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Indium tin oxide

About: Indium tin oxide is a research topic. Over the lifetime, 17857 publications have been published within this topic receiving 402127 citations. The topic is also known as: indium tin oxide.


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Journal ArticleDOI
TL;DR: In this paper, the effect of CdCl2 treatment on CdTe and CdS has been studied with X-ray diffraction and scanning electron microscopy, showing that an increase in the grain size and the loss of the preferred (111) growth orientation has been observed.

94 citations

Journal ArticleDOI
TL;DR: Amorphous Co3O4 nanoparticle/graphene composites were fabricated via layer-by-layer assembly onto indium tin oxide (ITO) coated conductive glass and applied as a catalyst for efficient oxygen evolution reaction in electrolytic water splitting as mentioned in this paper.
Abstract: Amorphous Co3O4 nanoparticle/graphene composites (Co3O4/GR) were fabricated via layer-by-layer (LBL) assembly onto indium tin oxide (ITO) coated conductive glass and applied as a catalyst for efficient oxygen evolution reaction in electrolytic water splitting. A thin uniform graphene layer was deposited onto the ITO surface through electrophoretic deposition (EPD), followed by subsequent deposition of a thin layer of Co3O4 nanoparticles onto the graphene surface by chemical bath deposition (CBD) to yield a transparent Co3O4/GR bi-layer. X-ray diffraction spectroscopy (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) were employed to characterise the fabricated composites. The layered Co3O4/GR composite is applied for electrocatalytic oxygen evolution reaction (OER) in 0.1 M KOH and exhibits remarkable catalytic activity with a high Faradaic efficiency (95%) and excellent long-term stability.

94 citations

Journal ArticleDOI
Ho-Chul Lee1, O Ok Park2
26 Jul 2004-Vacuum
TL;DR: In this paper, the authors measured carrier concentrations and mobilities of indium-tin-oxide (ITO) thin films by DC magnetron sputtering at various process temperatures using the Hall Technique.

93 citations

Journal ArticleDOI
TL;DR: In this paper, the degradation and failure of an organic light-emitting device are observed via optical microscopy and the degradation area is identified to be made up of three regions: (1) a dark spot at the center, (2) a nonemitting area forming the core and (3) a weakly emitting area surrounding the core.
Abstract: The degradation and failure of organic light-emitting device are observed via optical microscopy. The “degraded area” has been identified to be made up of three regions: (1) a dark spot at the center, (2) a nonemitting area forming the core, and (3) a weakly emitting area surrounding the core. It is found that due to metal migration, as evidenced from the secondary ion mass spectrometry profiles, the indium tin oxide/polymer interface roughens during operation. The intense local current at sharp points degrades the polymer causing the formation of the dark center. Further current stress caused the central core to carbonize which may lead to short and/or open circuits accompanied by fluctuations in the device current.

93 citations

Journal ArticleDOI
06 Jun 2006-Langmuir
TL;DR: The work function of indium tin oxide (ITO) substrates was modified with phosphonic acid molecular films and the absolute work functions of nitrophenyl- and cyanophenyl-phosphonic acid films in ITO were determined by Kelvin probe measurement to be 5.60 and 5.77 eV.
Abstract: The work function of indium tin oxide (ITO) substrates was modified with phosphonic acid molecular films. The ITO surfaces were treated prior to functionalization with a base cleaning procedure. The film growth and coverage were quantified by contact angle goniometry and XPS. Film orientation was determined by reflection/absorption infrared spectroscopy using ITO-on-Cr substrates. The absolute work functions of nitrophenyl- and cyanophenyl-phosphonic acid films in ITO were determined by Kelvin probe measurement to be 5.60 and 5.77 eV, respectively.

93 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023343
2022730
2021537
2020684
2019804
2018838