Related Experiment Video
Updated: May 22, 2025

A Protocol for Electrochemical Evaluations and State of Charge Diagnostics of a Symmetric Organic Redox Flow Battery
Published on: February 13, 2017
p-Type TiO2 Nanotubes: Quantum Confinement and Pt Single Atom Decoration Enable High Selectivity Photocatalytic
Hayoon Jung1,2, Hyesung Kim1, Johannes Will3
1Department of Materials Science and Engineering, WW4-LKO, Friedrich-Alexander-Universität Erlangen-Nürnberg, Martensstraße 7, 91058, Erlangen, Germany.
Abstract:
We synthesize p-type TiO2 nanotubes that allow band-gap adjustment by quantum confinement. These tubes therefore enable reductive photocatalytic reactions that are not thermodynamically possible on classic titania photocatalysts. Here, we demonstrate the direct photocatalytic nitrate reduction to ammonia without any need of hole scavengers. The quantum confinement effect (and thus the thermodynamic driving force) can be controlled by the thickness of the nanotube walls. Notably, the use of Pt single atoms as cocatalysts decorated on the TiO2 nanotubes additionally offers a superior ammonia production and a remarkable enhanced selectivity compared to Pt nanoparticles. Overall, the work not only highlights the potential of size-controlled modifications of electronic properties in extending the utility of a most classical photocatalyst but also exemplifies its use in technologically relevant reactions.
Related Concept Videos
P-N junction
Metal-Semiconductor Junctions
Schottky Barriers
Schottky barriers arise when a metal with a work function (Φm) contacts a semiconductor with a different work function (Φs). Initially, electrons transfer until the Fermi levels of the metal and semiconductor align at equilibrium. For instance, if Φm > Φs, the semiconductor Fermi level is higher than the metal's before contact. The...
Diode: Forward bias
The behavior of a diode in forward bias...
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...

