TY - JOUR
T1 - Tuning carbon nanotube-grafted core-shell-structured cobalt selenide@carbon hybrids for efficient oxygen evolution reaction
AU - Yuan, Menglei
AU - Wang, Meng
AU - Lu, Peilong
AU - Sun, Yu
AU - Dipazir, Sobia
AU - Zhang, Jingxian
AU - Li, Shuwei
AU - Zhang, Guangjin
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - The electrochemical oxygen evolution reaction (OER) is sparked extensive interest in efficient energy storage and conversion. Cobalt Selenide (CoSe2) is believed to be one of the promising candidates for OER based on Yang Shao-Horn's principle. However, owing to low exposure of active sites and/or low efficiency of electron transfer, the electrocatalytic activity of CoSe2 is far less than expected. In this work, a novel carbon nanotubes (CNT) grafted 3D core-shell structured CoSe2@C-CNT nanohybrid is developed by a general hydrothermal-calcination strategy. Zeolite imidazole frameworks (ZIF) was used as the precursor to synthesis of the materials. It is found that both the calcination temperature and the selenium content can significantly regulate the catalytic performance of the hybrids. The obtained best catalysts requires the overpotential of only 306 mV and 345 mV to reach a current density of 10 mA cm−2 and 50 mA cm−2 in 1.0 MKOH medium, respectively. It also exhibits a small Tafel slope of 46 mV dec−1 and excellent durability, which is superior to most of recently reported CoSe2-based and Co-based materials. These superior performances can be ascribed to synergistic effects of the highly active CoSe2 nanostructure, defect carbon species and the carbon nanotubes exist in the catalyst. Besides, the unique morphology leads to large electrochemical surface area of the catalyst, which is in favor of the exposure of active sites for OER. Due to high efficiency, low cost and excellent durability for OER, the prepared catalysts showed can be potentially used to substitute noble metals utilized in related energy storage and conversion devices.
AB - The electrochemical oxygen evolution reaction (OER) is sparked extensive interest in efficient energy storage and conversion. Cobalt Selenide (CoSe2) is believed to be one of the promising candidates for OER based on Yang Shao-Horn's principle. However, owing to low exposure of active sites and/or low efficiency of electron transfer, the electrocatalytic activity of CoSe2 is far less than expected. In this work, a novel carbon nanotubes (CNT) grafted 3D core-shell structured CoSe2@C-CNT nanohybrid is developed by a general hydrothermal-calcination strategy. Zeolite imidazole frameworks (ZIF) was used as the precursor to synthesis of the materials. It is found that both the calcination temperature and the selenium content can significantly regulate the catalytic performance of the hybrids. The obtained best catalysts requires the overpotential of only 306 mV and 345 mV to reach a current density of 10 mA cm−2 and 50 mA cm−2 in 1.0 MKOH medium, respectively. It also exhibits a small Tafel slope of 46 mV dec−1 and excellent durability, which is superior to most of recently reported CoSe2-based and Co-based materials. These superior performances can be ascribed to synergistic effects of the highly active CoSe2 nanostructure, defect carbon species and the carbon nanotubes exist in the catalyst. Besides, the unique morphology leads to large electrochemical surface area of the catalyst, which is in favor of the exposure of active sites for OER. Due to high efficiency, low cost and excellent durability for OER, the prepared catalysts showed can be potentially used to substitute noble metals utilized in related energy storage and conversion devices.
KW - Alkaline medium
KW - CoSe
KW - Oxygen evolution reaction
KW - Zeolite imidazole frameworks
UR - http://www.scopus.com/inward/record.url?scp=85052723738&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2018.08.104
DO - 10.1016/j.jcis.2018.08.104
M3 - 文章
C2 - 30176541
AN - SCOPUS:85052723738
SN - 0021-9797
VL - 533
SP - 503
EP - 512
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -