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Metal‐Organic Fragments with Adhesive Excipient and Their Utilization to Stabilize Multimetallic Electrocatalysts for High Activity and Robust Durability in Oxygen Evolution Reaction

Multimetallic electrocatalysts have shown great potential to improve electrocatalytic performance, but their deteriorations in activity and durability are yet to be overcome. Here, metal‐organic fragments with adhesive excipient to realize high activity with good durability in oxygen evolution react...

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Autores principales: Choi, Won Ho, Kim, Keon‐Han, Lee, Heebin, Choi, Jae Won, Park, Dong Gyu, Kim, Gi Hwan, Choi, Kyung Min, Kang, Jeung Ku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188218/
https://www.ncbi.nlm.nih.gov/pubmed/34105280
http://dx.doi.org/10.1002/advs.202100044
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author Choi, Won Ho
Kim, Keon‐Han
Lee, Heebin
Choi, Jae Won
Park, Dong Gyu
Kim, Gi Hwan
Choi, Kyung Min
Kang, Jeung Ku
author_facet Choi, Won Ho
Kim, Keon‐Han
Lee, Heebin
Choi, Jae Won
Park, Dong Gyu
Kim, Gi Hwan
Choi, Kyung Min
Kang, Jeung Ku
author_sort Choi, Won Ho
collection PubMed
description Multimetallic electrocatalysts have shown great potential to improve electrocatalytic performance, but their deteriorations in activity and durability are yet to be overcome. Here, metal‐organic fragments with adhesive excipient to realize high activity with good durability in oxygen evolution reaction (OER) are developed. First, a leaf‐like zeolitic–imidazolate framework (ZIF‐L) is synthesized. Then, ionized species in hydrogen plasma attack preferentially the organic linkers of ZIF‐L to derive cobalt–imidazole fragments (CIFs) as adhesive excipient, while they are designed to retain the coordinated cobalt nodes. Moreover, the vacant coordination sites at cobalt nodes and the unbound nitrogen at organic linkers induce high porosity and conductivity. The CIFs serve to stably impregnate trimetallic FeNiMo electrocatalysts (CIF:FeNiMo), and CIF:FeNiMo containing Fe contents of 22% and hexavalent Mo contents show to enable high activity with low overpotentials (203 mV at 10 mA cm(−2) and 238 mV at 100 mA cm(−2)) in OER. The near O K‐edge extended X‐ray absorption fine structure proves further that high activity for OER originates from the partially filled e(g) orbitals. Additionally, CIF:FeNiMo exhibit good durability, as demonstrated by high activity retention during at least 45 days in OER.
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spelling pubmed-81882182021-06-16 Metal‐Organic Fragments with Adhesive Excipient and Their Utilization to Stabilize Multimetallic Electrocatalysts for High Activity and Robust Durability in Oxygen Evolution Reaction Choi, Won Ho Kim, Keon‐Han Lee, Heebin Choi, Jae Won Park, Dong Gyu Kim, Gi Hwan Choi, Kyung Min Kang, Jeung Ku Adv Sci (Weinh) Research Articles Multimetallic electrocatalysts have shown great potential to improve electrocatalytic performance, but their deteriorations in activity and durability are yet to be overcome. Here, metal‐organic fragments with adhesive excipient to realize high activity with good durability in oxygen evolution reaction (OER) are developed. First, a leaf‐like zeolitic–imidazolate framework (ZIF‐L) is synthesized. Then, ionized species in hydrogen plasma attack preferentially the organic linkers of ZIF‐L to derive cobalt–imidazole fragments (CIFs) as adhesive excipient, while they are designed to retain the coordinated cobalt nodes. Moreover, the vacant coordination sites at cobalt nodes and the unbound nitrogen at organic linkers induce high porosity and conductivity. The CIFs serve to stably impregnate trimetallic FeNiMo electrocatalysts (CIF:FeNiMo), and CIF:FeNiMo containing Fe contents of 22% and hexavalent Mo contents show to enable high activity with low overpotentials (203 mV at 10 mA cm(−2) and 238 mV at 100 mA cm(−2)) in OER. The near O K‐edge extended X‐ray absorption fine structure proves further that high activity for OER originates from the partially filled e(g) orbitals. Additionally, CIF:FeNiMo exhibit good durability, as demonstrated by high activity retention during at least 45 days in OER. John Wiley and Sons Inc. 2021-03-24 /pmc/articles/PMC8188218/ /pubmed/34105280 http://dx.doi.org/10.1002/advs.202100044 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Choi, Won Ho
Kim, Keon‐Han
Lee, Heebin
Choi, Jae Won
Park, Dong Gyu
Kim, Gi Hwan
Choi, Kyung Min
Kang, Jeung Ku
Metal‐Organic Fragments with Adhesive Excipient and Their Utilization to Stabilize Multimetallic Electrocatalysts for High Activity and Robust Durability in Oxygen Evolution Reaction
title Metal‐Organic Fragments with Adhesive Excipient and Their Utilization to Stabilize Multimetallic Electrocatalysts for High Activity and Robust Durability in Oxygen Evolution Reaction
title_full Metal‐Organic Fragments with Adhesive Excipient and Their Utilization to Stabilize Multimetallic Electrocatalysts for High Activity and Robust Durability in Oxygen Evolution Reaction
title_fullStr Metal‐Organic Fragments with Adhesive Excipient and Their Utilization to Stabilize Multimetallic Electrocatalysts for High Activity and Robust Durability in Oxygen Evolution Reaction
title_full_unstemmed Metal‐Organic Fragments with Adhesive Excipient and Their Utilization to Stabilize Multimetallic Electrocatalysts for High Activity and Robust Durability in Oxygen Evolution Reaction
title_short Metal‐Organic Fragments with Adhesive Excipient and Their Utilization to Stabilize Multimetallic Electrocatalysts for High Activity and Robust Durability in Oxygen Evolution Reaction
title_sort metal‐organic fragments with adhesive excipient and their utilization to stabilize multimetallic electrocatalysts for high activity and robust durability in oxygen evolution reaction
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188218/
https://www.ncbi.nlm.nih.gov/pubmed/34105280
http://dx.doi.org/10.1002/advs.202100044
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