Covalent-organic frameworks: potential host materials for sulfur impregnation in lithium–sulfur batteries
Commercial development of lithium–sulfur (Li–S) batteries is severely hindered by their insufficient cyclability, which is due to the loss of soluble lithium polysulfide intermediates generated during the discharge processes. To overcome this problem, considerable efforts have been devoted to design...
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| Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 2; no. 23; pp. 8854 - 8858 |
|---|---|
| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
01.01.2014
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| Subjects | |
| Online Access | Get full text |
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| Abstract | Commercial development of lithium–sulfur (Li–S) batteries is severely hindered by their insufficient cyclability, which is due to the loss of soluble lithium polysulfide intermediates generated during the discharge processes. To overcome this problem, considerable efforts have been devoted to designing novel micro- or nano-structured host materials, aiming to trap soluble polysulfide within the network. Herein, we report a new approach to construct a sulfur electrode by impregnating sulfur into the nanopores of covalent-organic frameworks (COFs). Our results clearly demonstrate that by using a 2D COF as a host material,
e.g.
CTF-1 (CTF: covalent triazine-based framework), the thus-prepared cathode can show a remarkable positive effect on the capacity retention of Li–S batteries. Considering the unique features of COFs, such as highly flexible molecular design and a controllable pore size, this proof-of-principle study provides new opportunities for materials scientists for tailoring cathode materials in Li–S batteries. |
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| AbstractList | Commercial development of lithium–sulfur (Li–S) batteries is severely hindered by their insufficient cyclability, which is due to the loss of soluble lithium polysulfide intermediates generated during the discharge processes. To overcome this problem, considerable efforts have been devoted to designing novel micro- or nano-structured host materials, aiming to trap soluble polysulfide within the network. Herein, we report a new approach to construct a sulfur electrode by impregnating sulfur into the nanopores of covalent-organic frameworks (COFs). Our results clearly demonstrate that by using a 2D COF as a host material, e.g. CTF-1 (CTF: covalent triazine-based framework), the thus-prepared cathode can show a remarkable positive effect on the capacity retention of Li–S batteries. Considering the unique features of COFs, such as highly flexible molecular design and a controllable pore size, this proof-of-principle study provides new opportunities for materials scientists for tailoring cathode materials in Li–S batteries. Commercial development of lithium–sulfur (Li–S) batteries is severely hindered by their insufficient cyclability, which is due to the loss of soluble lithium polysulfide intermediates generated during the discharge processes. To overcome this problem, considerable efforts have been devoted to designing novel micro- or nano-structured host materials, aiming to trap soluble polysulfide within the network. Herein, we report a new approach to construct a sulfur electrode by impregnating sulfur into the nanopores of covalent-organic frameworks (COFs). Our results clearly demonstrate that by using a 2D COF as a host material, e.g. CTF-1 (CTF: covalent triazine-based framework), the thus-prepared cathode can show a remarkable positive effect on the capacity retention of Li–S batteries. Considering the unique features of COFs, such as highly flexible molecular design and a controllable pore size, this proof-of-principle study provides new opportunities for materials scientists for tailoring cathode materials in Li–S batteries. |
| Author | Liao, Huaping Wang, Cheng Ding, Huimin Ai, Xinping Li, Bijian |
| Author_xml | – sequence: 1 givenname: Huaping surname: Liao fullname: Liao, Huaping organization: Key Laboratory of Biomedical Polymers (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China – sequence: 2 givenname: Huimin surname: Ding fullname: Ding, Huimin organization: Key Laboratory of Biomedical Polymers (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China – sequence: 3 givenname: Bijian surname: Li fullname: Li, Bijian organization: Key Laboratory of Biomedical Polymers (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China – sequence: 4 givenname: Xinping surname: Ai fullname: Ai, Xinping organization: Key Laboratory of Biomedical Polymers (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China – sequence: 5 givenname: Cheng surname: Wang fullname: Wang, Cheng organization: Key Laboratory of Biomedical Polymers (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China |
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| Snippet | Commercial development of lithium–sulfur (Li–S) batteries is severely hindered by their insufficient cyclability, which is due to the loss of soluble lithium... Commercial development of lithium-sulfur (Li-S) batteries is severely hindered by their insufficient cyclability, which is due to the loss of soluble lithium... |
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| SubjectTerms | cathodes chemistry lithium lithium batteries nanopores porosity sulfur |
| Title | Covalent-organic frameworks: potential host materials for sulfur impregnation in lithium–sulfur batteries |
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