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Facile and solvothermal synthesis of rationally designed mesoporous NiCoSe2 nanostructure and its improved lithium and sodium storage properties

•Mesoporous NiCoSe2 has been prepared by a facile solvothermal synthesis technique.•The prepared NiCoSe2 has been attempted as an anode for LIBs and SIBs.•For LIBs, MNCS50 shows the discharge capacity of 387 mAh g−1 at 1600 mA g−1.•For SIBs, MNCS50 shows the discharge capacity of 293 mAh g−1 at 1000...

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Published in:Applied materials today 2020-12, Vol.21, p.100807, Article 100807
Main Authors: Santhoshkumar, P., Shaji, Nitheesha, Sim, Gyu Sang, Nanthagopal, Murugan, Park, Jae Woo, Lee, Chang Woo
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cited_by cdi_FETCH-LOGICAL-c300t-e6ad211f4b90d18ffa8ddffed9724b1dea96263cc25546b19f16beec6c24ce573
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container_title Applied materials today
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creator Santhoshkumar, P.
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description •Mesoporous NiCoSe2 has been prepared by a facile solvothermal synthesis technique.•The prepared NiCoSe2 has been attempted as an anode for LIBs and SIBs.•For LIBs, MNCS50 shows the discharge capacity of 387 mAh g−1 at 1600 mA g−1.•For SIBs, MNCS50 shows the discharge capacity of 293 mAh g−1 at 1000 mA g−1.•The MNCS50 exhibits a promising alternative in both LIBs and SIBs. Rechargeable metal ion batteries have attracted considerable attention in modern society because environmental issues are getting worse over time. They are highly expecting to play a vital role in day-to-day life in portable electronic devices (EVs) as well as hybrid electric vehicles (HEVs). Herein, we report the synthesis of bimetallic dichalcogenide by a solvothermal technique and systematically explore the effect of mesoporous NiCoSe2 (MNCS) nanostructures by controlling the ratio of surface-active agent during the synthesis process. The depth morphological evaluation using high-resolution field-emission transmission electron microscopy (HR FE-TEM) suggests that all the MNCS nanostructures display similar morphology with an extended network of material architecture when the ratio of surface active agent increased and thus interestingly play an important role in enhancement of surface area and porosity of the as-prepared electrode architecture. Interestingly, an obtained MNCS50 nanostructure displays a specific capacity of 557 and 398 mAh g−1 after 100 and 60 cycles for lithium ion batteries (LIBs) and sodium ion batteries (SIBs), respectively. The larger surface area and high porous nature of MNCS50 nanostructure affords more spaces to accommodate larger numbers of lithium (Li) and sodium (Na) ions during the discharge/charge process, and the nanostructured electrode material often enhances the electrical conductivity. These observations are indicating the use of nanostructured anode materials for LIBs and SIBs. [Display omitted]
doi_str_mv 10.1016/j.apmt.2020.100807
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Rechargeable metal ion batteries have attracted considerable attention in modern society because environmental issues are getting worse over time. They are highly expecting to play a vital role in day-to-day life in portable electronic devices (EVs) as well as hybrid electric vehicles (HEVs). Herein, we report the synthesis of bimetallic dichalcogenide by a solvothermal technique and systematically explore the effect of mesoporous NiCoSe2 (MNCS) nanostructures by controlling the ratio of surface-active agent during the synthesis process. The depth morphological evaluation using high-resolution field-emission transmission electron microscopy (HR FE-TEM) suggests that all the MNCS nanostructures display similar morphology with an extended network of material architecture when the ratio of surface active agent increased and thus interestingly play an important role in enhancement of surface area and porosity of the as-prepared electrode architecture. Interestingly, an obtained MNCS50 nanostructure displays a specific capacity of 557 and 398 mAh g−1 after 100 and 60 cycles for lithium ion batteries (LIBs) and sodium ion batteries (SIBs), respectively. The larger surface area and high porous nature of MNCS50 nanostructure affords more spaces to accommodate larger numbers of lithium (Li) and sodium (Na) ions during the discharge/charge process, and the nanostructured electrode material often enhances the electrical conductivity. These observations are indicating the use of nanostructured anode materials for LIBs and SIBs. 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Rechargeable metal ion batteries have attracted considerable attention in modern society because environmental issues are getting worse over time. They are highly expecting to play a vital role in day-to-day life in portable electronic devices (EVs) as well as hybrid electric vehicles (HEVs). Herein, we report the synthesis of bimetallic dichalcogenide by a solvothermal technique and systematically explore the effect of mesoporous NiCoSe2 (MNCS) nanostructures by controlling the ratio of surface-active agent during the synthesis process. The depth morphological evaluation using high-resolution field-emission transmission electron microscopy (HR FE-TEM) suggests that all the MNCS nanostructures display similar morphology with an extended network of material architecture when the ratio of surface active agent increased and thus interestingly play an important role in enhancement of surface area and porosity of the as-prepared electrode architecture. Interestingly, an obtained MNCS50 nanostructure displays a specific capacity of 557 and 398 mAh g−1 after 100 and 60 cycles for lithium ion batteries (LIBs) and sodium ion batteries (SIBs), respectively. The larger surface area and high porous nature of MNCS50 nanostructure affords more spaces to accommodate larger numbers of lithium (Li) and sodium (Na) ions during the discharge/charge process, and the nanostructured electrode material often enhances the electrical conductivity. These observations are indicating the use of nanostructured anode materials for LIBs and SIBs. 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Rechargeable metal ion batteries have attracted considerable attention in modern society because environmental issues are getting worse over time. They are highly expecting to play a vital role in day-to-day life in portable electronic devices (EVs) as well as hybrid electric vehicles (HEVs). Herein, we report the synthesis of bimetallic dichalcogenide by a solvothermal technique and systematically explore the effect of mesoporous NiCoSe2 (MNCS) nanostructures by controlling the ratio of surface-active agent during the synthesis process. The depth morphological evaluation using high-resolution field-emission transmission electron microscopy (HR FE-TEM) suggests that all the MNCS nanostructures display similar morphology with an extended network of material architecture when the ratio of surface active agent increased and thus interestingly play an important role in enhancement of surface area and porosity of the as-prepared electrode architecture. Interestingly, an obtained MNCS50 nanostructure displays a specific capacity of 557 and 398 mAh g−1 after 100 and 60 cycles for lithium ion batteries (LIBs) and sodium ion batteries (SIBs), respectively. The larger surface area and high porous nature of MNCS50 nanostructure affords more spaces to accommodate larger numbers of lithium (Li) and sodium (Na) ions during the discharge/charge process, and the nanostructured electrode material often enhances the electrical conductivity. These observations are indicating the use of nanostructured anode materials for LIBs and SIBs. [Display omitted]</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.apmt.2020.100807</doi></addata></record>
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Metal ion batteries
Negative electrode
Solvothermal
Surface active agent
title Facile and solvothermal synthesis of rationally designed mesoporous NiCoSe2 nanostructure and its improved lithium and sodium storage properties
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