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Stable, Efficient, Copper Coordination Polymer-Derived Heterostructured Catalyst for Oxygen Evolution under pH-Universal Conditions
Author(s) -
Ligang Wang,
Ning Ma,
Nian Wu,
Xiaoge Wang,
Junjie Xin,
Dingsheng Wang,
Jianhua Lin,
Xingguo Li,
Junliang Sun
Publication year - 2021
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.1c01424
Subject(s) - oxygen evolution , materials science , catalysis , copper , water splitting , chemical engineering , epitaxy , electron transfer , oxygen , coordination polymer , polymer , electrode , nanotechnology , photochemistry , electrochemistry , chemistry , metallurgy , organic chemistry , composite material , photocatalysis , layer (electronics) , engineering
The constructure of a heterostructured interface is an effective way to design highly durable and efficient water oxidation electrocatalysts. Herein, Cu/CuCN with heterointerfaces is the first synthesized case through a simple epitaxial-like growth method, displaying superior activity and stability under pH-universal media. Associated with high electron transport and transfer of the epitaxial interfacial area, the Cu/CuCN pre-catalyst is applied to deliver the oxygen evolution reaction (OER) with lower overpotentials of 250 mV (forward scan) and 380 mV (backward scan) at 10 mA cm -2 and demonstrates better intrinsic activity ( j ECSA of 1.0 mA cm -2 at 420 mV) and impressive stability (136 h) in 1.0 M KOH, which exceeds most previous catalysts. Even using a nominal voltage of 1.5 V of a AA battery can drive the overall water-splitting setup. Experiments combined with theoretical simulations further uncover the existence of CuO species at the heterointerface during basic OER, which is evidence of better OER performance with abundant active sites that accelerate the conversion kinetics.

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