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Twist-InducedOut-of-Plane Ferroelectricity in BilayerHafnia 双层铪中扭转诱导的面外铁电性
IF 10.8 1区 材料科学
Nano Letters Pub Date : 2026-10-14 DOI: 10.1021/acs.nanolett.6c04005
Jian Huang,Gwan Yeong Jung,Pravan Omprakash,Guodong Ren,Xin Li,Xilong Xu,Du Li,Xiaoshan Xu,Li Yang,Rohan Mishra
{"title":"Twist-Induced\u0000Out-of-Plane Ferroelectricity in Bilayer\u0000Hafnia","authors":"Jian Huang,Gwan Yeong Jung,Pravan Omprakash,Guodong Ren,Xin Li,Xilong Xu,Du Li,Xiaoshan Xu,Li Yang,Rohan Mishra","doi":"10.1021/acs.nanolett.6c04005","DOIUrl":"https://doi.org/10.1021/acs.nanolett.6c04005","url":null,"abstract":"Abstract Ferroelectric HfO2 is a promising candidate for next-generation memory devices due to its CMOS compatibility and ability to retain polarization at nanometer scales. However, the polar orthorhombic phase responsible for ferroelectricity is metastable and requires extrinsic stabilization, complicating integration with silicon. Here, we predict that twist-induced symmetry breaking in bilayer 1T-HfO2 enables robust, switchable out-of-plane (OOP) polarization. First-principles density functional theory shows that monolayer 1T-HfO2, cleaved from the (111) surface of cubic HfO2, is dynamically stable. Twisting two aligned monolayers forms a moiré superlattice that breaks interlayer symmetry and yields bistable OOP polarization. At a twist angle of 7.34°, the bilayer exhibits ∼16 μC/cm2 polarization, primarily from polar displacements within AB stacking domains. The polarization can be switched via interlayer sliding with a low energy barrier (∼8 meV per formula unit), enabling electric-field tunability in atomically thin ferroelectric devices.","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"4 1","pages":""},"PeriodicalIF":10.8,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149209323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interstitial Rare-Earth Doping of FAPbI3 Perovskite Nanocrystals under Mild Ambient Conditions 温和环境条件下FAPbI3钙钛矿纳米晶间稀土掺杂研究
IF 9.1 1区 材料科学
Nano Letters Pub Date : 2026-10-14 Epub Date: 2026-09-30 DOI: 10.1021/acs.nanolett.6c03556
Abdurrahman Ihsanuddin, Wei Zhu, Xinyu Zhao, Mazaya Basmalah, Xuliang Zhang, Chenyu Zhao, Fitri Aulia Permatasari, Ferry Iskandar, Jianyu Yuan
{"title":"Interstitial Rare-Earth Doping of FAPbI3 Perovskite Nanocrystals under Mild Ambient Conditions","authors":"Abdurrahman Ihsanuddin,&nbsp;Wei Zhu,&nbsp;Xinyu Zhao,&nbsp;Mazaya Basmalah,&nbsp;Xuliang Zhang,&nbsp;Chenyu Zhao,&nbsp;Fitri Aulia Permatasari,&nbsp;Ferry Iskandar,&nbsp;Jianyu Yuan","doi":"10.1021/acs.nanolett.6c03556","DOIUrl":"https://doi.org/10.1021/acs.nanolett.6c03556","url":null,"abstract":"<p>Therare-earth (RE) metal doping strategies have been investigatedfor many applications in perovskite materials. However, prior approachesto synthesizing RE-doped perovskite nanocrystals (PNCs) have predominantlyrequired harsh synthesis conditions, including an inert gas atmosphereand high temperatures. Here, we present a doping strategy using fourRE ions (La<sup>3+</sup>, Nd<sup>3+</sup>, Gd<sup>3+</sup>, and Er<sup>3+</sup>) doped into FAPbI<sub>3</sub> PNCs under mild conditions(50 °C) in an ambient atmosphere. Density functional theory calculationswere performed to rationalize the RE incorporation by evaluating theformation energy of possible dopant configurations within the FAPbI<sub>3</sub> lattice. The results demonstrated that RE ions were successfullyintroduced into interstitial sites in the FAPbI<sub>3</sub> latticeunder mild conditions. RE-doped FAPbI<sub>3</sub> PNCs were demonstratedto preserve the structure of α-FAPbI<sub>3</sub> PNCs, whileimproving the optical properties in colloidal and thin-film samples,delivering an enhanced power conversion efficiency of 18.65% in photovoltaicperformance together with improved stability relative to pristinePNCs.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"26 40","pages":"13948–13954"},"PeriodicalIF":9.1,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149173860","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Multiscale van der Waals Metallization via Peel-Front Strain Engineering 通过皮尔-弗朗斯工程实现多尺度van der Waals金属化
IF 9.1 1区 材料科学
Nano Letters Pub Date : 2026-10-14 Epub Date: 2026-09-22 DOI: 10.1021/acs.nanolett.6c03171
Han Yan, Zichao Ma, Shidi Zhou, Meng Liang, Changjian Zhou, Mansun Chan
{"title":"Multiscale van der Waals Metallization via Peel-Front Strain Engineering","authors":"Han Yan,&nbsp;Zichao Ma,&nbsp;Shidi Zhou,&nbsp;Meng Liang,&nbsp;Changjian Zhou,&nbsp;Mansun Chan","doi":"10.1021/acs.nanolett.6c03171","DOIUrl":"10.1021/acs.nanolett.6c03171","url":null,"abstract":"<p>Integrating van der Waals (vdW) devices into circuitsrequiresmetal electrodes and interconnects spanning nanometer to millimeterscales, yet mechanical deformation during electrode transfer compromisesgeometric integrity across this range. This work identifies strainlocalized at the carrier peel-front as a dominant factor influencingtransferred metal geometry. Evaluating the peel-front strain againstthickness-dependent strain tolerance of the carrier layer yields amechanics-based framework that predicts the carrier thickness forgeometry-preserving transfer. Operating within this regime preservesline continuity, edge definition, and dimensional accuracy from sub-100nm to millimeters in a single transfer. The impact of geometric preservationis evident in MoS<sub>2</sub> memristors with transferred electrodesas narrow as 80 nm, which improve switching durability by more thanan order of magnitude, and in field-effect transistors with a channellength of 70 nm and ultrascaled contact geometries. These resultsprovide a practical route toward scalable vdW metallization for 2Delectronics.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"26 40","pages":"13896–13903"},"PeriodicalIF":9.1,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149022301","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dynamic Sulfur Reservoir Programs Cation-Exchange Kinetics in PbS Quantum Dots for Short-Wave Infrared Imaging Chips 短波红外成像芯片中PbS量子点的动态硫储层程序-阳离子交换动力学
IF 9.1 1区 材料科学
Nano Letters Pub Date : 2026-10-14 Epub Date: 2026-10-05 DOI: 10.1021/acs.nanolett.6c03669
Bo-Yi Deng, Chengjie Deng, Yuxuan Liu, Hao Luo, Chenyu Zhang, Yang Liu, Daoli Zhang, Liang Gao, Haoliang Liu, Huarui Sun, Jianbing Zhang, Jiang Tang
{"title":"Dynamic Sulfur Reservoir Programs Cation-Exchange Kinetics in PbS Quantum Dots for Short-Wave Infrared Imaging Chips","authors":"Bo-Yi Deng,&nbsp;Chengjie Deng,&nbsp;Yuxuan Liu,&nbsp;Hao Luo,&nbsp;Chenyu Zhang,&nbsp;Yang Liu,&nbsp;Daoli Zhang,&nbsp;Liang Gao,&nbsp;Haoliang Liu,&nbsp;Huarui Sun,&nbsp;Jianbing Zhang,&nbsp;Jiang Tang","doi":"10.1021/acs.nanolett.6c03669","DOIUrl":"10.1021/acs.nanolett.6c03669","url":null,"abstract":"<p>Cation-exchange synthesis produces monodisperse PbS quantumdots(QDs), yet its central limitation─precursor preparation anddropwise injection─is usually treated as a practical issue.Here, we recast it as sulfur chemical-potential programming; thatis, ethyl ziram (EZ) serves as a dynamic sulfur reservoir (DSR) whosethermolysis continuously evolves sulfur activity during growth. Thisreservoir couples ZnS QD seeds with reservoir-fed growth, shiftingthe reaction from externally injected templates to an internally regulatedkinetic regime, where QD size is set by the balance between seed densityand EZ-derived sulfur replenishment. The DSR route yields short-waveinfrared PbS QDs tunable from 1200 to 2200 nm, with narrow size distributions,high reproducibility, and reduced synthetic burden. Photodetectorsshow 64.7% external quantum efficiency and 5.8 × 10<sup>12</sup> Jones detectivity, and 640 × 512 CMOS-integrated imaging chipsexhibit a 0.04% bad-pixel rate and 3.78% photoresponse nonuniformity,validating DSR as a strategy for high-quality QD synthesis.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"26 40","pages":"14002–14010"},"PeriodicalIF":9.1,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149088194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Quantum-Dot-Based Scanning Probe d-Band Hole Spectroscopy of Plasmonic Nanoparticles 基于量子点的等离子体纳米粒子扫描探针d带空穴光谱
IF 9.1 1区 材料科学
Nano Letters Pub Date : 2026-10-14 Epub Date: 2026-10-01 DOI: 10.1021/acs.nanolett.6c03990
Florian Küstner, Harald Ditlbacher, Andreas Hohenau, Dmitry N. Dirin, Maksym Kovalenko, Joachim R. Krenn
{"title":"Quantum-Dot-Based Scanning Probe d-Band Hole Spectroscopy of Plasmonic Nanoparticles","authors":"Florian Küstner,&nbsp;Harald Ditlbacher,&nbsp;Andreas Hohenau,&nbsp;Dmitry N. Dirin,&nbsp;Maksym Kovalenko,&nbsp;Joachim R. Krenn","doi":"10.1021/acs.nanolett.6c03990","DOIUrl":"https://doi.org/10.1021/acs.nanolett.6c03990","url":null,"abstract":"<p>Despite intense research efforts, quantitative energy-resolvedmeasurements on hot carriers generated due to plasmon decay in metalnanoparticles are rare. This concerns in particular excitations belowthe Fermi level, i.e., holes. Here, we use a metallized scanning probetip to measure photocurrents from plasmonic gold nanoparticles througha monolayer of colloidal lead sulfide quantum dots. Separating outcurrent contributions from quantum dot excitons and thermionic emission,we achieve quantitative measurements on the hole excitation quantumefficiency in the gold nanoparticles in the 1.9–2.6 eV energyrange. Therefore, we combine systematic experimental bias and wavelengthvariations and a comparison with the case of aluminum with extensivemodeling. The detection scheme can be extended to electron currentsand other energy ranges by simply using quantum dots with differentenergy levels.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"26 40","pages":"14040–14046"},"PeriodicalIF":9.1,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149173409","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Inhibition of Calendar Aging Induced Li Metal Corrosion Using Selected Area Insulating Layer Current Collectors 选定区域绝缘层集流器抑制历老化引起的锂金属腐蚀
IF 9.1 1区 材料科学
Nano Letters Pub Date : 2026-10-14 Epub Date: 2026-10-01 DOI: 10.1021/acs.nanolett.6c02391
Wenbo Zhang, Donglin Li, Sanzeeda Baig Shuchi, Chad Michael Serrao, Steven D. Liu, Elizabeth Zhang, Angela Cai, John Holoubek, Sang Cheol Kim, Sarah E. Holmes, Xin Chen, Jun Ho Lee, Renee Zhao, Zhenan Bao, Yi Cui
{"title":"Inhibition of Calendar Aging Induced Li Metal Corrosion Using Selected Area Insulating Layer Current Collectors","authors":"Wenbo Zhang,&nbsp;Donglin Li,&nbsp;Sanzeeda Baig Shuchi,&nbsp;Chad Michael Serrao,&nbsp;Steven D. Liu,&nbsp;Elizabeth Zhang,&nbsp;Angela Cai,&nbsp;John Holoubek,&nbsp;Sang Cheol Kim,&nbsp;Sarah E. Holmes,&nbsp;Xin Chen,&nbsp;Jun Ho Lee,&nbsp;Renee Zhao,&nbsp;Zhenan Bao,&nbsp;Yi Cui","doi":"10.1021/acs.nanolett.6c02391","DOIUrl":"https://doi.org/10.1021/acs.nanolett.6c02391","url":null,"abstract":"<p>Limetal is a promising anode for next-generation batteries, butits high per-cycle capacity loss hinders its commercial adoption.A major contributor is the corrosion of Li during calendar aging,which accelerates the generation of degradation byproducts, such asthe solid electrolyte interphase (SEI) and isolated Li (i-Li). Here,we reveal that Li corrosion is spatially heterogeneous: five timesmore capacity is lost at the edge overhang area of the current collectorthan at the center in the coin cell form factor. To address this,we developed a selected-area insulating layer (SAIL) that preventsLi plating in the overhang, yielding a 94% reduction in corrosion-inducedcapacity loss. Electron microscopy and titration gas chromatographywere employed to visualize the morphological heterogeneity and quantifythe disconnected Li loss at the center versus the overhang. Preventingdendritic Li plating in the overhang of the current collector cantherefore substantially mitigate calendar aging-induced capacity loss.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"26 40","pages":"13759–13766"},"PeriodicalIF":9.1,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149173526","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Confining Sn Nanocatalysts via Ship-in-a-Bottle Strategy: Local Alkaline Microenvironment Engineering for High-Selective and Durable Acidic CO2RR to Formic Acid 用瓶装策略限制锡纳米催化剂:高选择性和持久的酸性CO2RR到甲酸的局部碱性微环境工程
IF 9.1 1区 材料科学
Nano Letters Pub Date : 2026-10-14 Epub Date: 2026-09-29 DOI: 10.1021/acs.nanolett.6c02682
Xuhua Zhao, Jingying Li, Weizhou Wang, Mengqian Zhang, Haiwen Zhang, Hongdong Li, Lei Wang
{"title":"Confining Sn Nanocatalysts via Ship-in-a-Bottle Strategy: Local Alkaline Microenvironment Engineering for High-Selective and Durable Acidic CO2RR to Formic Acid","authors":"Xuhua Zhao,&nbsp;Jingying Li,&nbsp;Weizhou Wang,&nbsp;Mengqian Zhang,&nbsp;Haiwen Zhang,&nbsp;Hongdong Li,&nbsp;Lei Wang","doi":"10.1021/acs.nanolett.6c02682","DOIUrl":"https://doi.org/10.1021/acs.nanolett.6c02682","url":null,"abstract":"<p>Acidic CO<sub>2</sub> electroreduction (CO<sub>2</sub>RR) preventscarbonate formation but suffers from severe competition with the hydrogenevolution reaction. Herein, a nanoreactor-structured Sn@MCHS catalystis fabricated via a ship-in-a-bottle method, synergizing the catalyticactivity of metallic Sn with the microenvironment-modulating capabilityof hollow mesoporous carbon spheres (MCHS). This mesoporous shellacts as a physical barrier, restricting proton replenishment and retainingthe in situ generated OH<sup>–</sup>, thereby forming a localalkaline microenvironment. The nanoreactor enriches K<sup>+</sup> andstabilizes *OCHO. In the acidic CO<sub>2</sub> reduction system, theFE of the catalyst in an H-type cell reached 90.3%, and in a flowcell it reached 95.1%. It also demonstrated excellent stability forcontinuous operation for up to 96 h. This study established nanoscaleconfinement as a powerful strategy for constructing an electrocatalyticmicroenvironment, opening up a new path for designing highly selectiveand durable electrocatalysts.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"26 40","pages":"13776–13785"},"PeriodicalIF":9.1,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149173937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Probing andSensing Layer-Dependent van der WaalsInteraction via Induced Anisotropy 通过诱导各向异性探测和感知层相关范德华相互作用
IF 10.8 1区 材料科学
Nano Letters Pub Date : 2026-10-14 DOI: 10.1021/acs.nanolett.6c04684
Ting Wen,Shuang Cai,Ziluo Su,Yalan Wang,Jiaqi Wu,Jiaze Qin,Chenyin Jiao,Zenghui Wang,Zejuan Zhang,Shenghai Pei
{"title":"Probing and\u0000Sensing Layer-Dependent van der Waals\u0000Interaction via Induced Anisotropy","authors":"Ting Wen,Shuang Cai,Ziluo Su,Yalan Wang,Jiaqi Wu,Jiaze Qin,Chenyin Jiao,Zenghui Wang,Zejuan Zhang,Shenghai Pei","doi":"10.1021/acs.nanolett.6c04684","DOIUrl":"https://doi.org/10.1021/acs.nanolett.6c04684","url":null,"abstract":"Abstract Van der Waals (vdW) interaction, a fundamental force, plays an important role in two-dimensional (2D) systems by enabling atomically sharp assemblies and giving rise to many emergent phenomena. However, experimentally probing and sensing the evolution of vdW interaction between 2D layers remains challenging due to its extreme weakness, very short range, and the difficulty of keeping two atomic layers perfectly parallel while finely adjusting the interaction. Here, we demonstrate an optical strategy to indirectly probe vdW interactions by exploiting induced anisotropy in MoS2/NbIrTe4 heterostructures. We construct heterostructures using isotropic MoS2 and anisotropic NbIrTe4 to ensure perfect parallelism. We modulate and probe the vdW interaction by varying the NbIrTe4 thickness and monitor the vdW-interaction-induced anisotropy in MoS2. We find such induced anisotropy to strongly depend on the NbIrTe4 thickness and clearly observe its fast-decaying nature. This work provides a simple, noncontact approach for indirectly probing interlayer vdW interactions.","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"50 1","pages":""},"PeriodicalIF":10.8,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149209325","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Managing Proton-InvolvedKinetics via CooperativeAcceptance and Diffusion of Protons for Stable Acidic Water Oxidationunder Fluctuating Power 波动功率下稳定酸性水氧化中质子的协同接受和扩散动力学
IF 10.8 1区 材料科学
Nano Letters Pub Date : 2026-10-14 DOI: 10.1021/acs.nanolett.6c04041
Zhongfeng Wang,Mingming Wang,Hao Luo,Shaoyan Wang,Xiao Zhao
{"title":"Managing Proton-Involved\u0000Kinetics via Cooperative\u0000Acceptance and Diffusion of Protons for Stable Acidic Water Oxidation\u0000under Fluctuating Power","authors":"Zhongfeng Wang,Mingming Wang,Hao Luo,Shaoyan Wang,Xiao Zhao","doi":"10.1021/acs.nanolett.6c04041","DOIUrl":"https://doi.org/10.1021/acs.nanolett.6c04041","url":null,"abstract":"Abstract Practical application of RuO2 for the acidic oxygen evolution reaction (OER) is hindered by its sluggish kinetics and serious degradation. Here, we manage proton-involved kinetics via cooperative acceptance and diffusion of protons by constructing CrOx islands on the RuO2 surface. This architecture renders two distinct yet spatially coupled functions: interfacial Cr–OH groups at the perimeters act as proton acceptors to promote the deprotonation of OER intermediates, while the hydroxyl-rich CrOx islands dynamically restructure interfacial water networks with potentials to facilitate proton diffusion away from catalyst-electrolyte interfaces. This enhances the OER kinetics but, more critically, reduces the local acidification to secure operational stability under fluctuating power. Water electrolyzers with this CrOx/RuO2 need a low voltage of 1.61 V at 1 A cm–2 and operate for over 1600 h under square-wave loading conditions (cycling between 0.1 and 1 A cm–2, each for 12 h), exceeding that using RuO2 (stability &amp;lt;12 h).","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"52 1","pages":""},"PeriodicalIF":10.8,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149210030","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Strategy for Ultranarrow Light Down-Conversion for Displays Based on Bicolor-Emitting 2D Colloidal Heterostructures 基于双色发射二维胶体异质结构的显示器超窄光下转换策略。
IF 9.1 1区 材料科学
Nano Letters Pub Date : 2026-10-14 Epub Date: 2026-06-16 DOI: 10.1021/acs.nanolett.6c01589
Jisoo Oh, Jiho Roh, Clément Gureghian, Dario Mastrippolito, Mariarosa Cavallo, Marco Paye, Xiang Zhen Xu, Thomas E. Gage, Nicolas Menguy, Xavier Lafosse, Mathieu G. Silly, Debora Pierucci, Emmanuel Lhuillier, Juan I. Climente, Benjamin T. Diroll, Sandrine Ithurria
{"title":"Strategy for Ultranarrow Light Down-Conversion for Displays Based on Bicolor-Emitting 2D Colloidal Heterostructures","authors":"Jisoo Oh,&nbsp;Jiho Roh,&nbsp;Clément Gureghian,&nbsp;Dario Mastrippolito,&nbsp;Mariarosa Cavallo,&nbsp;Marco Paye,&nbsp;Xiang Zhen Xu,&nbsp;Thomas E. Gage,&nbsp;Nicolas Menguy,&nbsp;Xavier Lafosse,&nbsp;Mathieu G. Silly,&nbsp;Debora Pierucci,&nbsp;Emmanuel Lhuillier,&nbsp;Juan I. Climente,&nbsp;Benjamin T. Diroll,&nbsp;Sandrine Ithurria","doi":"10.1021/acs.nanolett.6c01589","DOIUrl":"10.1021/acs.nanolett.6c01589","url":null,"abstract":"<p>The demand for ultranarrow spectral emission below 10nm is criticalfor next-generation displays. Although current colloidal nanocrystalsare successful in light down-conversion applications, they fall shortin matching the stringent color purity requirements set by standardslike Rec. 2020. Achieving such narrow linewidths through materialengineering alone remains elusive, necessitating innovative lightmanagement strategies that avoid optical losses and maintain deviceefficiency. Here, we present a novel 2D colloidal heterostructuredesign, combining a CdSe core nanoplatelet, a CdS crown, and a CdZnSshell, to achieve bright bicolor emission in the solid state (green/red)emission with tunable intensity ratios controlled by excitation power(either optical or electrical). Integration of these nanoplateletsinto a dielectric cavity further narrows the emission linewidth tosub-2 nm while enhancing the photoluminescence intensity by up to200 times, meeting the Rec. 2020 color purity targets. This approachpaves the way for a strategy avoiding complex laser-based solutions.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"26 40","pages":"13730–13736"},"PeriodicalIF":9.1,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148262204","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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