Abstract

Chloride-induced corrosion is a major threat to excavated bronze artifacts, yet conventional alkaline desalination requires repeated solution replacement and generates secondary chemical waste. Herein, a series of BiOCl-loaded carbon nanofiber composites (CNFs@BiOCl-X) were prepared by KOH activation followed by hydrothermal growth of BiOCl, aiming to develop regenerable electrodes for chloride removal in capacitive deionization systems. Alkali activation regulated the surface roughness, oxygen-containing functional groups, hydrophilicity, and BiOCl loading of CNFs, while the three-dimensional conductive network helped immobilize BiOCl nanostructures and buffer the volume variation associated with reversible Bi/BiOCl conversion. Electrochemical analyses confirmed the pseudocapacitive chloride-storage behavior of the composites, with ion removal governed by the coupled effects of BiOCl redox activity, charge transfer, and interfacial ion transport. In a fixed-electrode membrane capacitive deionization system, CNFs@BiOCl-2 exhibited the best overall performance, delivering a salt adsorption capacity of 100.44 mg g−1 at 1.4 V and retaining 93.17% of its desalination capacity after 35 cycles at 1.2 V. For flow-electrode capacitive deionization, the higher BiOCl-loading CNFs@BiOCl-5 showed superior utilization of active sites and achieved 94.75% NaCl removal from a 1000 mg L−1 solution within 3 h, with an average desalination rate of 15.48 μg cm−2 min−1 and an energy consumption of 0.88 kWh kg−1-NaCl. These findings demonstrate that rationally matching BiOCl loading with electrode configuration enables efficient and sustainable chloride management, offering a promising electrochemical strategy for conservation electrolytes and related desalination applications.

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