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Division of Energy & Environmental Technology
1. Journal Articles
Design of Bronze-Rich Dual-Phasic TiO2 Embedded Amorphous Carbon Nanocomposites Derived from Ti-Metal-Organic Frameworks for Improved Lithium-Ion Storage
Ahn, Cheol Hyoun
;
Yang, Won Seok
;
Kim, Jeong Jae
;
Kim, Jae Hyun
;
Cho, Hyung Koun
Division of Energy & Environmental Technology
1. Journal Articles
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Title
Design of Bronze-Rich Dual-Phasic TiO2 Embedded Amorphous Carbon Nanocomposites Derived from Ti-Metal-Organic Frameworks for Improved Lithium-Ion Storage
Issued Date
2022-11
Citation
Ahn, Cheol Hyoun. (2022-11). Design of Bronze-Rich Dual-Phasic TiO2 Embedded Amorphous Carbon Nanocomposites Derived from Ti-Metal-Organic Frameworks for Improved Lithium-Ion Storage. Small Methods, 6(11). doi: 10.1002/smtd.202201066
Type
Article
Author Keywords
bronze/anatase heterojunctions
;
dual-phasic TiO2
;
interfacial storage
;
lithium-ion batteries
;
metal-organic frameworks
Keywords
ELECTROCHEMICAL ENERGY-STORAGE
;
ANODE MATERIALS
;
ANATASE TIO2
;
NANO-IONICS
;
CYCLE LIFE
;
PERFORMANCE
;
MIL-125
;
NANOWIRES
;
CONVERSION
;
STABILITY
ISSN
2366-9608
Abstract
Dual-phasic (DP)-TiO2-based composites are considered attractive anode materials for high lithium-ion storage because of the synergetic contribution from dual-phases in lithium-ion storage. However, a comprehensive investigation on more efficient architectures and platforms is necessary to develop lithium-storage devices with high-rate capability and long-term stability. Herein, for the first time, a rationally designed bronze-rich DP-TiO2-embedded amorphous carbon nanoarchitecture, denoted as DP-TiO2@C, from sacrificial Ti-metal-organic frameworks (Ti-MOFs) via a two-step pyrolysis process is proposed. The bronze/anatase DP-TiO2@C nanocomposites are successfully synthesized using a unique pyrolysis process, which decomposes individually the metal clusters and organic linkers of Ti-MOFs. DP-TiO2@C exhibits a significantly high density and even distribution of nanoparticles (<5 nm), enabling the formation of numerous heterointerfaces. Remarkably, the bronze-rich DP-TiO2@C shows high specific capacities of 638 and 194 mAh g(-1) at current densities of 0.1 and 5 A g(-1), respectively, owing to the contribution of the synergetic interfacial structure. In addition, reversible specific capacities are observed at a high rate (5 A g(-1)) during 6000 cycles. Thus, this study presents a new approach for the synthesis of DP-TiO2@C nanocomposites from a sacrificial Ti-MOF and provides insights into the efficient control of the volume ratio in DP-TiO2 anode architecture. © 2022 Wiley-VCH GmbH.
URI
http://hdl.handle.net/20.500.11750/17310
DOI
10.1002/smtd.202201066
Publisher
Wiley
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