Abstract
The quinhydrone/methanol treatment has been reported to yield outstanding passivation of the H-terminated Si(100) surface. Here, we report on the mechanism of this process by comparing the resulting surface to that of freshly etched H-terminated Si, of Si with chemically grown oxide, and of Si treated with hydroquinone/methanol solution of the same concentration. We find that the benzoquinone moieties of the quinhydrone react with the surface to yield a Si-hydroquinone surface termination, while the methanol molecules bind as well to form methoxy-terminated Si. The slightly negative-charged benzene ring of the hydroquinone acts to repel majority carrier electrons from the surface and inhabits the surface recombination. The higher the ratio of surface-bound hydroquinone to surface-bound methoxy species, the larger the minority carrier life-time measured by microwave photoconductivity. Thus, our results lead us to conclude that this treatment results in field effect passivation; remarkably, this effect is caused by a molecular monolayer alone.
| Original language | English |
|---|---|
| Article number | 084909 |
| Journal | Journal of Applied Physics |
| Volume | 113 |
| Issue number | 8 |
| DOIs | |
| State | Published - 28 Feb 2013 |
| Externally published | Yes |
Funding
This work was supported in part by grants from the Wolfson Family trust, the Nancy and Stephen Grand Center for Sensors & Security, the Leona M. and Harry B. Helmsley Charitable Trust, the Snyder Family Foundation, and the Israel Ministry of Science. DC holds the Rowland and Sylvia Schaefer Chair in Energy Research.
| Funders | Funder number |
|---|---|
| Israel Ministry of Science | |
| Nancy and Stephen Grand Center for Sensors & Security | |
| Wolfson Family trust | |
| Leona M. and Harry B. Helmsley Charitable Trust |