{"title":"通过高度可逆的 H+ 促进 Zn2+ 互钙化作用,晶格扩张的二氧化钛成为锌-离子水电池的优良阳极。","authors":"Chao Geng, Pengfei Zhang, Jin-Ming Wu, Jiayi Qin, Wei Wen","doi":"10.1021/acsnano.4c09999","DOIUrl":null,"url":null,"abstract":"<p><p>Aqueous Zn-ion batteries have garnered significant attention as promising and safe energy storage systems. Due to the inevitable dendrite and corrosion in metallic Zn anodes, alternative anodes of intercalation-type materials are desirable, but they still suffer from low energy efficiency, unsatisfactory capacity, and insufficient cycle life. Here, we develop a high-performance anode for aqueous Zn-ion batteries via a lattice expansion strategy in combination with a Zn<sup>2+</sup>/H<sup>+</sup> synergistic mechanism. The anatase TiO<sub>2</sub> with expanded lattice exhibits an appropriate deintercalation potential of 0.18 V vs Zn/Zn<sup>2+</sup> and a high reversible capacity (227 mAh g<sup>-1</sup> at 2.04 A g<sup>-1</sup>) with an outstanding rate capability and excellent cycle stability. The high electrochemical performance is attributed to a decrease in the Zn<sup>2+</sup>/H<sup>+</sup> diffusion barriers, which results from lattice expansion and also a H<sup>+</sup>-promoted Zn<sup>2+</sup> intercalation effect. The anode intercalates Zn<sup>2+</sup>/H<sup>+</sup> via a solid-solution mechanism with a minor volume change, which contributes to the high reversibility and thus high energy efficiency. When paired with different types of cathodes, including NV, I<sub>2</sub>, and activated carbon, to construct corresponding full cells, high specific energy, high specific power, long cycle life, and extremely high energy efficiency can be achieved. This study provides a prospect for developing high-performance Zn-ion batteries.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":" ","pages":""},"PeriodicalIF":15.8000,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lattice Expanded Titania as an Excellent Anode for an Aqueous Zinc-Ion Battery Enabled by a Highly Reversible H<sup>+</sup>-Promoted Zn<sup>2+</sup> Intercalation.\",\"authors\":\"Chao Geng, Pengfei Zhang, Jin-Ming Wu, Jiayi Qin, Wei Wen\",\"doi\":\"10.1021/acsnano.4c09999\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Aqueous Zn-ion batteries have garnered significant attention as promising and safe energy storage systems. Due to the inevitable dendrite and corrosion in metallic Zn anodes, alternative anodes of intercalation-type materials are desirable, but they still suffer from low energy efficiency, unsatisfactory capacity, and insufficient cycle life. Here, we develop a high-performance anode for aqueous Zn-ion batteries via a lattice expansion strategy in combination with a Zn<sup>2+</sup>/H<sup>+</sup> synergistic mechanism. The anatase TiO<sub>2</sub> with expanded lattice exhibits an appropriate deintercalation potential of 0.18 V vs Zn/Zn<sup>2+</sup> and a high reversible capacity (227 mAh g<sup>-1</sup> at 2.04 A g<sup>-1</sup>) with an outstanding rate capability and excellent cycle stability. The high electrochemical performance is attributed to a decrease in the Zn<sup>2+</sup>/H<sup>+</sup> diffusion barriers, which results from lattice expansion and also a H<sup>+</sup>-promoted Zn<sup>2+</sup> intercalation effect. The anode intercalates Zn<sup>2+</sup>/H<sup>+</sup> via a solid-solution mechanism with a minor volume change, which contributes to the high reversibility and thus high energy efficiency. When paired with different types of cathodes, including NV, I<sub>2</sub>, and activated carbon, to construct corresponding full cells, high specific energy, high specific power, long cycle life, and extremely high energy efficiency can be achieved. 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引用次数: 0
摘要
作为一种前景广阔的安全储能系统,锌离子水电池备受关注。由于金属锌阳极不可避免地会产生枝晶和腐蚀,因此采用插层型材料作为替代阳极是可取的,但它们仍然存在能量效率低、容量不理想和循环寿命不足等问题。在这里,我们通过晶格膨胀策略结合 Zn2+/H+ 协同机制,开发出一种用于水性 Zn 离子电池的高性能阳极。具有扩展晶格的锐钛矿二氧化钛的脱插电位为 0.18 V vs Zn/Zn2+,具有高可逆容量(227 mAh g-1 at 2.04 A g-1)、出色的速率能力和卓越的循环稳定性。高电化学性能归功于晶格膨胀导致的 Zn2+/H+ 扩散障碍的降低,以及 H+ 促进的 Zn2+ 插层效应。阳极通过固溶机制插层 Zn2+/H+,体积变化很小,因此具有很高的可逆性,因而能效很高。当与不同类型的阴极(包括 NV、I2 和活性炭)配对构建相应的全电池时,可实现高比能量、高比功率、长循环寿命和极高的能量效率。这项研究为开发高性能 Zn 离子电池提供了前景。
Lattice Expanded Titania as an Excellent Anode for an Aqueous Zinc-Ion Battery Enabled by a Highly Reversible H+-Promoted Zn2+ Intercalation.
Aqueous Zn-ion batteries have garnered significant attention as promising and safe energy storage systems. Due to the inevitable dendrite and corrosion in metallic Zn anodes, alternative anodes of intercalation-type materials are desirable, but they still suffer from low energy efficiency, unsatisfactory capacity, and insufficient cycle life. Here, we develop a high-performance anode for aqueous Zn-ion batteries via a lattice expansion strategy in combination with a Zn2+/H+ synergistic mechanism. The anatase TiO2 with expanded lattice exhibits an appropriate deintercalation potential of 0.18 V vs Zn/Zn2+ and a high reversible capacity (227 mAh g-1 at 2.04 A g-1) with an outstanding rate capability and excellent cycle stability. The high electrochemical performance is attributed to a decrease in the Zn2+/H+ diffusion barriers, which results from lattice expansion and also a H+-promoted Zn2+ intercalation effect. The anode intercalates Zn2+/H+ via a solid-solution mechanism with a minor volume change, which contributes to the high reversibility and thus high energy efficiency. When paired with different types of cathodes, including NV, I2, and activated carbon, to construct corresponding full cells, high specific energy, high specific power, long cycle life, and extremely high energy efficiency can be achieved. This study provides a prospect for developing high-performance Zn-ion batteries.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.