4.8 Article

Interfacing or Doping? Role of Ce in Highly Promoted Water Oxidation of NiFe-Layered Double Hydroxide

期刊

ADVANCED ENERGY MATERIALS
卷 11, 期 33, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202101281

关键词

cerium hydroxide nanoparticles; interface engineering; NiFe-LDH; oxygen evolution reaction; transition metal doping

资金

  1. Innovation and Technology Commission of Hong Kong
  2. Hong Kong Polytechnic University [1-BE0Y, Q-CDA3]
  3. Global Frontier Program through the Global Frontier Hybrid Interface Materials (GFHIM) of National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2013M3A6B1078882]

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Surface engineering of transition metal layered double hydroxides (LDHs) can enhance their catalytic activity for the oxygen evolution reaction (OER). The study on Ce-doped NiFe-LDHs and Ce(OH)(3) interfaced NiFe-LDHs reveals that Ce and Fe atoms facilitate the oxidation of Ni3+/4+ in NiFe-LDH, resulting in superior catalytic activity for water oxidation. The enhanced electron transfer between Ce(OH)(3) and the matrix in Ce@NiFe-LDH leads to better catalytic activity compared to CeNiFe-LDH, as demonstrated by first-principles density functional theory (DFT) calculations.
Surface engineering of transition metal layered double hydroxides (LDHs) provides an efficient way of enhancing their catalytic activity toward the oxygen evolution reaction (OER). However, the underlying mechanism of atomistic doping or heterogeneous interface with foreign atom is still ambiguous. Herein, a case study of NiFe-LDHs that are homogeneously doped with Ce (CeNiFe-LDH) and interfaced with Ce(OH)(3) (Ce@NiFe-LDH), which elucidates their electronic modulation, in situ evolution of active site, and catalytic reaction mechanisms by using X-ray photoelectronic spectroscopy, operando electrochemical Raman spectroscopy, and first-principles density functional theory (DFT) calculations, is reported. The results indicate that Ce and Fe atoms serve as the electron acceptors and facilitate the coupled oxidation of Ni3+/4+ in NiFe-LDH, and the activated oxyhydroxide phase of the catalysts exhibits superior catalytic activity for water oxidation. Especially, Ce@NiFe-LDH shows a stronger electron transfer between the loaded Ce(OH)(3) and the matrix, which leads to a better catalytic activity than CeNiFe-LDH. DFT calculations provide a clear picture with atomistic resolution for charge redistribution in the NiFe-LDH surface induced by Ce, which eventually leads to the optimal free energy landscape for the enhanced OER catalytic activity.

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