TY - JOUR
T1 - MoSe2 Embedded CNT-Reduced Graphene Oxide Composite Microsphere with Superior Sodium Ion Storage and Electrocatalytic Hydrogen Evolution Performances
AU - Park, Gi Dae
AU - Kim, Jung Hyun
AU - Park, Seung Keun
AU - Kang, Yun Chan
N1 - Funding Information:
This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (Grant 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 (Grant 20153030091450).
PY - 2017/3/29
Y1 - 2017/3/29
N2 - Highly porous MoSe2-reduced graphene oxide-carbon nanotube (MoSe2-rGO-CNT) powders were prepared by a spray pyrolysis process. The synergistic effect of CNTs and rGO resulted in powders containing ultrafine MoSe2 nanocrystals with a minimal degree of stacking. The initial discharge capacities of MoSe2-rGO-CNT, MoSe2-CNT, MoSe2-rGO, and bare MoSe2 powders for sodium ion storage were 501.6, 459.7, 460.2, and 364.0 mA h g-1, respectively, at 1.0 A g-1. The MoSe2-rGO-CNT composite powders had superior cycling and rate performances compared with the MoSe2-CNT, MoSe2-rGO composite, and bare MoSe2 powders. The electrocatalytic activity of MoSe2-rGO-CNT in the hydrogen evolution reaction (HER) was also compared with that of MoSe2-CNT, MoSe2-rGO, and bare MoSe2. MoSe2-rGO-CNT composite powders exhibited an overpotential of 0.24 V at a current density of 10 mA cm-2, which was less than that of MoSe2-CNT (0.26 V at 10 mA cm-2), MoSe2-rGO (0.32 V at 10 mA cm-2), and bare MoSe2 (0.33 V at 10 mA cm-2). Tafel slopes for the MoSe2-rGO-CNT, MoSe2-CNT, MoSe2-rGO, and bare MoSe2 powders were 53, 76, 86, and 115 mV dec-1, respectively. Because a large electrochemical surface area and ultrafine MoSe2 nanocrystals, the MoSe2-rGO-CNT composite possesses more active sites than the MoSe2-CNT, MoSe2-rGO composite, and bare MoSe2 powders with extensive stacking and large crystalline size, which provide greater catalytic HER activity.
AB - Highly porous MoSe2-reduced graphene oxide-carbon nanotube (MoSe2-rGO-CNT) powders were prepared by a spray pyrolysis process. The synergistic effect of CNTs and rGO resulted in powders containing ultrafine MoSe2 nanocrystals with a minimal degree of stacking. The initial discharge capacities of MoSe2-rGO-CNT, MoSe2-CNT, MoSe2-rGO, and bare MoSe2 powders for sodium ion storage were 501.6, 459.7, 460.2, and 364.0 mA h g-1, respectively, at 1.0 A g-1. The MoSe2-rGO-CNT composite powders had superior cycling and rate performances compared with the MoSe2-CNT, MoSe2-rGO composite, and bare MoSe2 powders. The electrocatalytic activity of MoSe2-rGO-CNT in the hydrogen evolution reaction (HER) was also compared with that of MoSe2-CNT, MoSe2-rGO, and bare MoSe2. MoSe2-rGO-CNT composite powders exhibited an overpotential of 0.24 V at a current density of 10 mA cm-2, which was less than that of MoSe2-CNT (0.26 V at 10 mA cm-2), MoSe2-rGO (0.32 V at 10 mA cm-2), and bare MoSe2 (0.33 V at 10 mA cm-2). Tafel slopes for the MoSe2-rGO-CNT, MoSe2-CNT, MoSe2-rGO, and bare MoSe2 powders were 53, 76, 86, and 115 mV dec-1, respectively. Because a large electrochemical surface area and ultrafine MoSe2 nanocrystals, the MoSe2-rGO-CNT composite possesses more active sites than the MoSe2-CNT, MoSe2-rGO composite, and bare MoSe2 powders with extensive stacking and large crystalline size, which provide greater catalytic HER activity.
KW - carbon nanotube
KW - hydrogen evolution reaction
KW - molybdenum diselenide
KW - reduced graphene oxide
KW - sodium ion batteries
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U2 - 10.1021/acsami.7b00147
DO - 10.1021/acsami.7b00147
M3 - Article
C2 - 28263546
AN - SCOPUS:85016582042
SN - 1944-8244
VL - 9
SP - 10673
EP - 10683
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 12
ER -