The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Hydrogen in aluminum: First-principles calculations of structure and thermodynamics
Abstract
Despite decades of study, several key aspects of the Al-H system remain the subject of considerable debate. In an effort to elucidate some of these unknowns, we perform a systematic study of this system using first-principles density-functional calculations. We show that generalized gradient approximation (GGA) calculations provide an accurate picture of energetics, phase stability and structure, diffusion, and defect binding in the Al-H system. A series of calculations for hydrides in the M-H systems (M=Al, Ba, Ca, K, Mg, La, Li, Na, Ni, Pd, Sc, Sr, Ti, V, and Y) also shows that the GGA calculations are a quantitatively accurate predictor of hydride formation energies. For Al-H, we find: (i) In agreement with experiment, the observed metastable hydride, ${\mathrm{AlH}}_{3}$ is found to have a small, negative formation enthalpy at ambient conditions, but a strongly positive formation free energy. (ii) Linear response calculations of ${\mathrm{AlH}}_{3}$ yield vibrational frequencies, phonon densities of states (DOS), and heat capacities in excellent agreement with experimental measurements, and suggest the need for a reinterpretation of measured phonon DOS. (iii) Atomic relaxation and anharmonic vibrational effects both play an important role in the tetrahedral versus octahedral interstitial site preference of H in Al. (iv) The calculated heat of solution of H in the preferred tetrahedral site is large and positive (+0.71 eV), consistent with experimental solubility data and with Al as an endothermic hydrogen absorber. (v) Interstitial H interacts strongly with Al vacancies $(\ensuremath{\square}),$ with a calculated H-$\ensuremath{\square}$ binding energy of 0.33 eV. (vi) In the absence of vacancies, the calculated migration energy of H between the tetrahedral and octahedral interstitial sites is 0.18 eV, but for H migrating away from an Al vacancy, the migration energy increases to 0.54 eV. Vacancy trapping of H can therefore provide an explanation for observed disparate H migration barriers.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Special points for Brillouin-zone integrations
Monkhorst, H. J., & Pack, J. D. (1976) · Physical Review B · doi:10.1103/physrevb.13.5188 · Cited by 71,721
Self-interaction correction to density-functional approximations for many-electron systems
Perdew, J. P., & Zunger, A. (1981) · Physical Review B · doi:10.1103/physrevb.23.5048 · Cited by 20,887
Reaction-rate theory: fifty years after Kramers
Hänggi, P., Talkner, P., & Borkovec, M. (1990) · Reviews of Modern Physics · doi:10.1103/revmodphys.62.251 · Cited by 6,154
Cited by
The Open Quantum Materials Database (OQMD): assessing the accuracy of DFT formation energies
Kirklin, S., Saal, J. E., Meredig, B., Thompson, A., Doak, J. W., Aykol, M., Rühl, S., & Wolverton, C. (2015) · npj Computational Materials · doi:10.1038/npjcompumats.2015.10 · Cited by 2,378
Self-citationHydrogen Storage Materials for Mobile and Stationary Applications: Current State of the Art
Lai, Q., Paskevicius, M., Sheppard, D. A., Buckley, C. E., Thornton, A. W., Hill, M. R., Gu, Q., Mao, J., Huang, Z., Liu, H. K., et al. (2015) · ChemSusChem · doi:10.1002/cssc.201500231 · Cited by 414
Metadata
- Authors
- Wolverton, C., Ozoliņš, V., & Asta, M.
- Venue
- Physical Review B
- Publisher
- American Physical Society (APS)
- Published
- 2004-04-12
- Volume
- 69
- Issue
- 14
- ISSN
- 1098-0121 (ISSN-L)
- 1550-235X
- OpenAlex
- W1968927688
- Cited by
- 345
- References
- 3
- FWCI
- 9.37
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Hydrogen in aluminum: First-principles calculations of structure and thermodynamics. https://app.cochat.ai/papers/10.1103/physrevb.69.144109
- The paper
- Wolverton, C., Ozoliņš, V., & Asta, M. (2004). Hydrogen in aluminum: First-principles calculations of structure and thermodynamics. Physical Review B. https://doi.org/10.1103/physrevb.69.144109
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.