Highly porous Co-doped NiO nanorods: facile hydrothermal synthesis and electrocatalytic oxygen evolution properties

被引:12
|
作者
Nguyen Duc Cuong [1 ,2 ]
Tran, Tien D. [3 ]
Nguyen, Quyen T. [3 ]
Ho Van Minh Hai [1 ]
Tran Thai Hoa [1 ]
Duong Tuan Quang [4 ]
Klysubun, Wantana [5 ]
Tran, Phong D. [3 ]
机构
[1] Hue Univ, Univ Sci, 77 Nguyen Hue, Hue City, Vietnam
[2] Hue Univ, Sch Hospitality & Tourism, 22 Lam Hoang, Hue City, Vietnam
[3] Vietnam Acad Sci & Technol, Univ Sci & Technol Hanoi, 18 Hoang Quoc Viet, Hanoi 100000, Vietnam
[4] Hue Univ, Univ Educ, 34 Lai Loi, Hue City, Vietnam
[5] Synchrotron Light Res Inst, 111 Moo 6,Univ Ave, Muang 30000, Nakhon Ratchasi, Thailand
来源
ROYAL SOCIETY OPEN SCIENCE | 2021年 / 8卷 / 09期
关键词
nickel oxide; Co dopant; highly porous nanorods; oxygen evolution reaction; synergistic effect; THERMAL-DECOMPOSITION; CONTROLLABLE SYNTHESIS; OXIDE; NANOSTRUCTURES; NANOPARTICLES; OXIDATION; MORPHOLOGY; STABILITY; FE;
D O I
10.1098/rsos.202352
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Highly porous 3d transition metal oxide nanostructures are opening up the exciting area of oxygen evolution reaction (OER) catalysts in alkaline medium thanks to their good thermal and chemical stability, excellent physiochemical properties, high specific surface area and abundant nanopores. In this paper, highly porous Co-doped NiO nanorods were successfully synthesized by a simple hydrothermal method. The porous rod-like nanostructures were preserved with the added cobalt dopant ranging from 1 to 5 at% but were broken into aggregated nanoparticles at higher concentrations of additional cobalt. The catalytic activity of Co-doped NiO nanostructures for OER in an alkaline medium was assayed. The 5%Co-NiO sample showed a drastically enhanced activity. This result could originate from the combination of advantageous characteristics of highly porous NiO nanorods such as large surface area and high porosity as well as the important role of Co dopant that could provide more catalytic active sites, leading to an enhanced catalytic activity of the nanocatalyst.
引用
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页数:12
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