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Enhanced Hydrogen Production from DNA‐Assembled Z‐Scheme TiO 2 –CdS Photocatalyst Systems
Author(s) -
Ma Ke,
Yehezkeli Omer,
Domaille Dylan W.,
Funke Hans H.,
Cha Jennifer N.
Publication year - 2015
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201504155
Subject(s) - photocatalysis , hydrogen production , catalysis , nucleation , nanocrystal , chemistry , chemical engineering , nanotechnology , materials science , photochemistry , organic chemistry , engineering
A wide range of inorganic nanostructures have been used as photocatalysts for generating H 2 . To increase activity, Z‐scheme photocatalytic systems have been implemented that use multiple types of photoactive materials and electron mediators. Optimal catalysis has previously been obtained by interfacing different materials through aggregation or epitaxial nucleation, all of which lowers the accessible active surface area. DNA has now been used as a structure‐directing agent to organize TiO 2 and CdS nanocrystals. A significant increase in H 2 production compared to CdS or TiO 2 alone was thus observed directly in solution with no sacrificial donors or applied bias. The inclusion of benzoquinone (BQ) equidistant between the TiO 2 and CdS through DNA assembly further increased H 2 production. While the use of a second quinone in conjunction with BQ showed no more improvement, its location within the Z‐scheme was found to strongly influence catalysis.