Out-diffusion and precipitation of copper in silicon: An electrostatic model
1Department of Materials Science, University of California at Berkeley and Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
Physical Review Letters
|December 2, 2000
Summary
Copper behavior in silicon depends on initial concentration. Below critical levels, copper moves to the surface; above, it precipitates within the bulk material due to electrostatic interactions.
Area of Science:
- Materials Science
- Semiconductor Physics
- Solid-State Chemistry
Background:
- Understanding copper behavior in silicon is crucial for semiconductor device fabrication and reliability.
- Interstitial and precipitated copper species significantly impact silicon's electrical properties.
Purpose of the Study:
- To investigate the partitioning of copper between interstitial and precipitated phases in silicon.
- To determine the critical copper concentration influencing its distribution.
- To elucidate the mechanisms governing copper diffusion and precipitation in silicon.
Main Methods:
- Intentional high-temperature copper contamination of silicon.
- Rapid quenching to room temperature to freeze-in concentrations.
- Analysis of mobile interstitial and precipitated copper species.
Main Results:
- Copper predominantly diffuses to the surface below a critical contamination level.
- For higher initial concentrations, copper mainly precipitates within the silicon bulk.
- The critical contamination threshold is defined as the acceptor concentration plus 10^16 cm^-3.
- Electrostatic interactions between interstitial copper and precipitates explain this behavior.
Conclusions:
- Copper distribution in silicon is concentration-dependent, transitioning from surface diffusion to bulk precipitation.
- Electrostatic forces play a key role in governing copper's phase partitioning in silicon.
- The findings provide insights into controlling metallic impurities in semiconductor materials.
Related Concept Videos
Precipitation and Co-precipitation
Precipitation and coprecipitation methods can be used to separate a mixture of ions in a solution. In qualitative inorganic analysis, ions that form sparingly soluble precipitates with the same reagent are separated based on the differences in solubility products. For example, consider the separation of Cu(II) and Fe(II) ions by precipitation as insoluble sulfides. First, copper(II) sulfide is precipitated by the addition of acidic H2S, where the dissociation of H2S is suppressed. Adding H2S...
Electrodeposition
Electrodeposition is a technique used to separate an analyte from interferents by electrochemical processes. Here, the analyte is a metal ion that can be deposited on an electrode immersed in the sample solution. The electrochemical setup consists of an anode and a cathode. When an electric current is applied to the setup, oxidation occurs at the anode. At the cathode, which consists of a large metal surface, metal ions undergo reduction and deposit onto the surface.
Electrodeposition can...
Electrodeposition can...
Carrier Transport
The generation of electrical current in semiconductors is fundamentally driven by two mechanisms: drift and diffusion. These processes are essential for the functionality and performance of semiconductor-based devices.
Drift Current:
The drift of charge carriers is started by an external electric field (E). Charged particles, such as electrons and holes, experience an acceleration between collisions with lattice atoms. For electrons, this results in a drift velocity (vd) given by:
Drift Current:
The drift of charge carriers is started by an external electric field (E). Charged particles, such as electrons and holes, experience an acceleration between collisions with lattice atoms. For electrons, this results in a drift velocity (vd) given by:
Electrochemical Systems
Electrochemical systems provide a fascinating insight into the dynamic interplay of charged species within various phases. One notable example is the interaction between a membrane permeable to K⁺ ions but not to Cl⁻ ions, separating an aqueous KCl solution from pure water. As K⁺ ions diffuse through the membrane, they generate net charges on each phase, leading to a potential difference between them.Similarly, when a piece of Zn is immersed in an aqueous ZnSO₄ solution, the Zn metal, composed...
The Electrical Double Layer
In the region where two bulk phases meet, an intricate electric charge distribution arises due to charge transfer, ion adsorption, molecular orientation, and charge distortion. This complex distribution is commonly referred to as the electrical double layer.When a solid electrode interfaces with ions in an electrolyte solution, the speed of electron transfer dictates the rates of oxidation and reduction. The electrode acquires a charge through the escape of atoms into the solution as cations or...
Processes at Electrodes
The electrode interacts with ions in the electrolyte solution at its interface. The rate of oxidation and reduction depends on the speed at which electrons can transfer through this interface. As ions attach to or leave the electrode surface, the electrode acquires a charge, and an electrical potential forms across the interface, making the process more difficult to reach equilibrium. The charge on the electrode affects the local ion concentrations in the solution, though thermal motion...


