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The nanoarchitectonic fabrication of multifunctional heterostructures that synergistically integrate photocatalytic environmental detoxification with electrochemical energy storage exemplifies an emerging frontier toward sustainable materials chemistry. Herein, a phytogenic-derived NiCo2O4/g-C3N4@rGO ternary heterostructure was synthesized to regulate electronic configuration, structural defects, and charge carrier transport through Ni/Co–O bonding and M–O–C interactions. The spectral and structural analyses revealed homogeneously distributed nanoparticles with an average crystallite size of ∼ 70 nm, a mesoporous heterostructure possessing a high specific surface area of 75.4 m2 g–1, a high defect density (nD = 1.74 × 1011 cm–2), a narrow optical bandgap (1.10 eV), and strong interfacial bonding with negative surface potential (ζ = −41.3 mV). Under natural solar radiation, the optimized heterostructure achieved 97% (4-NP), 96% (3-AP), and 92% (2,4-DNP) degradation of recalcitrant phenols, along with 71–81% total organic carbon (TOC) mineralization, subsequent pseudo-first-order kinetics, and stable activity over seven consecutive cycles. Statistical optimization via Box–Behnken design (BBD) recognized high predictive fidelity (R2 = 0.99), while GC–MS analysis elucidated a mineralization pathway primarily involving •OH and O2•– radicals. Electrochemical measurements revealed a pronounced supercapacitive response with dominant-diffusion contribution and enhanced surface contribution from corresponding individual components, with a specific capacitance of 1706 F g–1 at 4 A g–1 and significantly reduced charge-transfer resistance (Rct = 0.65 Ω), indicating improved accessibility of electroactive sites and favorable interfacial charge-transfer characteristics. The bifunctional heterostructure provides a promising platform for integrating various interfacial catalytic conversions with energy storage toward environmental remediation and energy conversion in the future.
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AGARWAL et al. (2026) studied this question.
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