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极端条件下金属超氢化物中扩散驱动的瞬态氢化作用

Diffusion-driven transient hydrogenation in metal superhydrides at extreme conditions.

作者信息

Zhou Yishan, Fu Yunhua, Yang Meng, Osmond Israel, Jana Rajesh, Nakagawa Takeshi, Moulding Owen, Buhot Jonathan, Friedemann Sven, Laniel Dominique, Meier Thomas

机构信息

Center for High-Pressure Science and Technology Advance Research, Beijing, China.

School of Earth and Space Sciences, Peking University, Beijing, China.

出版信息

Nat Commun. 2025 Jan 29;16(1):1135. doi: 10.1038/s41467-025-56033-3.

Abstract

In recent years, metal hydride research has become one of the driving forces of the high-pressure community, as it is believed to hold the key to superconductivity close to ambient temperature. While numerous novel metal hydride compounds have been reported and extensively investigated for their superconducting properties, little attention has been focused on the atomic and electronic states of hydrogen, the main ingredient in these novel compounds. Here, we present combined H- and La-NMR data on lanthanum superhydrides, LaH, (x = 10.2 - 11.1), synthesized after laser heating at pressures above 160 GPa. Strikingly, we found hydrogen to be in a highly diffusive state at room temperature, with diffusion coefficients in the order of 10cms. We found that this diffusive state of hydrogen results in a dynamic de-hydrogenation of the sample over the course of several weeks, approaching a composition similar to its precursor materials. Quantitative measurements demonstrate that the synthesized superhydrides continuously decompose over time. Transport measurements underline this conclusion as superconducting critical temperatures were found to decrease significantly over time as well. This observation sheds new light on formerly unanswered questions on the long-term stability of metal superhydrides.

摘要

近年来,金属氢化物研究已成为高压领域的驱动力之一,因为人们认为它是接近室温超导性的关键所在。尽管已经报道了许多新型金属氢化物化合物,并对其超导性能进行了广泛研究,但这些新型化合物的主要成分氢的原子和电子态却很少受到关注。在此,我们展示了在高于160 GPa的压力下激光加热合成的镧超氢化物LaHₓ(x = 10.2 - 11.1)的氢核磁共振(H-NMR)和镧核磁共振(La-NMR)联合数据。引人注目的是,我们发现氢在室温下处于高度扩散状态,扩散系数约为10⁻⁹ cm²/s。我们发现氢的这种扩散状态导致样品在几周内动态脱氢,接近其前驱体材料的成分。定量测量表明,合成的超氢化物会随时间持续分解。输运测量也支持这一结论,因为发现超导临界温度也会随时间显著降低。这一观察结果为金属超氢化物长期稳定性方面以前未解决的问题提供了新的线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ca/11779868/2f19ae3597b5/41467_2025_56033_Fig1_HTML.jpg

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