A pH-Tolerant Nickel–Vanadium Phosphonate Framework for Stable Aqueous Supercapacitor Cycling

We report a hybrid layered metal-phosphonate framework, [Ni(2,2’-bpy) 3 ] 2+ [(VO(H 2 O)) 2 (VO) 4 (μ-O) 2 (C 6 H 5 PO 3 ) 6 ] 2– ·2H 2 O, in which redox-active [(Ni(2,2’-bpy) 3 )] 2+ cations are embedded between anionic vanadium phosphonate layers [(VO(H 2 O)) 2 (VO) 4 (μ-O) 2 (C 6 H 5 PO 3 ) 6 ] 2– (with 2,2’-bpy = 2,2’-bipyridine). X-ray photoelectron spectroscopy reveals coexisting Ni 2+, V 2+, V 3+, and V 4+ /V 5+ species on the surface of the crystals, indicating a highly dynamic redox system. The material exhibits a main photoluminescence peak at 2.25 eV and strong short-range antiferromagnetic coupling between the V 4+ centers. Electrochemical characterization in aqueous media yields capacitances of 79 F/g in Na 2 SO 4 (pH 7) and 43 F/g in H 3 PO 4 (pH 4) at 1 A/g. In Na 2 SO 4 (pH 7), the material reaches about 300 F/g at a scan rate of 1 mV/s and retains capacity over more than 10,000 cycles. The crystals remain chemically stable between pH 2 and pH 10 for at least 1 week. Combined sustainable synthesis, robust redox activity, high capacitance, long cycle stability, and broad pH tolerance make these hybrid metal-phosphonate crystals promising candidates for next-generation aqueous energy-storage applications.