When it comes to an efficient catalytic oxygen evolution
reaction
(OER) in the production of renewable energy and chemicals, the construction
of heterogeneous structures is crucial to break the linear scalar
relationship of a single catalyst. This heterogeneous structure construction
helps creatively achieve high activity and stability. However, the
synthesis process of heterogeneous crystalline materials is often
complex and challenging to capture and reproduce, which limits their
application. Here, the dynamic process of structural changes in Co-MOFs in alkali was captured by in situ powder X-ray diffraction,
FT-IR spectroscopy, and Raman spectroscopy, and several self-reconfigured
MOF heterogeneous materials with different structures were stably
isolated. The created β-Co(OH)2/Co-MOF heterojunction
structure facilitates rapid mass–charge transfer and exposure
of active sites, which significantly enhanced OER activity. Experimental
results show that this heterogeneous structure achieves a low overpotential
of 333 mV at 10 mA cm–2. The findings provide new
insights and directions for the search for highly reactive cobalt-based
MOFs for sustainable energy technologies.