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Nature Communications logoLink to Nature Communications
. 2023 Sep 26;14:5991. doi: 10.1038/s41467-023-41777-7

Observation of non-superconducting phase changes in nitrogen doped lutetium hydrides

Xiangzhuo Xing 1,2,#, Chao Wang 1,2,#, Linchao Yu 1, Jie Xu 1, Chutong Zhang 1, Mengge Zhang 1, Song Huang 1, Xiaoran Zhang 1, Yunxian Liu 1,2, Bingchao Yang 1,2, Xin Chen 1,2, Yongsheng Zhang 1,2, Jiangang Guo 3, Zhixiang Shi 4, Yanming Ma 5,6,7, Changfeng Chen 8, Xiaobing Liu 1,2,
PMCID: PMC10522599  PMID: 37752133

Abstract

The recent report of near-ambient superconductivity and associated color changes in pressurized nitrogen doped lutetium hydride has triggered worldwide interest and raised major questions about the nature and underlying physics of these latest claims. Here we report synthesis and characterization of high-purity nitrogen doped lutetium hydride LuHxNy. We find that pressure conditions have notable effects on Lu-N and Lu-NH chemical bonding and the color changes likely stem from pressure-induced electron redistribution of nitrogen/vacancies and interaction with the LuH2 framework. No superconducting transition is found in all the phases at temperatures 1.8-300 K and pressures 0-38 GPa. Instead, we identify a notable temperature-induced resistance anomaly of electronic origin in LuHxNy, which is most pronounced in the pink phase and may have been erroneously interpreted as a sign of superconducting transition. This work establishes key benchmarks for nitrogen doped lutetium hydrides, allowing an in-depth understanding of its novel pressure-induced phase changes.

Subject terms: Superconducting properties and materials, Superconducting properties and materials


Near-ambient superconductivity and pressure-driven color changes were recently reported in nitrogen-doped lutetium hydride. Here, the authors synthesize LuHxNy and do not confirm the superconductivity. In addition, they find that the color changes likely stem from pressure-induced electron redistribution of nitrogen and vacancies.

Introduction

A recent study reported near-ambient superconductivity in a nitrogen doped lutetium hydride (Lu-N-H in short)1, which has triggered worldwide interest and raised major questions27. High-temperature superconductivity has been predicted even realized in metallic hydrogen and hydrogen-rich compounds (such as sulfur hydride8, rare-earth hydrides911, and alkaline-earth hydrides12,13), but megabar pressures are required to stabilize structures. The superconductivity in nitrogen doped lutetium hydride was claimed at much reduced pressures of 0.3-3 GPa, with maximum critical temperature Tc = 294 K at 1.3 GPa1. This discovery has sparked tremendous interest in the scientific community and beyond, ensuing studies quickly followed1437, which have thus far found no evidence supporting superconductivity in Lu-N-H systems.

It was reported that the presence of near-ambient superconductivity in the nitrogen doped lutetium hydride coincided with a visual color change of the sample from blue (0-0.3 GPa) through pink (0.3-3 GPa) to red (>3 GPa)1. Conspicuously, the superconducting state was only found in the pink phase. This is an intriguing phenomenon since all previously reported high-temperature superconductors show dark or black color in hydrogen-rich metallic systems913. Meanwhile, similar color changes were observed in LuH2 at pressures ranging from 2.5 GPa to 5 GPa14,26, but absent in LuHxNy samples at pressures of 0-6.5 GPa15,29. No superconducting transition was detected in LuH2 sample14 or LuHxNy sample up to 40.1 GPa15,28 at temperatures from 300 K to 10 K. Since all the samples in the reported works share the same crystal structure, their main distinctions are the sample color and nitrogen contents. Ming et al. detected nitrogen element at four locations in ten measurements as 0.07, 0.12, 0.19, and 1.38 wt.% in the LuHxNy samples15, while the claimed near-ambient superconductor was reported in lutetium hydrides with 0.8–0.9 wt.% nitrogen doping1. Since the superconductivity in hydrides may be highly sensitive to nitrogen doping38, producing and probing high-quality lutetium hydrides with well calibrated nitrogen doping is crucial to elucidating pertinent phenomena and the underlying mechanisms.

In this work, we synthesized pure bulk samples of nitrogen doped lutetium hydrides by high pressure and high temperature (HPHT) method. The samples exhibit uniform shinning blue color and have the same crystal structure and well-distributed nitrogen content as in previously reported samples1. Our in-situ high-pressure experiments revealed reversible color changes of nitrogen doped lutetium hydrides from shining blue to dark blue to purple and pink, finally into red. The critical pressures for these color changes are sensitive to the used pressure media, but the overall trends are consistent among all the cases. Our electrical measurements did not detect any signals of a superconducting transition at temperatures from 300 K to 1.8 K under pressures up to 38 GPa. There is an abnormal feature above 200 K during the warming-up electrical measurements on the purple, pink, and red phases, but the sample retains metallic behavior during the cooling-down measurements. The raw data taken in the warming-up measurements of the reported near-ambient superconductors1 exhibit the same anomalous resistance, which was interpreted as a sign of superconductivity after a background subtraction was applied. Our results from both warming-up and cooling-down cycles on the same sample show unambiguous evidence that there is no correlation between the pink phase and the claimed near-ambient superconductivity in nitrogen doped lutetium hydrides since otherwise the data obtained during the cooling-down cycle also should capture the same basic physics associated with the superconducting transition. Also, the fact the same resistance anomaly is also seen in the red phase, which was recognized to be non-superconducting1, further reinforces our conclusion about the lack of a superconducting transition in the sample.

Results and discussion

Synthesis, structure and composition of the produced LuHxNy sample

We performed HPHT experiments for synthesis of nitrogen doped lutetium hydrides (see Methods for details and a schematic diagram in Supplementary Fig. 1). Figure 1a shows the X-ray diffraction (XRD) pattern on a polished smooth surface of the shining blue sample (top inset) by a diffractometer with wavelength of 1.5406 Å. All the dominant peaks can be well indexed as a cubic structure with Fm3¯m space group, and no impurity phases such as LuN1-δHε and Lu2O3 phases are detected except for a small amount of lutetium left during the surface polishing in preparation for XRD measurements. The crystal structure is consistent with that of LuH239 and the reported near-ambient superconductors1. The sharp diffraction peaks indicate a better crystalline quality in our HPHT products compared to previous samples1.

Fig. 1. Structure and composition of the produced nitrogen doped lutetium hydride sample.

Fig. 1

The reported data of the near-ambient superconducting sample is plotted as black lines (bottom) for comparison. a Typical XRD pattern (red line) of our produced nitrogen doped lutetium hydride sample LuHxNy. The small peak marked by asterisk is from the residual lutetium. Top inset image is the measured bulk sample, around 1 mm in size. The XRD data of produced LuN1-δHε bulk sample (orange line) is also listed for comparison, in which the tiny peaks marked by rhombus come from unknown phase. b, c HRTEM image of the LuHxNy sample and the SAED pattern along the [11¯0] zone-axis. d Representative EDX spectra of the produced LuHxNy sample-I (red line) and sample-II (blue line). The spectrum of the Lu piece used in the starting materials is also shown for comparison. The carbon peaks are from the tape used for holding a tiny sample for EDX measurements. e A typical EDX mapping image for nitrogen elements at four different areas, 50 × 35 μm in size. f Typical Raman spectra of LuHxNy sample-I (red line) and sample-II (blue line) under ambient conditions. The peaks below 120 cm−1 are from the background. g Typical XPS spectrum of the N 1 s core level.

High-resolution transmission electron microscopy (HRTEM) measurements (Fig. 1b) reveal that the Lu atoms arrange in the (200), (111), and (11¯1¯) orientations with the lattice spacing of 0.252 nm, 0.288 nm, and 0.289 nm, respectively. The selected area electron diffraction (SAED) pattern along the [11¯0] zone-axis is shown in Fig. 1c, which is consistent with the result of our XRD measurement. The lattice parameter a is determined to be 5.040 Å, which is much smaller than that of LuH314, but is comparable to that of recently reported LuHxNy samples15. Thus, we attribute the composition of our HPHT produced samples as LuHxNy.

Energy dispersive X-ray spectroscopy (EDX) spectrum in Fig. 1d shows clear evidence for the incorporation of nitrogen in our LuHxNy samples, while the EDX mapping results indicate macroscopically uniform nitrogen distribution (Fig. 1e). We calculated the averaged nitrogen content in our LuHxNy sample-I based on 10 randomly spots and four EDX mapping results, containing low nitrogen contents with an averaged value of 0.2 wt.%. For sample-II, we randomly measured 15 spots, obtaining an averaged nitrogen content of 0.84 wt.%, at the same level with previously reported nitrogen doped lutetium hydrides (0.8–0.9 wt.%)1, indicating that these samples have similar nitrogen content. Details are given in Supplementary Tables 1 and 2.

Figure 1f displays typical Raman spectra of the LuHxNy samples with a 532 nm laser excitation. The obtained spectrum of sample-II is practically identical to that of the previously reported sample1 with characteristic peaks at 124 cm−1, 147 cm−1, 194 cm−1, 251 cm−1, and 1206 cm−1, while all the Raman peaks in the sample-I has a nearly uniform down-shift of about 5 cm−1. The peaks at 194 cm−1, 251 cm−1, and 1206 cm−1 are close to those in LuH214, thus likely coming from Lu-H framework or vacancy-associated vibration25, while the peaks at the lower wavenumbers of 124 cm−1 and 147 cm−1 are only observed in nitrogen doped lutetium hydrides that can be assigned to Lu-NH and Lu-N related vibrational modes (Supplementary Figs. 24). No Raman signals of LuN phase40 were detected in our produced samples. The scanning electron microscope and mapping measurements by Raman spectroscopy show a uniform polycrystalline structure of the produced LuHxNy samples (Supplementary Figs. 5 and 6). X-ray photoelectron spectroscopy (XPS) measurements further confirm incorporation of nitrogen in the produced samples. Figure 1g shows that the main peak of the N 1 s core level is located at 399.64 eV. This suggests that the dominant bonding configuration for nitrogen atoms and NH species is N-H bonding in the produced LuHxNy samples4143. The shoulder seen at the lower binding energy of 398.68 eV indicates that some nitrogen atoms partially bond with lutetium, which is close to the value observed in hydrogen-doped lutetium nitrides (Supplementary Fig.7).

Pressure-induced color changes in the LuHxNy sample

To investigate the color evolution of the nitrogen doped lutetium hydrides, we loaded the produced LuHxNy samples into standard diamond anvil cells without any medium or with different pressure media of nitrogen gas, water, silicon oil, and solid NaCl in the sample chambers. Our experimental results demonstrate that the color change with increasing pressure can be clearly seen in all the studied stress environments (Supplementary Figs. 813).

Figure 2a shows a systematic evolution pattern of color change of the LuHxNy sample in the silicon oil medium over a wide pressure range. With pressure increasing to 6.2 GPa, the initial shining blue color turns to royal blue, then to purplish blue at 8.2 GPa, further to purple at 10.5 GPa. The intriguing pink phase starts to show up at 16 GPa and remains over a span of about 7 GPa until the vivid red color appears at 23.5 GPa. During the decompression process, the color evolution is completely revisable, gradually from vivid red back to its original shinning blue after pressure is fully released. Figure 2b depicts the critical pressure and stable region for the color changes in LuHxNy samples in different pressure media. Our work reveals a previously unseen purple phase that is present in all the cases studied in our work, but was missed by Dasenbrock-Gammon et al. because of the very narrow pressure range for the transition from blue phase to pink phase in their work1. Our results establish a pressure-induced phase change sequence as indicated by their colors from phase I (blue) to phase II (purple), then phase III (pink), and eventually phase IV (red).

Fig. 2. Evolution of color changes of nitrogen doped lutetium hydrides with varying pressures.

Fig. 2

a Optical images of pressure-induced color changes of the produced LuHxNy samples during compression (upper images) and decompression (down images) processes in a DAC chamber with silicon oil as pressure medium. b Phase diagram of phase I (blue), phase II (purple), phase III (pink) and phase IV (red) of the LuHxNy samples in different pressure media. Two runs were carried out in silicon oil medium with Re-gasket thickness of 32 μm and 44 μm, respectively. The sample chamber with thick gasket underwent expansion, creating shear stresses, which helped reduce the critical pressures of color changes in the LuHxNy sample (Supplementary Fig. 10). c Optical images of the samples showcasing reduced critical pressures of the LuHxNy samples mixed with nanodiamonds by internal stress in the NaCl pressure medium.

The overall trend of pressure induced color variation in our work is fully consistent with that of the reported near-ambient superconductors1, but the critical pressures for color changes are higher in our work. This phenomenon is also observed in another independent work, where a dark-blue to pink-red color change occurs at pressure region of 11-21 GPa15. The much lower critical pressures (from 0.3 GPa to 3 GPa) in the previous work1 can be attributed to the composite nature of their samples containing dominant N-doped lutetium hydride and minority LuN1-δHε phase with different lattice parameters, and these mixed phase structures can introduce large and complex internal stresses between the constituent components under compression. Such complex stresses could lead to significant changes, including large reduction of critical pressure for phase transitions4447. This also explains the distinct critical pressures and stable regions of the differently colored phase in different pressure media that exert different stresses on the samples. To further verify this point, we introduce stresses by adding a small amount of nanodiamonds into LuHxNy powers in the NaCl pressure medium, as illustrated in Fig. 2c. Consequently, the pink and red phases occur at significantly reduced pressures of 5.1 GPa and 10.0 GPa, respectively. This suggests that the presence of minority LuN1-δHε phase, which doesn’t show any color change (Supplementary Fig. 14), mixed within dominant N-doped lutetium hydride in the samples of the previously report work1 is effective in pushing the critical pressure for the pink phase down to 0.3 GPa.

In-situ Raman spectrum of the LuHxNy sample under compression

We investigated the pressure-dependent Raman spectrum of the produced LuHxNy sample up to 30.75 GPa in the nitrogen gas medium, which has gone through the whole color change sequence (Fig. 3a and Supplementary Fig. 15). The strongest 1206 cm−1 peak (Fig. 1f) overlap at relatively low pressures with the Raman peaks at 1332 cm−1 from diamond anvils under compression, so we selected other characteristic peaks of 124 cm−1, 147 cm−1, 194 cm−1, and 251 cm−1 for comparison. The measured spectra are deconvoluted to analyze multipeak information1. Results in Fig. 3b show that all of these peaks gradually move upward in frequency at nearly the same rate, and the rate of decline decrease when it gets into the purple, pink and red phases. It is clearly seen in Fig. 3c that there is an accelerated rising rate for the intensity of N related peaks (124 cm−1 and 147 cm−1) when getting into the pink phase region and the intensity suddenly drop before the appearance of the red phase, while the Lu-H related peaks of 194 cm−1 and 251 cm−1 gradually decrease intensity at rising pressure through the purple and pink phases. The intensity of all peaks is more stable in the blue and red phases. It is interesting to note that the pressure driven changes of the intensity for Lu-N and Lu-NH related peaks in the pink phase are consistent with the appearance of the claimed superconductivity1.

Fig. 3. In-situ Raman spectrum of nitrogen doped lutetium hydrides at changing pressures.

Fig. 3

a Typical pressure-dependent Raman spectra of the produced LuHxNy (sample-II) with a 633 nm laser excitation. The spectral curves (cycles) are deconvoluted by Gaussian fitting (solid lines). b Pressure-dependent shift of the fitted Raman peaks. c Pressure-dependent intensity of the Raman peaks of 124 cm−1, 147 cm−1, 194 cm−1, and 251 cm−1.

These results offer strong evidence that the pressure conditions have major effects on the chemical interaction between nitrogen and the structural frame of lutetium hydrides in the pink phase region. Our further theoretical calculations provide evidence that the incorporation, distribution of N/NH can significantly influence the electron transfer between the existing vacancies and Lu-H framework (see Supplementary Figs. 1619). This may be a key reason for the gradual color evolution from its original blue to the ultimate red under compression.

Electrical transport measurements of the LuHxNy samples

We performed electrical transport measurements in the four phases over the temperature range of 1.8–300 K. Figure 4a show that LuHxNy samples exhibit typical metallic behaviors at ambient pressure. We further measured the temperature dependent resistance under pressure in five runs. Figure 4b shows pressure evolution of resistance at room temperature. In sample-I, the resistance in run 1 decreases with rising pressure up to 8.3 GPa and drops by an order of magnitude between 8.3 and 13.3 GPa, then stays nearly constant to the highest measured pressure of 29.9 GPa. In run 2, under rising pressure, the resistance first increases until pressure reaches 3.7 GPa, then gradually decreases up to pressure of 30.9 GPa (see Supplementary Fig. 20). Such diverse behaviors of resistance under pressure likely stem from the variation of the nitrogen contents taken from different parts of the original synthesized sample. In sample-II, the resistance gradually decreases up to pressure of 38.2 GPa (run 3–5), similar to that observed in run 2 of sample-I. In Fig. 4c, d, we present the resistance data during the cooling-down measurement, and the results show no sign of superconductivity in all four phases of LuHxNy samples (blue to red) from 300 K to 1.8 K. Our further experiments also preclude the possibility of the reported superconductivity1 from the secondary phase of LuN1-δHε in ref. 1. up to 31.29 GPa (see Supplementary Fig. 21).

Fig. 4. Temperature dependent electrical resistance of the LuHxNy samples at changing pressures.

Fig. 4

a Temperature dependence of resistivity at ambient pressure. Top inset shows the optical micrograph of LuHxNy sample with gold electrodes attached by silver paste. b Room temperature resistance of sample-I (top) and sample-II (bottom) at different pressures. The shading line is a guide to the eyes. c, d Evolution of the resistance with pressure at temperature ranging from 300 K to 1.8 K during cooling down process of sample-I (run 1) and sample-II (run 3), respectively.

The measured resistance curve should exhibit the same trend of variation with changing temperature during cooling-down or warming-up process with same cooling/warming rate if no temperature-driven phase transition occurs. Generally, data collected during warming-up are used for analysis because of the more homogeneous thermal equilibrium than in the cooling-down measurements. Surprisingly, we observed contrasting behaviors in the measured R(T) curves of LuHxNy samples during the cooling-down and warming-up electrical measurements (Supplementary Figs. 22-24), and the contrast is especially pronounced in the pink phase (III) that was claimed to host near-ambient superconductivity1.

It is interesting to note in Fig. 5a that, in the region of purple phase II (13.3 GPa) and pink phase III (22.3 GPa), a plateau in the resistance curve for sample-I develops and grows with rising pressure starting at about 260 K during the warming-up measurements, followed by a relatively sharp drop with reducing temperature; however, no zero-resistance state was observed down to 1.8 K. Such a feature significantly weakens when the sample turns to red color (phase IV). Such behaviors are possibly caused by pressure- or/and thermally driven influence on the electron transfer in LuHxNy due to the incorporation of N/NH and hydrogen vacancies48,49, as indicated by the Raman spectra shown in Fig. 3c. The onset temperature of the resistance anomaly in LuHxNy is sensitive to pressures and rises in the pink phase with increasing pressure (see Supplementary Fig. 25).

Fig. 5. Contrasting R(T) curves obtained in cooling-down and warming-up measurements.

Fig. 5

a Temperature dependence of resistance of sample-I (run 1) for phase I at 0.4 GPa, phase II at 13.3 GPa, phase III at 22.3 GPa and phase IV at 29.9 GPa. b Temperature dependence of resistance of sample-II (run 3) for phase I at 2.2 GPa, phase II at 13.0 GPa, phase III at 21.5 GPa and phase IV at 32.1 GPa. The raw resistance data on the pink phase (taken at lower pressure) from the recent work reporting on ambient superconductivity1 are included (panel III) to show a similar plateau observed in our warming-up curve, despite a shift in temperature where the turning point of the curve is located.

Similar resistance anomalies are also observed in sample-II (Fig. 5b) with the same N level as that in the claimed near-ambient superconductor1. The plateau in the resistance curve is observed even in the purple phase (II) at 13.0 GPa, and the hump structure becomes more pronounced (21.5 GPa) through the pink phase III and persists into the red phase IV above 32.1 GPa. We also measured R(T) with an applied magnetic field of 3 T at 26.1 GPa in run 2, the results show no shift in the critical pressure marking the turning point in the resistance curve, and this lack of response of resistance to applied magnetic field excludes the possibility of a superconducting transition for this abnormal behavior (Supplementary Fig. 23 j).

In conclusion, we have synthesized high-purity nitrogen doped lutetium hydrides (LuHxNy) using HPHT method, and the obtained samples exhibit the same crystal structure, composition and overall color changing trends as those of the recently reported near-ambient superconductor1. Our experimental and theoretical results provide convincing evidence of nitrogen incorporation in the LuHxNy samples. Our extensive and systematic resistance measurements indicate that there is no superconducting transition in all the blue, purple, pink and red phases of LuHxNy samples at temperatures of 1.8-300 K and pressures from 0.4 GPa to 38 GPa. These results demonstrate that the pressure/temperature-driven electron redistribution by incorporation of nitrogen/vacancies and its interaction with the LuH2 framework plays a crucial role in the remarkable visual color changes and anomalous electrical resistance behaviors seen in the experiments. The present work has shown unambiguous evidence that there is no correlation between the pink phase and near-ambient superconductivity in nitrogen doped lutetium hydrides, and further efforts should focus on elucidating the origin of the intriguing emergent N related bonding changes that may drive the sample color changes and the associated resistance anomalies.

Methods

Starting materials and HPHT synthesis

The polycrystalline samples of LuHxNy were synthesized using a China-type cubic-type high pressure apparatus. The high-pressure cell used in this study has two layers (layer 1 and layer 2) that were separated by a BN thin plate, as depicted by a schematic diagram in Supplementary Fig. 1. In layer 1, the Lu pieces (99.9 wt.% purity) with silver color were placed as the precursors. Layer 2 was filled with the mixture of NH4Cl (Aladdin 99.99 wt.% purity) and CaH2 (Aladdin 98.5 wt.% purity) in a molar ratio of 2:8 that was used as the source of nitrogen and hydrogen15. Lu pieces were commercially purchased from Hebei Rechen New Material Technology Co., Ltd. The cell assembly was then heated at 773 K for 5 ~ 7 hours under pressures of 3 GPa, followed by rapid cooling to room temperature. Finally, LuHxNy samples were obtained after pressure release. After the HPHT experiments, we carefully removed the surrounding h-BN materials and remaining lutetium on the surfaces (Supplementary Fig. 1b), and then retrieved the final products for characterization and further high-pressure experiments. The obtained HPHT products have a dominated shining blue phase and a very tiny amount of purple phase on the surface. We focus our study on the most interesting blue phase (Supplementary Fig. 1c). The LuN1-δHε samples were synthesized with the same conditions as LuHxNy. The starting materials are LuN powders (99.999 wt.% purity) that are commercially available from Shanghai Yien Chemical Reagent Co., Ltd.

Sample characterization

The crystal structure of produced samples was examined using an X-ray diffractometer (XRD) with Cu-Kα radiation (λ = 1.5406 Å, PANalytical X’pert3, Holland). High resolution transmission electron microscopy (HRTEM) images were obtained on a JEM2100 Plus transmission electron microscope at an acceleration voltage of 200 kV. Elemental analysis was made by a scanning electron microscope (SEM, Zeiss Sigma 500) equipped with energy dispersive x-ray (EDX) spectroscopy probe using an accelerating voltage of 5 kV. X-ray photoelectron spectroscopy (XPS) spectrums were taken by a Thermo Scientific (ESCALAB, 250Xi). During the experiments, the original surface of the studied samples was removed by etching techniques in order to avoiding the contamination of water and oxygen in air. Raman experiments were carried out on a high-resolution Raman spectrometer (Horiba, LabRAM HR revolution) with the excitation wavelength of 532 nm and 633 nm (grating: 1800 g/mm). The electrical transport measurement was carried out on a Quantum Design Physical Property Measurement System (PPMS).

In-situ high pressure measurements

High pressure resistivity measurements were conducted in a screw-pressure-type diamond-anvil-cell (DAC) made of non-magnetic Be-Cu alloy. A mixture of c-BN powder and epoxy was used as the insulating coating for the rhenium gaskets, which was pre-indented to 30 μm in thickness. Several pieces of LuH2±xNy grains with shinning blue color were selected under a microscope and loaded into the gasket hole. The Pt electrodes were attached to the sample with a four-probe van der Pauw method. NaCl was used as the pressure medium. Also, water, silicone oil, and nitrogen gas were used in the experiments of pressure induced color change. High-quality ruby balls ~10 μm in size were used for pressure calibration. The Raman peak position is taken from the center of the full width at half-maximum (FWHM), while the peak intensity is calculated after subtracting the background by considering the symmetry and FWHM of the peak.

Theoretical calculations

We used the Fm3¯m LuH2 as the prototype, and constructed LuH1.875 with H vacancies in a 2 × 2 × 2 supercell containing 96 atoms. Then one N atom and one NH cluster are inserted into interstitial sites to simulate N doped LuH1.875 systems, denoted as Lu32H60-N and Lu32H60-NH, respectively. The precise geometry relaxations and electronic structure calculations were carried out within the framework of density functional theory (DFT) as implemented in the Vienna ab initio simulation package (VASP)50. The electron–ion interactions are described by the generalized gradient approximation of Perdew-Burke-Ernzerhof (PBE)51 functional. The projector-augmented wave (PAW)52 pseudopotentials with the valence electrons 5p65d146s2 for Lu, 1s1 for H, and 2s22p3 for N were used. The energy cutoff of 550 eV and a Monkhorst-Pack scheme53 with a dense k-point spacing of 2π × 0.03 Å−1 were chosen in all the calculations. The electron localization function (ELF)54 was calculated to illustrate the electron distribution and chemical bonding. Phonon and Raman spectra were calculated within the PHONOPY code55.

Supplementary information

Peer Review File (561.9KB, pdf)

Acknowledgements

X.L. would like to thank the whole HPPMS team for the hard work. The authors would like to thank Xiaofeng Xu for fruitful discussion. This work was partly supported by the National Natural Science Foundation of China (Grant Nos. 12204265 X.X., 11974208 X.L., 52172212 X.C., and 52102335 C.W.), the Natural Science Foundation of Shandong Province (Grant Nos. ZR2023JQ001 X.L., ZR2020YQ05 X.L., ZR2022QA040 X.X., and ZR2021YQ03 X.C.), the Higher Educational Youth Innovation Science and Technology Program of Shandong Province (2022KJ183 Y.L.), the Young Scientists of Taishan Scholarship (tsqn202211128 X.L. and tsqn202306184 X.C.), and the Strategic Priority Research Program (B) of the Chinese Academy of Sciences (Grant No. XDB25000000 Z.S.).

Author contributions

X.L. and X.X. designed the experiments and gathered data. X.L., X.X., C.C., and Y.M. analyzed the data, organized the results and wrote the manuscript. X.X., L.Y., S.H., and X.L. synthesized the samples. X.X, C.W., J.X., M.Z., C.Z., and X.Z. performed sample characterization and high-pressure measurements. Y.L., X.C. and Y.Z. performed the theoretical calculations and analysis. B.Y., J.G., and Z.S. provided discussions. All authors contributed to editing and improving the manuscript.

Peer review

Peer review information

Nature Communications thanks the anonymous, reviewer(s) for their contribution to the peer review of this work. A peer review file is available.

Data availability

All data generated or analyzed in this study are included in this article and its Supplementary Information file. Additional data are available from the corresponding author upon request.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

These authors contributed equally: Xiangzhuo Xing, Chao Wang.

Supplementary information

The online version contains supplementary material available at 10.1038/s41467-023-41777-7.

References

  • 1.Dasenbrock-Gammon N, et al. Evidence of near-ambient superconductivity in a N-doped lutetium hydride. Nature. 2023;615:244. doi: 10.1038/s41586-023-05742-0. [DOI] [PubMed] [Google Scholar]
  • 2.Jin C, Ceperley D. Hopes raised for ambient superconductors. Nature. 2023;615:221. doi: 10.1038/d41586-023-00599-9. [DOI] [PubMed] [Google Scholar]
  • 3.Garisto D. Allegations of scientific misconduct mount as physicist makes his biggest claim yet. Physics. 2023;16:40. [Google Scholar]
  • 4.Sridhar S. True superconductivity at near ambient temperature has not been confirmed by Dasenbrock-Gammon. J. Phys. Chem. Solids. 2023;180:111381. [Google Scholar]
  • 5.Chen S. Muted response to new claim of a room-temperature superconductor. Physics. 2023;16:39. [Google Scholar]
  • 6.Liu G, Liu H. Hope and challenge of ternary hydrogen-based superconductors under pressure. Superconductivity. 2023;6:100046. [Google Scholar]
  • 7.Hirsch JE. Enormous variation in homogeneity of room temperature superconductor samples: a comment on Nature 615, 244. J. Supercond. Nov. Magn. 2023;36:1489–1494. [Google Scholar]
  • 8.Drozdov AP, Eremets MI, Troyan IA, Ksenofontov V, Shylin SI. Conventional superconductivity at 203 kelvin at high pressures in the sulfur hydride system. Nature. 2015;525:73–76. doi: 10.1038/nature14964. [DOI] [PubMed] [Google Scholar]
  • 9.Somayazulu M, et al. Evidence for superconductivity above 260 K in lanthanum superhydride at megabar pressures. Phys. Rev. Lett. 2019;122:027001. doi: 10.1103/PhysRevLett.122.027001. [DOI] [PubMed] [Google Scholar]
  • 10.Drozdov AP, et al. Superconductivity at 250 K in lanthanum hydride under high pressures. Nature. 2019;569:528. doi: 10.1038/s41586-019-1201-8. [DOI] [PubMed] [Google Scholar]
  • 11.Chen W, et al. High-temperature superconducting phases in cerium superhydride with a Tc up to 115 K below a pressure of 1 megabar. Phys. Rev. Lett. 2021;127:117001. doi: 10.1103/PhysRevLett.127.117001. [DOI] [PubMed] [Google Scholar]
  • 12.Ma L, et al. High-temperature superconducting phase in clathrate calcium hydride CaH6 up to 215 K at a pressure of 172 GPa. Phys. Rev. Lett. 2022;128:167001. doi: 10.1103/PhysRevLett.128.167001. [DOI] [PubMed] [Google Scholar]
  • 13.Li Z, et al. Superconductivity above 200 K discovered in superhydrides of calcium. Nat. Commun. 2022;13:2863. doi: 10.1038/s41467-022-30454-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Shan P, et al. Pressure-induced color change in the lutetium dihydride LuH2. Chin. Phys. Lett. 2023;40:046101. [Google Scholar]
  • 15.Ming X, et al. Absence of near-ambient superconductivity in LuH2±xNy. Nature. 2023;620:72–77. doi: 10.1038/s41586-023-06162-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Li Z, et al. Superconductivity above 70 K observed in lutetium polyhydrides. Sci. China-Phys. Mech. Astron. 2023;66:267411. [Google Scholar]
  • 17.Liu M, et al. On parent structures of near-ambient nitrogen-doped lutetium hydride superconductor. Phys. Rev. B. 2023;108:L020102. [Google Scholar]
  • 18.Zhang S, et al. Electronic and magnetic properties of Lu and LuH2. AIP Adv. 2023;13:065117. [Google Scholar]
  • 19.Xie F, et al. Lu-H-N phase diagram from first-principles calculations. Chin. Phys. Lett. 2023;40:057401. [Google Scholar]
  • 20.Sun Y, et al. Effect of nitrogen doping and pressure on the stability of cubic LuH3. Phys. Rev. B. 2023;108:L020101. [Google Scholar]
  • 21.Hilleke KP, et al. Structure, Stability and superconductivity of N-doped lutetium hydrides at kbar pressures. Phys. Rev. B. 2023;108:014511. [Google Scholar]
  • 22.Huo Z, et al. First-principles study on the superconductivity of N doped fcc-LuH3. Matter Radiat. Extremes. 2023;8:038402. [Google Scholar]
  • 23.Ferreira PP, et al. Search for ambient superconductivity in the Lu-N-H system. Nat. Commun. 2023;14:5367. doi: 10.1038/s41467-023-41005-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Lucrezi, R. et al. Temperature and quantum anharmonic lattice effects in lutetium trihydride: stability and superconductivity. Preprint at https://arxiv.org/abs/2304.06685 (2023). [DOI] [PMC free article] [PubMed]
  • 25.Moulding, O. et al. Trigonal to cubic structural transition in possibly N-doped LuH3 measured by Raman and X-ray diffraction. Preprint at https://arxiv.org/abs/2304.04310 (2023).
  • 26.Zhao X, et al. Pressure tuning of optical reflectivity in LuH2. Sci. Bull. 2023;68:883. doi: 10.1016/j.scib.2023.04.009. [DOI] [PubMed] [Google Scholar]
  • 27.Wang, N. et al. Percolation-induced resistivity drop in cold-pressed LuH2. Sci. China-Phys. Mech. Astron66, 297412 (2023).
  • 28.Zhang Y-J, et al. Pressure induced color change and evolution of metallic behavior in nitrogen-doped lutetium hydride. Sci. China-Phys. Mech. Astron. 2023;66:287411. [Google Scholar]
  • 29.Cai S, et al. No evidence of superconductivity in the compressed sample prepared from the lutetium foil and H2/N2 gas mixture. Matter Radiat. Extremes. 2023;8:048001. [Google Scholar]
  • 30.Kim, S.-W. et al. Microscopic theory of colour in lutetium hydride. Preprint at https://arxiv.org/abs/2304.07326 (2023). [DOI] [PMC free article] [PubMed]
  • 31.Tao X, et al. Leading components and pressure-induced color changes in lutetium-nitrogen-hydrogen system. Sci. Bull. 2023;68:1372–1378. doi: 10.1016/j.scib.2023.06.007. [DOI] [PubMed] [Google Scholar]
  • 32.Lv, R. et al. Physical origin of color changes in lutetium hydride under pressure. Preprint at https://arxiv.org/abs/2307.05024 (2023).
  • 33.Li, P. et al. Transformation of hexagonal Lu to cubic LuH2+x single-crystalline films. Chin. Phys. Lett.40, 087401 (2023).
  • 34.Liu, Z. et al. Pressure-induced color change arising from transformation between intra- and inter-band transitions in LuH2±xNy. Preprint at https://arxiv.org/abs/2305.06103 (2023).
  • 35.Guo, J. et al. Robust magnetism against pressure in non-superconducting samples prepared from lutetium foil and H2/N2 gas mixture. Preprint at https://arxiv.org/abs/2306.04302 (2023).
  • 36.Dangić, Ð. et al. Ab initio study of the structural, vibrational and optical properties of potential parent structures of nitrogen-doped lutetium hydride. Phys. Rev. B108, 064517 (2023).
  • 37.Di P, et al. The near room-temperature upsurge of electrical resistivity in Lu-H-N is not superconductivity, but a metal-to-poor-conductor transition. Matter Radiat. Extremes. 2023;8:058401. [Google Scholar]
  • 38.Ge Y, et al. Room-temperature superconductivity in boron- and nitrogen-doped lanthanum superhydride. Phys. Rev. B. 2021;104:214505. [Google Scholar]
  • 39.Pebler A, Wallace WE. Crystal structure of some lanthanide hydrides. J. Phys. Chem. 1962;66:148. [Google Scholar]
  • 40.Granville S, et al. Vibrational properties of rare-earth nitrides: Raman spectra and theory. Phys. Rev. B. 2009;79:054301. [Google Scholar]
  • 41.Asanova TI, et al. Studying the process of (NH4)2[IrCl6] thermal decomposition by X-Ray photoelectron spectroscopy and electron microscopy. J. Struct. Chem. 2020;61:388–399. [Google Scholar]
  • 42.Mozhchil RN, et al. Electronic, local atomic structure of lutetium tetraphenylporfyrin: XPS and XAFS spectroscopy stadies. J. Phys. Conf. Ser. 2019;1238:012002. [Google Scholar]
  • 43.Sitthiwet C, et al. Hydrogen sorption kinetics and suppression of NH3 emission of LiH-sandwiched LiNH2-LiH-TiF4-MWCNTs pellets upon cycling. J. Alloy. Compd. 2022;909:164673. [Google Scholar]
  • 44.Liu C, et al. Smooth flow in diamond: atomistic ductility and electronic conductivity. Phys. Rev. Lett. 2019;123:195504. doi: 10.1103/PhysRevLett.123.195504. [DOI] [PubMed] [Google Scholar]
  • 45.Liu C, et al. Superconductivity in compression-shear deformed diamond. Phys. Rev. Lett. 2020;124:147001. doi: 10.1103/PhysRevLett.124.147001. [DOI] [PubMed] [Google Scholar]
  • 46.Song X, et al. Stress-induced high-Tc superconductivity in solid molecular hydrogen. Proc. Natl Acad. Sci. USA. 2022;119:e2122691119. doi: 10.1073/pnas.2122691119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Gao Y, et al. Shear driven formation of nano-diamonds at sub-gigapascals and 300 K. Carbon. 2019;146:364–368. [Google Scholar]
  • 48.Vajda P, et al. Quenching and electron-irradiation effects in ordered β-PdH(D)0.63 around the resistivity anomaly near 50 K. Phys. Rev. B. 1986;33:2286–2291. doi: 10.1103/physrevb.33.2286. [DOI] [PubMed] [Google Scholar]
  • 49.Huiberts JN, et al. Logarithmic divergence of the electrical resistivity in the metal hydride YH3-δ. Phys. Rev. Lett. 1997;79:3724. [Google Scholar]
  • 50.Kresse G, Furthmüller J. Efficiency of ab-initio total energy calculations for metals and semiconductors using a plane-wave basis set. Comput. Mater. Sci. 1996;6:15–50. doi: 10.1103/physrevb.54.11169. [DOI] [PubMed] [Google Scholar]
  • 51.Perdew JP, Burke K, Ernzerhof M. Generalized gradient approximation made simple. Phys. Rev. Lett. 1996;77:3865–3868. doi: 10.1103/PhysRevLett.77.3865. [DOI] [PubMed] [Google Scholar]
  • 52.Kresse G, Joubert D. From ultrasoft pseudopotentials to the projector augmented-wave method. Phys. Rev. B. 1999;59:1758–1775. [Google Scholar]
  • 53.Monkhorst HJ, Pack JD. Special points for Brillouin-zone integrations. Phys. Rev. B. 1976;13:5188–5192. [Google Scholar]
  • 54.Becke AD, Edgecombe KE. A simple measure of electron localization in atomic and molecular systems. J. Chem. Phys. 1990;92:5397–5403. [Google Scholar]
  • 55.Togo A, Oba F, Tanaka I. First-principles calculations of the ferroelastic transition between rutile-type and CaCl2-type SiO2 at high pressures. Phys. Rev. B. 2008;78:134106. [Google Scholar]

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Data Availability Statement

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