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Small · 2023 ·Vol. 19 ·期 39 ·2302691 · IF 13.3

Improving Room-Temperature Li-Metal Battery Performance by In Situ Creation of Fast Li+ Transport Pathways in a Polymer-Ceramic Electrolyte

Jing Yu,Guodong Zhou,Yueqing Li,Yuhao Wang,Dengjie Chen,Francesco Ciucci

Composite polymer-ceramic electrolytes have shown considerable potential for high-energy-density Li-metal batteries as they combine the benefits of both polymers and ceramics. However, low ionic conductivity and poor contact with electrodes limit their practical usage. In this study, a highly conductive and stable composite electrolyte with a high ceramic loading is developed for high-energy-density Li-metal batteries. The electrolyte, produced through in situ polymerization and composed of a polymer called poly-1,3-dioxolane in a poly(vinylidene fluoride)/ceramic matrix, exhibits excellent room-temperature ionic conductivity of 1.2 mS cm −1 and high stability with Li metal over 1500 h. When tested in a Li|electrolyte|LiFePO 4 battery, the electrolyte delivers excellent cycling performance and rate capability at room temperature, with a discharge capacity of 137 mAh g −1 over 500 cycles at 1 C. Furthermore, the electrolyte not only exhibits a high Li + transference number of 0.76 but also significantly lowers contact resistance (from 157.8 to 2.1 Ω) relative to electrodes. When used in a battery with a high-voltage LiNi 0.8 Mn 0.1 Co 0.1 O 2 cathode, a discharge capacity of 140 mAh g −1 is achieved. These results show the potential of composite polymer-ceramic electrolytes in room-temperature solid-state Li-metal batteries and provide a strategy for designing highly conductive polymer-in-ceramic electrolytes with electrode-compatible interfaces.

研究领域: 材料科学 · 电化学 · 能源存储 · 固态电池 · 高分子化学 · 无机非金属材料
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Journal of Energy Chemistry · 2019 · IF 5.162

In-situ embedding zeolitic imidazolate framework derived Co–N–C bifunctional catalysts in carbon nanotube networks for flexible Zn–air batteries

Bo Lv,Sha Zeng,Wei Yang,Jian Qiao,Chao Zhang,Chengfeng Zhu,Minghai Chen,Jiangtao Di,Qingwen Li

Recently, the development of high-performance bifunctional oxygen catalysts integrated with flexible conductive scaffolds for rechargeable metal-air batteries has attracted considerable interest, driving by fast-growing wearable electronics . Herein, we report a flexible bifunctional oxygen catalyst thin film consisting of Co–N–C bifunctional catalysts embedding in carbon nanotube (CNT) networks. The catalyst is readily prepared by pyrolysis of cobalt-based zeolitic imidazolate frameworks (ZIF-67) that are in-situ synthesized in CNT networks. Such catalyst film demonstrates very high catalytic activities for oxygen reduction (onset potential: 0.91 V, and half-wave potential: 0.87 V vs. RHE) and oxygen evolution (10 mA cm −2 at 1.58 V) reactions, high methanol tolerance property, and long-term stability (97% current retention). Moreover, our integrated catalyst film shows very good structure flexibility and robustness. Based on the obtained film air electrodes, flexible Zn–air batteries demonstrate low charging and discharging overpotentials (0.82 V at 1 mA cm −1 ) and excellent structure stability in the bending tests . These results indicate that presently reported catalyst films are potential air electrodes for flexible metal–air batteries.

研究领域: 材料科学 · 电化学 · 纳米能源 · 先进功能材料 · 可再生能源
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TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA · 2025 ·Vol. 35 ·期 7 ·2341-2353 · IF 4.7

High-performance Li3YCl3Br3 halide solid electrolyte synthesized using wet-chemistry route for all-solid-state battery

Han-zhou LIU,Yan-chen LIU,Sheng-hao JING,Ya-qi HU,Zong-liang ZHANG,Si-liang LIU,Yang LIU,Zhi ZHUANG,Fan-qun LI,Fang-yang LIU

A dual-halide solid electrolyte, Li 3 YCl 3 Br 3 , was synthesized using a wet-chemistry route instead of the conventional mechanical ball-milling route. Li 3 YCl 3 B r3 exhibits an ion conductivity of 2.08 mS/cm and an electro- chemical stability window of 3.8 V. Additionally, an all-solid-state lithium-ion battery using Li 3 YCl 3 Br 3 and LiNi 0.83 Co 0.11 Mn 0.06 O 2 (NCM811) as the cathode material achieves a capacity retention of 93% after 200 cycles at 0.3 C and maintains a specific capacity of 115 mA·h/g during 2 C cycling. This exceptional performance is attributed to the high oxidative stability of Li 3 YCl 3 Br 3 and the in-situ formation of Y 2 O 3 inert protective layer on the NCM811 surface under high voltage. Consequently, the study demonstrates the feasibility of a simple, cost-effective wet-chemistry route for synthesizing multi-component halides, highlighting its potential for large-scale production of halide solid electrolytes for practical applications.

研究领域: 材料科学 · 电化学 · 固态离子学 · 能源存储 · 电池技术 · 无机非金属材料 · 纳米材料应用
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POLYMER TESTING · 2022 · IF 4.931

Preparation and properties of a fast curing carboxymethyl chitosan hydrogel for skin care

Yang-he Mo,Hui Wang,Shao-hua Jin,Ke-lin Peng,Zi-ming Yang,Pu-wang Li,Yu Chen

Fast curing hydrogels are highly valuable in the skin care industry. Multi-arm polyethylene glycol (PEG) is a commonly used crosslinking agent for the preparation of fast curing hydrogels. However, the hydrogel preparation using multi-arm PEG crosslinking agents usually requires the end group modifications of reactants, which makes the preparation process complicated and produces hydrogels with low curing rates. In the present study, a fast in situ curing hydrogel, 4-arm-PEG-succinimidyl carbonate/carboxymethyl chitosan (PEG-SC/CMCS), was prepared using 4-arm-PEG-SC as the crosslinking agent and carboxymethyl chitosan (CMCS), a derivative of natural polysaccharide with excellent comprehensive properties, as the framework without any end groups modified. The structure and properties of the prepared hydrogel were characterized by FTIR, XRD, SEM, rheology and swelling kinetics. The effects of reaction conditions on the structure and properties of hydrogel were investigated. The PEG-SC/CMCS hydrogel exhibited pH-sensitive swelling behaviors. Its application potential in skin care products is demonstrated with its excellent sustained-release performance of Vitamin C, a model drug for skin treatment, and high adsorption capacity of heavy metal ions that are easily deposited on skin surface. Our work has provided a new strategy for building multifunctional gel materials for skin care and offered a PEG-SC/CMCS hydrogel with great application potentials.

研究领域: 生物材料 · 高分子化学 · 药剂学 · 皮肤科学 · 组织工程 · 药物递送系统 · 环境毒理学
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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY · 2019 ·Vol. 19 ·期 1 ·57-65 · IF 1.093

Effects of Emulsifier Dosage and Curing Time on Self-Healing Microcapsules Containing Rejuvenator and Optimal Dosage in Asphalt Binders

Liu Wolong,Zhang Jiupeng,Liu Qi,Pei Jianzhong,Zhu Cunzhen,Liu Peng

Micro-damages always occur and accumulate in asphalt pavement materials under the effects of temperature, vehicle loads and other factors during service. Accordingly, self-healing microcapsules could be added into asphalt binder and repair micro-damages to prevent damage extension in time. In this study, the emulsified rejuvenator and melamine-urea-formaldehyde resin (MUF) were selected as the core and cyst wall materials, respectively, and in-situ polymerization method was applied to synthesize the novel microcapsules. The effects of emulsifier dosage and curing time were revealed on the particle size, dispersion, surface morphology and coating properties, and the optimum process parameters were determined for microcapsules. Then, the micro morphology, molecular structure, and thermal stability were further investigated to determine the optimal preparation of the microcapsules. Finally, the linear amplitude sweep (LAS) test was performed to evaluate the self-healing efficiency of the asphalt binder with different dosages of prepared microcapsule, and the optimal dosage of microcapsules was determined as 0.5%.

CAS / MDL: 25155-30-0
研究领域: 材料科学 · 土木工程 · 化学工程
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