Much of the earth’s water has a salt content that
is too
high for human consumption or agricultural use. Enhanced oil recovery
operations generate massive volumes of produced water waste with a
high mineral content that can substantially exacerbate water distress.
Current deionization techniques such as reverse osmosis function by
removing the water (majority phase) from the salt (minority phase)
and are thus exceedingly energy-intensive. Furthermore, these methods
are limited in their ability to selectively extract high-value ions
from produced water waste and brine streams. Hybrid capacitive deionization
holds promise for enabling both desalination and resource recovery.
In this work, we demonstrate the construction of a hybrid capacitive
deionization cell that makes use of tunnel-structured ζ-V2O5 as a redox-active positive electrode material.
By augmenting surface adsorption with Faradaic insertion processes,
a 50% improvement in the ion removal capacity for K and Li ions is
obtained as compared to a capacitive high-surface-area carbon electrode.
The extracted ions are accommodated in surface sites and interstitial
sites within the one-dimensional tunnel framework of ζ-V2O5. The kinetics of ion removal depend on the free
energy of hydration, which governs the ease of desolvation at the
electrode/electrolyte interface. The overall ion removal capacity
additionally depends on the solid-state diffusion coefficient. ζ-V2O5 positive electrodes show substantial selectivity
for Li+ removal from mixed flow streams and enrichment
of the Li-ion concentration from produced water waste derived from
the Permian Basin.