Abstract

The electrosorption capacity of an electrode strongly depends on the surface properties of the electrode material, such as the surface area, pore microstructure, and pore size distribution. Carbon-based electrode materials for capacitive deionization (CDI) or electrosorption processes suffer from problems with high manufacturing costs, poor electrical conductivity, and poor wettability. The thin-film coating of SiO2 on porous biomass carbon may provide an alternative electrode material for double-layer applications. In this paper, the activated porous biomass carbon (AWSC) was first obtained through a simple potassium hydroxide (KOH) activation of wheat straw carbon (WSC) as the precursor, and then thin-film SiO2 coated AWSC (SiO2@AWSC) was prepared by a sol-gel coating process. Scanning electron microscope (SEM) imaging of SiO2@AWSC demonstrated that a SiO2 thin-film was deposited on the surface of AWSC without changing the opening structure. Compared to WSC, the Brunauer-Emmett-Teller (BET) surface area of SiO2@AWSC was greatly increased, and presented obvious micropore and mesopore distributions. Further electrochemical analyses were performed via cyclic voltammetry, galvanostatic charge/discharge, and electrochemical impedance. The electrochemical results showed that SiO2@AWSC electrodes showed increased electrosorption capacitance, which were attributed to a large specific surface area, a porous structure, and enhanced wettability.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.