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- Publisher Website: 10.1016/j.jallcom.2018.11.159
- Scopus: eid_2-s2.0-85056617485
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Article: Metal organic frameworks derived CoSe2 @N-Doped-carbon-nanorods as highly efficient electrocatalysts for oxygen evolution reaction
| Title | Metal organic frameworks derived CoSe<inf>2</inf>@N-Doped-carbon-nanorods as highly efficient electrocatalysts for oxygen evolution reaction |
|---|---|
| Authors | |
| Keywords | Cobalt diselenide Metal-organic frameworks Nanorods Oxygen evolution reaction |
| Issue Date | 2019 |
| Citation | Journal of Alloys and Compounds, 2019, v. 778, p. 134-140 How to Cite? |
| Abstract | The development of highly efficient and long-term durable electrocatalyst for oxygen evolution reaction is still a great challenge to attain renewable and clean energy. Herein, CoSe2@N-Doped-carbon-nanorods named as CoSe2@NC nanorods have been conveniently synthesized by in-situ selenization of a novel N-doped metal organic frameworks under N2 atmosphere. CoSe2@NC nanorods show highly efficient electrocatalytic performance for oxygen evolution reaction at a low overpotential of 310 mV for 10 mA cm−2 current density in 1.0 M KOH aqueous solution, which are comparable to the state-of-the-art RuO2 and IrO2 catalysts. The remarkable electrocatalytic performance can be attributed to the unique N-doped MOFs derived well-defined architecture with large active surface area, high conductivity of carbon and well-distributed active sites. In addition, CoSe2@NC nanorods exhibit long-term stability without obvious decay after 1000 cyclic voltammetry cycles. |
| Persistent Identifier | http://hdl.handle.net/10722/351387 |
| ISSN | 2023 Impact Factor: 5.8 2023 SCImago Journal Rankings: 1.103 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lu, Jitao | - |
| dc.contributor.author | Wang, Suqing | - |
| dc.contributor.author | Ding, Caifeng | - |
| dc.contributor.author | Lv, Wei | - |
| dc.contributor.author | Zeng, Yue | - |
| dc.contributor.author | Liu, Nan | - |
| dc.contributor.author | Wang, Huiqin | - |
| dc.contributor.author | Meng, Qingguo | - |
| dc.contributor.author | Liu, Qingyun | - |
| dc.date.accessioned | 2024-11-20T03:55:59Z | - |
| dc.date.available | 2024-11-20T03:55:59Z | - |
| dc.date.issued | 2019 | - |
| dc.identifier.citation | Journal of Alloys and Compounds, 2019, v. 778, p. 134-140 | - |
| dc.identifier.issn | 0925-8388 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/351387 | - |
| dc.description.abstract | The development of highly efficient and long-term durable electrocatalyst for oxygen evolution reaction is still a great challenge to attain renewable and clean energy. Herein, CoSe2@N-Doped-carbon-nanorods named as CoSe2@NC nanorods have been conveniently synthesized by in-situ selenization of a novel N-doped metal organic frameworks under N2 atmosphere. CoSe2@NC nanorods show highly efficient electrocatalytic performance for oxygen evolution reaction at a low overpotential of 310 mV for 10 mA cm−2 current density in 1.0 M KOH aqueous solution, which are comparable to the state-of-the-art RuO2 and IrO2 catalysts. The remarkable electrocatalytic performance can be attributed to the unique N-doped MOFs derived well-defined architecture with large active surface area, high conductivity of carbon and well-distributed active sites. In addition, CoSe2@NC nanorods exhibit long-term stability without obvious decay after 1000 cyclic voltammetry cycles. | - |
| dc.language | eng | - |
| dc.relation.ispartof | Journal of Alloys and Compounds | - |
| dc.subject | Cobalt diselenide | - |
| dc.subject | Metal-organic frameworks | - |
| dc.subject | Nanorods | - |
| dc.subject | Oxygen evolution reaction | - |
| dc.title | Metal organic frameworks derived CoSe<inf>2</inf>@N-Doped-carbon-nanorods as highly efficient electrocatalysts for oxygen evolution reaction | - |
| dc.type | Article | - |
| dc.description.nature | link_to_subscribed_fulltext | - |
| dc.identifier.doi | 10.1016/j.jallcom.2018.11.159 | - |
| dc.identifier.scopus | eid_2-s2.0-85056617485 | - |
| dc.identifier.volume | 778 | - |
| dc.identifier.spage | 134 | - |
| dc.identifier.epage | 140 | - |
| dc.identifier.isi | WOS:000455179500018 | - |
