Self-Templated Formation of P2-type K0.6CoO2 Microspheres for High Reversible Potassium-Ion Batteries
Layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored for sodium-ion batteries. However, their application to potassium-ion batteries (PIBs) is hampered because of the poor cycling stability and low rate capab...
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Published in | Nano letters Vol. 18; no. 2; pp. 1522 - 1529 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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American Chemical Society
14.02.2018
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Abstract | Layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored for sodium-ion batteries. However, their application to potassium-ion batteries (PIBs) is hampered because of the poor cycling stability and low rate capability due to the larger ionic size of K+ than of Li+ or Na+. Herein, a facile self-templated strategy was used to synthesize unique P2-type K0.6CoO2 microspheres that consist of aggregated primary nanoplates as PIB cathodes. The unique K0.6CoO2 microspheres with aggregated structure significantly enhanced the kinetics of the K+ intercalation/deintercation and also minimized the parasitic reactions between the electrolyte and K0.6CoO2. The P2-K0.6CoO2 microspheres demonstrated a high reversible capacity of 82 mAh g–1 at 10 mA g–1, high rate capability of 65 mAh g–1 at 100 mA g–1, and long cycle life (87% capacity retention over 300 cycles). The high reversibility of the P2-K0.6CoO2 full cell paired with a hard carbon anode further demonstrated the feasibility of PIBs. This work not only successfully demonstrates exceptional performance of P2-type K0.6CoO2 cathodes and microspheres K0.6CoO2∥hard carbon full cells, but also provides new insights into the exploration of other layered metal oxides for PIBs. |
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AbstractList | We report that layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored for sodium-ion batteries. However, their application to potassium-ion batteries (PIBs) is hampered because of the poor cycling stability and low rate capability due to the larger ionic size of K+ than of Li+ or Na+. Herein, a facile self-templated strategy was used to synthesize unique P2-type K0.6CoO2 microspheres that consist of aggregated primary nanoplates as PIB cathodes. The unique K0.6CoO2 microspheres with aggregated structure significantly enhanced the kinetics of the K+ intercalation/deintercation and also minimized the parasitic reactions between the electrolyte and K0.6CoO2. The P2-K0.6CoO2 microspheres demonstrated a high reversible capacity of 82 mAh g–1 at 10 mA g–1, high rate capability of 65 mAh g–1 at 100 mA g–1, and long cycle life (87% capacity retention over 300 cycles). The high reversibility of the P2-K0.6CoO2 full cell paired with a hard carbon anode further demonstrated the feasibility of PIBs. Lastly, this work not only successfully demonstrates exceptional performance of P2-type K0.6CoO2 cathodes and microspheres K0.6CoO2∥hard carbon full cells, but also provides new insights into the exploration of other layered metal oxides for PIBs. Layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored for sodium-ion batteries. However, their application to potassium-ion batteries (PIBs) is hampered because of the poor cycling stability and low rate capability due to the larger ionic size of K+ than of Li+ or Na+. Herein, a facile self-templated strategy was used to synthesize unique P2-type K0.6CoO2 microspheres that consist of aggregated primary nanoplates as PIB cathodes. The unique K0.6CoO2 microspheres with aggregated structure significantly enhanced the kinetics of the K+ intercalation/deintercation and also minimized the parasitic reactions between the electrolyte and K0.6CoO2. The P2-K0.6CoO2 microspheres demonstrated a high reversible capacity of 82 mAh g–1 at 10 mA g–1, high rate capability of 65 mAh g–1 at 100 mA g–1, and long cycle life (87% capacity retention over 300 cycles). The high reversibility of the P2-K0.6CoO2 full cell paired with a hard carbon anode further demonstrated the feasibility of PIBs. This work not only successfully demonstrates exceptional performance of P2-type K0.6CoO2 cathodes and microspheres K0.6CoO2∥hard carbon full cells, but also provides new insights into the exploration of other layered metal oxides for PIBs. Layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored for sodium-ion batteries. However, their application to potassium-ion batteries (PIBs) is hampered because of the poor cycling stability and low rate capability due to the larger ionic size of K+ than of Li+ or Na+. Herein, a facile self-templated strategy was used to synthesize unique P2-type K0.6CoO2 microspheres that consist of aggregated primary nanoplates as PIB cathodes. The unique K0.6CoO2 microspheres with aggregated structure significantly enhanced the kinetics of the K+ intercalation/deintercation and also minimized the parasitic reactions between the electrolyte and K0.6CoO2. The P2-K0.6CoO2 microspheres demonstrated a high reversible capacity of 82 mAh g-1 at 10 mA g-1, high rate capability of 65 mAh g-1 at 100 mA g-1, and long cycle life (87% capacity retention over 300 cycles). The high reversibility of the P2-K0.6CoO2 full cell paired with a hard carbon anode further demonstrated the feasibility of PIBs. This work not only successfully demonstrates exceptional performance of P2-type K0.6CoO2 cathodes and microspheres K0.6CoO2∥hard carbon full cells, but also provides new insights into the exploration of other layered metal oxides for PIBs.Layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored for sodium-ion batteries. However, their application to potassium-ion batteries (PIBs) is hampered because of the poor cycling stability and low rate capability due to the larger ionic size of K+ than of Li+ or Na+. Herein, a facile self-templated strategy was used to synthesize unique P2-type K0.6CoO2 microspheres that consist of aggregated primary nanoplates as PIB cathodes. The unique K0.6CoO2 microspheres with aggregated structure significantly enhanced the kinetics of the K+ intercalation/deintercation and also minimized the parasitic reactions between the electrolyte and K0.6CoO2. The P2-K0.6CoO2 microspheres demonstrated a high reversible capacity of 82 mAh g-1 at 10 mA g-1, high rate capability of 65 mAh g-1 at 100 mA g-1, and long cycle life (87% capacity retention over 300 cycles). The high reversibility of the P2-K0.6CoO2 full cell paired with a hard carbon anode further demonstrated the feasibility of PIBs. This work not only successfully demonstrates exceptional performance of P2-type K0.6CoO2 cathodes and microspheres K0.6CoO2∥hard carbon full cells, but also provides new insights into the exploration of other layered metal oxides for PIBs. |
Author | Wang, Chunsheng Chen, Ji Deng, Tao Hou, Singyuk Eidson, Nico Chen, Long Zhou, Xiuquan Luo, Chao Fan, Xiulin |
AuthorAffiliation | Department of Chemistry and Biochemistry Department of Chemical and Biomolecular Engineering |
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Author_xml | – sequence: 1 givenname: Tao surname: Deng fullname: Deng, Tao – sequence: 2 givenname: Xiulin surname: Fan fullname: Fan, Xiulin – sequence: 3 givenname: Chao surname: Luo fullname: Luo, Chao – sequence: 4 givenname: Ji orcidid: 0000-0003-0326-8304 surname: Chen fullname: Chen, Ji – sequence: 5 givenname: Long surname: Chen fullname: Chen, Long – sequence: 6 givenname: Singyuk surname: Hou fullname: Hou, Singyuk – sequence: 7 givenname: Nico surname: Eidson fullname: Eidson, Nico – sequence: 8 givenname: Xiuquan orcidid: 0000-0002-1361-3880 surname: Zhou fullname: Zhou, Xiuquan – sequence: 9 givenname: Chunsheng orcidid: 0000-0002-8626-6381 surname: Wang fullname: Wang, Chunsheng email: cswang@umd.edu |
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Snippet | Layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored for sodium-ion... We report that layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored... |
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SubjectTerms | bio-inspired Cathode material charge transport defects ENERGY STORAGE energy storage (including batteries and capacitors) high reversibility K0.6CoO2 layered metal oxides MATERIALS SCIENCE potassium-ion battery synthesis (novel materials) synthesis (scalable processing) synthesis (self-assembly) |
Title | Self-Templated Formation of P2-type K0.6CoO2 Microspheres for High Reversible Potassium-Ion Batteries |
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