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In situ cross-linking construction of 3D mesoporous bimetallic phosphide-in-carbon superstructure with atomic interface toward enhanced sodium ion storage performance

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27640%2F21%3A10247491" target="_blank" >RIV/61989100:27640/21:10247491 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/61989100:27740/21:10247491

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/pii/S1385894720335737" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1385894720335737</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.cej.2020.127449" target="_blank" >10.1016/j.cej.2020.127449</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    In situ cross-linking construction of 3D mesoporous bimetallic phosphide-in-carbon superstructure with atomic interface toward enhanced sodium ion storage performance

  • Popis výsledku v původním jazyce

    Constructing heterostructures are capable of offering fascinating performance for electronics owing to the built-in charge transfer driving force. However, exploring a universal methodology to rationally design and control-lable synthesis of heterostructure with high stability of interface is a big challenge. Also the synergistic effect of the heterointerface in the composites remains to be clarified. Here, we report three-dimensional (3D) FeP/CoP heterostructure embedded within N-doped carbon aerogel (FeP/CoP-NA) through an in situ cross-linking and phosphorization process. In such a 3D hybrid, the FeP/CoP heterocrystals are wrapped by N-doped carbon which form a core-shell structure. Benefiting from the unique porous network induced by N-doped carbon, the con-ducting highway is built to promote the ion and electron fast diffusion. This structure can accommodate the volume change of FeP/CoP, which prevent the agglomeration and act as the protecting layer to maintain the integrity of the interface. Impressively, the atomic interface between FeP/CoP is successfully constructed, which could not only introduce enhanced capacitive contribution to facilitate electron transport, but also provide extra active sites to adsorb more Na+ proved by both experiments and density functional theory (DFT) calculations. As expected, FeP/CoP-NA electrode demonstrates an excellent rate capability of 342 mAh g(-1) at a current of 5 A g(-1) current density. , a high specific capacity of 525 mAh g(-1) at 0.2 A g(-1), and a long cycling stability over 8000 cycles at high

  • Název v anglickém jazyce

    In situ cross-linking construction of 3D mesoporous bimetallic phosphide-in-carbon superstructure with atomic interface toward enhanced sodium ion storage performance

  • Popis výsledku anglicky

    Constructing heterostructures are capable of offering fascinating performance for electronics owing to the built-in charge transfer driving force. However, exploring a universal methodology to rationally design and control-lable synthesis of heterostructure with high stability of interface is a big challenge. Also the synergistic effect of the heterointerface in the composites remains to be clarified. Here, we report three-dimensional (3D) FeP/CoP heterostructure embedded within N-doped carbon aerogel (FeP/CoP-NA) through an in situ cross-linking and phosphorization process. In such a 3D hybrid, the FeP/CoP heterocrystals are wrapped by N-doped carbon which form a core-shell structure. Benefiting from the unique porous network induced by N-doped carbon, the con-ducting highway is built to promote the ion and electron fast diffusion. This structure can accommodate the volume change of FeP/CoP, which prevent the agglomeration and act as the protecting layer to maintain the integrity of the interface. Impressively, the atomic interface between FeP/CoP is successfully constructed, which could not only introduce enhanced capacitive contribution to facilitate electron transport, but also provide extra active sites to adsorb more Na+ proved by both experiments and density functional theory (DFT) calculations. As expected, FeP/CoP-NA electrode demonstrates an excellent rate capability of 342 mAh g(-1) at a current of 5 A g(-1) current density. , a high specific capacity of 525 mAh g(-1) at 0.2 A g(-1), and a long cycling stability over 8000 cycles at high

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10302 - Condensed matter physics (including formerly solid state physics, supercond.)

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/EF16_013%2F0001791" target="_blank" >EF16_013/0001791: IT4Innovations národní superpočítačové centrum - cesta k exascale</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2021

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Chemical engineering journal

  • ISSN

    1385-8947

  • e-ISSN

  • Svazek periodika

    413

  • Číslo periodika v rámci svazku

    June

  • Stát vydavatele periodika

    CH - Švýcarská konfederace

  • Počet stran výsledku

    9

  • Strana od-do

  • Kód UT WoS článku

    000638225400005

  • EID výsledku v databázi Scopus

    2-s2.0-85094556666