Electronic phase transitions and superconductivity in ferroelectric Sn$_2$P$_2$Se$_6$ under pressure
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arXiv
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2024
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| _version_ | 1866913244275277824 |
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| author | Zhang, He Zhong, Wei Yu, Xiaohui Yue, Binbin Hong, Fang |
| author_facet | Zhang, He Zhong, Wei Yu, Xiaohui Yue, Binbin Hong, Fang |
| contents | Since there is both strong electron-phonon coupling during a ferroelectric/FE transition and superconducting/SC transition, it has been an important topic to explore superconductivity from the FE instability. Sn$_2$P$_2$Se$_6$ arouses broad attention due to its unique FE properties. Here, we reported the electronic phase transitions and superconductivity in this compound based on high-pressure electrical transport measurement, optical absorption spectroscopy and Raman based structural analysis. Upon compression, the conductivity of Sn$_2$P$_2$Se$_6$ was elevated monotonously, an electronic phase transition occurred near 5.4 GPa, revealed by optical absorption spectroscopy, and the insulating state is estimated to be fully suppressed near 15 GPa. Then, it started to show the signature of superconductivity near 15.3 GPa. The zero-resistance state was presented from 19.4 GPa, and the superconductivity was enhanced with pressure continuously. The magnetic field effect further confirmed the SC behavior and this compound had a $T_c$ of 5.4 K at 41.8 GPa with a zero temperature upper critical field of 6.55 T. The Raman spectra confirmed the structural origin of the electronic transition near 5.4 GPa, which should due to the transition from the paraelectric phase to the incommensurate phase, and suggested a possible first-order phase transition when the sample underwent the semiconductor-metal transition near 15 GPa. This work demonstrates the versatile physical properties in ferroelectrics and inspires the further investigation on the correlation between FE instability and SC in M$_2$P$_2$X$_6$ family. |
| format | Preprint |
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arxiv_https___arxiv_org_abs_2402_16427 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | Electronic phase transitions and superconductivity in ferroelectric Sn$_2$P$_2$Se$_6$ under pressure Zhang, He Zhong, Wei Yu, Xiaohui Yue, Binbin Hong, Fang Superconductivity Materials Science Since there is both strong electron-phonon coupling during a ferroelectric/FE transition and superconducting/SC transition, it has been an important topic to explore superconductivity from the FE instability. Sn$_2$P$_2$Se$_6$ arouses broad attention due to its unique FE properties. Here, we reported the electronic phase transitions and superconductivity in this compound based on high-pressure electrical transport measurement, optical absorption spectroscopy and Raman based structural analysis. Upon compression, the conductivity of Sn$_2$P$_2$Se$_6$ was elevated monotonously, an electronic phase transition occurred near 5.4 GPa, revealed by optical absorption spectroscopy, and the insulating state is estimated to be fully suppressed near 15 GPa. Then, it started to show the signature of superconductivity near 15.3 GPa. The zero-resistance state was presented from 19.4 GPa, and the superconductivity was enhanced with pressure continuously. The magnetic field effect further confirmed the SC behavior and this compound had a $T_c$ of 5.4 K at 41.8 GPa with a zero temperature upper critical field of 6.55 T. The Raman spectra confirmed the structural origin of the electronic transition near 5.4 GPa, which should due to the transition from the paraelectric phase to the incommensurate phase, and suggested a possible first-order phase transition when the sample underwent the semiconductor-metal transition near 15 GPa. This work demonstrates the versatile physical properties in ferroelectrics and inspires the further investigation on the correlation between FE instability and SC in M$_2$P$_2$X$_6$ family. |
| title | Electronic phase transitions and superconductivity in ferroelectric Sn$_2$P$_2$Se$_6$ under pressure |
| topic | Superconductivity Materials Science |
| url | https://arxiv.org/abs/2402.16427 |