Broadband Hot‐Electron Collection for Solar Water Splitting with Plasmonic Titanium Nitride
Year: 2017
Type: article
Abstract: The use of hot electrons generated from the decay of surface plasmons is a novel concept that promises to increase the conversion yield in solar energy technologies. Titanium nitride (TiN) is an emerging plasmonic material that offers compatibility with complementary metal‐oxide‐semiconductor (CMOS) technology, corrosion resistance, as well as mechanical strength and durability, thus outperforming noble metals in terms of cost, mechanical, chemical, and thermal stability. Here, it is shown that plasmonic TiN can inject into TiO 2 twice as many hot electrons as Au nanoparticles. TiO 2 nanowires decorated with TiN nanoparticles show higher photocurrent enhancement than decorated with Au nanoparticles for photo‐electrochemical water splitting. Experimental and theoretical evidence highlight the superior performance of TiN in hot carrier collection due to several factors. First, TiN nanoparticles provide broadband absorption efficiency over the wavelength range 500–1200 nm combined with high field enhancement due to its natural cubic morphology. Second, TiN forms an Ohmic junction with TiO 2 , thus enabling efficient electron collection compared to Au nanoparticles. Since TiN nanoparticles have strong plasmon resonances in the red, the entire solar spectrum is covered when complemented with Au nanocrystals. These findings show that transition metal nitrides enable plasmonic devices with enhanced performance for solar energy conversion.
Source: Advanced Optical Materials
Language: English
Subfield: Atomic and Molecular Physics, and Optics
Field: Physics and Astronomy
Domain: Physical Sciences
Open Access status: bronze
Funders: National Science Foundation, Volkswagen Foundation, Fondazione Cariplo, Ministero dell’Istruzione, dell’Università e della Ricerca, Regione Lombardia, Materials Research Science and Engineering Center, Harvard University, Multidisciplinary University Research Initiative, Division of Materials Research, Army Research Office
OpenAlex ID: W2592752843
