2021
DOI: 10.1016/j.apcatb.2021.120386
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Synthesis of 3D heterostructure Co-doped Fe2P electrocatalyst for overall seawater electrolysis

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Cited by 156 publications
(91 citation statements)
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“…However, due to the higher redox potential of Cl À /Cl 2 (Cl À /ClO À in alkaline solution), CER is less thermodynamically favorable than OER. Specifically, the potential seawater electrolyzers, 33,[53][54][55][56][57][58][59][60][61][62] Fe 0.01 -Ni&Ni 0.2 Mo 0.8 N8Fe 0.01 &Mo-NiO delivers a record-high current density of 688 mA cm À2 at the voltage of 1.7 V. Compared to our previous study of a two-electrode electrolyzer using NiMoN as the cathode and NiFeN/NiMoN as the anode, the current density of Fe 0.01 -Ni&Ni 0.2 Mo 0.8 N8Fe 0.01 &Mo-NiO at 1.7 V is about 2.2 times as large. 33 These results reveal the excellent seawater electrolysis performance of Fe 0.01 -Ni&Ni 0.2 Mo 0.8 N8Fe 0.01 &Mo-NiO and again underscore the importance of utilizing electrochemical reconstruction for the design of highly active bifunctional catalysts.…”
Section: Papermentioning
confidence: 99%
“…However, due to the higher redox potential of Cl À /Cl 2 (Cl À /ClO À in alkaline solution), CER is less thermodynamically favorable than OER. Specifically, the potential seawater electrolyzers, 33,[53][54][55][56][57][58][59][60][61][62] Fe 0.01 -Ni&Ni 0.2 Mo 0.8 N8Fe 0.01 &Mo-NiO delivers a record-high current density of 688 mA cm À2 at the voltage of 1.7 V. Compared to our previous study of a two-electrode electrolyzer using NiMoN as the cathode and NiFeN/NiMoN as the anode, the current density of Fe 0.01 -Ni&Ni 0.2 Mo 0.8 N8Fe 0.01 &Mo-NiO at 1.7 V is about 2.2 times as large. 33 These results reveal the excellent seawater electrolysis performance of Fe 0.01 -Ni&Ni 0.2 Mo 0.8 N8Fe 0.01 &Mo-NiO and again underscore the importance of utilizing electrochemical reconstruction for the design of highly active bifunctional catalysts.…”
Section: Papermentioning
confidence: 99%
“…Heteroatom doping directly and continuously fine‐tunes electronic structure and HER activity of the catalyst without changing the chemical composition. [ 183 , 184 , 185 , 186 , 187 , 188 , 189 , 190 , 191 , 192 , 193 , 194 , 195 ] Therefore, heteroatom doping is an effective strategy widely used to optimize HER activity. Transition metal doping (Fe, [ 196 ] Co, [ 197 , 198 ] Ni, [ 199 ] Zn, [ 200 ] and Mo [ 201 ] ) modifies the local electronic environment and can also optimize the interatomic distances and coordination numbers of active sites.…”
Section: Strategies To Improve Her Electrocatalystsmentioning
confidence: 99%
“…X‐rays analysis revealed that the Co surface oxidizes to a higher valance state during water oxidation, but Fe preserves its charge due to covalent interaction with P. The M─P bond creates oxide/hydroxide active layers on the Co–Fe surface and optimizes the Fe active sites for OER intermediates. [ 46 ] In multimetal catalysts, the stoichiometry of each metal has a remarkable influence on the electronic structure of hybrid material. Ni sites are considered more selective for OER in Ni–Co bimetallic catalyst because its 3 d band has a higher superposition with p ‐orbital.…”
Section: Rational Design Of Anode Materials For Seawater Oxidationmentioning
confidence: 99%