Junming Li
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Junming Li has a total of 31 co-authors. Here are the top co-authors by number of shared publications:
- Xinghua Liang
Guangxi Key Laboratory of Automobile Components and Vehicle Technology, Guangxi University of Science and Technology, Liuzhou 545006, China
3 shared publications - Qiankun Hun
Guangxi Key Laboratory of Automobile Components and Vehicle Technology, Guangxi University of Science & Technology, Liuzhou 545006, China
2 shared publications - Wendong Qin
Guangxi Key Laboratory of Automobile Components and Vehicle Technology, Guangxi University of Science & Technology, Liuzhou 545006, China
2 shared publications - Yifeng Guo
School of Mechanical Engineering, Chengdu University, Chengdu 610106, China
2 shared publications - Youping Sun
College of Mechanical and Automotive Engineering, Guangxi University of Science and Technology, Liuzhou, China
2 shared publications - Aijun Fu
Guangxi Key Laboratory of Automobile Components and Vehicle Technology, Guangxi University of Science & Technology, Liuzhou 545006, China
1 shared publication
Latest Publications
- 1 October 2025
- Published by Springer Nature in Journal of Materials Engineering and Performance
- Vol. 35 (8) , 7234-7248
Comparison in Microstructure, Mechanical Properties, and Fatigue Behavior of Q690D High-Strength Steel and its Welded Joint
- 1 October 2025
- Published by Springer Nature in Journal of Materials Engineering and Performance
- Vol. 35 (8) , 7234-7248
Comparison in Microstructure, Mechanical Properties, and Fatigue Behavior of Q690D High-Strength Steel and its Welded Joint
- Open Access
Preparation and Failure Behavior of Gel Electrolytes for Multilayer Structure Lithium Metal Solid-State Batteries
High safety gel polymer electrolyte (GPE) is used in lithium metal solid state batteries, which has the advantages of high energy density, wide temperature range, high safety, and is considered as a subversive new generation battery technology. However, solid-state lithium batteries with multiple layers and large capacity currently have poor cycle life and a large gap between the actual output cycle capacity retention rate and the theoretical level. In this paper, polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP)/polyacrylonitrile (PAN)—lithium perchlorate (LiClO4)—lithium lanthanum zirconium tantalate (LLZTO) gel polymer electrolytes was prepared by UV curing process using a UV curing machine at a speed of 0.01 m/min for 10 s, with the temperature controlled at 30 °C and wavelength 365 nm. In order to study the performance and failure mechanism of multilayer solid state batteries, single and three layers of solid state batteries with ceramic/polymer composite gel electrolyte were assembled. The results show that the rate and cycle performance of single-layer solid state battery with gel electrolyte are better than those of three-layer solid state battery. As the number of cycles increases, the interface impedance of both single-layer and three-layer electrolyte membrane solid-state batteries shows an increasing trend. Specifically, the three-layer battery impedance increased from 17 Ω to 42 Ω after 100 cycles, while the single-layer battery showed a smaller increase, from 2.2 Ω to 4.8 Ω, indicating better interfacial stability. After 100 cycles, the interface impedance of multi-layer solid-state batteries increases by 9.61 times that of single-layer batteries. After 100 cycles, the corresponding capacity retention rates were 48.9% and 15.6%, respectively. This work provides a new strategy for large capacity solid state batteries with gel electrolyte design.
Open AccessPreparation and Failure Behavior of Gel Electrolytes for Multilayer Structure Lithium Metal Solid-State Batteries
High safety gel polymer electrolyte (GPE) is used in lithium metal solid state batteries, which has the advantages of high energy density, wide temperature range, high safety, and is considered as a subversive new generation battery technology. However, solid-state lithium batteries with multiple layers and large capacity currently have poor cycle life and a large gap between the actual output cycle capacity retention rate and the theoretical level. In this paper, polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP)/polyacrylonitrile (PAN)—lithium perchlorate (LiClO4)—lithium lanthanum zirconium tantalate (LLZTO) gel polymer electrolytes was prepared by UV curing process using a UV curing machine at a speed of 0.01 m/min for 10 s, with the temperature controlled at 30 °C and wavelength 365 nm. In order to study the performance and failure mechanism of multilayer solid state batteries, single and three layers of solid state batteries with ceramic/polymer composite gel electrolyte were assembled. The results show that the rate and cycle performance of single-layer solid state battery with gel electrolyte are better than those of three-layer solid state battery. As the number of cycles increases, the interface impedance of both single-layer and three-layer electrolyte membrane solid-state batteries shows an increasing trend. Specifically, the three-layer battery impedance increased from 17 Ω to 42 Ω after 100 cycles, while the single-layer battery showed a smaller increase, from 2.2 Ω to 4.8 Ω, indicating better interfacial stability. After 100 cycles, the interface impedance of multi-layer solid-state batteries increases by 9.61 times that of single-layer batteries. After 100 cycles, the corresponding capacity retention rates were 48.9% and 15.6%, respectively. This work provides a new strategy for large capacity solid state batteries with gel electrolyte design.
- Open Access
Fabrication and Performance Study of 3D-Printed Ceramic-in-Gel Polymer Electrolytes
Solid-state electrolytes (SSEs) have emerged as a promising solution for next-generation lithium-ion batteries due to their excellent safety and high energy density. However, their practical application is still hindered by critical challenges such as their low ionic conductivity and high interfacial resistance at room temperature. The innovative application of 3D printing in the field of electrochemistry, particularly in solid-state electrolytes, endows energy storage devices with attractive characteristics. In this study, ceramic-in-gel polymer electrolytes (GPEs) based on PVDF-HFP/PAN@LLZTO were fabricated using a direct ink writing (DIW) 3D printing technique. Under the optimal printing conditions (printing speed of 40 mm/s and fill density of 70%), the printed electrolyte exhibited a uniform and dense sponge-like porous structure, achieving a high ionic conductivity of 5.77 × 10−4 S·cm−1, which effectively facilitated lithium-ion transport. A structural analysis indicated that the LLZTO fillers were uniformly dispersed within the polymer matrix, significantly enhancing the electrochemical stability of the electrolyte. When applied in a LiFePO4|GPEs|Li cell configuration, the electrolyte delivered excellent electrochemical performance, with high initial discharge capacities of 168 mAh·g−1 at 0.1 C and 166 mAh·g−1 at 0.2 C, and retained 92.8% of its capacity after 100 cycles at 0.2 C. This work demonstrates the great potential of 3D printing technology in fabricating high-performance GPEs. It provides a novel strategy for the structural design and industrial scalability of lithium-ion batteries.
Open AccessFabrication and Performance Study of 3D-Printed Ceramic-in-Gel Polymer Electrolytes
Solid-state electrolytes (SSEs) have emerged as a promising solution for next-generation lithium-ion batteries due to their excellent safety and high energy density. However, their practical application is still hindered by critical challenges such as their low ionic conductivity and high interfacial resistance at room temperature. The innovative application of 3D printing in the field of electrochemistry, particularly in solid-state electrolytes, endows energy storage devices with attractive characteristics. In this study, ceramic-in-gel polymer electrolytes (GPEs) based on PVDF-HFP/PAN@LLZTO were fabricated using a direct ink writing (DIW) 3D printing technique. Under the optimal printing conditions (printing speed of 40 mm/s and fill density of 70%), the printed electrolyte exhibited a uniform and dense sponge-like porous structure, achieving a high ionic conductivity of 5.77 × 10−4 S·cm−1, which effectively facilitated lithium-ion transport. A structural analysis indicated that the LLZTO fillers were uniformly dispersed within the polymer matrix, significantly enhancing the electrochemical stability of the electrolyte. When applied in a LiFePO4|GPEs|Li cell configuration, the electrolyte delivered excellent electrochemical performance, with high initial discharge capacities of 168 mAh·g−1 at 0.1 C and 166 mAh·g−1 at 0.2 C, and retained 92.8% of its capacity after 100 cycles at 0.2 C. This work demonstrates the great potential of 3D printing technology in fabricating high-performance GPEs. It provides a novel strategy for the structural design and industrial scalability of lithium-ion batteries.
- Open Access
- 9 June 2025
- Published by MDPI AG in Applied Sciences
- Vol. 15 (12) , 6471
Tube-Based Robust Model Predictive Control for Autonomous Vehicle with Complex Road Scenarios
This study proposes a Tube-based Robust Model Predictive Control (Tube-RMPC) strategy for autonomous vehicle control to address model parameter uncertainties and variations in road–tire adhesion coefficients in complex road scenarios. More specifically, the proposed approach improves the representation of vehicle dynamic behavior by introducing a unified vehicle–tire modeling framework. To facilitate computational tractability and algorithmic implementation, the model is systematically linearized and discretized. Furthermore, the Tube-based Robust Model Predictive Control strategy is developed to improve adaptability to uncertainty in the road surface adhesion coefficient. The Tube-based Robust Model Predictive controller ensures robustness by establishing a robust invariant tube around the nominal trajectory, effectively mitigating road surface variations and enhancing stability. Finally, a co-simulation platform integrating CarSim and Simulink is employed to validate the proposed method’s effectiveness. The experimental results demonstrate that Tube-RMPC improves the path-tracking performance, reducing the maximum tracking error by up to 9.17% on an S-curve and 2.25% in a double lane change, while significantly lowering RMSE and enhancing yaw stability compared to MPC and PID.
- 9 June 2025
- Published by MDPI AG in Applied Sciences
- Vol. 15 (12) , 6471
Open AccessTube-Based Robust Model Predictive Control for Autonomous Vehicle with Complex Road Scenarios
This study proposes a Tube-based Robust Model Predictive Control (Tube-RMPC) strategy for autonomous vehicle control to address model parameter uncertainties and variations in road–tire adhesion coefficients in complex road scenarios. More specifically, the proposed approach improves the representation of vehicle dynamic behavior by introducing a unified vehicle–tire modeling framework. To facilitate computational tractability and algorithmic implementation, the model is systematically linearized and discretized. Furthermore, the Tube-based Robust Model Predictive Control strategy is developed to improve adaptability to uncertainty in the road surface adhesion coefficient. The Tube-based Robust Model Predictive controller ensures robustness by establishing a robust invariant tube around the nominal trajectory, effectively mitigating road surface variations and enhancing stability. Finally, a co-simulation platform integrating CarSim and Simulink is employed to validate the proposed method’s effectiveness. The experimental results demonstrate that Tube-RMPC improves the path-tracking performance, reducing the maximum tracking error by up to 9.17% on an S-curve and 2.25% in a double lane change, while significantly lowering RMSE and enhancing yaw stability compared to MPC and PID.
- Open Access
Composite Polymer Electrolyte Based on PAN/TPU for Lithium-Ion Batteries Operating at Room Temperature
Lithium-ion batteries have garnered significant attention owing to their exceptional energy density, extended lifespan, rapid charging capabilities, eco-friendly characteristics, and extensive application potential. These remarkable features establish them as a critical focus for advancing next-generation battery technologies. However, the commonly used organic liquid electrolytes in batteries are explosive, volatile, and possess specific toxic properties, resulting in persistent safety concerns that remain to be addressed. Composite polymer electrolytes (CPEs) exhibit enhanced safety and stable electrochemical performance, emerging as one of the most promising alternatives. However, single polymers often need to meet the multifaceted performance requirements of batteries. In this study, a composite polymer electrolyte was prepared using solution casting, consisting of a blend of polyurethane (TPU) and polyacrylonitrile (PAN), along with the ceramic filler Li1.3Al0.3Ti1.7(PO4)3 (LATP) and lithium perchlorate (LiClO4). The optimal formulation, which included 40 wt% TPU, 60 wt% PAN, and 10 wt% LATP, exhibited a commendable ionic conductivity of 2.1 × 10−4 S cm−1, a lithium-ion transference number (tLi+) of 0.60, and notable electrochemical stability at 30 °C. The LiFePO4/Li battery assembled with this CPE demonstrated excellent cycling stability and rate capability at room temperature. It delivered a discharge specific capacity of 130 mAh g−1 at 1C. Under a charge–discharge rate of 0.2C, the battery achieved a discharge specific capacity of 168 mAh g−1, retaining 98% of its capacity after 100 cycles at 25 °C. Additionally, the CPE exhibited robust safety performance. Consequently, this composite polymer electrolyte holds significant promise for application in lithium-ion batteries.
Open AccessComposite Polymer Electrolyte Based on PAN/TPU for Lithium-Ion Batteries Operating at Room Temperature
Lithium-ion batteries have garnered significant attention owing to their exceptional energy density, extended lifespan, rapid charging capabilities, eco-friendly characteristics, and extensive application potential. These remarkable features establish them as a critical focus for advancing next-generation battery technologies. However, the commonly used organic liquid electrolytes in batteries are explosive, volatile, and possess specific toxic properties, resulting in persistent safety concerns that remain to be addressed. Composite polymer electrolytes (CPEs) exhibit enhanced safety and stable electrochemical performance, emerging as one of the most promising alternatives. However, single polymers often need to meet the multifaceted performance requirements of batteries. In this study, a composite polymer electrolyte was prepared using solution casting, consisting of a blend of polyurethane (TPU) and polyacrylonitrile (PAN), along with the ceramic filler Li1.3Al0.3Ti1.7(PO4)3 (LATP) and lithium perchlorate (LiClO4). The optimal formulation, which included 40 wt% TPU, 60 wt% PAN, and 10 wt% LATP, exhibited a commendable ionic conductivity of 2.1 × 10−4 S cm−1, a lithium-ion transference number (tLi+) of 0.60, and notable electrochemical stability at 30 °C. The LiFePO4/Li battery assembled with this CPE demonstrated excellent cycling stability and rate capability at room temperature. It delivered a discharge specific capacity of 130 mAh g−1 at 1C. Under a charge–discharge rate of 0.2C, the battery achieved a discharge specific capacity of 168 mAh g−1, retaining 98% of its capacity after 100 cycles at 25 °C. Additionally, the CPE exhibited robust safety performance. Consequently, this composite polymer electrolyte holds significant promise for application in lithium-ion batteries.
- 6 October 2023
- Published by Springer Nature in Journal of Materials Engineering and Performance
- Vol. 33 (21) , 11981-11991
The Effect of Rolling Reduction on the Microstructure, Mechanical, and Damping Properties of Mg-1.0 wt.% Al Alloy
- 6 October 2023
- Published by Springer Nature in Journal of Materials Engineering and Performance
- Vol. 33 (21) , 11981-11991
The Effect of Rolling Reduction on the Microstructure, Mechanical, and Damping Properties of Mg-1.0 wt.% Al Alloy