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Quantum and Classical Orientational Ordering in Solid Hydrogen

Condensed Matter · Submitted 14 May 1996

abstract compiled · 2026-09-23 · no language-model review

The authors' main claim Phases II and III are orientationally ordered, while the ordering objects in phase II are angular momenta of rotating molecules, and in phase III the molecules themselves.

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arXiv IDcond-mat/9605083 (version 2)
Pith IDKRCNDUUQ, Pith's permanent record of this paper and its review
CitationA.F. Goncharov, H.-K. Mao, I.I. Mazin, M. Hanfland, R.J. Hemley. "Quantum and Classical Orientational Ordering in Solid Hydrogen." arXiv:cond-mat/9605083 (1996). https://pith.science/paper/KRCNDUUQ
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The paper's own sentences, arranged. Each label is drawn from a closed vocabulary; the number beside it is the probability the classifier gave that label. Numbers in the tables are the authors', checked by code. No sentence in this record was written by a model.

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Compiled by classifier-1.13-20260917 via OpenRouter, question bank abstract-p1-20260923, 2026-09-23: 1 request, 4,170 input tokens, $0.0002 reported.

What the abstract itself states, as probabilities: claims first 0.04 · states limitation 0.05 · human participants 0.01 · controlled comparison 0.03 · randomized assignment 0.01 · states quantitative result 0.12 · compares with prior results 0.08 · mentions code or data availability 0.02.

The abstract, sentence by sentence

arXiv listing abstract v2. Results and the main claim are underlined; .

We present a unified view of orientational ordering in phases I, II, and III of solid hydrogen. Phases II and III are orientationally ordered, while the ordering objects in phase II are angular momenta of rotating molecules, and in phase III the molecules themselves. This concept provides quantitative explanation of the vibron softening, libron and roton spectra, and increase of the IR vibron oscillator strength in phase III. The temperature dependence of the effective charge parallels the frequency shifts of the IR and Raman vibrons. All three quantities are linear in the order parameter.

background contribution method result interpretation main claim

What the classifier reports for each sentence. The number is the probability it gave the label.
#sentencerolethe authors' own workstates the main conclusionstrength
s0 We present a unified view of orientational ordering in phases I, II, and III of solid hydrogen. contribution 1.00 0.87 0.24 asserted 0.97
s1 Phases II and III are orientationally ordered, while the ordering objects in phase II are angular momenta of rotating molecules, and in phase III the molecules themselves. result 0.52 0.42 0.44 asserted 1.00
s2 This concept provides quantitative explanation of the vibron softening, libron and roton spectra, and increase of the IR vibron oscillator strength in phase III. result 0.51 0.79 0.20 asserted 1.00
s3 The temperature dependence of the effective charge parallels the frequency shifts of the IR and Raman vibrons. result 0.99 0.73 0.07 asserted 1.00
s4 All three quantities are linear in the order parameter. result 0.97 0.73 0.11 asserted 1.00

What kind of paper the classifier reports this is: theoretical result 1.00 · evidence from argument 0.53.

What was examined, and what was not

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  • arXiv listing abstract v2
not examined
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  • figures and tables
  • references and citing sentences
  • relations to other papers
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  • P abstract
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  • S sections
  • T body sentences
  • C citations
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Every quoted sentence on this record is the authors'. Every label is from Pith's closed vocabulary, with the probability shown beside it. Every number in the measurements table is the authors', checked by code. Record as JSON

The paper
Original abstract

We present a unified view of orientational ordering in phases I, II, and III of solid hydrogen. Phases II and III are orientationally ordered, while the ordering objects in phase II are angular momenta of rotating molecules, and in phase III the molecules themselves. This concept provides quantitative explanation of the vibron softening, libron and roton spectra, and increase of the IR vibron oscillator strength in phase III. The temperature dependence of the effective charge parallels the frequency shifts of the IR and Raman vibrons. All three quantities are linear in the order parameter.

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