Materials and Interface Designs for Batteries

A special issue of Batteries (ISSN 2313-0105). This special issue belongs to the section "Battery Materials and Interfaces: Anode, Cathode, Separators and Electrolytes or Others".

Deadline for manuscript submissions: closed (31 January 2024) | Viewed by 20193

Special Issue Editors


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Guest Editor
Key Laboratory of Surface and Interface Science and Technology, School of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002, China
Interests: preparation and application of energy materials

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Guest Editor
School of Iron and Steel, Soochow University, Suzhou 215000, China
Interests: battery materials (Li/Na/K ion batteries, et al.); physical chemistry of metallurgy; hydrometallurgy; comprehensive utilization of metallurgical resources

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Guest Editor
School of Chemistry and Chemical Engineering, Jishou University, Jishou 416000, China
Interests: design, preparation, structural characterization and application of new energy materials (aqueous or non-aqueous lithium/sodium/potassium/zinc ion batteries, zinc-air batteries); hydrometallurgy and recycling of solid waste resources

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Guest Editor
College of Materials Science and Engineering, Zhejiang University of Technology, Hangzhou 310014, China
Interests: energy material; nanomaterial; catalytic material
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

This Special Issue is focused on “Materials and Interface Designs for Batteries”. Electrode materials and their interface with electrolytes significantly determine the performance of batteries. The electrode material design of batteries is not only about the size and morphology of the materials, but also about the chemical bond strength, atomic migration, structural change, and volume expansion. Interface design mainly includes the regulation of electronic properties (band structure, state density) and ionic properties (ion migration). In general, understanding the structure and interface evolution of electrodes at the molecular level, rational design and regulation of the structure, and interface of electrochemical energy materials are the basis for significantly improving the performance of batteries.

Potential topics include but are not limited to:

  • Li/Na/K/Zn-ion batteries;
  • Li/Na/K/Zn metal batteries;
  • Li/Na/K/Zn-Air batteries;
  • Li/Na/K-S batteries;
  • Cathode, anode, and electrolytes;
  • All-solid-state battery and quasi-solid-state battery;
  • Novel battery systems;
  • Electrochemical test method.

Dr. Yuanhua Xiao
Prof. Dr. Ling Wu
Prof. Dr. Xianwen Wu
Prof. Dr. Yiping Tang
Guest Editors

Manuscript Submission Information

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Keywords

  • batteries
  • structure design
  • nanomaterials
  • composite materials
  • coating materials
  • interlayer materials
  • interface engineering
  • interfacial modification

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Published Papers (8 papers)

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Research

12 pages, 3772 KiB  
Article
Freeze-Drying-Assisted Preparation of High-Compaction-Density LiMn0.69Co0.01Fe0.3PO4 Cathode Materials with High-Capacity and Long Life-Cycle for Lithium Ion Batteries
by Shaojun Liu, Jingang Zheng, Hao Huang, Hongyang Li, Han Zhang, Lixiang Li, Baigang An, Yuanhua Xiao and Chengguo Sun
Batteries 2024, 10(4), 114; https://doi.org/10.3390/batteries10040114 - 25 Mar 2024
Viewed by 2158
Abstract
As a successor to LiFePO4, the research interest in LiMn1−yFeyPO4 has been sustained due to its higher working voltage and safety features. However, its further application is limited by the low compaction density caused by uncontrolled [...] Read more.
As a successor to LiFePO4, the research interest in LiMn1−yFeyPO4 has been sustained due to its higher working voltage and safety features. However, its further application is limited by the low compaction density caused by uncontrolled particle size. In this study, the high-quality LiMn0.69Co0.01Fe0.3PO4 (LMFP) materials were prepared using the freeze-drying method to process the LMFP precursor synthesized through a solvothermal crystallization method followed by a calcination process at different temperatures (400–550 °C). The results demonstrate that the obtained particles exhibit a spheroidal shape with a low specific surface area after secondary crystallization calcination at 700 °C. The compaction density increased from 1.96 g/cm3 for LMFP precursor (LMFP-M1) to 2.18, 2.27, 2.34, and 2.43 g/cm3 for samples calcined at 400, 450, 500 and 550 °C, respectively, achieving a maximum increase of 24%. The full cell constructed with the high-compaction-density material calcined at 500 °C displayed discharge capacities of 144.1, 143.8, and 142.6 mAh/g at 0.5, 1, and 3 C rates, respectively, with a retention rate of 99% at 3 C rate. After undergoing charging and discharging cycles at a rate of 1 C for up to 800 cycles, the capacity retention rate was found to be 90%, indicating an expected full cell life span exceeding 2500 cycles. Full article
(This article belongs to the Special Issue Materials and Interface Designs for Batteries)
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12 pages, 5557 KiB  
Article
Bimetal-Initiated Concerted Zn Regulation Enabling Highly Stable Aqueous Zn-Ion Batteries
by Hong Yin, Yuliang Liu, Yifeng Zhu, Fengxiang Ye, Guangliang Xu, Mengfang Lin and Wenbin Kang
Batteries 2024, 10(3), 70; https://doi.org/10.3390/batteries10030070 - 20 Feb 2024
Cited by 2 | Viewed by 2282
Abstract
Aqueous zinc ion batteries are highly sought after for the next generation of sustainable energy storage systems. However, their development is significantly impeded by the presence of undesired zinc dendrites, which greatly reduce their cycle life. It is well-received that surface passivation by [...] Read more.
Aqueous zinc ion batteries are highly sought after for the next generation of sustainable energy storage systems. However, their development is significantly impeded by the presence of undesired zinc dendrites, which greatly reduce their cycle life. It is well-received that surface passivation by introducing foreign metals represents a compelling measure to enhance the stability of Zn anodes. Nevertheless, the vast potential of effecting concerted interplay between multiple metal elements for enhanced overall performance in Zn ion batteries remains elusive, due to the overwhelming challenge in creating uniform textures from hetero-units and understanding the mechanism underlying the synergistic performance gain. In this work, an innovative bimetallic overlaying strategy is proposed that renders possible the synergy between AgZn3 and CuZn5 in effecting uniform Zn deposition in a laterally confined and compact manner. The seeded growth of Zn on the bimetal-modulated interface effectively reduces the nucleation potential barrier, yielding a low nucleation overpotential (25 mV). In full cell testing with a commercial MnO2 applied as the cathode, superb cycling stability, surpassing the results reported in previous works, is achieved. The cell delivers an outstanding remaining capacity of 215 mA h g−1 after 300 cycles with almost no capacity degradation observed. The simple and highly efficient bimetal design, which synergizes the strengths of distinct metals, has the potential to drive innovations in the development of multicomponent aqueous Zn batteries with exceptional performance. Full article
(This article belongs to the Special Issue Materials and Interface Designs for Batteries)
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16 pages, 9562 KiB  
Article
Acrylate Copolymer-Reinforced Hydrogel Electrolyte for Strain Sensors and Flexible Supercapacitors
by Ruixue Liu, Wenkang Liu, Jichao Chen, Xiangli Bian, Kaiqi Fan, Junhong Zhao and Xiaojing Zhang
Batteries 2023, 9(6), 304; https://doi.org/10.3390/batteries9060304 - 31 May 2023
Cited by 4 | Viewed by 1604
Abstract
Ionic conductive hydrogels with good conductivity and biocompatibility have become one of the research highlights in the field of wearable flexible sensors and supercapacitors. In this work, poly(methacrylic acid–methyl methacrylate)-reinforced poly(sodium acrylate–vinyl phosphonic acid) composite hydrogels (P(AAS-VPA)/PMMS) were designed and tested for strain [...] Read more.
Ionic conductive hydrogels with good conductivity and biocompatibility have become one of the research highlights in the field of wearable flexible sensors and supercapacitors. In this work, poly(methacrylic acid–methyl methacrylate)-reinforced poly(sodium acrylate–vinyl phosphonic acid) composite hydrogels (P(AAS-VPA)/PMMS) were designed and tested for strain sensor or supercapacitor applications. The results showed recoverability for 20 cycles of tension and compression experiments, an excellent breaking strain of 2079%, and ionic conductivity of 0.045 S·cm−1, demonstrating strong support for the application of the P(AAS-VPA)/PMMS hydrogel in strain sensors and supercapacitors. The composite hydrogel exhibited outstanding sensing and monitoring capability with high sensitivity (GF = 4.0). The supercapacitor based on the P(AAS-VPA)/PMMS composite hydrogel showed excellent capacitance performance (area capacitance 100.8 mF·cm−2 and energy density 8.96 μWh·cm−2) at ambient temperature and even −30 °C (25.3 mF·cm−2 and 2.25 μWh·cm−2). The hydrogel has stable electrochemical stability (1000 cycles, Coulomb efficiency > 97%) and exhibits electrochemical properties similar to those in the normal state under different deformations. The excellent results demonstrate the great potential of the P(AAS-VPA)/PMMS composite hydrogel in the field of strain sensors and flexible supercapacitors. Full article
(This article belongs to the Special Issue Materials and Interface Designs for Batteries)
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13 pages, 3206 KiB  
Article
Zn-Co-Mo-rGO Ultra-Thin Nanosheets Arrays-Based Electrode Materials for Asymmetric Supercapacitor
by Shuang Liu, Siwei He, Yanhong Xiang, Xiaochun Peng, Lizhi Xiong and Jianhua Wu
Batteries 2023, 9(3), 158; https://doi.org/10.3390/batteries9030158 - 2 Mar 2023
Cited by 6 | Viewed by 1974
Abstract
The design of electrode materials for supercapacitors (SCs) with high specific capacity and high energy density has always been a research hotspot. In this paper, ternary metal oxides Zn-Co-Mo-rGO (ZCMG) and Zn-Co-Mo (ZCM) based electrode materials were prepared by one-step hydrothermal method. Compared [...] Read more.
The design of electrode materials for supercapacitors (SCs) with high specific capacity and high energy density has always been a research hotspot. In this paper, ternary metal oxides Zn-Co-Mo-rGO (ZCMG) and Zn-Co-Mo (ZCM) based electrode materials were prepared by one-step hydrothermal method. Compared with the ZCM, SEM and TEM results demonstrates the ultra-thin nanosheets grown vertically on the nickel foam for ZCMG. Owing to synergistic effect of the multi-component composites, the as-prepared electrode with ZCMG exhibits the specific capacity of 713 C g−1 (1189 F g−1) at 1 A g−1, which was higher than that of ZCM without rGO (492 F g−1, 295 C g−1). The assembled ZCMG//AC (activated carbon) asymmetric supercapacitor (ASC) delivers the maximum specific capacity of 68 C g−1 (45 F g−1) at 1 A g−1. After 1000 cycles, it still has a high-capacity retention rate of 95%. Furthermore, the ASC exhibited an energy density of 14 Wh kg−1 at 750 W kg−1, and it can retain 5.23 Wh kg−1, even at 7500 W kg−1. Full article
(This article belongs to the Special Issue Materials and Interface Designs for Batteries)
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13 pages, 3059 KiB  
Article
In-Situ Photoelectron Spectroscopy Investigation of Sulfurization-Induced Sodiophilic Sites with Model Systems of α-sexithiophene and p-sexiphenyl
by Yuan Liu, Xu Lian, Chonglai Jiang, Zejun Sun, Jinlin Yang, Yishui Ding and Wei Chen
Batteries 2023, 9(1), 21; https://doi.org/10.3390/batteries9010021 - 27 Dec 2022
Cited by 4 | Viewed by 2620
Abstract
Uncontrollable sodium dendrite growth results in poor cycling performance and severe safety issues, hindering practical applications of sodium metal batteries (SMBs). To stabilize sodium metal anodes (SMAs), various strategies have been developed including employing anode hosts and electrolyte additives to establish protective layers. [...] Read more.
Uncontrollable sodium dendrite growth results in poor cycling performance and severe safety issues, hindering practical applications of sodium metal batteries (SMBs). To stabilize sodium metal anodes (SMAs), various strategies have been developed including employing anode hosts and electrolyte additives to establish protective layers. Nevertheless, the understanding of interaction mechanisms between protective materials and SMAs is still limited, which is crucial for the rational design of protective materials. In this work, we investigated the interaction mechanism between sodium metal and sulfur-containing functional groups with comparative model systems of α-sexithiophene (6T) and p-sexiphenyl (6P) through in-situ photoelectron spectroscopy investigations and density functional theory (DFT) calculations. Our results show that sodium atoms tend to interact with sulfur atoms and their connected carbon atoms simultaneously as well as the aromatic carbon atoms of the end groups of 6T molecules, while no chemical interaction between Na and 6P molecules is observed. The observed sulfurization-induced sodiophilic sites can shed light on the rational design of sulfur-containing protective materials and the relevant interface engineering to stabilize SMAs. Full article
(This article belongs to the Special Issue Materials and Interface Designs for Batteries)
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19 pages, 5863 KiB  
Article
Effect of Sample Interval on the Parameter Identification Results of RC Equivalent Circuit Models of Li-ion Battery: An Investigation Based on HPPC Test Data
by Hehui Zhang, Chang Deng, Yutong Zong, Qingsong Zuo, Haipeng Guo, Shuai Song and Liangxing Jiang
Batteries 2023, 9(1), 1; https://doi.org/10.3390/batteries9010001 - 20 Dec 2022
Cited by 12 | Viewed by 4529
Abstract
The validity of the equivalent circuit model (ECM), which is crucial for the development of lithium-ion batteries (LIBs) and state evaluation, is primarily dependent on the precision of the findings of parameter identification. In this study, the commonly used first-order RC (1-RC) circuit [...] Read more.
The validity of the equivalent circuit model (ECM), which is crucial for the development of lithium-ion batteries (LIBs) and state evaluation, is primarily dependent on the precision of the findings of parameter identification. In this study, the commonly used first-order RC (1-RC) circuit and second-order RC (2-RC) circuit models were selected for parameter identification. A time series of voltage with different sample intervals were used for function fitting based on the least square method, which were extracted from the hybrid pulse power characteristic (HPPC) test data of a commercial square punch LIB, and the sample intervals were set to be 0.1 s, 0.2 s, 0.5 s, and 1.0 s to evaluate the effect of sample interval on the parameter identification results. When the sample interval is more than 0.5 s, the results reveal that the 2-RC circuit model’s goodness of fit marginally declines, and for some data scenarios, the bias between the fitted terminal voltage curve and test curve increases obviously. With all of the sample intervals under consideration, the 1-RC circuit model’s imitative effect is satisfactory. This work demonstrates that the sample interval of data samples, in addition to the method itself, affects the accuracy and robustness of parameter identification, with the 1-RC circuit model showing larger advantages under low sample frequency compared to the 2-RC circuit model. Full article
(This article belongs to the Special Issue Materials and Interface Designs for Batteries)
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14 pages, 4060 KiB  
Article
Tuning the Architecture of Hierarchical Porous CoNiO2 Nanosheet for Enhanced Performance of Li-S Batteries
by Lili Chai, Huizi Ye, Zhengguang Hu, Fengliang Liu, Liyun Qin, Zhiqi Zhang, Xianxin Lai, Yong Zhao and Li Wang
Batteries 2022, 8(12), 262; https://doi.org/10.3390/batteries8120262 - 29 Nov 2022
Cited by 1 | Viewed by 1814
Abstract
As the desired components and crystal structure of a transition metal oxide catalyst are selected, architecture is a dominating factor affecting its electrocatalytic performance for applications in lithium-sulfur (Li-S) batteries. Nano-compounds with a hollow architecture are undoubtedly the ideal catalysts for enhancing cathodic [...] Read more.
As the desired components and crystal structure of a transition metal oxide catalyst are selected, architecture is a dominating factor affecting its electrocatalytic performance for applications in lithium-sulfur (Li-S) batteries. Nano-compounds with a hollow architecture are undoubtedly the ideal catalysts for enhancing cathodic performance for more exposed active sites and shortened path lengths than are other architectures. Additionally, the internal stress in hollow architecture is favorable for further performance enhancement, due to its regulation effects of driving the d-band center of the transition metal in the active sites to migrate toward the Fermi level, which will promote the chemical adsorption and catalytic conversion of the polysulfides (PSs). To this point, we select hierarchical porous dual transition metal oxide CoNiO2 nano-boxes (CoNiO2(B)) as the conceptual model; meanwhile, CoNiO2 nano-flakes (CoNiO2(F)) with identical stoichiometry and crystal structure are also analyzed as a comparison. Li-S batteries based on CoNiO2(B) deliver superior energy storage features, including a reversible discharge capacity of 1232 mAh g−1 at 0.05 C and a stable cycle performance with decay rate of 0.1% each cycle even after 300 cycles at 1 C. This research presents an alternative scheme for booting the performance of Li-S batteries. Full article
(This article belongs to the Special Issue Materials and Interface Designs for Batteries)
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11 pages, 8456 KiB  
Article
Microstructure Modulation of Zn Doped VO2(B) Nanorods with Improved Electrochemical Properties towards High Performance Aqueous Batteries
by Dewei Liu, Qijie Zhang, Xiaohong Chen, Haiyang Dai, Xuezhen Zhai, Jing Chen, Gaoshang Gong, Cui Shang and Xuzhe Wang
Batteries 2022, 8(10), 172; https://doi.org/10.3390/batteries8100172 - 9 Oct 2022
Cited by 5 | Viewed by 2012
Abstract
Vanadium dioxide with monoclinic structure is theoretically a promising layered cathode material for aqueous metal-ion batteries due to its excellent specific capacity. However, its poor cycling stability limits its application as an electrode material. In this study, a series of Zn-doped VO2 [...] Read more.
Vanadium dioxide with monoclinic structure is theoretically a promising layered cathode material for aqueous metal-ion batteries due to its excellent specific capacity. However, its poor cycling stability limits its application as an electrode material. In this study, a series of Zn-doped VO2 (V1−xZnxO2) nanorods were successfully fabricated by the technology of one-step hydrothermal synthesis. The XRD result indicated that there was a slight lattice distortion caused by doped Zn2+ with a larger ion radius. The positron lifetime spectrum showed that there were vacancy cluster defects in all the samples. The electrochemical measurement demonstrated the enhancement of the specific capacitance of V1−xZnxO2 electrodes compared with the undoped sample. In addition, the discharge capacitance of the sample remained around 86% after 1000 charge/discharge cycles. This work proves that Zn2+ doping is a valid tactic for the application of nano-VO2(B) in energy storage electrode materials. Full article
(This article belongs to the Special Issue Materials and Interface Designs for Batteries)
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