</sub></small> (gCNTO) heterostructure nanoparticle with high porosity and high conductivity, we were able to provide ample space and numerous active/catalytic sites during the reaction process. Our findings indicate that Li<small><sub>2</sub></small>O is the product of the photo-assisted lithium–oxygen battery. Under illumination, the battery can be rechargeable for over 1000 hours at 0.05 mA cm<small><sup>−2</sup></small> with a small polarization gap. The photocathode delivers an ultra-high discharge capacity of 29.7 mA h cm<small><sup>−2</sup></small> at 0.5 mA cm<small><sup>−2</sup></small>, resulting in a specific energy of approximately 515.12 W h kg<small><sup>−1</sup></small><small><sub>cell</sub></small>. The performance is superior to the battery with Li<small><sub>2</sub></small>O<small><sub>2</sub></small> as a discharge product in the dark. This study paves the way for the rapid development of high-energy-density photo-assisted Li–O<small><sub>2</sub></small> batteries.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":null,"pages":null},"PeriodicalIF":8.3000,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Z-Scheme g-C3N4/TiO2 heterojunction for a high energy density photo-assisted Li–O2 battery†\",\"authors\":\"Zhichao Xue, Yingyi Ru, Qiang Li, Xiaolong Liang, Ying Ma, Hong Sun and Ying Lv\",\"doi\":\"10.1039/D4TC01832J\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A lithium–oxygen battery based on the formation of lithium oxide (Li<small><sub>2</sub></small>O) can theoretically achieve a high energy density through a four-electron reaction. This is more challenging to accomplish than the one- and two-electron reactions that produce lithium superoxide (LiO<small><sub>2</sub></small>) and lithium peroxide (Li<small><sub>2</sub></small>O<small><sub>2</sub></small>), respectively. A stable cathode with a sufficient supply of electrons and Li cations to form Li<small><sub>2</sub></small>O must be developed to achieve a four-electron reaction for a lithium–oxygen battery. Herein, by utilizing a composite 3D-printed cathode composed of a g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>/TiO<small><sub>2</sub></small> (gCNTO) heterostructure nanoparticle with high porosity and high conductivity, we were able to provide ample space and numerous active/catalytic sites during the reaction process. Our findings indicate that Li<small><sub>2</sub></small>O is the product of the photo-assisted lithium–oxygen battery. Under illumination, the battery can be rechargeable for over 1000 hours at 0.05 mA cm<small><sup>−2</sup></small> with a small polarization gap. The photocathode delivers an ultra-high discharge capacity of 29.7 mA h cm<small><sup>−2</sup></small> at 0.5 mA cm<small><sup>−2</sup></small>, resulting in a specific energy of approximately 515.12 W h kg<small><sup>−1</sup></small><small><sub>cell</sub></small>. The performance is superior to the battery with Li<small><sub>2</sub></small>O<small><sub>2</sub></small> as a discharge product in the dark. This study paves the way for the rapid development of high-energy-density photo-assisted Li–O<small><sub>2</sub></small> batteries.</p>\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":8.3000,\"publicationDate\":\"2024-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/tc/d4tc01832j\",\"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":"1","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/tc/d4tc01832j","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
基于氧化锂(Li2O)形成的锂氧电池理论上可以通过四电子反应实现高能量密度。这比分别产生超氧化锂(LiO2)和过氧化锂(Li2O2)的单电子反应和双电子反应更具挑战性。要实现锂氧电池的四电子反应,必须开发出一种具有足够电子和锂阳离子的稳定阴极,以形成 Li2O。在此,我们利用由具有高孔隙率和高导电性的 g-C3N4/TiO2 (gCNTO)异质结构纳米粒子组成的复合 3D 打印阴极,在反应过程中提供了充足的空间和大量的活性/催化位点。我们的研究结果表明,Li2O 是光辅助锂氧电池的产物。在光照下,电池在 0.05 mA cm-2 的极化间隙很小的条件下可充电 1000 小时以上。光电阴极在 0.5 mA cm-2 的条件下可提供 29.7 mA h cm-2 的超高放电容量,从而产生约 515.12 W h kg-1cell 的比能量。其性能优于以 Li2O2 作为黑暗中放电产物的电池。这项研究为快速开发高能量密度光助二氧化锰锂电池铺平了道路。
Z-Scheme g-C3N4/TiO2 heterojunction for a high energy density photo-assisted Li–O2 battery†
A lithium–oxygen battery based on the formation of lithium oxide (Li2O) can theoretically achieve a high energy density through a four-electron reaction. This is more challenging to accomplish than the one- and two-electron reactions that produce lithium superoxide (LiO2) and lithium peroxide (Li2O2), respectively. A stable cathode with a sufficient supply of electrons and Li cations to form Li2O must be developed to achieve a four-electron reaction for a lithium–oxygen battery. Herein, by utilizing a composite 3D-printed cathode composed of a g-C3N4/TiO2 (gCNTO) heterostructure nanoparticle with high porosity and high conductivity, we were able to provide ample space and numerous active/catalytic sites during the reaction process. Our findings indicate that Li2O is the product of the photo-assisted lithium–oxygen battery. Under illumination, the battery can be rechargeable for over 1000 hours at 0.05 mA cm−2 with a small polarization gap. The photocathode delivers an ultra-high discharge capacity of 29.7 mA h cm−2 at 0.5 mA cm−2, resulting in a specific energy of approximately 515.12 W h kg−1cell. The performance is superior to the battery with Li2O2 as a discharge product in the dark. This study paves the way for the rapid development of high-energy-density photo-assisted Li–O2 batteries.
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.