Surface studies of crystalline and amorphous Zn-In-Sn-O transparent conducting oxides
Identifieur interne : 001454 ( Main/Repository ); précédent : 001453; suivant : 001455Surface studies of crystalline and amorphous Zn-In-Sn-O transparent conducting oxides
Auteurs : RBID : Pascal:12-0296700Descripteurs français
- Pascal (Inist)
- Spectre photoélectron UV, Dépôt physique phase vapeur, Couche mince, Dépôt laser pulsé, Niveau coeur, Niveau énergie, Energie liaison, Niveau Fermi, Structure électronique, Addition étain, Travail sortie, Potentiel ionisation, Sonde Kelvin, Addition antimoine, Oxyde d'indium, Oxyde d'étain, Oxyde de zinc, Addition aluminium, Spectre photoélectron RX, In2O3, SnO2, ZnO, 8115C, 8115F, 7320, 7320A.
English descriptors
- KwdEn :
- Aluminium additions, Antimony additions, Binding energy, Core levels, Electronic structure, Energy levels, Fermi level, Indium oxide, Ionization potential, Kelvin probe, Physical vapor deposition, Pulsed laser deposition, Thin films, Tin additions, Tin oxide, Ultraviolet photoelectron spectra, Work functions, X-ray photoelectron spectra, Zinc oxide.
Abstract
X-ray and ultraviolet photoelectron spectroscopy (UPS) studies were made of in situ RF magnetron-sputtered crystalline (c) and amorphous (a) Zn-In-Sn-O (ZITO) thin films, ex situ pulsed laser deposited c- and a-ZITO thin films, and bulk ZITO ceramics. Cosubstitution of Zn and Sn for In results in an increase of the In core level binding energy at a given Fermi level compared to that measured in undoped and Sn-doped In2O3 (ITO). In plots of work function vs. Fermi level, in situ c-ZITO and a-ZITO films have low ionization potentials (7.0-7.7 eV) that are similar to undoped In2O3. In contrast, dry-air-annealed in situ films, ex situ films, and bulk ceramics have higher ionization potentials (7.7-8.1 eV) that are more similar to ITO and match well with previous work on air-exposed surfaces. Kelvin Probe measurements were made of select a-ZITO films exposed to air and ultraviolet/ozone-treated so as to measure work functions under conditions commonly employed for device fabrication. Results (4.8-5.3 eV) were in good agreement with the UPS work functions of oxygen-exposed materials and with literature values. Lastly, a parallelogram plot of work function vs. Fermi level shows that a wider range of work functions is achievable in ZITO materials as compared to other transparent conducting oxides (Sb-doped SnO2, Al-doped ZnO, Sn-doped In2O3), making ZITO more versatile for applications.
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Pascal:12-0296700Le document en format XML
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<term>Electronic structure</term>
<term>Energy levels</term>
<term>Fermi level</term>
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<term>Kelvin probe</term>
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<term>Pulsed laser deposition</term>
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<term>Couche mince</term>
<term>Dépôt laser pulsé</term>
<term>Niveau coeur</term>
<term>Niveau énergie</term>
<term>Energie liaison</term>
<term>Niveau Fermi</term>
<term>Structure électronique</term>
<term>Addition étain</term>
<term>Travail sortie</term>
<term>Potentiel ionisation</term>
<term>Sonde Kelvin</term>
<term>Addition antimoine</term>
<term>Oxyde d'indium</term>
<term>Oxyde d'étain</term>
<term>Oxyde de zinc</term>
<term>Addition aluminium</term>
<term>Spectre photoélectron RX</term>
<term>In2O3</term>
<term>SnO2</term>
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<front><div type="abstract" xml:lang="en">X-ray and ultraviolet photoelectron spectroscopy (UPS) studies were made of in situ RF magnetron-sputtered crystalline (c) and amorphous (a) Zn-In-Sn-O (ZITO) thin films, ex situ pulsed laser deposited c- and a-ZITO thin films, and bulk ZITO ceramics. Cosubstitution of Zn and Sn for In results in an increase of the In core level binding energy at a given Fermi level compared to that measured in undoped and Sn-doped In<sub>2</sub>
O<sub>3</sub>
(ITO). In plots of work function vs. Fermi level, in situ c-ZITO and a-ZITO films have low ionization potentials (7.0-7.7 eV) that are similar to undoped In<sub>2</sub>
O<sub>3</sub>
. In contrast, dry-air-annealed in situ films, ex situ films, and bulk ceramics have higher ionization potentials (7.7-8.1 eV) that are more similar to ITO and match well with previous work on air-exposed surfaces. Kelvin Probe measurements were made of select a-ZITO films exposed to air and ultraviolet/ozone-treated so as to measure work functions under conditions commonly employed for device fabrication. Results (4.8-5.3 eV) were in good agreement with the UPS work functions of oxygen-exposed materials and with literature values. Lastly, a parallelogram plot of work function vs. Fermi level shows that a wider range of work functions is achievable in ZITO materials as compared to other transparent conducting oxides (Sb-doped SnO<sub>2</sub>
, Al-doped ZnO, Sn-doped In<sub>2</sub>
O<sub>3</sub>
), making ZITO more versatile for applications.</div>
</front>
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<fC01 i1="01" l="ENG"><s0>X-ray and ultraviolet photoelectron spectroscopy (UPS) studies were made of in situ RF magnetron-sputtered crystalline (c) and amorphous (a) Zn-In-Sn-O (ZITO) thin films, ex situ pulsed laser deposited c- and a-ZITO thin films, and bulk ZITO ceramics. Cosubstitution of Zn and Sn for In results in an increase of the In core level binding energy at a given Fermi level compared to that measured in undoped and Sn-doped In<sub>2</sub>
O<sub>3</sub>
(ITO). In plots of work function vs. Fermi level, in situ c-ZITO and a-ZITO films have low ionization potentials (7.0-7.7 eV) that are similar to undoped In<sub>2</sub>
O<sub>3</sub>
. In contrast, dry-air-annealed in situ films, ex situ films, and bulk ceramics have higher ionization potentials (7.7-8.1 eV) that are more similar to ITO and match well with previous work on air-exposed surfaces. Kelvin Probe measurements were made of select a-ZITO films exposed to air and ultraviolet/ozone-treated so as to measure work functions under conditions commonly employed for device fabrication. Results (4.8-5.3 eV) were in good agreement with the UPS work functions of oxygen-exposed materials and with literature values. Lastly, a parallelogram plot of work function vs. Fermi level shows that a wider range of work functions is achievable in ZITO materials as compared to other transparent conducting oxides (Sb-doped SnO<sub>2</sub>
, Al-doped ZnO, Sn-doped In<sub>2</sub>
O<sub>3</sub>
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<s5>07</s5>
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<s5>08</s5>
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<s5>08</s5>
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<s5>09</s5>
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<s5>09</s5>
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<s5>10</s5>
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<s5>10</s5>
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<s5>11</s5>
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<s5>11</s5>
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<s5>12</s5>
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<s5>12</s5>
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<s5>13</s5>
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<s5>13</s5>
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<s5>13</s5>
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<s5>14</s5>
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<s5>14</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE"><s0>Oxyde d'indium</s0>
<s5>15</s5>
</fC03>
<fC03 i1="15" i2="X" l="ENG"><s0>Indium oxide</s0>
<s5>15</s5>
</fC03>
<fC03 i1="15" i2="X" l="SPA"><s0>Indio óxido</s0>
<s5>15</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE"><s0>Oxyde d'étain</s0>
<s5>16</s5>
</fC03>
<fC03 i1="16" i2="X" l="ENG"><s0>Tin oxide</s0>
<s5>16</s5>
</fC03>
<fC03 i1="16" i2="X" l="SPA"><s0>Estaño óxido</s0>
<s5>16</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE"><s0>Oxyde de zinc</s0>
<s5>17</s5>
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<fC03 i1="17" i2="X" l="ENG"><s0>Zinc oxide</s0>
<s5>17</s5>
</fC03>
<fC03 i1="17" i2="X" l="SPA"><s0>Zinc óxido</s0>
<s5>17</s5>
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<s5>29</s5>
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<s4>INC</s4>
<s5>46</s5>
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<s5>47</s5>
</fC03>
<fC03 i1="22" i2="3" l="FRE"><s0>ZnO</s0>
<s4>INC</s4>
<s5>48</s5>
</fC03>
<fC03 i1="23" i2="3" l="FRE"><s0>8115C</s0>
<s4>INC</s4>
<s5>71</s5>
</fC03>
<fC03 i1="24" i2="3" l="FRE"><s0>8115F</s0>
<s4>INC</s4>
<s5>72</s5>
</fC03>
<fC03 i1="25" i2="3" l="FRE"><s0>7320</s0>
<s4>INC</s4>
<s5>73</s5>
</fC03>
<fC03 i1="26" i2="3" l="FRE"><s0>7320A</s0>
<s4>INC</s4>
<s5>74</s5>
</fC03>
<fN21><s1>226</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>
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