TY - JOUR
T1 - Synergetic Cobalt-Copper-Based Bimetal–Organic Framework Nanoboxes toward Efficient Electrochemical Oxygen Evolution
AU - Cheng, Weiren
AU - Wu, Zhi-Peng
AU - Luan, Deyan
AU - Zang, Shuang-Quan
AU - Lou, Xiong Wen (David)
PY - 2021/12/6
Y1 - 2021/12/6
N2 - The development of efficient oxygen electrocatalysts and understanding their underlying catalytic mechanism are of significant importance for the high-performance energy conversion and storage technologies. Herein, we report novel CoCu-based bimetallic metal–organic framework nanoboxes (CoCu-MOF NBs) as promising catalysts toward efficient electrochemical oxygen evolution reaction (OER), fabricated via a successive cation and ligand exchange strategy. With the highly exposed bimetal centers and the well-designed architecture, the CoCu-MOF NBs show excellent OER activity and stability, with a small overpotential of 271 mV at 10 mA cm−2 and a high turnover frequency value of 0.326 s−1 at an overpotential of 300 mV. In combination of quasi in situ X-ray absorption fine structure spectroscopy and density-functional theory calculations, the post-formed CoCu-based oxyhydroxide analogue during OER is believed to account for the high OER activity of CoCu-MOF NBs, where the electronic synergy between Co and neighbouring Cu atoms promotes the O−O bond coupling toward fast OER kinetics. © 2021 Wiley-VCH GmbH
AB - The development of efficient oxygen electrocatalysts and understanding their underlying catalytic mechanism are of significant importance for the high-performance energy conversion and storage technologies. Herein, we report novel CoCu-based bimetallic metal–organic framework nanoboxes (CoCu-MOF NBs) as promising catalysts toward efficient electrochemical oxygen evolution reaction (OER), fabricated via a successive cation and ligand exchange strategy. With the highly exposed bimetal centers and the well-designed architecture, the CoCu-MOF NBs show excellent OER activity and stability, with a small overpotential of 271 mV at 10 mA cm−2 and a high turnover frequency value of 0.326 s−1 at an overpotential of 300 mV. In combination of quasi in situ X-ray absorption fine structure spectroscopy and density-functional theory calculations, the post-formed CoCu-based oxyhydroxide analogue during OER is believed to account for the high OER activity of CoCu-MOF NBs, where the electronic synergy between Co and neighbouring Cu atoms promotes the O−O bond coupling toward fast OER kinetics. © 2021 Wiley-VCH GmbH
KW - bimetallic synergy
KW - electrocatalysis
KW - hollow nanostructure
KW - MOFs
KW - OER
UR - http://www.scopus.com/inward/record.url?scp=85118498591&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85118498591&origin=recordpage
U2 - 10.1002/anie.202112775
DO - 10.1002/anie.202112775
M3 - RGC 21 - Publication in refereed journal
C2 - 34661372
SN - 1433-7851
VL - 60
SP - 26397
EP - 26402
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 50
ER -