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Updated: Jun 28, 2026

Preparation of Polyoxometalate-based Photo-responsive Membranes for the Photo-activation of Manganese Oxide Catalysts
Published on: August 7, 2018
Single-atom Electronic Bridge Facilitates Cascade Electron Transfer From Encapsulated Polyoxometalate to
Shengqian Yu1, Zicheng Wang1, Yihong Xie1
1Key Laboratory of Functional Inorganic Material Chemistry (MOE), School of Chemistry and Material Science, Heilongjiang University, Harbin, 150080, China.
Abstract:
The POM@MOF system, integrating the exceptional properties of polyoxometalates (POM) and metal-organic frameworks (MOF), exhibits considerable catalytic potential. However, the absence of stable and well-defined electron-transfer pathways between the two components hampers charge separation and transport, thereby limiting its catalytic efficiency. Here, we constructed a Ni single-atom electronic bridge (SAEB) between POM and MOF, based on our previously-reported PMo11W@rht-MOF-1 composite. Spherical aberration-corrected transmission electron microscopy and X-ray absorption spectroscopy analyses revealed not only the hierarchical dispersion of single-atom Ni, POM, and MOF, but also the formation of chemical bonds between Ni and both POM and MOF. This precisely engineered Ni-SAEB facilitated cascade electron transfer from the encapsulated PMo11W to rht-MOF-1 framework, as confirmed by femtosecond transient absorption spectroscopy and in situ X-ray photoelectron spectroscopy. Further investigations demonstrated that the Ni-SAEB/POM@MOF system simultaneously harnessed the "electronic sponge" effect of POM and the CO2 adsorption-conversion capability of MOF. Consequently, the Ni-SAEB/PMo11W@rht-MOF-1 composite achieved a CO2-to-CO photocatalytic conversion rate of 3 mmol g-1 h-1, markedly surpassing that of PMo11W@rht-MOF-1 without Ni-SAEB. This work establishes the SAEB strategy as a versatile catalytic concept, where single atoms serve as both surface catalytic centers and interfacial cascade electron mediators, with broad scientific significance.
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