TY - JOUR
T1 - Yolk-shell carbon microspheres with controlled yolk and void volumes and shell thickness and their application as a cathode material for Li-S batteries
AU - Hong, Young Jun
AU - Lee, Jung Kul
AU - Chan Kang, Yun
N1 - Funding Information:
This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (NRF-2015R1A2A1A15056049). This work was supported by the Energy Efficiency & Resources Core Technology Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP), granted financial resource from the Ministry of Trade, Industry & Energy, Republic of Korea (201320200000420 and 20153030091450
Publisher Copyright:
© The Royal Society of Chemistry.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017
Y1 - 2017
N2 - Carbon yolk-shell microspheres are ideal sulfur host materials for Li-S batteries because they can accommodate the volume expansion of sulfur during charge-discharge cycles. In this study, yolk-shell structured carbon microspheres are prepared by spray pyrolysis, and their formation mechanism is investigated. SnO2/carbon-carbon core-shell microspheres, prepared by one-step spray pyrolysis using a solution containing tin(ii) oxalate, polyvinylpyrrolidone (PVP), and sucrose, are used as precursor microspheres; the shell and core are formed from PVP and sucrose, respectively. Carbon yolk-shell microspheres with a carbon-void-carbon configuration are prepared by the elimination of SnO2 using Se under a reducing atmosphere. The carbon yolk-shell microspheres prepared from the solution containing sucrose have more filled yolk than the microspheres prepared from the solution without sucrose. The first discharge and charge capacities of the sulfur infiltrated carbon yolk-shell microspheres with a filled yolk at a current density of 0.1 A g−1 are 1503 and 1368 mA h g−1, respectively. The discharge capacity of the microspheres after the 150th cycle at a current density of 0.5 A g−1 is 602 mA h g−1. The microspheres have high reversible discharge capacities of 817, 735, 626, 513, and 340 mA h g−1 at the current densities of 0.5, 1, 2, 4, and 10 A g−1, respectively. The sulfur-infiltrated carbon yolk-shell microspheres with the filled yolk show superior rate performance compared to the hollow microspheres with negligible yolk.
AB - Carbon yolk-shell microspheres are ideal sulfur host materials for Li-S batteries because they can accommodate the volume expansion of sulfur during charge-discharge cycles. In this study, yolk-shell structured carbon microspheres are prepared by spray pyrolysis, and their formation mechanism is investigated. SnO2/carbon-carbon core-shell microspheres, prepared by one-step spray pyrolysis using a solution containing tin(ii) oxalate, polyvinylpyrrolidone (PVP), and sucrose, are used as precursor microspheres; the shell and core are formed from PVP and sucrose, respectively. Carbon yolk-shell microspheres with a carbon-void-carbon configuration are prepared by the elimination of SnO2 using Se under a reducing atmosphere. The carbon yolk-shell microspheres prepared from the solution containing sucrose have more filled yolk than the microspheres prepared from the solution without sucrose. The first discharge and charge capacities of the sulfur infiltrated carbon yolk-shell microspheres with a filled yolk at a current density of 0.1 A g−1 are 1503 and 1368 mA h g−1, respectively. The discharge capacity of the microspheres after the 150th cycle at a current density of 0.5 A g−1 is 602 mA h g−1. The microspheres have high reversible discharge capacities of 817, 735, 626, 513, and 340 mA h g−1 at the current densities of 0.5, 1, 2, 4, and 10 A g−1, respectively. The sulfur-infiltrated carbon yolk-shell microspheres with the filled yolk show superior rate performance compared to the hollow microspheres with negligible yolk.
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U2 - 10.1039/C6TA08328E
DO - 10.1039/C6TA08328E
M3 - Article
AN - SCOPUS:85010460652
SN - 2050-7488
VL - 5
SP - 988
EP - 995
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 3
ER -