OH−/H+ dual-ion energy assisted electricity effective photoelectrochemical water splitting

Abstract

Photoelectrochemical (PEC) water splitting is an emerging technology to store the solar energy in the chemical bonds of molecular hydrogen. Among several photo electrodes used for PEC water splitting, α-Fe2O3 is a promising material due to its suitable bandgap, chemical stability, and abundance. Despite these, the position of its conduction band does not allow spontaneous movement of photo-generated electrons to cause the water reduction. This demands the application of a minimum electrical bias of ∼1.5 V vs. SHE to increase the energy of the conduction band such that it will be energetically above the H2O/H2 redox level. We show that by utilizing the energy of neutralization, the minimum electrical voltage required for PEC water splitting can be brought down to ∼0.8 V. By employing an OH−/H+dual-ion configuration. OH−/H+dual-ion assisted PEC water splitting required only 0.95 V to produce a current density of 10 mA/cm2, and for achieving the same rate in a conventional symmetric ion configuration, at least a doubling of the applied electrical bias (∼1.8 V) is required.

Keywords

• OH-/H+ dual-ion electrolyte
• Energy of neutralization
• Photoelectrochemical water splitting
• Semiconductor electrode