The high capacity of silver (Ag) anodes positions them as a promising avenue for addressing pressing water purification challenges through capacitive deionization (CDI). However, it faces significant challenges such as severe volume expansion and particle crushing, leading to rapid electrochemical failure. Herein, hierarchical hybrid structures comprising highly dispersed ultrafine Ag anchored in carbon nanolayers were prepared using a temperature-mediated strategy. The coordination effect of organic precursors reduces the surface energy of Ag nanoparticles, effectively preventing aggregation during heat treatment. Carbon layer encapsulation synergized with particle size control effectively suppresses the absolute volumetric strain of the electrode in the electrochemical reaction, enhancing electrochemical stability. When used as a CDI anode, AgNC-500 demonstrated an excellent Cl- capturing capacity of 159.96 mg g-1 and a rate of 27.53 mg g−1 min−1. Furthermore, the capacity exhibited excellent stability with negligible degradation over 50 cycles. This study offers crucial insights for advancing the development of highly stable conversion electrodes.
Read full abstract