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Electronic Tuning of Co, Ni‐Based Nanostructured (Hydr)oxides for Aqueous Electrocatalysis
Author(s) -
Kuang Min,
Han Peng,
Huang Linsong,
Cao Na,
Qian Linping,
Zheng Gengfeng
Publication year - 2018
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201804886
Subject(s) - electrocatalyst , materials science , electrochemistry , aqueous solution , reactivity (psychology) , catalysis , nanotechnology , electronic structure , fuel cells , chemical engineering , chemistry , organic chemistry , electrode , computational chemistry , engineering , medicine , alternative medicine , pathology
Co, Ni‐based (hydr)oxides with stoichiometric or nonstoichiometric composites are playing significant roles in renewable energy technologies, such as electrocatalytic reactions for transforming earth abundant resources into value‐added chemicals. In the past several years, attributed to the development of novel synthesis strategies, characterization techniques, and theoretical calculations, the rational design and realization of a variety of Co, Ni‐based (hydr)oxides with exciting performances have been demonstrated. Particularly, the electrocatalytic reactivities of these Co, Ni‐based (hydr)oxides are highly dependent on their surface electronic structures, which can be well tuned by their nanostructures and compositions. This Review summarizes recent research advances in regulating electronic structures toward the optimization of electrochemical reactivity in aqueous solutions. These research works mainly focus on three important clean energy reactions: i) water oxidation, ii) oxygen reduction, and iii) carbon dioxide reduction, where the developments of advanced electrocatalysts can enable the production of value‐added chemicals or fuels. Furthermore, the electronic structure–property relationships behind the enhanced electrocatalytic properties of these Co, Ni‐based (hydr)oxides are also discussed.

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