Synthesis and Electrochemical Properties of TiO2-Ti3C2 Quantum Dots with a Layered Structure as Efficient Sulfur Hosts for High-Performance Lithium-Sulfur BatteriesSynthesis and Electrochemical Properties of TiO2-Ti3C2 Quantum Dots with a Layered Structure as Efficient Sulfur Hosts for High-Performance Lithium-Sulfur Batteries
- Other Titles
- Synthesis and Electrochemical Properties of TiO2-Ti3C2 Quantum Dots with a Layered Structure as Efficient Sulfur Hosts for High-Performance Lithium-Sulfur Batteries
- Authors
- Joohyun Kim; B.S. Reddy; Youna Choi; Hojun Na; Kwonkoo Cho
- Issue Date
- Dec-2024
- Publisher
- 한국신뢰성학회
- Keywords
- TiO2; Ti3C2; MXene; Sulfur; Lithium-sulfur batteries
- Citation
- 신뢰성 응용연구, v.24, no.4, pp 325 - 334
- Pages
- 10
- Indexed
- KCI
- Journal Title
- 신뢰성 응용연구
- Volume
- 24
- Number
- 4
- Start Page
- 325
- End Page
- 334
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/75316
- DOI
- 10.33162/JAR.2024.12.24.4.325
- ISSN
- 1738-9895
2733-8320
- Abstract
- Purpose: An ideal sulfur-supporting material for lithium-sulfur (Li-S) batteries would exhibit both minimal volume expansion and high electrical conductivity because these properties are essential for improving cycling stability, and enable implementation in large-scale applications.
Methods: In this work, we developed TiO2 quantum dots on Ti3C2 (QDs TiO2-Ti3C2) MXene nanosheets using a simple hydrothermal synthesis. The sulfur was loaded in the QDs TiO2-Ti3C2 MXene via a simple melt-diffusion method.
Results: The TiO2 quantum dots increased the interlayer space and prevented restacking of the MXene nanosheets. The QDs TiO2-Ti3C2@S electrode showed a higher initial capacity at a C-rate of 0.5, 921.6 mAh/g, compared with the corresponding value for the Ti3C2@S (499.0 mAh/g). Moreover, the QDs TiO2-Ti3C2@S electrode demonstrated excellent cyclic stability, retaining a capacity of 342.7 mAh/g after 150 cycles.
Conclusion: The QDs TiO2-Ti3C2@S electrode showed significantly enhanced long-term cyclability and rate capability, demonstrating a new prospect for the development of rapid and stable Li-S batteries.
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