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Amorphous nickel-cobalt complexes hybridized with 1T-phase molybdenum disulfide via hydrazine-induced phase transformation for water splitting.


ABSTRACT: Highly active and robust eletcrocatalysts based on earth-abundant elements are desirable to generate hydrogen and oxygen as fuels from water sustainably to replace noble metal materials. Here we report an approach to synthesize porous hybrid nanostructures combining amorphous nickel-cobalt complexes with 1T phase molybdenum disulfide (MoS2) via hydrazine-induced phase transformation for water splitting. The hybrid nanostructures exhibit overpotentials of 70?mV for hydrogen evolution and 235?mV for oxygen evolution at 10?mA?cm-2 with long-term stability, which have superior kinetics for hydrogen- and oxygen-evolution with Tafel slope values of 38.1 and 45.7?mV?dec-1. Moreover, we achieve 10?mA?cm-2 at a low voltage of 1.44?V for 48?h in basic media for overall water splitting. We propose that such performance is likely due to the complete transformation of MoS2 to metallic 1T phase, high porosity and stabilization effect of nickel-cobalt complexes on 1T phase MoS2.

SUBMITTER: Li H 

PROVIDER: S-EPMC5436140 | biostudies-literature | 2017 May

REPOSITORIES: biostudies-literature

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Amorphous nickel-cobalt complexes hybridized with 1T-phase molybdenum disulfide via hydrazine-induced phase transformation for water splitting.

Li Haoyi H   Chen Shuangming S   Jia Xiaofan X   Xu Biao B   Lin Haifeng H   Yang Haozhou H   Song Li L   Wang Xun X  

Nature communications 20170509


Highly active and robust eletcrocatalysts based on earth-abundant elements are desirable to generate hydrogen and oxygen as fuels from water sustainably to replace noble metal materials. Here we report an approach to synthesize porous hybrid nanostructures combining amorphous nickel-cobalt complexes with 1T phase molybdenum disulfide (MoS<sub>2</sub>) via hydrazine-induced phase transformation for water splitting. The hybrid nanostructures exhibit overpotentials of 70 mV for hydrogen evolution a  ...[more]

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