Related Experiment Video
Updated: May 2, 2026

Hydrogen Charging of Aluminum using Friction in Water
Published on: January 28, 2020
Hydrogen passivation of impurities in Al(2)O(3)
Minseok Choi1, Anderson Janotti, Chris G Van de Walle
1Materials Department, University of California , Santa Barbara, California 93106, United States.
Abstract:
Carbon and nitrogen are contaminant impurities in Al2O3 dielectrics grown by atomic layer deposition, leading to deleterious effects in device performance. We investigate whether these impurities can be passivated using hydrogen. The role of atomic hydrogen in the electronic properties is addressed by examining formation energies and charge-state transition levels of C-H and N-H complexes. Combined with calculated band alignment, we then assess the impact on Al2O3/semiconductor interfaces. We find that hydrogen is indeed an effective passivating agent: it removes carbon-related carrier traps and passivates negative fixed charge associated with nitrogen.
Related Concept Videos
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Hydroboration-Oxidation of Alkenes
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...

