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NiCoFe‐Layered Double Hydroxides/N‐Doped Graphene Oxide Array Colloid Composite as an Efficient Bifunctional Catalyst for Oxygen Electrocatalytic Reactions
Author(s) -
Zhou Daojin,
Cai Zhao,
Lei Xiaodong,
Tian Weiliang,
Bi Yongmin,
Jia Yin,
Han Nana,
Gao Tengfei,
Zhang Qian,
Kuang Yun,
Pan Junqing,
Sun Xiaoming,
Duan Xue
Publication year - 2018
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201701905
Subject(s) - bifunctional , graphene , oxygen evolution , materials science , catalysis , oxide , inorganic chemistry , hydroxide , layered double hydroxides , electrochemistry , colloid , chemical engineering , bifunctional catalyst , electrode , nanotechnology , chemistry , organic chemistry , metallurgy , engineering
Ternary NiCoFe‐layered double hydroxide (NiCo III Fe‐LDH) with Co 3+ is grafted on nitrogen‐doped graphene oxide (N‐GO) by an in situ growth route. The array‐like colloid composite of NiCo III Fe‐LDH/N‐GO is used as a bifunctional catalyst for both oxygen evolution/reduction reactions (OER/ORR). The NiCo III Fe‐LDH/N‐GO array has a 3D open structure with less stacking of LDHs and an enlarged specific surface area. The hierarchical structure design and novel material chemistry endow high activity propelling O 2 redox. By exposing more amounts of Ni and Fe active sites, the NiCo III Fe‐LDH/N‐GO illustrates a relatively low onset potential (1.41 V vs reversible hydrogen electrode) in 0.1 mol L −1 KOH solution under the OER process. Furthermore, by introducing high valence Co 3+ , the onset potential of this material in ORR is 0.88 V. The overvoltage difference is 0.769 V between OER and ORR. The key factors for the excellent bifunctional catalytic performance are believed to be the Co with a high valence, the N‐doping of graphene materials, and the highly exposed Ni and Fe active sites in the array‐like colloid composite. This work further demonstrates the possibility to exploit the application potential of LDHs as OER and ORR bifunctional electrochemical catalysts.
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