LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Heavy metal-free, near-infrared colloidal quantum dots for efficient photoelectrochemical hydrogen generation

Photo by viazavier from unsplash

Abstract Photoelectrochemical (PEC) hydrogen generation based on colloidal quantum dots (QDs) is very promising because of its high solar energy to fuel conversion efficiency and low fabrication costs. However, its… Click to show full abstract

Abstract Photoelectrochemical (PEC) hydrogen generation based on colloidal quantum dots (QDs) is very promising because of its high solar energy to fuel conversion efficiency and low fabrication costs. However, its commercial development is hindered by various challenges, including the widespread use of toxic heavy metal–based QDs as sensitizers. We report an environmentally friendly, high efficiency PEC device in which the photoanode consists of a mesoporous TiO 2 film sensitized with heavy metal-free, near-infrared (NIR) colloidal CuInSe x S 2−x (CISeS) QDs. To reduce surface-related traps, we grew an ultrathin ZnS shell on the CISeS core QDs by cation exchange. The PEC cell based on this core/shell CISeS/ZnS QDs exhibits suppressed charge recombination and a saturated photocurrent density of ~5.3 mA/cm 2 under one sun illumination (AM 1.5 G, 100 mW/cm 2 ). In addition, the as-prepared PEC device shows an outstanding stability, exhibiting a drop of only 23% after 9 h illumination. The success in using such core/shell CISeS/ZnS QDs paves the way to realize environment-friendly, high efficiency and cost-effective PEC devices for hydrogen production.

Keywords: hydrogen; heavy metal; hydrogen generation; colloidal quantum; quantum dots

Journal Title: Nano Energy
Year Published: 2017

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.