Ji‐Wook Jang 교수

Solar water splitting is a promising approach to transform sunlight into renewable, sustainable and green hydrogen energy. There are three representative ways of transforming solar radiation into molecular hydrogen, which are the photocatalytic (PC), photoelectrochemical (PEC), and photovoltaic-electrolysis (PV-EC) routes. Having the future perspective of green hydrogen economy in mind, this review article discusses devices and systems for solar-to-hydrogen production including comparison of the

Abstract The last few decades’ extensive research on the photoelectrochemical (PEC) water splitting has projected it as a promising approach to meet the steadily growing demand for cleaner and renewable energy in a sustainable and economically viable fashion. Among many potential photocatalysts, hematite (α‐Fe 2 O 3 ) emerges as a highly promising photoanode material with favorable characteristics including visible light absorption (a suitable band gap energy), earth abundance, chemical stabilit

Considering their superior charge-transfer characteristics, easy tenability of energy levels, and low production cost, organic semiconductors are ideal for photoelectrochemical (PEC) hydrogen production. However, organic-semiconductor-based photoelectrodes have not been extensively explored for PEC water-splitting because of their low stability in water. Herein, we report high-performance and stable organic-semiconductors photoanodes consisting of p-type polymers and n-type non-fullerene materia

Abstract Widespread application of solar water splitting for energy conversion is largely dependent on the progress in developing not only efficient but also cheap and scalable photoelectrodes. Metal oxides, which can be deposited with scalable techniques and are relatively cheap, are particularly interesting, but high efficiency is still hindered by the poor carrier transport properties (i.e., carrier mobility and lifetime). Here, a mild hydrogen treatment is introduced to bismuth vanadate (BiV

As a photocathode for CO2 reduction, zinc-blende zinc telluride (ZnTe) was directly formed on a Zn/ZnO nanowire substrate by a simple dissolution-recrystallization mechanism without any surfactant. With the most negative conduction-band edge among p-type semiconductors, this new photocatalyst showed efficient and stable CO formation in photoelectrochemical CO2 reduction at -0.2--0.7 V versus RHE without a sacrificial reagent.

Electrocatalytic nitrate reduction reaction (NO₃RR) presents an innovative approach for sustainable NH₃ production. However, selective NH₃ production is hindered by the multiple intermediates involved in the NO₃RR process and the competitive hydrogen evolution reaction. Hence, the development of highly efficient NO₃RR catalysts is paramount. Herein, we report highly efficient bimetallic catalysts derived from hydroxy double salt (HDS). Under