High-activity lattice oxygen
Activates lattice oxygen via metal electronegativity modulation to enhance water oxidation activity while maintaining stability, overcoming the trade-off between activity and durability.
Liu, Yuehua · Fangfang, Feng · Lingyi, Rao · Qun, Liao · Zhaohui, Li · Xingxing, Zheng · Zifeng, Wu · Ze, Zhang · Fu, Xionghui · Zhu, Yi · Zhang, Yuanming
Journal of Alloys and Compounds 2026
By tuning metal electronegativity, the lattice oxygen activation degree is modulated to induce the lattice oxygen mechanism, enhancing OER activity while maintaining catalyst stability, breaking the usual trade-off.
Co-BiVO₄ achieves a photocurrent density of 3.64 mA cm⁻², 2.9-fold higher than pure BiVO₄ and much higher than most reported BiVO₄ without cocatalysts.
Higher metal electronegativity upshifts the O 2p energy center, enhances M–O bond covalency, and increases lattice oxygen activation, leading to better OER activity in the order Co > Fe > Zn.