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

Kód výsledku v 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>

Nalezeny alternativní kódy

RIV/60461373:22310/20:43920497

Výsledek na webu

<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>

Jazyk výsledku

angličtina

Název v původním jazyce

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

Popis výsledku v původním jazyce

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.

Název v anglickém jazyce

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

Popis výsledku anglicky

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.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10403 - Physical chemistry

Projekt

<a href="/cs/project/GX19-26896X" target="_blank" >GX19-26896X: Elektrochemie 2D Nanomateriálů</a><br>

Návaznosti

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

Rok uplatnění

2020

Kód důvěrnosti údajů

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

Název periodika

SUSTAINABLE ENERGY & FUELS

ISSN

2398-4902

e-ISSN

—

Svazek periodika

4

Číslo periodika v rámci svazku

7

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

7

Strana od-do

3732-3738

Kód UT WoS článku

000544657200050

EID výsledku v databázi Scopus

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