Y. X. Zuo
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Y. X. Zuo has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
C. C. Zuo
College of Mechanical Science and EngineeringJilin University, Changchun 130022, China
1 shared publication- Chuncheng Zuo
College of Mechanical and Electrical Engineering, Jiaxing University, Jiaxing 314000, China
1 shared publication - Fulei Shi
College of Mechanical Science and Engineering, Jilin University, Changchun 130022, China
1 shared publication - Guoqiang Wang
School of Mechanical and Aerospace Engineering, Jilin University, Changchun 130025, China
1 shared publication - Jie Wei
College of Mechanical Science and Engineering, Jilin University, Changchun 130022, China
1 shared publication - Luyou Shi
College of Mechanical Science and Engineering, Jilin University, Changchun, China
1 shared publication
Latest Publications
- 14 December 2015
- Published by Taylor & Francis in Materials Research Innovations
- Vol. 19 (sup10) , S10-168
Gel polymer electrolytes with high ionic conductivity for the electrical double layer capacitors
Symmetrical electrical double layer capacitors with ionic liquid potassium hydroxide (KOH)-based poly(acrylic acid) gel polymer electrolytes and activated charcoal electrodes were constructed and characterised. The optimised composition of gel polymer electrolytes exhibits high room temperature ionic conductivity of 0.46 S cm−1 with good mechanical and dimensional stability, which is suitable for their application as electrolyte in electrical double layer capacitors. Analysis shows that the maximum value of capacitance was 0.343 F cm−2, and this value corresponds to an energy density equal to 0.111 J cm−2. Electrical double layer capacitor exhibits large capacitance and high energy density. The results indicate that the gel polymer electrolyte used in our study is promising and is suitable as a solid electrolyte for high-performance all-solid-state electrochemical devices.
- 14 December 2015
- Published by Taylor & Francis in Materials Research Innovations
- Vol. 19 (sup10) , S10-168
Gel polymer electrolytes with high ionic conductivity for the electrical double layer capacitors
Symmetrical electrical double layer capacitors with ionic liquid potassium hydroxide (KOH)-based poly(acrylic acid) gel polymer electrolytes and activated charcoal electrodes were constructed and characterised. The optimised composition of gel polymer electrolytes exhibits high room temperature ionic conductivity of 0.46 S cm−1 with good mechanical and dimensional stability, which is suitable for their application as electrolyte in electrical double layer capacitors. Analysis shows that the maximum value of capacitance was 0.343 F cm−2, and this value corresponds to an energy density equal to 0.111 J cm−2. Electrical double layer capacitor exhibits large capacitance and high energy density. The results indicate that the gel polymer electrolyte used in our study is promising and is suitable as a solid electrolyte for high-performance all-solid-state electrochemical devices.
- Open Access
Phase Behavior of Copolymers Confined in Multi-Walled Nanotubes: Insights from Simulations
In this paper, the self-assembly process of diblock copolymers confined in multi-walled cylindrical nanotubes is systematically investigated using a molecular dynamics (MD) method. The dependence of resultant morphologies on the degree of confinement and on the interaction strength between nanotubes and copolymers is studied comprehensively. When the wall surfaces are not preferential, results indicate that geometric confinement significantly influences copolymer conformations. In addition, the thickness of the helical lamellar structure increases with interaction strength and confinement size. In cases where the nanotubes are strongly attracted to one copolymer block, the confinement effect weakens as geometric space increases. Findings explain the dependence of chain conformation on the degree of confinement and the strength of surface preferences.
Open AccessPhase Behavior of Copolymers Confined in Multi-Walled Nanotubes: Insights from Simulations
In this paper, the self-assembly process of diblock copolymers confined in multi-walled cylindrical nanotubes is systematically investigated using a molecular dynamics (MD) method. The dependence of resultant morphologies on the degree of confinement and on the interaction strength between nanotubes and copolymers is studied comprehensively. When the wall surfaces are not preferential, results indicate that geometric confinement significantly influences copolymer conformations. In addition, the thickness of the helical lamellar structure increases with interaction strength and confinement size. In cases where the nanotubes are strongly attracted to one copolymer block, the confinement effect weakens as geometric space increases. Findings explain the dependence of chain conformation on the degree of confinement and the strength of surface preferences.