Journal
ADVANCED FUNCTIONAL MATERIALS
Volume 31, Issue 15, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202009743
Keywords
host modification; kinetic activity; layered double hydroxide; oxygen evolution reaction; thermodynamic activity
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Funding
- National Natural Science Foundation of China [21922501, 21871021, 21521005]
- Beijing Natural Science Foundation [2192040]
- Fundamental Research Funds for the Central Universities [XK1802-6, XK1803-05]
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This study demonstrates a strategy to optimize the oxygen evolution reaction activity of LDHs by introducing transition and main group metal atoms, which can enhance the intrinsic activity and kinetics of LDHs. Experimental and theoretical results show that suitable dopants can lower the activation energy barrier and promote electron transfers, providing insights for the rational design of high-performing OER electrocatalysts.
Layered double hydroxides (LDHs) are regarded as an earth-abundant and highly efficient electrocatalyst for oxygen evolution reaction (OER). In this work, a systematic strategy is demonstrated to simultaneously optimize the OER thermodynamic and kinetic activity via introducing a series of transition and main group metal atoms into the NiFe-LDH host layers. Typically, V, Co, and Cr dopants largely promote the intrinsic activity of NiFe-LDH through the effective electron transfer from Fe3+ in NiFe-LDH laminate to the doping metals, while the introduction of V, Ti, and Mn into NiFe-LDH facilitates the kinetics of water oxidation due to the increased conductivity induced by dopants. Furthermore, the detailed experiments and density functional theory calculations illustrate that the presence of suitable heteroatoms (V) lowers the activation energy barrier for OER rate-limiting step as well as promotes the electron transfers by effective electronic modification. This work provides an effective strategy to modulate the OER activity of LDHs and determine their performance trends for a more rational design of high-performed OER electrocatalysts.
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