R&D of IR Detectors and Emitters

Total Page:16

File Type:pdf, Size:1020Kb

R&D of IR Detectors and Emitters Soreq nanodots and nanocrystals for infrared photodetectors Yossi Paltiel Solid State Physics Group Soreq NRC III-V compounds Most of our work Are bulk devices for MWIR Quantum detectors SWIR- Nano-crystals MWIR- Nanodots LWIR-Quantum wells THz Quantum wells Bulk problems and possible solution • Low temperature operation • Wide band wavelength response • Restricted flexibility in choosing the peak wavelength Nano Why Nano and Meso? Call for Research Proposals in Advanced Materials and Nanotechnology, Israel- Ukraine Cooperation Impressive A lot of money Using Quantum effects in the world of high temperatures (300K) Nanodots in lasers and detectors Light prorogation E H ¾ Theoretically, high temperature operations. 1D QW energy shift as a function of L 105 InSb ¾ Long lifetime 104 dE 1000 ¾ Normal light absorption 100 10 ¾ Narrow absorption lines 1 0 5 10 15 20 25 30 35 40 ¾ Changing dots size will change the blue shift and could give L [nm] multispectral detection Nano crystals for shorter wavelength Uri Banin room T precursors In/GaCl3 and P/As(SiMe3)3 P = P O liquid surfactant, stirring and at o InCl3+As(SiMe3)3 InAs + 3Me3SiCl “high T,” 250-300 C Wavelength (nm) Quantum confinement in 1600 1200 800 600 InAs nanocrystals 2.4 nm Optical spectra 2.9 nm ) . u . a ( 3.3 nm ) . y u . a nsit Quantum Dot e 4.0 nm t n ance ( E 4.6 nm b 1Pe Absor inescence I 1Se 5.0 nm Eg Lum 5.8 nm 1Sh 6.4 nm 1Ph r 1.01.52.02.5 Energy (eV) Transport and dissipation The molecules used 1.4 InAs - NPs AA112C4S2 AAC1325S3 1.2 1334 1466 1.0 ce 0.8 an rb so 0.6 Ab 0.4 HS-(CH2)10-SH DT 0.2 0.0 1000 1100 1200 1300 1400 1500 1600 1700 Wavelength (nm) HS- (CH ) -SH EDT 2 2 5nm and 6 nm InAs nanocrystals HS-CH -φ-CH -SH BDMT Au 2 2 Au 5nm GaAs n-GaAs 50nm AlGaAs semi- insulating GaAs semi-insulating substrate FTIR spectra of GaAs slides with 1,10 Decanethiol Monolayer and with InAs 6 nm NPs connected 0.0025 1,10 Decanethiol+InAs 1/2h 1260 1,10 Decanethiol+InAs 10 Decanethiol+InAs 1h 16(1,10 Decanethiol+InAs one step) 0.0020 1,10 Decanethiol 1,10 Decanethiol e 0.0015 anc rb o s b 0.0010 A 0.0005 0.0000 1340 1320 1300 1280 1260 1240 1220 1200 -1 -0.30 Wavenumber (cm ) GaAs insulator; 1,4 Ethanedithiol (EDT); EDT+InAs(AAC1325S3); 40V; 4 min. CH2 Vibration mode -0.35 -0.40 D (V) -0.45 CP Contact Potential Difference -0.50 (Kelvin Probe)- Traps -0.55 0 500 1000 1500 2000 Time (s) Soreq MOCVD (MOVPE) growth system Growth Machine- Thomas Swan with Vertical Reactor Substrates –Te doped InSb (100) or (100) 20 ooffff towartowardsds (111)(111),, up to 2” wafers Metal Organics- TMSb, TMIn Dopants- Zn for p-type, S or Si for n-type, DEZn and H2S/H2 or SiH4/H2 Soreq Growth methods Stranski-Krastanov growth mode γ 2 > γ 12 + γ 1 + µ1 (d ) γ 1 − surface free energy of deposited material γ − Conventional method 2 surface free energy of substrate γ 12 − interface energy µ1 (d ) − strain energy of the γ 2 < γ 12 + γ 1 + µ1 (d ) layer (SK) Droplet heteroepitaxy (DHE) growth mode First stage of the growth: group III element nano-droplets Interest in the last years formation on the substrate M. Gherasimova et al. Second stage of the growth: APL 85 2346 (2004) reaction of these droplets with one or more group V elements in the gas phase (DHE) Soreq InSb dots on different substrates InSb/GaAs Density: 1x1010 cm-2 Size distribution: 15-40nm Q factor: ~0.35 InSb/GaSb Density: 4x1010 cm-2 Size distribution: 15-50nm Q factor: ~0.1 Growing on InSb/InAs SOG Density: 8x1010 cm-2 Size distribution: 15-25nm Q factor: ~0.4 Soreq PL signal of InSb nanodots on GaAs Eg (InSb) =0.23eV (5.4 µ m) 1 10-6 1 10-6 50 18-20 nm Number of dots 15-40nm dots -7 8 10 PL signal 8 10-7 12-30nm dots 40 12-30nm dots with cap 22-25 nm InSb -7 6 10-7 6 10 10K 30 100mW Bulk -7 30-35 nm 4 10 830nm laser 4 10-7 40-45 nm 20 ~50 nm 2 10-7 -7 2 10 10 0 100 0 100 0 3500 4000 4500 5000 5500 3500 4000 4500 5000 5500 Wavelength [nm] Wavelength [nm] Size and density Blue shift 1 757 dots dots cap 0.8 dots cap dots 332 dots cap x 5 0.6 280 0.4 0.2 136 dots Dots and cap Dots+cap X5 0 3000 4000 5000 Wavelength [nm] Soreq Main idea- Well or dots as a gate FET transistor with Sb based nanodots acting as a gate Ohmic contacts Ohmic contacts FET Infrared radiation Amplified current change Potential change A Photon excites an electron to produce a E = hν measurable voltage QWIP QDIP and - e Voltage MESFET QD First excited bias state x50 Ground state Contact Contact QW Barriers Contact FET Contact Contact FET QD QWIP QDIP QWIP - Mature working technology working at 70K, needs grating. Everything under control. QDIP - Theoretically could work at higher temperatures and absorb normal light. Currently no seen advantages over QWIP. FET QD – Taking all the advantages of the QDIP with improved signal to noise ratio and wider material options. Single photon detector at 77K – A. J. Shields et al., APL 76 3673 (2000) Transistor response to a thin layer of InAsSb (Chiaro, Ron aaman) Accepted for publication in IEEE sensors journal 295B InAsSb#2 black body and Ge filter -4 7 10 -4 6 10 -4 5 10 -4 4 10 I light off 1 [A] -4 The detector on a test chip fabricated in Chiaro 3 10 I Ge 1 [A] 300K I light off 003 [A] -4 2 10 I Ge 003 [A] I light off 03 [A] -4 1 10 I Ge 03 [A] 0 0 10 -4 -2 0 2 4 Voltage [V] Room temperature response Amplified response detectors response 2 150 Laser power transistor only respose 100 50 0 0 -50 -100 1.3 µ m laser no voltage 300K 8 10-6 1 10-7 -2 -150 layer photoresponse 0 5 10 15 20 25 30 time [ms] detectors response Room temperature zero voltage AC 1 squre response black body with Ge filter -6 -8 response of the FET with 10nm 4 10 77K 5 10 InAsSb absorber deposited on the gate area .A 1.3 µm laser modulated by a chopper 0 100 0 -4 -2 0 2 4 Voltage [V] Photo response of the thin InAsSb layer compared with the full detector response, When illuminated with a filtered 1000C blackbody radiation presenting a gain of 100. Nano gold local field enhancement With and WO the nanogold Local field enhancement aa132ss3 Blue shift and nano enhancment aa132ss3 inas nano 10k 100mw different wavelength 8 102 1 103 1 DT+ nano gold solution peak DT 10K 2 532nm 8 10 630nm 6 102 10K solution 830nm Nano gold 6 102 2 4 10 0.5 4 102 2 2 10 2 102 0 100 0 100 0 1000 1200 1400 1600 1800 1000 1200 1400 1600 1800 Wavelength [nm] Wavelength [nm] Building new molecules combined with metal nano particles and semiconductor nano Future work GaAs Building artificial molecules with local field enhancement Combination of the two InAs InSb 10K GaAs 0.0004 100mW 830nm laser Dual peak 16_4_06 PL [mV] 0.0002 0.0000 1.0 1.5 2.0 2.5 3.0 3.5 4.0 4.5 5.0 Wavelength [ µm] PL signal from the two nano structures Two different worlds? Mesoscopic and nano physics Bulk Most works use one option only: •Semiconductor bulk properties •Quantum ideal calculations nickel 3 Angstroms = 0.3 nm In the real life they all coupled to the bulk environment Very complex relations between our robust world and the nano world The environment effects on quantum properties •Strain •Doping • Bend alignment • Discreet levels coupled to continuum •Life time • Dissipation • Conservation laws InAs nano Are the dots free? molecules GaAs substrate 532nm 820nm Transport from the substrate to the Distance to the substrate nono crystal aa132ss3 inas nano 10k 100mw 532nm dt gaas.InGaAs sensor aa112 inas nano on gold 10k 100mw 820nm Avrage 3 10-7 TM PL BDMT 2 DT H O PL EDT 6 10 2 BMDT 10K PL DT EDT CO 2 10-7 2 2 4 10 532nm 100mW 1 10-7 2 102 0 0 10 0 100 1000 1100 1200 1300 1400 1500 1600 1000 1200 1400 1600 1800 Wavelength [nm] wavelength [nm] life time , transport properties , coupling 820nm - coupling 520nm- transport Future work DNA transport studies 2 DT 530nm EDT 820nm BDMT solution 1 DT EDT BDMT molecule 10K 530nm 00 1000 1200 1400 1600 1800 2000 wavelength [nm] life time , transport properties , coupling Future work DNA transport studies Coupling between the np and the GaAs substrate 1. There is coupling between the np and the GaAs as is evident by the SPV and PL studies. 2. The coupling varies with the molecules- In the order- BDMT>EDT>DT 3. Transport of charges interactions between nano particles polarization aa132ss3 inas nano 10k 100mw 532nm dt TE-TM 4 102 TE TM 10K 2 102 0 100 1000 1200 1400 1600 wavelength [nm] Soreq Substrate effects 1.Lattice mismatch (strain) 2.Energy band-gap alignment Type-I Type-II Staggered Type-III InSb/GaAs InSb/GaSb (Type-II Misaligned) InSb/InAs I.T.
Recommended publications
  • Professor Uri Banin, Curriculum Vitae
    PROFESSOR URI BANIN, CURRICULUM VITAE Email: [email protected]; Website: http://chem.ch.huji.ac.il/~nano/ EDUCATION: 1986-1989: The Hebrew University, Jerusalem, B.Sc. Summa Cum Laude, chemistry and physics 1989-1994: The Hebrew University, Jerusalem, Ph.D. Summa Cum Laude, physical chemistry 1994-1997: University of California at Berkeley, Department of Chemistry, Post Doctoral Research with Professor A. Paul Alivisatos. Topic: Physical Chemistry of Semiconductor Nanocrystals; EMPLOYMENT HISTORY: 2010-: Incumbent of the Alfred & Erica Larisch Memorial Chair 2009-2015: Scientific founder and chief scientific officer of Qlight Nanotech, start-up company in Jeru- salem. Qlight develops use of semiconductor nanocrystals in display and lighting applications. Qlight was fully purchased by Merck in 7/2015. Banin continues to serve as scientific advisor to the company 2004-: Full Professor, The Hebrew University of Jerusalem 2003-2004: Visiting professor in sabbatical stay at the University of California, Berkeley 2001-2010: Founding director, Hebrew University Center for Nanoscience and Nanotechnology 2001-2004: Associate Professor, The Hebrew University of Jerusalem 1997-2001: Senior Lecturer, Alon Fellow, The Hebrew University of Jerusalem OTHER MAIN APPOINTMENTS: 2013-: Associate Editor, Nano Letters 2010-: Member of the scientific advisory committee of the Italian Institute of Technology (IIT) 2010-2011: Member of the Managing Committee of the Hebrew University 2009: Chairman of the Scientific Committee and co-chairperson of the
    [Show full text]
  • How to Dope a Semiconductor Nanocrystal? Uri Banin Institute Of
    Abstract #2152, 224th ECS Meeting, © 2013 The Electrochemical Society How to dope a semiconductor nanocrystal? Uri Banin Institute of Chemistry and the Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel Doping of bulk semiconductors, the process of intentional introduction of impurity atoms into a crystal discovered back in the 1940s, is a key enabling route for tuning their properties. Its introduction allowed the wide-spread application of semiconductors in electronic and electro- optic components. Controlling the size and dimensionality of semiconductor structures is an additional powerful way to tune their properties via quantum confinement effects. In this respect, colloidal semiconductor nanocrystals have emerged as a family of materials with size dependent optical and electronic properties that have attracted significant attention due to their unique attributes and potential applications. Impurity doping in such colloidal nanocrystals still remains an open challenge. From the Figure 1: Effects of doping in semiconductor synthesis side, the introduction of a few impurity atoms nanocrystals. Shown is a sketch for n-doped into a nanocrystal which contains only a few hundred nanocrystal quantum dot with confined energy atoms may lead to their expulsion to the surface or levels, red and green lines correspond to the compromise the crystal structure. From a physical QD and impurity levels, respectively. Left: viewpoint, impurities inherently create a heavily doped The level diagram for a single impurity nanocrystal under strong quantum confinement, and the effective mass model, Right: Impurity levels electronic and optical properties in such circumstances are develop into impurity bands as the number of still unresolved.
    [Show full text]
  • Gold-Tipped Nanocrystals Developed by Hebrew University 17 June 2004
    Gold-tipped nanocrystals developed by Hebrew University 17 June 2004 "Nanodumbells" – gold-tipped nanocrystals which resultant structure resembles a nanodumbbell, in can be used as highly-efficient building blocks which the central, nanocrystal, semiconductor part for devices in the emerging nanotechnology of the rod is linked via a strong chemical bond to revolution – have been developed by researchers the gold tips. These nanodumbbells provide strong at the Hebrew University of Jerusalem. chemical bonds between the gold and the The technology, developed by a research group semiconductor, leading to good electrical headed by Prof. Uri Banin of the Department of connectivity. This provides the path towards solving Physical Chemistry and the Center for the problem of wiring the nanocrystals intro Nanoscience and Nanotechnology of the Hebrew electrical circuitry. University, is described in an article in the current issue of Science magazine. The chemical bonding quality of the gold also helps solve the difficulties involved in manufacturing The nanodumbells – shaped somewhat like mini- simultaneously up to billions of circuits. By adding weightlifting bars – offer a solution to problems of to the nanodumbbell solution specific "linker" building new, nanocrystal transistors, the basic molecules, the gold tips are attracted to each other, component of computer chips. thus creating self-assembling chain structures of nanocrystals, linked end-to-end. This strategy can Semiconductor nanocrystals are tiny particles with serve as the basis for future manufacturing that will dimensions of merely a few nanometers. A connect billions of nanorods to nanoelectronic nanometer (nm) is one-billionth of a meter, or circuitry. It is also possible to create other shapes, about a hundred-thousandth of the diameter of a such as tetrapods, in which four arms expand from human hair.
    [Show full text]
  • Heavily Doped Semiconductor Nanocrystals
    Heavily doped semiconductor nanocrystals Uri Banin Institute of Chemistry & the Center for Nanoscience and Nanotechnology The Hebrew University of Jerusalem, Jerusalem 91904, Israel Doping of bulk semiconductors, the process of intentional introduction of impurity atoms into a crystal discovered back in the 1940s, is a key enabling route for tuning their properties. Its introduction allowed the wide-spread application of semiconductors in electronic and electro-optic components. Controlling the size and dimensionality of semiconductor structures is an additional powerful way to tune their properties via quantum confinement effects. In this respect, colloidal semiconductor nanocrystals have emerged as a family of materials with size dependent optical and electronic properties that have attracted significant attention due to their unique attributes and potential applications. Impurity doping in such colloidal nanocrystals still remains an open challenge. From the synthesis side, the introduction of a few impurity atoms into a nanocrystal which contains only a few hundred atoms may lead to their expulsion to the surface or compromise the crystal structure. From a physical viewpoint, impurities inherently create a heavily doped nanocrystal under strong quantum confinement, and the electronic and optical properties in such circumstances are still unresolved. We developed a solution based method to dope semiconductor nanocrystals with metal impurities providing control of the band gap and Fermi energy. A combination of optical measurements, scanning tunnelling spectroscopy and theory revealed the emergence of a confined impurity band and band-tailing effects. Successful control of doping and its understanding provide n- and p-doped semiconductor nanocrystals which greatly enhance the potential application of such materials in solar cells, thin-film transistors, and optoelectronic devices prepared by facile bottom-up methods.
    [Show full text]
  • Surface Versus Impurity Doping Contributions in Inas Nanocrystals Field Effect Transistor Performance
    Surface versus Impurity Doping Contributions in InAs Nanocrystals Field Effect Transistor Performance Durgesh C. Tripathi §, ║, Lior Asor †, ‡, ║, Gil Zaharoni †, ‡, Uri Banin*, †, ‡ and Nir Tessler*, § § The Zisapel Nano-Electronics Center, Department of Electrical Engineering, Technion – Israel Institute of Technology, Haifa 32000, Israel † The Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel ‡ The Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel 1 ABSTRACT The electrical functionality of an array of semiconductor nanocrystals depends critically on the free carriers that may arise from impurity or surface doping. Herein, we used InAs nanocrystals thin films as a model system to address the relative contributions of these doping mechanisms by comparative analysis of as-synthesized and Cu-doped nanocrystal based field effect transistor (FET) characteristics. By applying FET simulation methods used in conventional semiconductor FETs, we elucidate surface and impurity-doping contributions to the overall performance of InAs NCs based FETs. As-synthesized InAs nanocrystal based FETs show n-type characteristics assigned to the contribution of surface electrons accumulation layer that can be considered as an actual electron donating doping level with specific doping density and is energetically located just below the conduction band. The Cu-doped InAs NCs FETs show enhanced n-type conduction as expected from the Cu impurities location as an interstitial n-dopant in InAs nanocrystals. The simulated curves reveal the additional contribution from electrons within an impurity sub band close to the conduction band onset of the InAs NCs. The work therefore demonstrates the utility of the bulk FET simulation methodology also to NC based FETs.
    [Show full text]
  • Education Professional Ctivities
    Name: Taleb Mokari Date (12, 11, 2014) CURRICULUM VITAE • Personal Details Name: Taleb Mokari Address and telephone number at work: Department of Chemistry, BGU, 08-6428615 Address and telephone number at home: Yalin More Natan 19, Beer-sheva, 0523404450 Education B.Sc. studies in Chemistry 1998 – 2000: Hebrew University, Jerusalem, M. Sc. Studies 10/2000–10/2002 : Department of Physical Chemistry - Hebrew University, Jerusalem, Master studies with Prof. Uri Banin: The thesis’ topic “Synthesis and characterization of semiconductor nanocrystals quantum rods (CdSe) and rod/shell (CdSe/ZnS)” Ph.D. studies in the Chemistry: 12/2003 –5/2006: graduated with distinction. Summa cum Laude Department of Physical Chemistry - Hebrew University, Jerusalem, Ph.D Studies with Prof. Uri Banin: the thesis’ topic “Development of composite of nanocrystals with Semiconductor-Insulator and Semiconductor-Metal interfaces” Professional Activities A) Positions in academic administration: 10/2012- present: Member of the "Young Israel Academy". 12/2011- present: Associate Professor, Department of Chemistry, Ben-Gurion University of the Negev. 10/2009- 12/2011: Senior Lecturer, Department of Chemistry, Ben-Gurion University of the Negev. 9/2007-9/2009 : staff scientist at the Molecular Foundry, Material Sciences Division, Lawrence Berkeley National Laboratory. 09/2006-6/2007 : Fulbright-commercial and Industrial club -Ilan Ramon Postdoctoral Fellow, the group of Professor Peidong Yang, Department of Chemistry, University of California- Berkeley 1 B) Professional functions outside universities/institutions 1. 2008: Member of US Department of Energy Evaluation Committee of Brookhaven National Laboratory, 2. 2012: Member of the organizing committee of the Israel chemical Society conference 3. 2014: Member of Fulbright committee for Postdoctoral fellowships 4.
    [Show full text]
  • Qlight Nanotech – Overview
    קפיצה קוונטית מהמעבדה להייטק: ננוגבישים מוליכים למחצה לתאורה ולמסכים אורי בנין המכון לכימיה והמרכז לננומדע ולננוטכנולוגיה יום חדשנות טכנולוגית בתחום החומרים המתקדמים Nanocrystal Science and Technology 30 nm Bulk Tunable colors through band size, composition & gap shape control Synthesis – scalable manufacturing • Cost effective scalable wet chemical synthesis applicable to different Semiconductors • Chemically processable through surface providing flexible manipulations in solutions, plastic films, electrodes Qlight Nanotech – Overview • A Hebrew University spin-off company founded in 2009 • Based on inventions from professor Uri Banin lab • Strategic cooperation with Merck KGaA, fully owned by Merck since summer 2015 • Labs located in Jerusalem, Israel (in the Safra Campus) • Team of highly qualified scientists Qlight develops innovative nanocrystal enabled products for flat panel displays and solid state lighting markets The story of Qlight Nanotech: From Bright Idea to Successful Company • 2001 – Professor Uri Banin research on Nanorods • 2008 – Nofar project of OCS on Nanorods switchable display • 2009 – Qlight established as a company on campus • 2012 – First equity investment by Merck • 2013 – Second equity investment by Merck • 2014 – Blue-Chip JDA partners • 2015 – Qlight acquired by Merck Qlight Nanotech – Nanotechnology Company of the Year 2014 Award presented by Chief Scientist of Israel, Ministry of Economy A World of Displays… Indoor Outdoor Mobile Liquid crystal display (LCD) operation principle Liquid Crystal Display schematic Challenges: • Better colors • Low energy consumption & long battery life ABEF: Active Brightness Enhancement Film; The ABEF converts blue LED light into RGB light. Illustration of ABEF film: quantum rods are excited by blue LEDs to give R-G-B light ABEF: Outstanding Display Colors – OLED like colors with LCD • Highly saturated Red, Green and Blue colors are obtained due to the narrow emission bands.
    [Show full text]
  • Chemically Reversible Isomerization of Inorganic Clusters
    Chemically reversible isomerization of inorganic clusters Curtis B. Williamson†§, Douglas R. Nevers†§, Andrew Nelson‡, Ido Hadar‖, Uri Banin‖*, Tobias Hanrath†*, and Richard D. Robinson‡* †Robert F. Smith School of Chemical and Biomolecular Engineering, ‡Department of Materials Science and Engineering, Cornell University, Ithaca, USA ‖Institute of Chemistry and the Center for Nanoscience and Nanotechnology, The Hebrew University, Jerusalem 91904, Israel *corresponding authors Curtis B. Williamson Cornell University [email protected] Douglas R. Nevers Cornell University [email protected] Andrew Nelson Cornell University [email protected] Ido Hadar The Hebrew University [email protected] Uri Banin* The Hebrew University [email protected] Tobias Hanrath* Cornell University [email protected] Richard D. Robinson* Cornell University [email protected] 1 Abstract Structural transformations in molecules and solids have generally been studied in isolation, while intermediate systems have eluded characterization. We show that a pair of CdS cluster isomers provides an advantageous experimental platform to study isomerization in well-defined atomically precise systems. The clusters coherently interconvert over an ~1 eV energy barrier with a 140 meV shift in their excitonic energy gaps. There is a diffusionless, displacive reconfiguration of the inorganic core (solid-solid transformation) with first order (isomerization-like) transformation kinetics. Driven by a distortion of the ligand binding motifs, the presence of hydroxyl species changes the surface energy via physisorption, which determines “phase” stability in this system. This reaction possesses essential characteristics of both solid-solid transformations and molecular isomerizations, and bridges these disparate length scales. Phase transitions in solids and molecular isomerizations occupy different extremes for structural rearrangements of a set of atoms proceeding along mechanistic pathways.
    [Show full text]
  • How to Dope a Semiconductor Nanocrystal Yorai Amit, Adam Faust
    ECS Transactions, 58 (7) 127-133 (2013) 10.1149/05807.0127ecst ©The Electrochemical Society How to Dope a Semiconductor Nanocrystal Yorai Amit,a,b Adam Faust, a,b Oded Millo,b,c Eran Rabani,d Anatoly I. Frenkel,e and Uri Banin*a,b aThe Institute of Chemistry, bThe Center for Nanoscience and Nanotechnology, and cThe Racah Institute of Physics, , Hebrew University, Jerusalem 91904, Israel dSchool of Chemistry, Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 69978, Israel eThe Department of Physics, Yeshiva University, New York, New York 10016, United States *To Whom Correspondence should be addressed. E-mail: [email protected] The doping of colloidal semiconductor nanocrystals (NCs) presents an additional knob beyond size and shape for controlling the electronic properties. An important problem for impurity doping is associated with resolving the location and structural surrounding of the dopant within the small NCs, in light of tendency for driving of the impurity atom to the surface of the NC. A post-synthesis diffusion-based doping approach for introducing metal impurities into InAs NCs is described and characterized. This enables accurate correlation between the emerged electronic properties and the doping process. Optical absorption spectroscopy and scanning tunneling spectroscopy (STS) measurements revealed the n-type and p-type behavior of the doped NCs, depending on the identity of selected impurities. X-ray absorption fine structure (XAFS) spectroscopy measurements demonstrated the interstitial location of Cu within the InAs NCs, acting as an n-type dopant, which was found to occupy a single unique hexagonal interstitial site within the NC lattice for a wide range of doping levels.
    [Show full text]
  • Crossover from Auger Recombination to Charge Transfer † § ‡ ‡ ‡ Yuval Ben-Shahar, John P
    Letter Cite This: Nano Lett. 2018, 18, 5211−5216 pubs.acs.org/NanoLett Charge Carrier Dynamics in Photocatalytic Hybrid Semiconductor− Metal Nanorods: Crossover from Auger Recombination to Charge Transfer † § ‡ ‡ ‡ Yuval Ben-Shahar, John P. Philbin, Francesco Scotognella, Lucia Ganzer, Giulio Cerullo,*, § ∥ † Eran Rabani,*, , and Uri Banin*, † The Institute of Chemistry and Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel ‡ IFN-CNR, Dipartimento di Fisica, Politecnico di Milano, Milan 20133, Italy § Department of Chemistry, University of California and Lawrence Berkeley National Laboratory, Berkeley, California 94720-1460, United States ∥ The Sackler Institute for Computational Molecular and Materials Science, Tel Aviv University, Tel Aviv, Israel 69978 *S Supporting Information ABSTRACT: Hybrid semiconductor−metal nanoparticles (HNPs) manifest unique, synergistic electronic and optical properties as a result of combining semiconductor and metal physics via a controlled interface. These structures can exhibit spatial charge separation across the semiconductor−metal junction upon light absorption, enabling their use as photocatalysts. The combination of the photocatalytic activity of the metal domain with the ability to generate and accommodate multiple excitons in the semiconducting domain can lead to improved photocatalytic performance because injecting multiple charge carriers into the active catalytic sites can increase the quantum yield. Herein, we show a significant metal domain
    [Show full text]
  • Nanotechnology for Catalysis and Solar Energy Conversion
    Nanotechnology Nanotechnology 32 (2021) 042003 (28pp) https://doi.org/10.1088/1361-6528/abbce8 Roadmap Nanotechnology for catalysis and solar energy conversion U Banin1 , N Waiskopf1, L Hammarström2 , G Boschloo2, M Freitag2, E M J Johansson2,JSá2 , H Tian2 , M B Johnston3 , L M Herz3 , R L Milot4, M G Kanatzidis5 ,WKe5, I Spanopoulos5, K L Kohlstedt5 , G C Schatz5 , N Lewis6 , T Meyer7 , A J Nozik8,9 , M C Beard8 , F Armstrong10 , C F Megarity10, C A Schmuttenmaer11,12 , V S Batista11,13 and G W Brudvig11,13 1 The Institute of Chemistry and the Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel 2 Department of Chemistry—Ångström Laboratory, Uppsala University, Box 523, SE-75120 Uppsala, Sweden 3 Department of Physics, University of Oxford, Clarendon Laboratory, Parks Road, Oxford OX1 3PU, United Kingdom 4 Department of Physics, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, United Kingdom 5 Department of Chemistry, Northwestern University, Evanston, IL 60208, United States of America 6 Division of Chemistry and Chemical Engineering, and Beckman Institute, 210 Noyes Laboratory, 127-72 California Institute of Technology, Pasadena, CA 91125, United States of America 7 University of North Carolina at Chapel Hill, Department of Chemistry, United States of America 8 National Renewable Energy Laboratory, United States of America 9 University of Colorado, Boulder, CO, Department of Chemistry, 80309, United States of America 10 Department of Chemistry, University of Oxford, Oxford, United Kingdom 11 Department of Chemistry, Yale University, 225 Prospect St, New Haven, CT, 06520-8107, United States of America E-mail: [email protected], [email protected], [email protected], m- [email protected], [email protected], [email protected], nslewis@its.
    [Show full text]
  • Colloidal Quantum Dot Molecules Manifesting Quantum Coupling at Room Temperature
    ARTICLE https://doi.org/10.1038/s41467-019-13349-1 OPEN Colloidal quantum dot molecules manifesting quantum coupling at room temperature Jiabin Cui 1,2,3, Yossef E. Panfil1,2,3, Somnath Koley1,2,3, Doaa Shamalia1,2, Nir Waiskopf1,2, Sergei Remennik2, Inna Popov2, Meirav Oded1,2 & Uri Banin 1,2* Coupling of atoms is the basis of chemistry, yielding the beauty and richness of molecules. We utilize semiconductor nanocrystals as artificial atoms to form nanocrystal molecules that 1234567890():,; are structurally and electronically coupled. CdSe/CdS core/shell nanocrystals are linked to form dimers which are then fused via constrained oriented attachment. The possible nano- crystal facets in which such fusion takes place are analyzed with atomic resolution revealing the distribution of possible crystal fusion scenarios. Coherent coupling and wave-function hybridization are manifested by a redshift of the band gap, in agreement with quantum mechanical simulations. Single nanoparticle spectroscopy unravels the attributes of coupled nanocrystal dimers related to the unique combination of quantum mechanical tunneling and energy transfer mechanisms. This sets the stage for nanocrystal chemistry to yield a diverse selection of coupled nanocrystal molecules constructed from controlled core/shell nano- crystal building blocks. These are of direct relevance for numerous applications in displays, sensing, biological tagging and emerging quantum technologies. 1 Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel. 2 The Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel. 3These authors contributed equally: Jiabin Cui, Yossef E. Panfil, Somnath Koley. *email: [email protected] NATURE COMMUNICATIONS | (2019) 10:5401 | https://doi.org/10.1038/s41467-019-13349-1 | www.nature.com/naturecommunications 1 ARTICLE NATURE COMMUNICATIONS | https://doi.org/10.1038/s41467-019-13349-1 olloidal semiconductor quantum dots (CQDs) that con- hetero-plane-attachment in the fusion process.
    [Show full text]