{"title":"Inorganic hole transport layers for perovskite light-emitting diodes: from material design to interfacial kinetics regulation","authors":"Lunyao Pan, Cheng Yan, Shixiu Sun, Zhennan Tian, Tianxiang Li, Qiao Luo, Taiyu Li, Weiqing Yang, Wen Li, Ding Zheng and Junsheng Yu","doi":"10.1039/D6TC00523C","DOIUrl":"https://doi.org/10.1039/D6TC00523C","url":null,"abstract":"<p >Perovskite light-emitting diodes (PeLEDs) have emerged as a promising technology for next-generation displays. However, the widely employed organic hole transport layers (HTLs) in PeLEDs suffer from inherent drawbacks, such as thermal instability and low carrier mobility, which severely constrain their commercial viability. Although inorganic HTLs offer a robust solution, a systematic framework linking their physicochemical properties to interfacial dynamics is lacking. This review critically assesses the state-of-the-art inorganic HTLs, comprehensively categorizing them into copper-based compounds, nickel oxides, transition metal oxides, and emerging candidates. Beyond material categorization, we dissect the critical interface regulation mechanisms essential for high-performance devices. These specifically involve mitigating interfacial carrier accumulation to suppress non-radiative recombination, leveraging HTLs as growth templates to modulate perovskite crystallization kinetics, and immobilizing metal ions to inhibit detrimental migration. By elucidating these physicochemical interactions, we provide theoretical insights and design guidelines for engineering stable, high-efficiency inorganic HTLs for PeLEDs.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 20","pages":" 8442-8456"},"PeriodicalIF":5.1,"publicationDate":"2026-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148039712","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Balakrishnappa Venugopal, Christian Anders, Bommanahalli Shivalingegowda Ranjitha, Bishwajit Paul, Ganga Periyasamy, Mohamed Alaasar, Gurumurthy Hegde and Govindaswamy Shanker
{"title":"Molecular redesign unlocks 99.89% light-driven control of azobiphenyl liquid crystals","authors":"Balakrishnappa Venugopal, Christian Anders, Bommanahalli Shivalingegowda Ranjitha, Bishwajit Paul, Ganga Periyasamy, Mohamed Alaasar, Gurumurthy Hegde and Govindaswamy Shanker","doi":"10.1039/D6TC00725B","DOIUrl":"https://doi.org/10.1039/D6TC00725B","url":null,"abstract":"<p >Two series consisting of 14 unsymmetric azocholesterol dimers linking chiral cholesterol to photoswitchable azobenzene <em>via</em> spacers of varying length (<em>n</em> = 3–9) with terminal cyano (<strong>ACN-<em>n</em></strong>, electron-withdrawing) or ester (<strong>ACEt-<em>n</em></strong>, electron-donating) groups were synthesized. Differential scanning calorimetry (DSC), polarizing optical microscopy (POM), and X-ray diffraction (XRD) reveal enantiotropic chiral nematic (N*) phases for most derivatives in the cyano series and diverse polymorphism (N*, SmC*, SmA*) in the ester series, with spacer parity and terminal polarity dictating phase sequence and thermal stability. All compounds exhibit reversible photoisomerization in solution, with the ester derivative <strong>ACEt-5</strong> showing nearly quantitative <em>E</em> → <em>Z</em> conversion (99.89%). A prototype optical storage device based on the structurally related cyano dimer <strong>ACN-8</strong> (5 wt% in E7) demonstrates efficient switching under 365 nm UV irradiation, with a photo-stationary state reached in about 150 s and thermal back-relaxation occurring over approximately 160 min, highlighting the strong device relevant photo-responsiveness of this molecular design in a guest–host system. Density functional theory (DFT) elucidates structure–property relationships <em>via</em> HOMO–LUMO gaps, electrostatic potentials, and polarizability trends, revealing molecular design principles for tunable photoresponsive liquid crystalline materials.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 22","pages":" 9443-9458"},"PeriodicalIF":5.1,"publicationDate":"2026-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148208704","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tao Geng, Defei Yu, Fanyue Zhao, Huachao Zai, Guilin Liu and Guocheng Lv
{"title":"Research progress of single crystal perovskite growth","authors":"Tao Geng, Defei Yu, Fanyue Zhao, Huachao Zai, Guilin Liu and Guocheng Lv","doi":"10.1039/D6TC00682E","DOIUrl":"https://doi.org/10.1039/D6TC00682E","url":null,"abstract":"<p >Single crystals are attracting increasing interest in photovoltaics research due to their superior material properties. In contrast to polycrystalline thin films that currently dominate high-efficiency device development, single-crystal perovskites, characterized by their grain-boundary-free bulk structure, exhibit a potential ability superior to polycrystalline perovskites. This review summarizes key advancements in the field, hinging on the successful synthesis of micron-thick single-crystal sheets <em>via</em> several preparation techniques such as the Bridgman growth method. Through evolution from the initial MAPbI<small><sub>3</sub></small> system to mixed-cation compositions (<em>e.g.</em>, FA<small><sub>0.95</sub></small>Cs<small><sub>0.05</sub></small>PbI<small><sub>3</sub></small>), coupled with interface engineering and surface passivation strategies, the power conversion efficiency (PCE) of PSSCs has achieved a remarkable leap from single digits to a record 25.8%, accompanied by enhanced operational stability. However, to realize their commercial viability, several critical challenges must be addressed. As we illustrated in this review, further challenges, for instance, reducing the crystal thickness to below 10 micrometers, ensuring robust mechanical and electrical contact between the single crystal and charge transport layers, and developing scalable fabrication techniques for large-area and uniform single crystals, are worthy of further investigations. Despite these hurdles, the considerable potential demonstrated by PSSCs lays a solid foundation for their emergence as a next-generation photovoltaic technology boasting both high performance and exceptional durability.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 23","pages":" 9901-9922"},"PeriodicalIF":5.1,"publicationDate":"2026-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148261435","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
J. Jency Rubia, Julaiba Tahsina Mazumder, Lubna Aamir, Chacko Jacob, Tarikul Islam, Harshal B. Nemade and Ravindra Kumar Jha
{"title":"Physical vapor deposited nanomaterials for gas sensing: design strategies, performance limits and machine learning prospects","authors":"J. Jency Rubia, Julaiba Tahsina Mazumder, Lubna Aamir, Chacko Jacob, Tarikul Islam, Harshal B. Nemade and Ravindra Kumar Jha","doi":"10.1039/D6TC00534A","DOIUrl":"https://doi.org/10.1039/D6TC00534A","url":null,"abstract":"<p >Physical vapor deposition (PVD) has been known for producing high-quality thin films for large-area electronics. The application of these films includes fabrication of memory devices, solar cells, photodetectors, light-emitting diodes (LEDs), light amplification by stimulated emission of radiation (LASER), solid-state sensors, <em>etc.</em> A wide range of functional materials, such as pure metals, metal oxides, transition metal dichalcogenides (TMDCs), their alloys, nanocomposites, nanohybrids and heterostructures, can be deposited with precise control over film thickness, composition, and morphology by PVD. This review explores PVD methods for fabricating thin films tailored for gas sensing applications. It highlights how controlled deposition parameters influence sensor performance metrics such as sensitivity, selectivity, response/recovery times, and stability. Various transduction principles, like resistive, capacitive, optical, acoustic, <em>etc.</em>, have been covered to explain and highlight the role of quality films produced by PVD techniques for gas sensing. This review provides an overview of the critical role, challenges, and promising future of PVD in depositing innovative gas-sensing materials and tuning their electrical properties for improved sensing behaviour. Special attention is given to future perspectives, including the correlation between PVD fabrication and machine learning for the development of next-generation intelligent sensing platforms.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 22","pages":" 9385-9442"},"PeriodicalIF":5.1,"publicationDate":"2026-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148208703","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Visual detection of the topology freezing transition temperature of vitrimers based on fluorescein-soaked coatings from photonic crystals and vitrimers","authors":"Chengjia Xiong, Qiang Tan and Zihan Yang","doi":"10.1039/D6TC01113F","DOIUrl":"https://doi.org/10.1039/D6TC01113F","url":null,"abstract":"<p >The topology freezing transition temperature (<em>T</em><small><sub>v</sub></small>) of vitrimers is a key parameter for their application. Common methods for detection of <em>T</em><small><sub>v</sub></small> include the use of rheology and dynamic mechanical analysis under external force, but external force may affect <em>T</em><small><sub>v</sub></small>. Herein, a visual detection method for <em>T</em><small><sub>v</sub></small> is proposed based on fluorescein-soaked photonic coatings from lower photonic crystals (PCs) and upper vitrimers. Because PCs have photonic band gaps (or structural colors), by combining different structural colors of PCs and the fluorescence of vitrimers soaked with fluorescein, when the heating temperature is higher than <em>T</em><small><sub>v</sub></small> of the vitrimer, the ester (or carboxyl) group of fluorescein undergoes ester exchange with the ester group in vitrimers, and the color and fluorescence intensity of photonic coatings show great changes. <em>T</em><small><sub>v</sub></small> of vitrimers is easily obtained according to these obvious changes and it is unaffected by the use of a different fluorescein. Accurate fluorescence spectra can be measured to further identify the <em>T</em><small><sub>v</sub></small> of vitrimers. The lower PCs enhance the sensitivity of <em>T</em><small><sub>v</sub></small> detection for vitrimers. The visual detection method is simple, non-damaging, and accurate, has good reliability and universality, and does not require expensive equipment.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 23","pages":" 9932-9942"},"PeriodicalIF":5.1,"publicationDate":"2026-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148261437","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Transient extreme ultraviolet spectroscopy: a probe of ultrafast charge dynamics in solid-state materials","authors":"Tyler Goodman and Wei Xiong","doi":"10.1039/D5TC04525H","DOIUrl":"https://doi.org/10.1039/D5TC04525H","url":null,"abstract":"<p >Over the past two decades, transient extreme ultraviolet spectroscopy (Tr-XUV) has evolved into a unique probe of ultrafast electronic dynamics. In this review, we summarize several advances and applications of this technique to study solid-state materials. We first discuss how this technique enables understanding of small polaron formation in varying chemical environments, a central application in the early development of the technique. We then describe emerging directions where Tr-XUV has provided distinctive insight, including charge transfer across interfaces and charge localization through giant resonances. Lastly, we discuss instances where its combination with other ultrafast spectroscopies facilitates a more complete physical picture. Together, these advances demonstrate that ultrafast core-level spectroscopy in the extreme ultraviolet regime reveals a comprehensive framework for nonequilibrium dynamics that establishes it as a versatile frontier technique for materials science.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 22","pages":" 9334-9349"},"PeriodicalIF":5.1,"publicationDate":"2026-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148208701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yu Zhou, Youcheng Huang, Hangzhou Wang, Chenguang Kong, Shumin Jiang, Guohao Zhang, Yanting Tang, Chaolin Wang, Jun Shi and Kun Wu
{"title":"A mechanically robust self-healing polysiloxane via Fe3+-dopamine metal coordination for flexible sensors","authors":"Yu Zhou, Youcheng Huang, Hangzhou Wang, Chenguang Kong, Shumin Jiang, Guohao Zhang, Yanting Tang, Chaolin Wang, Jun Shi and Kun Wu","doi":"10.1039/D5TC04540A","DOIUrl":"https://doi.org/10.1039/D5TC04540A","url":null,"abstract":"<p >In recent years, wearable electronic devices based on polydimethylsiloxane (PDMS) have garnered increasing attention. However, the limited mechanical strength of PDMS itself and its poor self-healing properties after prolonged use restrict its application in flexible sensors. Here, we propose a novel approach to successfully prepare a self-healing polydimethylsiloxane material (Si-DOPA<small><sub><em>x</em></sub></small>-Fe<small><sub><em>y</em></sub></small>) with enhanced mechanical properties by introducing a metallic coordination network. The obtained Si-DOPA<small><sub><em>x</em></sub></small>-Fe<small><sub><em>y</em></sub></small> exhibited a maximum tensile strength of 652 kPa and an elongation at break of 133%. When fracture damage occurred, Si-DOPA<small><sub>3</sub></small>-Fe<small><sub>0.6</sub></small> achieved a self-healing efficiency of 90.3% after 8 hours of repair at room temperature. Based on Si-DOPA<small><sub>3</sub></small>-Fe<small><sub>0.6</sub></small>, we combined it with AgNWs to prepare Si-DOPA<small><sub>3</sub></small>-Fe<small><sub>0.6</sub></small>-AgNWs for measuring human physiological activity in real time. According to experimental results, Si-DOPA<small><sub>3</sub></small>-Fe<small><sub>0.6</sub></small>-AgNWs had a sensitivity of 4.6 and a linear response coefficient <em>R</em><small><sup>2</sup></small> of 0.999 within the 0–60% strain range, indicating good stability and sensitivity for this flexible sensor. This research not only advances the development of polysiloxanes in flexible electronic sensing but also holds promise for broad applications in medical health monitoring and human–machine interface fields, laying the foundation for next-generation smart material development.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 24","pages":" 10661-10675"},"PeriodicalIF":5.1,"publicationDate":"2026-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148314685","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yangang Zhao, Hao Zhang, Keying Feng, Xiangfu Shi, Na Liu, Zong-Quan Wu and Zheng Chen
{"title":"“Colorless to other colors” electrochromic polymer materials: structural design strategies and current development status","authors":"Yangang Zhao, Hao Zhang, Keying Feng, Xiangfu Shi, Na Liu, Zong-Quan Wu and Zheng Chen","doi":"10.1039/D6TC00127K","DOIUrl":"https://doi.org/10.1039/D6TC00127K","url":null,"abstract":"<p >Electrochromic materials have attracted extensive attention due to their ability to achieve rapid and reversible regulation of optical properties under low-voltage driving. Endowed with advantages such as high energy conversion efficiency, low energy consumption, and excellent functional expandability, they have been successfully applied in intelligent fields including architectural smart windows, electric vehicles, and space shuttles. Among them, polymer-based electrochromic materials have become a key research and development focus because of their rich color-changing varieties, fast color switching, and feasibility of roll-to-roll processing. According to their color-changing characteristics, polymer-based electrochromic materials are mainly classified into two categories: “colored to other colors (including colorless)” and “colorless to other colors”. These two types of materials not only show distinct contrasts in color-changing features but also form a perfect complementary relationship in practical applications. The “colorless to other colors” electrochromic polymers, as new types of materials that have developed rapidly in the past 20 years, possess significant scientific research interest and practical application value. However, up to now, there has been a lack of detailed analysis and reports on the design, development, and research progress of such materials. Therefore, this review will sort out and introduce the development status of these materials from the perspective of the structure–property relationship between material structure and electrochromic characteristics, summarize the strategies for designing and developing such polymer materials, and discuss the future development trends of these materials.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 20","pages":" 8394-8441"},"PeriodicalIF":5.1,"publicationDate":"2026-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148039711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Xiaoyi Hou, Ying He, Dengdeng Ai, Jianglong Kang, Lijuan Ma and Jiatai Wang
{"title":"Synergistic N-doped carbon encapsulation in porous CoSe2 nanospheres for enhancing the anode performance of sodium-ion batteries","authors":"Xiaoyi Hou, Ying He, Dengdeng Ai, Jianglong Kang, Lijuan Ma and Jiatai Wang","doi":"10.1039/D6TC00643D","DOIUrl":"https://doi.org/10.1039/D6TC00643D","url":null,"abstract":"<p >Transition metal selenides (TMSes) are considered one of the most promising anode materials for advancing sodium-ion batteries (SIBs) due to their high specific capacity and energy density. However, they suffer from significant volume expansion and poor conductivity, which lead to unsatisfactory electrochemical performance. In this work, CoSe<small><sub>2</sub></small>@NC composites with an N-doped carbon (NC) coating were fabricated <em>via</em> a self-assembly strategy combined with chemical vapor deposition. The obtained sample exhibits a uniform porous spherical architecture with an ultrathin N-doped carbon shell, thereby effectively buffering the volumetric strain of CoSe<small><sub>2</sub></small> and accelerating the electron/ion transport kinetics. Specifically, the CoSe<small><sub>2</sub></small>@NC anode delivers a high initial discharge specific capacity of 513.7 mAh g<small><sup>−1</sup></small> and retains 431.3 mAh g<small><sup>−1</sup></small> after 100 cycles, demonstrating excellent capacity retention. CV and EIS analyses confirm that the N-doped carbon coating significantly enhances pseudocapacitive contributions (82.5% at 1 mV s<small><sup>−1</sup></small>) and facilitates the Na<small><sup>+</sup></small> insertion/extraction kinetics. This work presents a practical methodology for the rational design and fabrication of advanced metal selenide anodes for sodium-ion batteries.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 24","pages":" 10823-10832"},"PeriodicalIF":5.1,"publicationDate":"2026-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148314701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}