The one-pot synthesis of porous Ni0.85Se nanospheres on graphene as an efficient and durable electrocatalyst for overall water splitting

The design and preparation of highly efficient and durable non-noble metal electrocatalysts for overall water splitting is pivotal for actualizing large-scale water splitting via electrolysis. Herein, porous Ni0.85Se nanospheres anchored on reduced graphene oxide (RGO) (Ni0.85Se/RGO) were synthesize...

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Veröffentlicht in:New journal of chemistry 2020-10, Vol.44 (40), p.17313-17322
Hauptverfasser: Liu, Guigui, Chao Shuai, Mo, Zunli, Guo, Ruibin, Liu, Nijuan, Niu, Xiaohui, Dong, Qibing, Wang, Jia, Gao, Qinqin, Chen, Ying, Liu, Wentong
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Sprache:eng
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Zusammenfassung:The design and preparation of highly efficient and durable non-noble metal electrocatalysts for overall water splitting is pivotal for actualizing large-scale water splitting via electrolysis. Herein, porous Ni0.85Se nanospheres anchored on reduced graphene oxide (RGO) (Ni0.85Se/RGO) were synthesized via a one-step hydrothermal method. Following explorations of the hydrothermal temperature and reaction time, the optimized Ni0.85Se/RGO exhibited extraordinary oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) performance in 1.0 M KOH solution, providing an overpotential as small as 320 mV at a current density of 30 mA cm−2 and a low Tafel slope of 91 mV dec−1 for the OER, and an overpotential of 169 mV at a current density of 10 mA cm−2 and a low Tafel slope of 65 mV dec−1 for the HER. A current density of 10 mA cm−2 at 1.64 V and high stability can be obtained upon using Ni0.85Se/RGO as both the cathode and anode for overall water splitting under alkaline conditions; this was attributed to the merits of both the porous structure of Ni0.85Se and the high conductivity of RGO. This work provides a meaningful exploration of the synthesis of 3d-transition-metal-chalcogenide- and carbon-based composite electrocatalysts via a hydrothermal reaction for water splitting, and provides a general method.
ISSN:1144-0546
1369-9261
DOI:10.1039/d0nj04197a