In
capacitive deionization (CDI), coion repulsion and Faradaic
reactions during charging reduce the charge efficiency (CE), thus
limiting the salt adsorption capacity (SAC) and energy efficiency.
To overcome these issues, membrane CDI (MCDI) based on the enhanced
permselectivity of the anode and cathode is proposed using the ion-exchange
polymer as the independent membrane or coating. To develop a novel
and cost-effective MCDI system, we fabricated an integrated membrane
electrode using a thin layer of the inorganic ion-exchange material
coated on the activated carbon (AC) electrode, which effectively improves
the ion selectivity. Montmorillonite (MT, Al2O9Si3) and hydrotalcite (HT, Mg6Al2(CO3)(OH)16·4H2O) were selected
as the main active anion- and cation-exchange materials, respectively,
for the cathode and anode. The HT–MT MCDI system employing
HT–AC and MT–AC electrodes obtained a CE of 90.5% and
an SAC of 15.8 mg g–1 after 100 consecutive cycles
(50 h); these values were considerably higher than those of the traditional
CDI system employing pristine AC electrodes (initially, a CE of 55%
and an SAC of 10.2 mg g–1, which attenuated continuously
to zero, and even “inverted work” occurs after 50 h,
i.e., desorption during charging and adsorption during discharging).
The HT–MT MCDI system showed moderate tolerance to organic
matters during desalination and retained 84% SAC and 89% CE after
70 cycles in 50–200 mg L–1 sodium alginate.
This study demonstrates a simple and cost-effective method for fabricating
high-CE electrodes for desalination with great application potential.