This review demonstrates that engineering the interfacial sites in a catalyst enables precise control over the reaction pathway for direct ethanol synthesis from COx (CO/CO2) and H2. The tailored interface structure facilita...
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Ni–O–Ca Interfacial Electron Transfer Channels Engineered From Electroplating Sludge for Ultrafast 4‐Nitrophenol Reduction
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The Ni-plating sludge was converted into a Ni@Ca-195/20 catalyst with abundant oxygen vacancies and Ni–O–Ca heterointerfaces via the solvothermal method, which was used to efficiently catalyze the hydrogenation reduction of 4-nitrophenol.
Abstract
The catalytic reduction of 4-nitrophenol (4-NP), a persistent environmental pollutant faces dual challenges reliance on noble metals and inefficient utilization of hydrogen radicals (H*). Meanwhile, nickel-containing sludge generated by the electroplating industry, classified as hazardous waste has long posed significant disposal conundrums. Herein, we developed a noble metal-free pyroxene-type CaNi(Si2O6) catalyst, synthesized from electroplating sludge, that simultaneously addresses these challenges through dynamically reconstructed Ni–O–Ca interface with oxygen vacancies and interfacial electron transfer channels. Ni@Ca-195/20 establishes a self-sustaining catalytic system, achieving a remarkable conversion of 96.8% with 0.1 mM NaBH4 and 0.05 mg catalyst, while maintaining stability over 31 cycles in low concentration regimes. Integrated characterization combined with catalytic performance evaluation reveals an interfacial electron transfer mechanism: the engineered interface enables in situ reduction of Ni2+ generates metallic electron-deficient Niδ+ species, enhancing 4-NP− and BH4 − adsorption through dual-site coordination. Oxygen vacancies accelerate BH4 − hydrolysis, while electron transfer channels sustain H* flux via Ca2+ modulated charge equilibration. This work establishes a waste-to-functionality paradigm for designing defect-engineered catalysts while advancing sustainable remediation of nitroaromatic pollutants.
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