Hierarchical carbon microflowers supported defect-rich Co3S4 nanoparticles: An efficient electrocatalyst for water splitting

Developing highly efficient and cost-effective bifunctional electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) represents a judicious way to produce massive hydrogen fuel through electrochemical water splitting. Herein, defect-rich Co3S4 particles with a diame...

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Published in:Carbon (New York) 2020-04, Vol.160, p.133-144
Main Authors: Zhu, Xiaojing, Dai, Jiale, Li, Ligui, Zhao, Dengke, Wu, Zexing, Tang, Zhenghua, Ma, Li-Jun, Chen, Shaowei
Format: Article
Language:English
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Summary:Developing highly efficient and cost-effective bifunctional electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) represents a judicious way to produce massive hydrogen fuel through electrochemical water splitting. Herein, defect-rich Co3S4 particles with a diameter less than 5 nm were in-situ grown on nitrogen-doped hierarchical carbon microflowers (Co3S4@FNC) through a simple hydrothermal method, in which an unconventional vulcanization process with the strongly coordinating ligand ethylenediamine and formaldehyde serving as structure-directive agents is resorted to effectively control the morphology of catalysts. The resultant Co3S4@FNC-Co3 comprises dense Co3S4 nanoparticles supported on ultrathin nitrogen-doped carbon nanosheets with a thickness of ca. 20 nm, as well as abundant defects on Co3S4 nanoparticles and highly porous textures on carbon microflowers. These nanostructure merits lead to efficient catalytic activities, featuring a small overpotential of only 250 mV and 140 mV for OER and HER electrocatalysis at 10 mV cm−2. When Co3S4@FNC-Co3 is utilized as a bifunctional catalyst in an alkaline water electrolyzer, a bias of only 1.580 V is able to complement overall water splitting at 10 mA cm−2. Results in present work may suggest a paradigm in the design and engineering of high-performance electrocatalysts based on nanocomposites of transition metal sulfides and carbons. [Display omitted]
ISSN:0008-6223
1873-3891
DOI:10.1016/j.carbon.2019.12.072