Interactions between metal−organic frameworks (MOFs) and nucleic acids are of great importance in molecular assembly. However, current MOF−nucleic acid interactions lack diversity and are normally realized in an uncontrollable manner. Herein, the interaction of zirconium-based MOFs (Zr-MOFs) with nucleic acids is enabled by the formation of Zr−O−P bonds and further manipulated by a phosphate-induced site-occupying effect. Covering Zr ions in clusters of MOFs with phosphates impedes the formation of Zr−O−P bonds with nucleic acids, rendering the MOF−nucleic acid interaction tunable and stimulus-responsive. Notably, the experimental results demonstrate that various phosphates, Zr-MOFs, and nucleic acids can all be adopted in the tunable interaction. On the basis of these findings, fluorescent DNA and typical Zr-MOFs are proposed as functional probe−quencher pairs to establish molecular sensing and logic systems. Accordingly, alkaline phosphatase and inorganic pyrophosphatase can be quantified simultaneously, and the overall relation of different phosphates and phosphatases is facilely displayed. The work provides a general strategy for modulating MOF−nucleic acid interactions, which is conducive to the development of molecular intelligent systems.

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The hard carbon (HC) has been emerging as one of the most promising anode materials for sodium-ion batteries (SIBs). Incorporation of cations into the HC lattice proved to be effective to regulate their d-interlayer spacing with a modified SIB performance. However, the complexity and high cost of current synthetic processes limited its large-scale application in SIBs. Through the natural hyperaccumulation process, a cost-effective and scale-up-driven procedure to produce Ca-ion self-incorporated HC materials was proposed by applying tamarind fruits as the precursor with the enrichment of Ca ions. In virtue of one-step pyrolysis, the self-incorporated and well-distributed Ca ions in tamarind fruits had successfully served as the buffer layer to expand the d-interlayer spacing of HC materials. Furthermore, the natural porosity hierarchy could be largely preserved by the optimization of calcination temperature. As a result, the Ca-rich HC material had exhibited the optimized cycling performance (326.7 mA h g–1 at 50 mA g–1 and capacity retention rate of 89.40% after 250 cycles) with a high initial Coulombic efficiency of 70.39%. This work provided insight into applying the hyperaccumulation effect of biomass precursors to produce doped HC materials with ion self-incorporation and the optimized d-interlayer spacing, navigating its large-scale application for high-performance SIBs.

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