TY - JOUR
T1 - Constructing NiCo/Fe3O4 Heteroparticles within MOF-74 for Efficient Oxygen Evolution Reactions
AU - Wang, Xiaolu
AU - Xiao, Hai
AU - Li, Ang
AU - Li, Zhi
AU - Liu, Shoujie
AU - Zhang, Qinghua
AU - Gong, Yue
AU - Zheng, Lirong
AU - Zhu, Youqi
AU - Chen, Chen
AU - Wang, Dingsheng
AU - Peng, Qing
AU - Gu, Lin
AU - Han, Xiaodong
AU - Li, Jun
AU - Li, Yadong
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/11/14
Y1 - 2018/11/14
N2 - Metal-organic frameworks (MOF) have recently emerged as versatile precursors to fabricate functional MOF derivatives for oxygen evolution reactions (OER). Herein, we developed a controlled partial pyrolysis strategy to construct robust NiCo/Fe3O4 heteroparticles within MOF-74 for efficient OER using trimetallic NiCoFe-MOF-74 as precursor. The partial pyrolysis method preserves the framework structure of MOF for effective substrates diffusion while producing highly active nanoparticles. The as-prepared NiCo/Fe3O4/MOF-74 delivered remarkably stable OER current with an overpotential as low as 238 mV at 10.0 mA cm-2 and an Tafel slop of 29 mV/dec, outperforming those of pristine NiCoFe-MOF-74, totally decomposed MOF derivatives, and most reported non-noble metal based electrocatalysts. The key for the formation of NiCo/Fe3O4/MOF-74 nanostructures is that the metals can be decomposed from NiCoFe-MOF-74 in the order of Ni, Co, and Fe under controlled heat treatment. Density functional theory calculations reveals that the underlying NiCo promotes the OER activity of Fe3O4 through exchange stabilization of active oxygen species.
AB - Metal-organic frameworks (MOF) have recently emerged as versatile precursors to fabricate functional MOF derivatives for oxygen evolution reactions (OER). Herein, we developed a controlled partial pyrolysis strategy to construct robust NiCo/Fe3O4 heteroparticles within MOF-74 for efficient OER using trimetallic NiCoFe-MOF-74 as precursor. The partial pyrolysis method preserves the framework structure of MOF for effective substrates diffusion while producing highly active nanoparticles. The as-prepared NiCo/Fe3O4/MOF-74 delivered remarkably stable OER current with an overpotential as low as 238 mV at 10.0 mA cm-2 and an Tafel slop of 29 mV/dec, outperforming those of pristine NiCoFe-MOF-74, totally decomposed MOF derivatives, and most reported non-noble metal based electrocatalysts. The key for the formation of NiCo/Fe3O4/MOF-74 nanostructures is that the metals can be decomposed from NiCoFe-MOF-74 in the order of Ni, Co, and Fe under controlled heat treatment. Density functional theory calculations reveals that the underlying NiCo promotes the OER activity of Fe3O4 through exchange stabilization of active oxygen species.
UR - http://www.scopus.com/inward/record.url?scp=85056521136&partnerID=8YFLogxK
U2 - 10.1021/jacs.8b08744
DO - 10.1021/jacs.8b08744
M3 - Article
C2 - 30352508
AN - SCOPUS:85056521136
SN - 0002-7863
VL - 140
SP - 15336
EP - 15341
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 45
ER -