Yirui Ma, Zaichun Liu, Xinhua Zheng, Nawab Ali Khan, Ruihao Luo, Zhengxin Zhu, Zuodong Zhang, Kai Zhang, Weiping Wang, Yahan Meng, Zehui Xie, Touqeer Ahmad, Wei Chen
{"title":"Permanent Lithiophilic Layer for Anode-Free Lithium-Hydrogen Gas Battery","authors":"Yirui Ma, Zaichun Liu, Xinhua Zheng, Nawab Ali Khan, Ruihao Luo, Zhengxin Zhu, Zuodong Zhang, Kai Zhang, Weiping Wang, Yahan Meng, Zehui Xie, Touqeer Ahmad, Wei Chen","doi":"10.1002/aenm.202501912","DOIUrl":null,"url":null,"abstract":"The necessity for high-performance energy storage systems propels extensive research into diverse battery technologies. Among them, the lithium-hydrogen gas (Li//H<sub>2</sub>) battery, characterized by high energy density and low cost, is emerging as a promising candidate. Implementing a large areal capacity for the Li metal anode in an anode-free Li//H<sub>2</sub> battery design is essential for achieving higher energy density and further reducing manufacturing costs. Here the study reports a permanent Li-SiO<sub>x</sub> lithiophilic layer in-situ generated on a Cu substrate during the Li//H<sub>2</sub> battery initial charge that facilitates homogeneous Li nucleation and drives the formation of a dense and thick Li deposition layer. The study manages to maintain the lithiation state to avoid the repetition of lithiation/de-lithiation and significantly reduce the Li nucleation barrier. The anode-free Cu@Li-SiO<sub>x</sub>//H<sub>2</sub> battery with a high areal capacity of 5 mAh cm<sup>−2</sup> exhibits promising cycling stability with a Coulombic efficiency of up to 99.1% under a current density of 1 mA cm<sup>−2</sup>. Moreover, the significantly reduced Li nucleation barrier results in an increased round-trip energy efficiency reaching up to 93.20%. This work proposes a novel strategy for constructing a lithiophilic layer to enhance the practical feasibility of large areal capacity anode-free Li//H<sub>2</sub> batteries.","PeriodicalId":111,"journal":{"name":"Advanced Energy Materials","volume":"27 1","pages":""},"PeriodicalIF":24.4000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Energy Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/aenm.202501912","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The necessity for high-performance energy storage systems propels extensive research into diverse battery technologies. Among them, the lithium-hydrogen gas (Li//H2) battery, characterized by high energy density and low cost, is emerging as a promising candidate. Implementing a large areal capacity for the Li metal anode in an anode-free Li//H2 battery design is essential for achieving higher energy density and further reducing manufacturing costs. Here the study reports a permanent Li-SiOx lithiophilic layer in-situ generated on a Cu substrate during the Li//H2 battery initial charge that facilitates homogeneous Li nucleation and drives the formation of a dense and thick Li deposition layer. The study manages to maintain the lithiation state to avoid the repetition of lithiation/de-lithiation and significantly reduce the Li nucleation barrier. The anode-free Cu@Li-SiOx//H2 battery with a high areal capacity of 5 mAh cm−2 exhibits promising cycling stability with a Coulombic efficiency of up to 99.1% under a current density of 1 mA cm−2. Moreover, the significantly reduced Li nucleation barrier results in an increased round-trip energy efficiency reaching up to 93.20%. This work proposes a novel strategy for constructing a lithiophilic layer to enhance the practical feasibility of large areal capacity anode-free Li//H2 batteries.
高性能储能系统的需求推动了对各种电池技术的广泛研究。其中,锂-氢气体(Li//H2)电池具有高能量密度和低成本的特点,是一种很有前途的候选电池。在无阳极锂//H2电池设计中,实现大面积容量的锂金属阳极对于实现更高的能量密度和进一步降低制造成本至关重要。本研究报告了在Li//H2电池初始充电过程中,在Cu衬底上原位生成的永久性Li- siox亲锂层,促进了均匀的Li成核,并驱动了致密厚Li沉积层的形成。该研究成功地保持了锂化状态,避免了锂化/去锂化的重复,并显著降低了锂成核屏障。该无阳极Cu@Li-SiOx//H2电池具有5 mAh cm−2的高面容量,在电流密度为1 mA cm−2的情况下,库仑效率高达99.1%,具有良好的循环稳定性。此外,Li成核势垒的显著降低导致往返能量效率提高,最高可达93.20%。本研究提出了一种构建亲锂层的新策略,以提高大面积容量无阳极Li//H2电池的实际可行性。
期刊介绍:
Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small.
With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics.
The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.