Co1-xS embedded in porous carbon derived from metal organic framework as a highly efficient electrocatalyst for oxygen evolution reaction
[Display omitted] Here, we report a two-step conversion method to fabricate a composite of Co1-xS embedded in porous carbon framework (Co1-xS@C) derived from metal organic frameworks (MOFs). The as-prepared porous dodecahedron Co1-xS@C composite catalyst exhibits excellent electrocatalytic performan...
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Published in | Chinese chemical letters Vol. 30; no. 1; pp. 229 - 233 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.01.2019
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Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
Here, we report a two-step conversion method to fabricate a composite of Co1-xS embedded in porous carbon framework (Co1-xS@C) derived from metal organic frameworks (MOFs). The as-prepared porous dodecahedron Co1-xS@C composite catalyst exhibits excellent electrocatalytic performance towards oxygen evolution reaction (OER).
Developing active, robust, and cost-efficient electrocatalysts is critical for oxygen evolution reaction (OER). Here, a novel composite catalyst of Co1-xS embedded in porous dodecahedron carbon hybrid was synthesized by a two-step conversion protocol of a cobalt-based metal-organic framework (ZIF-67). The porous dodecahedron Co1-xS@C composite catalyst was prepared by direct oxidation of ZIF-67 followed by sulfurization reaction. The Co1-xS@C composite exhibit superior OER performance, including a low overpotential of 260mV for 10mA/cm2, a small Tafel slope of ∼85mV/dec, outstanding stability over 80h and almost 100% Faradaic efficiency. The various material characterizations indicate that the excellent activity and strong stability of Co1-xS@C might be attributed to good conductivity of Co1-xS, mesoporous nanostructure, and synergistic effect of Co1-xS encapsulated within porous carbon. This work provides a novel strategy for designing and synthesizing advanced composite electrocatalysts |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2018.03.020 |