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Optical shaping of the polarization anisotropy in a laterally coupled quantum dot dimer

Light(Science & Applications) 2020年第1期9卷 1047-1056页

作者： Heedae Kim Kwangseuk Kyhm Robert A.Taylor Jong Su Kim Jin Dong Song sungkyun park School of Physics Northeast Normal University130024 ChangchunChina Clarendon Laboratory Department of PhysicsUniversity of OxfordOxford OX13PUUK Department of Opto-mechatronics Pusan Nat’l UniversityBusan 609-735Republic of Korea Department of Physics Yeungnam UniversityGyeongsan 712-749Republic of Korea Nano-Photonics Research Center KISTSeoul 136-791Republic of Korea Department of Physics Pusan Nat’l UniversityBusan 609-735Republic of Korea

We find that the emission from laterally coupled quantum dots is strongly polarized along the coupled direction[110],and its polarization anisotropy can be shaped by changing the orientation of the polarized *** the nonresonant excitation is linearly polarized perpendicular to the coupled direction[110],excitons(X_(1) and X_(2))and local biexcitons(X_(1)X_(1) and X_(2)X_(2))from the two separate quantum dots(QD_(1) and QD_(2))show emission anisotropy with a small degree of polarization(10%).On the other hand,when the excitation polarization is parallel to the coupled direction [110],the polarization anisotropy of excitons,local biexcitons,and coupled biexcitons(X_(1)X_(2))is enhanced with a degree of polarization of 74%.We also observed a consistent anisotropy in the time-resolved *** decay rate of the polarized photoluminescence intensity along the coupled direction is relatively high,but the anisotropic decay rate can be modified by changing the orientation of the polarized *** energy difference is also observed between the polarized emission spectra parallel and perpendicular to the coupled direction,and it increases by up to three times by changing the excitation polarization orientation from [110] to [110].These results suggest that the dipole-dipole interaction across the two separate quantum dots is mediated and that the anisotropic wavefunctions of the excitons and biexcitons are shaped by the excitation polarization.

关键词： anisotropy quantum polarized

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Spectroscopic Understanding of Structural and Electrical Property Variations in Dopant-Free ZnO Films

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Journal of Materials Science & Technology 2017年第6期33卷 523-526页

作者： Hyegyeong Kim JiWoong Kim Dooyong Lee Won-Jae Lee Jong-Seong Bae Jaekwang Lee sungkyun park Department of Physics Pusan National University Department of Nano Engineering & Electronic Research Center Dong-Eui University Busan Center Korea Basic Science Institute

Physical property variation in dopant-free ZnO films was investigated. Film annealing under various environments（O_2, in-Air, N2 and vacuum） resulted in better crystallinity than in the as-grown film. In particular, the film annealed under the N_2 environment showed better crystallinity and electrical properties than films annealed in other environments. Based on spectroscopic analysis, we found a correlation between physical（structural, electrical） and chemical properties： The crystallinity of ZnO films is closely related to ZnO bonding, whereas carrier concentration is associated with VO（oxygen vacancy）.

关键词： ZnO films Annealing Oxygen vacancies Environmental stability

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Real-Time Tunable Gas Sensing Platform Based on SnO_(2) Nanoparticles Activated by Blue Micro-Light-Emitting Diodes

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Nano-Micro Letters 2024年第12期16卷 103-119页

作者： Gi Baek Nam Jung-El Ryu Tae Hoon Eom Seung Ju Kim Jun Min Suh Seungmin Lee sungkyun Choi Cheon Woo Moon Seon Ju park Soo Min Lee Byungsoo Kim Sung Hyuk park Jin Wook Yang Sangjin Min Sohyeon park Sung Hwan Cho Hyuk Jin Kim Sang Eon Jun Tae Hyung Lee Yeong Jae Kim Jae Young Kim Young Joon Hong Jong-In Shim Hyung-Gi Byun Yongjo park Inkyu park Sang-Wan Ryu Ho Won Jang Department of Materials Science and Engineering Seoul National UniversitySeoul 08826Republic of Korea Research Laboratory of Electronics Department of Mechanical EngineeringMassachusetts Institute of TechnologyCambridgeMA 02139USA Ming Hsieh Department of Electrical and Computer Engineering University of Southern CaliforniaLos AngelesCA 90089USA Department of Display Materials Engineering Soonchunhyang UniversityAsan 31538Republic of Korea Department of Photonics and Nanoelectronics BK21 FOUR ERICA-ACE CenterHanyang University ERICAAnsan 15588Republic of Korea Department of Nanotechnology and Advanced Materials Engineering Sejong UniversitySeoul 05006Republic of Korea Department of Electronics Information and Communication EngineeringKangwon National UniversitySamcheok 25913Republic of Korea Advance Institute of Convergence Technology Seoul National UniversitySuwon 16229Republic of Korea Department of Mechanical Engineering Korea Advanced Institute of Science and TechnologyDaejeon 34141Republic of Korea Department of Physics Chonnam National UniversityGwangju 500-757Republic of Korea

Micro-light-emitting diodes(μLEDs)have gained significant interest as an activation source for gas sensors owing to their advantages,including room temperature operation and low power ***,despite these benefits,challenges still exist such as a limited range of detectable gases and slow *** this study,we present a blueμLED-integrated light-activated gas sensor array based on SnO_(2)nanoparticles(NPs)that exhibit excellent sensitivity,tunable selectivity,and rapid detection with micro-watt level power *** optimal power forμLED is observed at the highest gas response,supported by finite-difference time-domain ***,we first report the visible light-activated selective detection of reducing gases using noble metal-decorated SnO_(2)*** noble metals induce catalytic interaction with reducing gases,clearly distinguishing NH3,H2,and ***-time gas monitoring based on a fully hardwareimplemented light-activated sensing array was demonstrated,opening up new avenues for advancements in light-activated electronic nose technologies.

关键词： Micro-LED Gas sensor array Low power consumption Metal decoration Real-time detection

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用于电化学能量转换反应的非贵金属单原子催化剂

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Chinese Journal of Catalysis 2023年第7期50卷 195-214页

作者： Sang Eon Jun sungkyun Choi Jaehyun Kim Ki Chang Kwon Sun Hwa park Ho Won Jang 首尔国立大学先进材料研究所材料科学与工程系首尔韩国韩国标准与科学研究院跨学科材料测量研究所大田韩国首尔国立大学融合技术高级研究所水原韩国

非贵金属单原子催化剂(NNMSAC)被认为是贵金属单原子催化剂的经济替代品,同时保留了源自单原子位点独特电子结构的高催化活性.通过金属-载体充分的相互作用,NNMSAC可以在各种电催化反应中发挥关键作用,具有与贵金属单原子催化剂相当的... 详细信息

非贵金属单原子催化剂(NNMSAC)被认为是贵金属单原子催化剂的经济替代品,同时保留了源自单原子位点独特电子结构的高催化活性.通过金属-载体充分的相互作用,NNMSAC可以在各种电催化反应中发挥关键作用,具有与贵金属单原子催化剂相当的高原子利用效率和选择性.为此,本文首先综述了NNMSAC在调节反应选择性、金属-载体相互作用和催化活性中心方面的特点.随后,详细介绍了用于析氢反应、析氧反应、氧还原反应、二氧化碳还原反应和氮还原反应的代表性NNMSAC(Co,Ni,Fe,Cu和双金属SAC)催化剂.最后,展望了NNMSAC在几何、电子和电化学性能方面进一步发展所面临的挑战.

关键词：单原子催化剂非贵金属电催化水裂解 CO_(2)还原

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