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摘要:
Transition metal chalcogenides will be in situ transformed into metal oxyhydroxides during oxygen evo-lution reaction (OER) process in alkaline medium.However,most of these compounds only undergo sur-face reconstruction under operating conditions,which contains a large percentage of inactive atoms in the core,thus limiting the exposure of the active sites.Here,we synthesize a Ni-Mo-Se precatalyst with three-dimensional hierarchical structure and develop a facile on-site electrochemical activation strategy for achieving deep reconstruction of the precatalyst.Using the combination of multiple spectroscopic characterizations and high resolution electron microscopy techniques,we unravel that the Ni-Mo-Se pre-catalyst is deeply reconstructed into γ-NiOOH with co-leaching of Mo and Se after the anodic oxidation.Such flower-like γ-NiOOH is constituted by distorted ultrathin nanosheets with a thickness of ~ 4.5 nm and contains abundant intercalated species such as water and OH-/CO32-,thus offering a large quantity of accessible active sites.To reach the current density of 10 mAcm-2,the derived electrode requires an overpotential of only 244 mV,outperforming almost all the reported analogues.This work highlights the reconstruction chemistry and provides a simple method for the preparation of efficient OER electrocatalyst.
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篇名 Selenization triggers deep reconstruction to produce ultrathin γ-NiOOH toward the efficient water oxidation
来源期刊 能源化学 学科
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年,卷(期) 2021,(12) 所属期刊栏目
研究方向 页码范围 651-658
页数 8页 分类号
字数 语种 英文
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能源化学
双月刊
2095-4956
10-1287/O6
大连市中山路457号
eng
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2804
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7996
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