Intercalation-Induced Irreversible Lattice Distortion in Layered Double Hydroxides

插层(化学) 析氧 材料科学 层状双氢氧化物 催化作用 金属 化学物理 无机化学 电化学 化学 物理化学 电极 氢氧化物 生物化学 冶金
作者
Deok Ki Cho,Hyun Woo Lim,Andi Haryanto,Bingyi Yan,Chan Woo Lee,Jin Young Kim
出处
期刊:ACS Nano [American Chemical Society]
卷期号:18 (31): 20459-20467 被引量:80
标识
DOI:10.1021/acsnano.4c04832
摘要

Inducing strain in the lattice effectively enhances the intrinsic activity of electrocatalysts by shifting the metal’s d-band center and tuning the binding energy of reaction intermediates. NiFe-layered double hydroxides (NiFe LDHs) are promising electrocatalysts for the oxygen evolution reaction (OER) due to their cost-effectiveness and high catalytic activity. The distorted β-NiOOH phase produced by the Jahn–Teller effect under the oxidation polarization is known to exhibit superior catalytic activity, but it eventually transforms to the undistorted γ-NiOOH phase during the OER process. Such a reversible lattice distortion limits the OER activity. In this study, we propose a facile boron tungstate (BWO) anion intercalation method to induce irreversible lattice distortion in NiFe LDHs, leading to significantly enhanced OER activity. Strong interactions with BWO anions induce significant stress on the LDH’s metal-hydroxide slab, leading to an expansion of metal–oxygen bonds and subsequent lattice distortion. In situ Raman spectroscopy revealed that lattice-distorted NiFe LDHs (D-NiFe LDHs) stabilize the β-NiOOH phase under the OER conditions. Consequently, D-NiFe LDHs exhibited low OER overpotentials (209 and 276 mV for 10 and 500 mA cm –2, respectively), along with a modest Tafel slope (33.4 mV dec –1 ). Moreover, D-NiFe LDHs demonstrated excellent stability at 500 mA cm –2 for 50 h, indicating that the lattice distortion of the LDHs is irreversible. The intercalation-induced lattice strain reported in this study can provide a general strategy to enhance the activity of electrocatalysts.
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