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CuAg nanoparticles (CuAgNPs) were electrochemically formed in situ on pre‐anodized, screen‐printed carbon electrodes (SPCEs) that possessed many oxygen‐containing functional groups capable of adsorbing metal ions, namely Cu2+ and Ag+. Pre‐anodization was achieved using continuous cyclic voltammetry in the range of potential 0.3–2.0 V under a scan rate of 50 mV/s. Cu2+ and Ag+ ions were adsorbed on...
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