Muhammad Akbar, Iqra Moeez, Young Hwan Kim, Mingony Kim, Jiwon Jeong, Eunbyoul Lee, Ali Hussain Umar Bhatti, Jae-Ho Park, Kyung Yoon Chung
{"title":"新型掺锡nasicon型Na3.2Zr2Si2.2P0.8O12固体电解质的离子电导率提高的固态钠电池","authors":"Muhammad Akbar, Iqra Moeez, Young Hwan Kim, Mingony Kim, Jiwon Jeong, Eunbyoul Lee, Ali Hussain Umar Bhatti, Jae-Ho Park, Kyung Yoon Chung","doi":"10.1002/cey2.717","DOIUrl":null,"url":null,"abstract":"<p>Solid electrolytes face challenges in solid-state sodium batteries (SSSBs) because of limited ionic conductivity, increased interfacial resistance, and sodium dendrite issues. In this study, we adopted a unique Sn<sup>4+</sup> doping strategy for Na<sub>3.2</sub>Zr<sub>2</sub>Si<sub>2.2</sub>P<sub>0.8</sub>O<sub>12</sub> (NZSP) that caused a partial structural transition from the monoclinic (<i>C</i>2/<i>c</i>) phase to the rhombohedral (<i>R</i>-3<i>c</i>) phase in Na<sub>3.2</sub>Zr<sub>1.9</sub>Sn<sub>0.1</sub>Si<sub>2.2</sub>P<sub>0.8</sub>O<sub>12</sub> (NZSnSP1). X-ray diffraction (XRD) patterns and high-resolution transmission electron microscopy analyses were used to confirm this transition, where rhombohedral NZSnSP1 showed an increase in the Na2–O bond length compared with monoclinic NZSnSP1, increasing its triangular bottleneck areas and noticeably enhancing Na<sup>+</sup> ionic conductivity, a higher Na transference number, and lower electronic conductivity. NZSnSP1 also showed exceptionally high compatibility with Na metal with an increased critical current density, as evidenced by symmetric cell tests. The SSSB, fabricated using Na<sub>0.9</sub>Zn<sub>0.22</sub>Fe<sub>0.3</sub>Mn<sub>0.48</sub>O<sub>2</sub> (NZFMO), Na metal, and NZSnSP1 as the cathode, anode, and the solid electrolyte and separator, respectively, maintains 65.86% of retention in the reversible capacity over 300 cycles within a voltage range of 2.0–4.0 V at 25°C at 0.1 C. The in-situ X-ray diffraction and X-ray absorption analyses of the P and Zr K-edges confirmed that NZSnSP1 remained highly stable before and after electrochemical cycling. This crystal structure modification strategy enables the synthesis of ideal solid electrolytes for practical SSSBs.</p>","PeriodicalId":33706,"journal":{"name":"Carbon Energy","volume":"7 5","pages":""},"PeriodicalIF":24.2000,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cey2.717","citationCount":"0","resultStr":"{\"title\":\"Novel Sn-Doped NASICON-Type Na3.2Zr2Si2.2P0.8O12 Solid Electrolyte With Improved Ionic Conductivity for a Solid-State Sodium Battery\",\"authors\":\"Muhammad Akbar, Iqra Moeez, Young Hwan Kim, Mingony Kim, Jiwon Jeong, Eunbyoul Lee, Ali Hussain Umar Bhatti, Jae-Ho Park, Kyung Yoon Chung\",\"doi\":\"10.1002/cey2.717\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Solid electrolytes face challenges in solid-state sodium batteries (SSSBs) because of limited ionic conductivity, increased interfacial resistance, and sodium dendrite issues. In this study, we adopted a unique Sn<sup>4+</sup> doping strategy for Na<sub>3.2</sub>Zr<sub>2</sub>Si<sub>2.2</sub>P<sub>0.8</sub>O<sub>12</sub> (NZSP) that caused a partial structural transition from the monoclinic (<i>C</i>2/<i>c</i>) phase to the rhombohedral (<i>R</i>-3<i>c</i>) phase in Na<sub>3.2</sub>Zr<sub>1.9</sub>Sn<sub>0.1</sub>Si<sub>2.2</sub>P<sub>0.8</sub>O<sub>12</sub> (NZSnSP1). X-ray diffraction (XRD) patterns and high-resolution transmission electron microscopy analyses were used to confirm this transition, where rhombohedral NZSnSP1 showed an increase in the Na2–O bond length compared with monoclinic NZSnSP1, increasing its triangular bottleneck areas and noticeably enhancing Na<sup>+</sup> ionic conductivity, a higher Na transference number, and lower electronic conductivity. NZSnSP1 also showed exceptionally high compatibility with Na metal with an increased critical current density, as evidenced by symmetric cell tests. The SSSB, fabricated using Na<sub>0.9</sub>Zn<sub>0.22</sub>Fe<sub>0.3</sub>Mn<sub>0.48</sub>O<sub>2</sub> (NZFMO), Na metal, and NZSnSP1 as the cathode, anode, and the solid electrolyte and separator, respectively, maintains 65.86% of retention in the reversible capacity over 300 cycles within a voltage range of 2.0–4.0 V at 25°C at 0.1 C. The in-situ X-ray diffraction and X-ray absorption analyses of the P and Zr K-edges confirmed that NZSnSP1 remained highly stable before and after electrochemical cycling. 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Novel Sn-Doped NASICON-Type Na3.2Zr2Si2.2P0.8O12 Solid Electrolyte With Improved Ionic Conductivity for a Solid-State Sodium Battery
Solid electrolytes face challenges in solid-state sodium batteries (SSSBs) because of limited ionic conductivity, increased interfacial resistance, and sodium dendrite issues. In this study, we adopted a unique Sn4+ doping strategy for Na3.2Zr2Si2.2P0.8O12 (NZSP) that caused a partial structural transition from the monoclinic (C2/c) phase to the rhombohedral (R-3c) phase in Na3.2Zr1.9Sn0.1Si2.2P0.8O12 (NZSnSP1). X-ray diffraction (XRD) patterns and high-resolution transmission electron microscopy analyses were used to confirm this transition, where rhombohedral NZSnSP1 showed an increase in the Na2–O bond length compared with monoclinic NZSnSP1, increasing its triangular bottleneck areas and noticeably enhancing Na+ ionic conductivity, a higher Na transference number, and lower electronic conductivity. NZSnSP1 also showed exceptionally high compatibility with Na metal with an increased critical current density, as evidenced by symmetric cell tests. The SSSB, fabricated using Na0.9Zn0.22Fe0.3Mn0.48O2 (NZFMO), Na metal, and NZSnSP1 as the cathode, anode, and the solid electrolyte and separator, respectively, maintains 65.86% of retention in the reversible capacity over 300 cycles within a voltage range of 2.0–4.0 V at 25°C at 0.1 C. The in-situ X-ray diffraction and X-ray absorption analyses of the P and Zr K-edges confirmed that NZSnSP1 remained highly stable before and after electrochemical cycling. This crystal structure modification strategy enables the synthesis of ideal solid electrolytes for practical SSSBs.
期刊介绍:
Carbon Energy is an international journal that focuses on cutting-edge energy technology involving carbon utilization and carbon emission control. It provides a platform for researchers to communicate their findings and critical opinions and aims to bring together the communities of advanced material and energy. The journal covers a broad range of energy technologies, including energy storage, photocatalysis, electrocatalysis, photoelectrocatalysis, and thermocatalysis. It covers all forms of energy, from conventional electric and thermal energy to those that catalyze chemical and biological transformations. Additionally, Carbon Energy promotes new technologies for controlling carbon emissions and the green production of carbon materials. The journal welcomes innovative interdisciplinary research with wide impact. It is indexed in various databases, including Advanced Technologies & Aerospace Collection/Database, Biological Science Collection/Database, CAS, DOAJ, Environmental Science Collection/Database, Web of Science and Technology Collection.