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Formation and dissolution of D-N complexes in dilute nitrides
Deuterium (hydrogen) incorporation in dilute nitrides (e.g., GaAsN and GaPN) modifies dramatically the crystal's electronic and structural properties and represents a prominent example of defect engineering in semiconductors. However, the microscopic origin of D-related effects is still an expe...
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Published in: | Physical review. B, Condensed matter and materials physics Condensed matter and materials physics, 2007-11, Vol.76 (20), Article 205323 |
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creator | Berti, Marina Bisognin, Gabriele De Salvador, Davide Napolitani, Enrico Vangelista, Silvia Polimeni, Antonio Capizzi, Mario Boscherini, Federico Ciatto, Gianluca Rubini, Silvia Martelli, Faustino Franciosi, Alfonso |
description | Deuterium (hydrogen) incorporation in dilute nitrides (e.g., GaAsN and GaPN) modifies dramatically the crystal's electronic and structural properties and represents a prominent example of defect engineering in semiconductors. However, the microscopic origin of D-related effects is still an experimentally unresolved issue. In this paper, we used nuclear reaction analyses and/or channeling, high resolution x-ray diffraction, photoluminescence, and x-ray absorption fine structure measurements to determine how the stoichiometric [D]/[N] ratio and the local structure of the N-D complexes parallel the evolution of the GaAsN electronic and strain properties upon irradiation and controlled removal of D. The experimental results provide the following picture: (i) Upon deuteration, nitrogen-deuterium complexes form with [D]/[N]=3, leading to a neutralization of the N electronic effects in GaAs and to a strain reversal (from tensile to compressive) of the N-containing layer. (ii) A moderate annealing at 250 deg. C gives [D]/[N]=2 and removes the compressive strain, therefore the lattice parameter approaches that of the N-free alloy, whereas the N-induced electronic properties are still passivated. (iii) Finally, annealings at higher temperature (330 deg. C) dissolve the deuterium-nitrogen complexes, and consequently the electronic properties and the tensile strain of the as-grown GaAsN lattice are recovered. Therefore, we conclude that the complex responsible for N passivation contains two deuterium atoms per nitrogen atom, while strain reversal in deuterated GaAsN is due to a complex with a third, less tightly bound deuterium atom. |
doi_str_mv | 10.1103/PhysRevB.76.205323 |
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However, the microscopic origin of D-related effects is still an experimentally unresolved issue. In this paper, we used nuclear reaction analyses and/or channeling, high resolution x-ray diffraction, photoluminescence, and x-ray absorption fine structure measurements to determine how the stoichiometric [D]/[N] ratio and the local structure of the N-D complexes parallel the evolution of the GaAsN electronic and strain properties upon irradiation and controlled removal of D. The experimental results provide the following picture: (i) Upon deuteration, nitrogen-deuterium complexes form with [D]/[N]=3, leading to a neutralization of the N electronic effects in GaAs and to a strain reversal (from tensile to compressive) of the N-containing layer. (ii) A moderate annealing at 250 deg. C gives [D]/[N]=2 and removes the compressive strain, therefore the lattice parameter approaches that of the N-free alloy, whereas the N-induced electronic properties are still passivated. (iii) Finally, annealings at higher temperature (330 deg. C) dissolve the deuterium-nitrogen complexes, and consequently the electronic properties and the tensile strain of the as-grown GaAsN lattice are recovered. Therefore, we conclude that the complex responsible for N passivation contains two deuterium atoms per nitrogen atom, while strain reversal in deuterated GaAsN is due to a complex with a third, less tightly bound deuterium atom.</description><identifier>ISSN: 1098-0121</identifier><identifier>EISSN: 1550-235X</identifier><identifier>DOI: 10.1103/PhysRevB.76.205323</identifier><language>eng</language><publisher>United States</publisher><subject>ABSORPTION ; ANNEALING ; CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY ; CRYSTAL DEFECTS ; DEUTERIUM ; ELECTRONIC STRUCTURE ; FINE STRUCTURE ; GALLIUM ARSENIDES ; HYDROGEN ; IMPURITIES ; LATTICE PARAMETERS ; NITRIDES ; NITROGEN ; NITROGEN COMPLEXES ; NUCLEAR REACTION ANALYSIS ; PHOTOLUMINESCENCE ; SEMICONDUCTOR MATERIALS ; STRAINS ; X RADIATION ; X-RAY DIFFRACTION ; X-RAY SPECTRA</subject><ispartof>Physical review. 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B, Condensed matter and materials physics</title><description>Deuterium (hydrogen) incorporation in dilute nitrides (e.g., GaAsN and GaPN) modifies dramatically the crystal's electronic and structural properties and represents a prominent example of defect engineering in semiconductors. However, the microscopic origin of D-related effects is still an experimentally unresolved issue. In this paper, we used nuclear reaction analyses and/or channeling, high resolution x-ray diffraction, photoluminescence, and x-ray absorption fine structure measurements to determine how the stoichiometric [D]/[N] ratio and the local structure of the N-D complexes parallel the evolution of the GaAsN electronic and strain properties upon irradiation and controlled removal of D. The experimental results provide the following picture: (i) Upon deuteration, nitrogen-deuterium complexes form with [D]/[N]=3, leading to a neutralization of the N electronic effects in GaAs and to a strain reversal (from tensile to compressive) of the N-containing layer. (ii) A moderate annealing at 250 deg. C gives [D]/[N]=2 and removes the compressive strain, therefore the lattice parameter approaches that of the N-free alloy, whereas the N-induced electronic properties are still passivated. (iii) Finally, annealings at higher temperature (330 deg. C) dissolve the deuterium-nitrogen complexes, and consequently the electronic properties and the tensile strain of the as-grown GaAsN lattice are recovered. Therefore, we conclude that the complex responsible for N passivation contains two deuterium atoms per nitrogen atom, while strain reversal in deuterated GaAsN is due to a complex with a third, less tightly bound deuterium atom.</description><subject>ABSORPTION</subject><subject>ANNEALING</subject><subject>CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY</subject><subject>CRYSTAL DEFECTS</subject><subject>DEUTERIUM</subject><subject>ELECTRONIC STRUCTURE</subject><subject>FINE STRUCTURE</subject><subject>GALLIUM ARSENIDES</subject><subject>HYDROGEN</subject><subject>IMPURITIES</subject><subject>LATTICE PARAMETERS</subject><subject>NITRIDES</subject><subject>NITROGEN</subject><subject>NITROGEN COMPLEXES</subject><subject>NUCLEAR REACTION ANALYSIS</subject><subject>PHOTOLUMINESCENCE</subject><subject>SEMICONDUCTOR MATERIALS</subject><subject>STRAINS</subject><subject>X RADIATION</subject><subject>X-RAY DIFFRACTION</subject><subject>X-RAY SPECTRA</subject><issn>1098-0121</issn><issn>1550-235X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNo1kE9LxDAUxIMouK5-AU8Fz6n50zTtwYOurgqLiih4C2nywkbaZkmiuN_e6urpzWOGYfghdEpJSSnh50_rbXqGz6tS1iUjgjO-h2ZUCIIZF2_7kyZtgwll9BAdpfROCK3ais3QxTLEQWcfxkKPtrA-pdB__P7BFdf4oTBh2PTwBanw4-RPJhSjz9FbSMfowOk-wcnfnaPX5c3L4g6vHm_vF5crbJgUGVNbVbbTppbtNKNuJOjKMKZr13TOcsmJ7LhztuaVdqCNJlKD5ZQ24DqjJZ-js11vSNmrZHwGszZhHMFkxSgRTDbtlGK7lIkhpQhObaIfdNwqStQPJvWPScla7TDxb5hvXaE</recordid><startdate>20071101</startdate><enddate>20071101</enddate><creator>Berti, Marina</creator><creator>Bisognin, Gabriele</creator><creator>De Salvador, Davide</creator><creator>Napolitani, Enrico</creator><creator>Vangelista, Silvia</creator><creator>Polimeni, Antonio</creator><creator>Capizzi, Mario</creator><creator>Boscherini, Federico</creator><creator>Ciatto, Gianluca</creator><creator>Rubini, Silvia</creator><creator>Martelli, Faustino</creator><creator>Franciosi, Alfonso</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>20071101</creationdate><title>Formation and dissolution of D-N complexes in dilute nitrides</title><author>Berti, Marina ; Bisognin, Gabriele ; De Salvador, Davide ; Napolitani, Enrico ; Vangelista, Silvia ; Polimeni, Antonio ; Capizzi, Mario ; Boscherini, Federico ; Ciatto, Gianluca ; Rubini, Silvia ; Martelli, Faustino ; Franciosi, Alfonso</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c275t-1d44dbac679098687ea4c22a6f8bfd37307b3ffd634afeaca07aed3118efbca73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>ABSORPTION</topic><topic>ANNEALING</topic><topic>CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY</topic><topic>CRYSTAL DEFECTS</topic><topic>DEUTERIUM</topic><topic>ELECTRONIC STRUCTURE</topic><topic>FINE STRUCTURE</topic><topic>GALLIUM ARSENIDES</topic><topic>HYDROGEN</topic><topic>IMPURITIES</topic><topic>LATTICE PARAMETERS</topic><topic>NITRIDES</topic><topic>NITROGEN</topic><topic>NITROGEN COMPLEXES</topic><topic>NUCLEAR REACTION ANALYSIS</topic><topic>PHOTOLUMINESCENCE</topic><topic>SEMICONDUCTOR MATERIALS</topic><topic>STRAINS</topic><topic>X RADIATION</topic><topic>X-RAY DIFFRACTION</topic><topic>X-RAY SPECTRA</topic><toplevel>online_resources</toplevel><creatorcontrib>Berti, Marina</creatorcontrib><creatorcontrib>Bisognin, Gabriele</creatorcontrib><creatorcontrib>De Salvador, Davide</creatorcontrib><creatorcontrib>Napolitani, Enrico</creatorcontrib><creatorcontrib>Vangelista, Silvia</creatorcontrib><creatorcontrib>Polimeni, Antonio</creatorcontrib><creatorcontrib>Capizzi, Mario</creatorcontrib><creatorcontrib>Boscherini, Federico</creatorcontrib><creatorcontrib>Ciatto, Gianluca</creatorcontrib><creatorcontrib>Rubini, Silvia</creatorcontrib><creatorcontrib>Martelli, Faustino</creatorcontrib><creatorcontrib>Franciosi, Alfonso</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Physical review. B, Condensed matter and materials physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Berti, Marina</au><au>Bisognin, Gabriele</au><au>De Salvador, Davide</au><au>Napolitani, Enrico</au><au>Vangelista, Silvia</au><au>Polimeni, Antonio</au><au>Capizzi, Mario</au><au>Boscherini, Federico</au><au>Ciatto, Gianluca</au><au>Rubini, Silvia</au><au>Martelli, Faustino</au><au>Franciosi, Alfonso</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Formation and dissolution of D-N complexes in dilute nitrides</atitle><jtitle>Physical review. B, Condensed matter and materials physics</jtitle><date>2007-11-01</date><risdate>2007</risdate><volume>76</volume><issue>20</issue><artnum>205323</artnum><issn>1098-0121</issn><eissn>1550-235X</eissn><abstract>Deuterium (hydrogen) incorporation in dilute nitrides (e.g., GaAsN and GaPN) modifies dramatically the crystal's electronic and structural properties and represents a prominent example of defect engineering in semiconductors. However, the microscopic origin of D-related effects is still an experimentally unresolved issue. In this paper, we used nuclear reaction analyses and/or channeling, high resolution x-ray diffraction, photoluminescence, and x-ray absorption fine structure measurements to determine how the stoichiometric [D]/[N] ratio and the local structure of the N-D complexes parallel the evolution of the GaAsN electronic and strain properties upon irradiation and controlled removal of D. The experimental results provide the following picture: (i) Upon deuteration, nitrogen-deuterium complexes form with [D]/[N]=3, leading to a neutralization of the N electronic effects in GaAs and to a strain reversal (from tensile to compressive) of the N-containing layer. (ii) A moderate annealing at 250 deg. C gives [D]/[N]=2 and removes the compressive strain, therefore the lattice parameter approaches that of the N-free alloy, whereas the N-induced electronic properties are still passivated. (iii) Finally, annealings at higher temperature (330 deg. C) dissolve the deuterium-nitrogen complexes, and consequently the electronic properties and the tensile strain of the as-grown GaAsN lattice are recovered. Therefore, we conclude that the complex responsible for N passivation contains two deuterium atoms per nitrogen atom, while strain reversal in deuterated GaAsN is due to a complex with a third, less tightly bound deuterium atom.</abstract><cop>United States</cop><doi>10.1103/PhysRevB.76.205323</doi></addata></record> |
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subjects | ABSORPTION ANNEALING CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY CRYSTAL DEFECTS DEUTERIUM ELECTRONIC STRUCTURE FINE STRUCTURE GALLIUM ARSENIDES HYDROGEN IMPURITIES LATTICE PARAMETERS NITRIDES NITROGEN NITROGEN COMPLEXES NUCLEAR REACTION ANALYSIS PHOTOLUMINESCENCE SEMICONDUCTOR MATERIALS STRAINS X RADIATION X-RAY DIFFRACTION X-RAY SPECTRA |
title | Formation and dissolution of D-N complexes in dilute nitrides |
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