1 research outputs found
Self-Driven Photoelectrochemical Splitting of H<sub>2</sub>S for S and H<sub>2</sub> Recovery and Simultaneous Electricity Generation
A novel,
facile self-driven photoelectrocatalytic (PEC) system
was established for highly selective and efficient recovery of H<sub>2</sub>S and simultaneous electricity production. The key ideas were
the self-bias function between a WO<sub>3</sub> photoanode and a Si/PVC
photocathode due to their mismatched Fermi levels and the special
cyclic redox reaction mechanism of I<sup>โ</sup>/I<sub>3</sub><sup>โ</sup>. Under solar light, the system facilitated the
separation of holes in the photoanode and electrons in the photocathode,
which then generated electricity. Cyclic redox reactions were produced
in the photoanode region as follows: I<sup>โ</sup> was transformed
into I<sub>3</sub><sup>โ</sup> by photoholes or hydroxyl radicals,
H<sub>2</sub>S was oxidized to S by I<sub>3</sub><sup>โ</sup>, and I<sub>3</sub><sup>โ</sup> was then reduced to I<sup>โ</sup>. Meanwhile, H<sup>+</sup> was efficiently converted
to H<sub>2</sub> in the photocathode region. In the system, H<sub>2</sub>S was uniquely oxidized to sulfur but not to polysulfide (S<sub><i>x</i></sub><sup>nโ</sup>) because of the mild
oxidation capacity of I<sub>3</sub><sup>โ</sup>. High recovery
rates for S and H<sub>2</sub> were obtained up to โผ1.04 mg
h<sup>โ1</sup> cm<sup>โ1</sup> and โผ0.75 mL h<sup>โ1</sup> cm<sup>โ1</sup>, respectively, suggesting
that H<sub>2</sub>S was completely converted into H<sub>2</sub> and
S. In addition, the output power density of the system reached โผ0.11
mW cm<sup>โ2</sup>. The proposed PEC-H<sub>2</sub>S system
provides a self-sustaining, energy-saving method for simultaneous
H<sub>2</sub>S treatment and energy recovery