将较小的稀土阳离子和混合价锰掺入作为提高 A 位有序四元过氧化物 LnCu3Mn1+xTi3-xO12 (Ln = La、Nd;x = 0、0.3)中铁磁有序温度的双重策略

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Dalton Transactions Pub Date : 2024-09-20 DOI:10.1039/D4DT01859A
Lalit Kumar, Sujan Sen and Tapas Kumar Mandal
{"title":"将较小的稀土阳离子和混合价锰掺入作为提高 A 位有序四元过氧化物 LnCu3Mn1+xTi3-xO12 (Ln = La、Nd;x = 0、0.3)中铁磁有序温度的双重策略","authors":"Lalit Kumar, Sujan Sen and Tapas Kumar Mandal","doi":"10.1039/D4DT01859A","DOIUrl":null,"url":null,"abstract":"<p >High-<em>T</em><small><sub>C</sub></small> ferro-/ferrimagnetic quadruple perovskites constitute an important class of oxides that has garnered a lot of research attention in recent times, but their synthesis is commonly achieved under high-pressure conditions. Thus, the development of high-<em>T</em><small><sub>C</sub></small> quadruple perovskites that can be synthesized under ambient pressure can be a key to the above problem. Herein, we report ambient pressure synthesis of a series of new A-site ordered quadruple perovskites, LnCu<small><sub>3</sub></small>Mn<small><sub>1+<em>x</em></sub></small>Ti<small><sub>3−<em>x</em></sub></small>O<small><sub>12</sub></small> (Ln = La, Nd; <em>x</em> = 0, 0.3), by coupled aliovalent-cation manipulation in CaCu<small><sub>3</sub></small>Ti<small><sub>4</sub></small>O<small><sub>12</sub></small>. The effect of smaller lanthanide Nd incorporation in place of La has been investigated. Furthermore, 30% mixed valency of Mn per Mn<small><sup>3+</sup></small> has been introduced in place of Ti<small><sup>4+</sup></small> following similar strategies adopted to achieve giant magnetoresistive manganites La<small><sub>0.7</sub></small>A<small><sub>0.3</sub></small>MnO<small><sub>3</sub></small> (A = Ca, Sr, Ba) from LaMnO<small><sub>3</sub></small>. Mn is present in the 3+ state for <em>x</em> = 0 and in a mixed valent state (3+ and 4+) for <em>x</em> = 0.3, whereas Cu exists in the 2+ state in all the compounds. While LaCu<small><sub>3</sub></small>MnTi<small><sub>3</sub></small>O<small><sub>12</sub></small> and LaCu<small><sub>3</sub></small>Mn<small><sub>1.3</sub></small>Ti<small><sub>2.7</sub></small>O<small><sub>12</sub></small> show the onset of ferrimagnetic order at ∼60 and 110 K, respectively, the corresponding Nd analogs, NdCu<small><sub>3</sub></small>MnTi<small><sub>3</sub></small>O<small><sub>12</sub></small> and NdCu<small><sub>3</sub></small>Mn<small><sub>1.3</sub></small>Ti<small><sub>2.7</sub></small>O<small><sub>12</sub></small>, exhibit enhanced <em>T</em><small><sub>C</sub></small>'s of ∼80 and 140 K, respectively. This work reveals an effective strategy of mixed-valent Mn incorporation in the B-sublattice and smaller rare-earth cation incorporation to achieve higher ferrimagnetic ordering temperatures in quadruple perovskites.</p>","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":" 40","pages":" 16661-16670"},"PeriodicalIF":3.3000,"publicationDate":"2024-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Smaller rare-earth cation and mixed valent Mn incorporation as a dual strategy to enhance ferrimagnetic ordering temperatures in A-site ordered quadruple perovskites, LnCu3Mn1+xTi3−xO12 (Ln = La, Nd; x = 0, 0.3)†\",\"authors\":\"Lalit Kumar, Sujan Sen and Tapas Kumar Mandal\",\"doi\":\"10.1039/D4DT01859A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >High-<em>T</em><small><sub>C</sub></small> ferro-/ferrimagnetic quadruple perovskites constitute an important class of oxides that has garnered a lot of research attention in recent times, but their synthesis is commonly achieved under high-pressure conditions. Thus, the development of high-<em>T</em><small><sub>C</sub></small> quadruple perovskites that can be synthesized under ambient pressure can be a key to the above problem. Herein, we report ambient pressure synthesis of a series of new A-site ordered quadruple perovskites, LnCu<small><sub>3</sub></small>Mn<small><sub>1+<em>x</em></sub></small>Ti<small><sub>3−<em>x</em></sub></small>O<small><sub>12</sub></small> (Ln = La, Nd; <em>x</em> = 0, 0.3), by coupled aliovalent-cation manipulation in CaCu<small><sub>3</sub></small>Ti<small><sub>4</sub></small>O<small><sub>12</sub></small>. The effect of smaller lanthanide Nd incorporation in place of La has been investigated. Furthermore, 30% mixed valency of Mn per Mn<small><sup>3+</sup></small> has been introduced in place of Ti<small><sup>4+</sup></small> following similar strategies adopted to achieve giant magnetoresistive manganites La<small><sub>0.7</sub></small>A<small><sub>0.3</sub></small>MnO<small><sub>3</sub></small> (A = Ca, Sr, Ba) from LaMnO<small><sub>3</sub></small>. Mn is present in the 3+ state for <em>x</em> = 0 and in a mixed valent state (3+ and 4+) for <em>x</em> = 0.3, whereas Cu exists in the 2+ state in all the compounds. While LaCu<small><sub>3</sub></small>MnTi<small><sub>3</sub></small>O<small><sub>12</sub></small> and LaCu<small><sub>3</sub></small>Mn<small><sub>1.3</sub></small>Ti<small><sub>2.7</sub></small>O<small><sub>12</sub></small> show the onset of ferrimagnetic order at ∼60 and 110 K, respectively, the corresponding Nd analogs, NdCu<small><sub>3</sub></small>MnTi<small><sub>3</sub></small>O<small><sub>12</sub></small> and NdCu<small><sub>3</sub></small>Mn<small><sub>1.3</sub></small>Ti<small><sub>2.7</sub></small>O<small><sub>12</sub></small>, exhibit enhanced <em>T</em><small><sub>C</sub></small>'s of ∼80 and 140 K, respectively. This work reveals an effective strategy of mixed-valent Mn incorporation in the B-sublattice and smaller rare-earth cation incorporation to achieve higher ferrimagnetic ordering temperatures in quadruple perovskites.</p>\",\"PeriodicalId\":71,\"journal\":{\"name\":\"Dalton Transactions\",\"volume\":\" 40\",\"pages\":\" 16661-16670\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-09-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Dalton Transactions\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/dt/d4dt01859a\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/dt/d4dt01859a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

摘要

高热导率铁磁性四元过氧化物是一类重要的氧化物,近年来受到了大量研究的关注,但它们的合成通常是在高压条件下实现的。因此,开发可在常压下合成的高TC四元过氧化物是解决上述问题的关键。在此,我们报告了通过在 CaCu3Ti4O12 中耦合别价阳离子操作,在常压下合成了一系列新的 A 位有序四元包晶 LnCu3Mn1+xTi3-xO12 (Ln = La, Nd; x = 0, 0.3)。我们还研究了用较小的镧系元素钕代替镧的效果。此外,根据从 LaMnO3 中获得巨磁阻锰矿 La0.7A0.3MnO3(A = Ca、Sr、Ba)所采用的类似策略,还引入了 30% 的 Mn 混合价 Mn3+ 来代替 Ti4+。锰在 x = 0 时呈 3+ 态,在 x = 0.3 时呈混合价态(3+ 和 4+),而铜在所有化合物中均呈 2+ 态。LaCu3MnTi3O12 和 LaCu3Mn1.3Ti2.7O12 分别在开氏 60 度和 110 度时出现铁磁阶,而相应的钕类似物 NdCu3MnTi3O12 和 NdCu3Mn1.3Ti2.7O12 则在开氏 80 度和 140 度时表现出更高的磁导率。这项研究揭示了在 B 亚晶格中掺入混价锰和掺入较少稀土的有效策略,从而在四元过氧化物中实现更高的铁磁有序温度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Smaller rare-earth cation and mixed valent Mn incorporation as a dual strategy to enhance ferrimagnetic ordering temperatures in A-site ordered quadruple perovskites, LnCu3Mn1+xTi3−xO12 (Ln = La, Nd; x = 0, 0.3)†

High-TC ferro-/ferrimagnetic quadruple perovskites constitute an important class of oxides that has garnered a lot of research attention in recent times, but their synthesis is commonly achieved under high-pressure conditions. Thus, the development of high-TC quadruple perovskites that can be synthesized under ambient pressure can be a key to the above problem. Herein, we report ambient pressure synthesis of a series of new A-site ordered quadruple perovskites, LnCu3Mn1+xTi3−xO12 (Ln = La, Nd; x = 0, 0.3), by coupled aliovalent-cation manipulation in CaCu3Ti4O12. The effect of smaller lanthanide Nd incorporation in place of La has been investigated. Furthermore, 30% mixed valency of Mn per Mn3+ has been introduced in place of Ti4+ following similar strategies adopted to achieve giant magnetoresistive manganites La0.7A0.3MnO3 (A = Ca, Sr, Ba) from LaMnO3. Mn is present in the 3+ state for x = 0 and in a mixed valent state (3+ and 4+) for x = 0.3, whereas Cu exists in the 2+ state in all the compounds. While LaCu3MnTi3O12 and LaCu3Mn1.3Ti2.7O12 show the onset of ferrimagnetic order at ∼60 and 110 K, respectively, the corresponding Nd analogs, NdCu3MnTi3O12 and NdCu3Mn1.3Ti2.7O12, exhibit enhanced TC's of ∼80 and 140 K, respectively. This work reveals an effective strategy of mixed-valent Mn incorporation in the B-sublattice and smaller rare-earth cation incorporation to achieve higher ferrimagnetic ordering temperatures in quadruple perovskites.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
期刊最新文献
Synthesis, crystal structures and urease inhibition of Ni(II) complexes constructed from Schiff bases with 2,2'-bipyridine as co-ligands. Luminescence of BaFBr nanoplates codoped with Eu2+/3. Structurally characterized Ni(II) complex exhibiting potent anti-Candida activity: biomolecular interaction mechanism and in silico ADMET insights. Optimization of Xantphos-type ligands for highly linear-selective hydroformylation of allyl alcohol and alkenes. Structure-performance relationship in copper phthalocyanine-based supercapacitor electrodes: influence of substituent geometry from molecular design to electrochemical function.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1