Mirosław Mączka*, Anna Gagor, Dagmara Stefanska, Jerzy Hanuza, Edyta Kucharska and Jan K. Zareba*,
{"title":"二价甲基肼─一种构建杂化钙钛矿的超小有机阳离子","authors":"Mirosław Mączka*, Anna Gagor, Dagmara Stefanska, Jerzy Hanuza, Edyta Kucharska and Jan K. Zareba*, ","doi":"10.1021/acs.chemmater.5c00919","DOIUrl":null,"url":null,"abstract":"<p >Hybrid lead halide perovskites exhibit remarkable optoelectronic properties that can be tailored by incorporating diverse organic cations. Monoprotonated methylhydrazine (MHy<sup>+</sup>) has emerged as an effective cation for constructing perovskites with unique properties due to its intrinsic ability to form Pb–N coordination bonds, small size, and high dielectric permittivity. In this work, we enter the uncharted territory of hybrid perovskites comprising ultrasmall diprotonated amines. We show that methylhydrazine can exist in a diprotonated form (MHy<sup>2+</sup>) in hybrid perovskites, enabling the design of compounds with enhanced nonlinear optical responses, unconventional crystal architectures, and tunable emission properties. Using strongly acidic conditions at elevated temperatures, we obtained three distinct MHy<sup>2+</sup>-based lead halides: polar MHy<sup>II</sup>Pb<sub>2</sub>Cl<sub>6</sub>·2H<sub>2</sub>O (<i>P</i>2<sub>1</sub>) and MHy<sub>2</sub><sup>II</sup>MHy<sup>I</sup>Pb<sub>2</sub>Br<sub>8</sub>Br (<i>Pna</i>2<sub>1</sub>), as well as centrosymmetric GAMHy<sup>II</sup>PbBr<sub>5</sub> (<i>P</i>2<sub>1</sub>/<i>m</i>), where GA<sup>+</sup> stands for guanidinium. Structural study reveals that MHy<sup>2+</sup> drives unprecedented architectures, including Br<sup>–</sup>/Pb<sup>2+</sup>-deficient trilayered Dion-Jacobson phase in MHy<sub>2</sub><sup>II</sup>MHy<sup>I</sup>Pb<sub>2</sub>Br<sub>8</sub>Br with mixed mono/diprotonated cation coexistence. MHy<sup>II</sup>Pb<sub>2</sub>Cl<sub>6</sub>·2H<sub>2</sub>O, a compound which involves only MHy<sup>2+</sup> as an organic constituent, exhibits a warm white emission (CIE 0.32, 0.38 at 80 K) through dual bound/self-trapped exciton recombination and demonstrates a second-harmonic generation (SHG) efficiency of 0.51 × KDP, nearly three times higher than MHy<sup>+</sup>-based analogues. MHy<sub>2</sub><sup>II</sup>MHy<sup>I</sup>Pb<sub>2</sub>Br<sub>8</sub>Br shows a narrow purplish-blue emission (fwhm of 8 nm) and SHG activity comparable to those of extant 2D MHy<sup>+</sup> perovskites. This discovery expands the toolkit for a hybrid perovskite design, establishing methylhydrazine as an ultrasmall amine capable of incorporating two different protonation states and opening avenues for developing advanced optoelectronic materials with enhanced nonlinear optical properties and tunable emissions.</p>","PeriodicalId":33,"journal":{"name":"Chemistry of Materials","volume":"37 14","pages":"5195–5205"},"PeriodicalIF":7.0000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.chemmater.5c00919","citationCount":"0","resultStr":"{\"title\":\"Divalent Methylhydrazinium─An Ultrasmall Organic Cation for Construction of Hybrid Perovskites\",\"authors\":\"Mirosław Mączka*, Anna Gagor, Dagmara Stefanska, Jerzy Hanuza, Edyta Kucharska and Jan K. Zareba*, \",\"doi\":\"10.1021/acs.chemmater.5c00919\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Hybrid lead halide perovskites exhibit remarkable optoelectronic properties that can be tailored by incorporating diverse organic cations. Monoprotonated methylhydrazine (MHy<sup>+</sup>) has emerged as an effective cation for constructing perovskites with unique properties due to its intrinsic ability to form Pb–N coordination bonds, small size, and high dielectric permittivity. In this work, we enter the uncharted territory of hybrid perovskites comprising ultrasmall diprotonated amines. We show that methylhydrazine can exist in a diprotonated form (MHy<sup>2+</sup>) in hybrid perovskites, enabling the design of compounds with enhanced nonlinear optical responses, unconventional crystal architectures, and tunable emission properties. Using strongly acidic conditions at elevated temperatures, we obtained three distinct MHy<sup>2+</sup>-based lead halides: polar MHy<sup>II</sup>Pb<sub>2</sub>Cl<sub>6</sub>·2H<sub>2</sub>O (<i>P</i>2<sub>1</sub>) and MHy<sub>2</sub><sup>II</sup>MHy<sup>I</sup>Pb<sub>2</sub>Br<sub>8</sub>Br (<i>Pna</i>2<sub>1</sub>), as well as centrosymmetric GAMHy<sup>II</sup>PbBr<sub>5</sub> (<i>P</i>2<sub>1</sub>/<i>m</i>), where GA<sup>+</sup> stands for guanidinium. Structural study reveals that MHy<sup>2+</sup> drives unprecedented architectures, including Br<sup>–</sup>/Pb<sup>2+</sup>-deficient trilayered Dion-Jacobson phase in MHy<sub>2</sub><sup>II</sup>MHy<sup>I</sup>Pb<sub>2</sub>Br<sub>8</sub>Br with mixed mono/diprotonated cation coexistence. MHy<sup>II</sup>Pb<sub>2</sub>Cl<sub>6</sub>·2H<sub>2</sub>O, a compound which involves only MHy<sup>2+</sup> as an organic constituent, exhibits a warm white emission (CIE 0.32, 0.38 at 80 K) through dual bound/self-trapped exciton recombination and demonstrates a second-harmonic generation (SHG) efficiency of 0.51 × KDP, nearly three times higher than MHy<sup>+</sup>-based analogues. MHy<sub>2</sub><sup>II</sup>MHy<sup>I</sup>Pb<sub>2</sub>Br<sub>8</sub>Br shows a narrow purplish-blue emission (fwhm of 8 nm) and SHG activity comparable to those of extant 2D MHy<sup>+</sup> perovskites. This discovery expands the toolkit for a hybrid perovskite design, establishing methylhydrazine as an ultrasmall amine capable of incorporating two different protonation states and opening avenues for developing advanced optoelectronic materials with enhanced nonlinear optical properties and tunable emissions.</p>\",\"PeriodicalId\":33,\"journal\":{\"name\":\"Chemistry of Materials\",\"volume\":\"37 14\",\"pages\":\"5195–5205\"},\"PeriodicalIF\":7.0000,\"publicationDate\":\"2025-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/pdf/10.1021/acs.chemmater.5c00919\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry of Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.chemmater.5c00919\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Materials","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.chemmater.5c00919","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Divalent Methylhydrazinium─An Ultrasmall Organic Cation for Construction of Hybrid Perovskites
Hybrid lead halide perovskites exhibit remarkable optoelectronic properties that can be tailored by incorporating diverse organic cations. Monoprotonated methylhydrazine (MHy+) has emerged as an effective cation for constructing perovskites with unique properties due to its intrinsic ability to form Pb–N coordination bonds, small size, and high dielectric permittivity. In this work, we enter the uncharted territory of hybrid perovskites comprising ultrasmall diprotonated amines. We show that methylhydrazine can exist in a diprotonated form (MHy2+) in hybrid perovskites, enabling the design of compounds with enhanced nonlinear optical responses, unconventional crystal architectures, and tunable emission properties. Using strongly acidic conditions at elevated temperatures, we obtained three distinct MHy2+-based lead halides: polar MHyIIPb2Cl6·2H2O (P21) and MHy2IIMHyIPb2Br8Br (Pna21), as well as centrosymmetric GAMHyIIPbBr5 (P21/m), where GA+ stands for guanidinium. Structural study reveals that MHy2+ drives unprecedented architectures, including Br–/Pb2+-deficient trilayered Dion-Jacobson phase in MHy2IIMHyIPb2Br8Br with mixed mono/diprotonated cation coexistence. MHyIIPb2Cl6·2H2O, a compound which involves only MHy2+ as an organic constituent, exhibits a warm white emission (CIE 0.32, 0.38 at 80 K) through dual bound/self-trapped exciton recombination and demonstrates a second-harmonic generation (SHG) efficiency of 0.51 × KDP, nearly three times higher than MHy+-based analogues. MHy2IIMHyIPb2Br8Br shows a narrow purplish-blue emission (fwhm of 8 nm) and SHG activity comparable to those of extant 2D MHy+ perovskites. This discovery expands the toolkit for a hybrid perovskite design, establishing methylhydrazine as an ultrasmall amine capable of incorporating two different protonation states and opening avenues for developing advanced optoelectronic materials with enhanced nonlinear optical properties and tunable emissions.
期刊介绍:
The journal Chemistry of Materials focuses on publishing original research at the intersection of materials science and chemistry. The studies published in the journal involve chemistry as a prominent component and explore topics such as the design, synthesis, characterization, processing, understanding, and application of functional or potentially functional materials. The journal covers various areas of interest, including inorganic and organic solid-state chemistry, nanomaterials, biomaterials, thin films and polymers, and composite/hybrid materials. The journal particularly seeks papers that highlight the creation or development of innovative materials with novel optical, electrical, magnetic, catalytic, or mechanical properties. It is essential that manuscripts on these topics have a primary focus on the chemistry of materials and represent a significant advancement compared to prior research. Before external reviews are sought, submitted manuscripts undergo a review process by a minimum of two editors to ensure their appropriateness for the journal and the presence of sufficient evidence of a significant advance that will be of broad interest to the materials chemistry community.