TY - JOUR
T1 - Porosity-controlled TiNb2O7 microspheres with partial nitridation as a practical negative electrode for high-power lithium-ion batteries
AU - Park, Hyunjung
AU - Wu, Hao Bin
AU - Song, Taeseup
AU - Lou, Xiong Wen
AU - Paik, Ungyu
N1 - Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].
PY - 2015/4/1
Y1 - 2015/4/1
N2 - Titanium niobium oxide (TiNb2O7) has been recognized as a promising anode material for lithium-ion batteries (LIBs) in view of its potential to operate at high rates with improved safety and high theoretical capacity of 387 mAh g-1. However, it suffers from poor Li+ ion diffusivity and low electronic conductivity originated from its wide band gap energy (Eg > 2 eV). Here, porous TiNb2O7 microspheres (PTNO MSs) are prepared via a facile solvothermal reaction. PTNO MSs have a particle size of ≈1.2 μm and controllable pore sizes in the range of 5-35 nm. Ammonia gas nitridation treatment is conducted on PTNO MSs to introduce conducting Ti1-xNbxN layer on the surface and form nitridated PTNO (NPTNO) MSs. The porous structure and conducting Ti1-xNbxN layer enhance the transport kinetics associated with Li+ ions and electrons, which leads to significant improvement in electrochemical performance. As a result, the NPTNO electrode shows a high discharge capacity of ≈265 mAh g-1, remarkable rate capability (≈143 mAh g-1 at 100 C) and durable long-term cyclability (≈91% capacity retention over 1000 cycles at 5 C). These results demonstrate the great potential of TiNb2O7 as a practical high-rate anode material for LIBs. Porosity controlled TiNb2O7 microspheres are successfully prepared via a facile solvothermal reaction. Ammonia gas treatment is then carried out to enhance conductivity with a Ti1-XNbXN layer formed on the surface. These partially nitridated TiNb2O7 microspheres show a superior rate capability of ≈143 mAh g-1 at 100 C and durable long-term cyclability of ≈91% capacity retention over 1000 cycles at 5 C. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
AB - Titanium niobium oxide (TiNb2O7) has been recognized as a promising anode material for lithium-ion batteries (LIBs) in view of its potential to operate at high rates with improved safety and high theoretical capacity of 387 mAh g-1. However, it suffers from poor Li+ ion diffusivity and low electronic conductivity originated from its wide band gap energy (Eg > 2 eV). Here, porous TiNb2O7 microspheres (PTNO MSs) are prepared via a facile solvothermal reaction. PTNO MSs have a particle size of ≈1.2 μm and controllable pore sizes in the range of 5-35 nm. Ammonia gas nitridation treatment is conducted on PTNO MSs to introduce conducting Ti1-xNbxN layer on the surface and form nitridated PTNO (NPTNO) MSs. The porous structure and conducting Ti1-xNbxN layer enhance the transport kinetics associated with Li+ ions and electrons, which leads to significant improvement in electrochemical performance. As a result, the NPTNO electrode shows a high discharge capacity of ≈265 mAh g-1, remarkable rate capability (≈143 mAh g-1 at 100 C) and durable long-term cyclability (≈91% capacity retention over 1000 cycles at 5 C). These results demonstrate the great potential of TiNb2O7 as a practical high-rate anode material for LIBs. Porosity controlled TiNb2O7 microspheres are successfully prepared via a facile solvothermal reaction. Ammonia gas treatment is then carried out to enhance conductivity with a Ti1-XNbXN layer formed on the surface. These partially nitridated TiNb2O7 microspheres show a superior rate capability of ≈143 mAh g-1 at 100 C and durable long-term cyclability of ≈91% capacity retention over 1000 cycles at 5 C. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
KW - anodes
KW - lithium-ion batteries
KW - microspheres
KW - TiNb2O7
UR - https://www.scopus.com/pages/publications/84928213554
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-84928213554&origin=recordpage
U2 - 10.1002/aenm.201401945
DO - 10.1002/aenm.201401945
M3 - RGC 21 - Publication in refereed journal
SN - 1614-6832
VL - 5
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 8
M1 - 1401945
ER -