Oxygen vacancies effects in a‐IGZO: Formation mechanisms, hysteresis, and negative bias stress effects. Issue 6 (2nd March 2017)

• Record Type: Journal Article
• Authors: de Jamblinne de Meux, Albert; Bhoolokam, Ajay; Pourtois, Geoffrey; Genoe, Jan; Heremans, Paul
• Is Part Of: Physica status solidi. Volume 214:Issue 6(2017)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2017-03-02
• Subjects: a‐IGZO -- amorphous oxide semiconductors -- bias stress -- hysteresis -- oxygen vacancies; Solid state physics -- Periodicals; Solids -- Industrial applications -- Periodicals; 530.41
• DOI: 10.1002/pssa.201600889
• Languages: English
• ISSNs: 1862-6300

Abstract

Abstract : The amorphous oxide semiconductor Indium‐Gallium‐Zinc‐Oxide (a‐IGZO) has gained a large technological relevance as a semiconductor for thin‐film transistors in active‐matrix displays. Yet, major questions remain unanswered regarding the atomic origin of threshold voltage control, doping level, hysteresis, negative bias stress (NBS), and negative bias illumination stress (NBIS). We undertake a systematic study of the effects of oxygen vacancies on the properties of a‐IGZO by relating experimental observations to microscopic insights gained from first‐principle simulations. It is found that the amorphous nature of the semiconductor allows unusually large atomic relaxations. In some cases, oxygen vacancies are found to behave as perfect shallow donors without the formation of structural defects. Once structural defects are formed, their transition states can vary upon charge and discharge cycles. We associate this phenomenon to a possible presence of hysteresis in the transfer curve of the devices. Under NBS, the creation of oxygen vacancies becomes energetically very stable, hence thermodynamically very likely. This generation process is correlated with the occurrence of the negative bias stress instabilities observed in a‐IGZO transistors. While oxygen vacancies can therefore be related to NBS and hysteresis, it appears unlikely from our results that they are direct causes of NBIS, contrary to common belief.