TY - JOUR
T1 - Simple and cost effective fabrication of 3D porous core-shell Ni nanochains@NiFe layered double hydroxide nanosheet bifunctional electrocatalysts for overall water splitting
AU - Cai, Zhengyang
AU - Bu, Xiuming
AU - Wang, Ping
AU - Su, Wenqiang
AU - Wei, Renjie
AU - Ho, Johnny C.
AU - Yang, Junhe
AU - Wang, Xianying
N1 - Funding Information:
We greatly appreciate the nancial supports from the National Natural Science Foundation of China (51572173, 51602197, 51771121 and 51702212), Science and Technology Commission of Shanghai Municipality (16060502300, 16JC402200 and 18511110600), Innovation Program of Shanghai Municipal Education Commission (2019-01-07-00-07-E00015), Program of Shanghai Academic Research Leader (19XD1422900), Shanghai Eastern Scholar Program (QD2016014) and General Research Fund (CityU 11275961) of the Research Grants Council of Hong Kong SAR, China.
Funding Information:
Showcasing joint research from the laboratories of Dr Ping Wang & Dr XianYing Wang at School of Materials Science and Technology, University of Shanghai for Science and Technology, Shanghai, P. R. China and Dr Johnny C. Ho at Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong, P. R. China.
Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - Highly efficient, durable and cost-effective electrocatalysts are highly desired for overall water splitting (OWS). Herein, we report the easy fabrication of 3D porous core-shell Ni nanochains@NiFe layered double hydroxide (LDH) nanosheets with extraordinary oxygen evolution reaction (OER), hydrogen evolution reaction (HER) and OWS performance. In specific, a simple magnetic field-assisted method is used for the in situ growth of Ni nanochain cores with large surface areas, allowing the subsequent vertical growth of few-layered NiFe LDH nanosheets to form densely packed shells. Benefiting from the meticulously designed nanoarchitecture, the electrocatalyst possesses rich exposed active sites, plentiful charge transfer channels and high porosity for the release of gas bubbles. The OER performance and durability of the electrocatalyst are far better than those of both commercial RuO2 and IrO2, while its HER performance is competitive with the performance of the benchmark Pt/C electrode in alkaline electrolytes. When these catalysts are further employed as anode and cathode electrodes, small cell voltages of 1.53 and 1.78 V can be achieved at current densities of 10 and 100 mA cm-2 for a long-term OWS reaction. Towards the commercial use, we design an electrolytic overall-water-splitting cell pack, which demonstrates a linear relationship between the numbers of packing cells and the increase of current density under a given voltage.
AB - Highly efficient, durable and cost-effective electrocatalysts are highly desired for overall water splitting (OWS). Herein, we report the easy fabrication of 3D porous core-shell Ni nanochains@NiFe layered double hydroxide (LDH) nanosheets with extraordinary oxygen evolution reaction (OER), hydrogen evolution reaction (HER) and OWS performance. In specific, a simple magnetic field-assisted method is used for the in situ growth of Ni nanochain cores with large surface areas, allowing the subsequent vertical growth of few-layered NiFe LDH nanosheets to form densely packed shells. Benefiting from the meticulously designed nanoarchitecture, the electrocatalyst possesses rich exposed active sites, plentiful charge transfer channels and high porosity for the release of gas bubbles. The OER performance and durability of the electrocatalyst are far better than those of both commercial RuO2 and IrO2, while its HER performance is competitive with the performance of the benchmark Pt/C electrode in alkaline electrolytes. When these catalysts are further employed as anode and cathode electrodes, small cell voltages of 1.53 and 1.78 V can be achieved at current densities of 10 and 100 mA cm-2 for a long-term OWS reaction. Towards the commercial use, we design an electrolytic overall-water-splitting cell pack, which demonstrates a linear relationship between the numbers of packing cells and the increase of current density under a given voltage.
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U2 - 10.1039/c9ta07282a
DO - 10.1039/c9ta07282a
M3 - Article
AN - SCOPUS:85072932423
SN - 2050-7488
VL - 7
SP - 21722
EP - 21729
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 38
ER -