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Metal-organic-frameworks on 3D-printed electrodes:in situelectrochemical transformation towards the oxygen evolution reaction

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F20%3APU138313" target="_blank" >RIV/00216305:26620/20:PU138313 - isvavai.cz</a>

  • Alternative codes found

    RIV/60461373:22310/20:43920497

  • Result on the web

    <a href="https://pubs.rsc.org/en/content/articlelanding/2020/SE/D0SE00503G#!divAbstract" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2020/SE/D0SE00503G#!divAbstract</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d0se00503g" target="_blank" >10.1039/d0se00503g</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Metal-organic-frameworks on 3D-printed electrodes:in situelectrochemical transformation towards the oxygen evolution reaction

  • Original language description

    Metal-organic framework (MOF) derived materials are important alternatives for electrochemical energy storage and conversion, due to their highly large surface area, abundant active sites, and diversity in composition and structure. In this work, a controllable electrochemical transformation of ZIF-67 into active porous metal oxides is employed for the oxygen evolution reaction (OER). ZIF-67 is directly coated onto the surface of three-dimensional (3D) printed titanium (Ti) electrodes using a step-by-stepin situgrowth and then converted into cobalt oxide (Co3O4) by electrochemical cycling, designated as ZIF-67/Ti-E electrode. Raman spectroscopy, scanning electron microscopy (SEM), and cyclic voltammetry (CV) have been used to verify the electrochemical transformation from octahedral ZIF-67 to thin sheet-shaped Co3O4. This large-surface-area Co3O4, as well as the existence of Co(IV)species right before water oxidation, plays a critical role in enhanced OER performance under alkaline electrolysis conditions. The optimized ZIF-67/Ti-E electrode has demonstrated a better OER performance with a low overpotential of 360 mV at a current density of 10 mA cm(-2)and excellent durability, compared with its counterparts produced by the widely popular calcination method. Our method provides a simplein situ, fast, mild, and energy-efficient approach to employ MOF-derived materials as promising OER catalysts using scaled-up 3D-printed electrodes.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10403 - Physical chemistry

Result continuities

  • Project

    <a href="/en/project/GX19-26896X" target="_blank" >GX19-26896X: 2D Nanomaterials Electrochemistry</a><br>

  • Continuities

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

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    SUSTAINABLE ENERGY & FUELS

  • ISSN

    2398-4902

  • e-ISSN

  • Volume of the periodical

    4

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    7

  • Pages from-to

    3732-3738

  • UT code for WoS article

    000544657200050

  • EID of the result in the Scopus database