<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Tabassum H</submitter><pubmed_abstract>To cater for the demands of electrochemical energy storage system, the development of cost effective, durable and highly efficient electrode materials is desired. Here, a novel electrode material based on redox active β-Co(OH)&lt;sub>2&lt;/sub> and B, N co-doped graphene nanohybrid is presented for electrochemical supercapacitor by employing a facile metal-organic frameworks (MOFs) route through pyrolysis and hydrothermal treatment. The Co(OH)&lt;sub>2&lt;/sub> could be firmly stabilized by dual protection of N-doped carbon polyhedron (CP) and B/N co-doped graphene (BCN) nanosheets. Interestingly, the porous carbon and BCN nanosheets greatly improve the charge storage, wettability, and redox activity of electrodes. Thus the hybrid delivers specific capacitance of 1263 F g&lt;sup>-1&lt;/sup> at a current density of 1A g&lt;sup>-1&lt;/sup> with 90% capacitance retention over 5000 cycles. Furthermore, the new aqueous asymmetric supercapacitor (ASC) was also designed by using Co(OH)&lt;sub>2&lt;/sub>@CP@BCN nanohybrid and BCN nanosheets as positive and negative electrodes respectively, which leads to high energy density of 20.25 Whkg&lt;sup>-1&lt;/sup>. This device also exhibits excellent rate capability with energy density of 15.55 Whkg&lt;sup>-1&lt;/sup> at power density of 9331 Wkg&lt;sup>-1&lt;/sup> coupled long termed stability up to 6000 cycles.</pubmed_abstract><journal>Scientific reports</journal><pagination>43084</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5327408</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Hierarchical Cobalt Hydroxide and B/N Co-Doped Graphene Nanohybrids Derived from Metal-Organic Frameworks for High Energy Density Asymmetric Supercapacitors.</pubmed_title><pmcid>PMC5327408</pmcid><pubmed_authors>Tabassum H</pubmed_authors><pubmed_authors>Mahmood A</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhao R</pubmed_authors><pubmed_authors>Liang Z</pubmed_authors><pubmed_authors>Qiu B</pubmed_authors><pubmed_authors>Zou R</pubmed_authors><pubmed_authors>Xia W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hierarchical Cobalt Hydroxide and B/N Co-Doped Graphene Nanohybrids Derived from Metal-Organic Frameworks for High Energy Density Asymmetric Supercapacitors.</name><description>To cater for the demands of electrochemical energy storage system, the development of cost effective, durable and highly efficient electrode materials is desired. Here, a novel electrode material based on redox active β-Co(OH)&lt;sub>2&lt;/sub> and B, N co-doped graphene nanohybrid is presented for electrochemical supercapacitor by employing a facile metal-organic frameworks (MOFs) route through pyrolysis and hydrothermal treatment. The Co(OH)&lt;sub>2&lt;/sub> could be firmly stabilized by dual protection of N-doped carbon polyhedron (CP) and B/N co-doped graphene (BCN) nanosheets. Interestingly, the porous carbon and BCN nanosheets greatly improve the charge storage, wettability, and redox activity of electrodes. Thus the hybrid delivers specific capacitance of 1263 F g&lt;sup>-1&lt;/sup> at a current density of 1A g&lt;sup>-1&lt;/sup> with 90% capacitance retention over 5000 cycles. Furthermore, the new aqueous asymmetric supercapacitor (ASC) was also designed by using Co(OH)&lt;sub>2&lt;/sub>@CP@BCN nanohybrid and BCN nanosheets as positive and negative electrodes respectively, which leads to high energy density of 20.25 Whkg&lt;sup>-1&lt;/sup>. This device also exhibits excellent rate capability with energy density of 15.55 Whkg&lt;sup>-1&lt;/sup> at power density of 9331 Wkg&lt;sup>-1&lt;/sup> coupled long termed stability up to 6000 cycles.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Feb</publication><modification>2024-02-14T23:37:54.911Z</modification><creation>2019-03-27T02:37:25Z</creation></dates><accession>S-EPMC5327408</accession><cross_references><pubmed>28240224</pubmed><doi>10.1038/srep43084</doi></cross_references></HashMap>