Specific Process Knowledge/Wafer cleaning/RCA: Difference between revisions

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[[Image:RCA-bænk_RR2_0.JPG|300x300px|thumb|RCA bench: positioned in cleanroom B1. <br /> RCA1 - RCA2 - HF - BHF(pre-dep wafers)]]
[[Image:RCA-bænk_RR2_0.JPG|300x300px|thumb|RCA bench: positioned in cleanroom B1. <br /> RCA1 - RCA2 - HF - BHF(pre-dep wafers)]]


The RCA cleaning procedure was originally developed by the Radio Corporation of America (RCA) as part of manufacturing electron tube components. This process has since been adapted to silicon semiconductor processing. RCA is a two-step process (RCA1 and RCA2), and RCA1 should always be made before RCA2 because removing organic contaminants is a requirement before metal contaminants can be removed effectively.<br>  
The RCA cleaning procedure was originally developed by the Radio Corporation of America (RCA) as part of manufacturing electron tube components. This process has since been adapted to silicon semiconductor processing. RCA is a two-step process (RCA1 and RCA2, sometimes referred to as SC-1 and SC-2 (Standard Clean)), and RCA1 should always be made before RCA2 because removing organic contaminants is a requirement before metal contaminants can be removed effectively.<br>  


RCA1 is a powerful oxidizer and will thus remove organic contaminants. The ammonium hydroxide in RCA1 also has good solvating power as it can complex metals such as Cu, Ag, Ni, Co and Cd into solution. RCA2 forms soluble complexes with heavy metals and also shows cleaning action similar to that of piranha solutions. Furthermore, solutions of hydrochloric acid, which is a major constituent of RCA2, has proven effective at removing alkali metal ions. It is important that the chemicals used are very clean. RCA mixtures are therefore only used for up to a few batches (boats) of wafers and once an RCA mixture has cooled down it should not be reheated/reused. A new mixture should be made instead. Since RCA1 and RCA2 can oxidize silicon to silicon dioxide, an HF dip can be used to remove the thin oxide formed during RCA clean.<br \>
RCA1 is a powerful oxidizer and will thus remove organic contaminants. The ammonium hydroxide in RCA1 also has good solvating power as it can complex metals such as Cu, Ag, Ni, Co and Cd into solution. RCA2 forms soluble complexes with heavy metals and also shows cleaning action similar to that of piranha solutions. Furthermore, solutions of hydrochloric acid, which is a major constituent of RCA2, has proven effective at removing alkali metal ions. RCA2 is effective at removing metal hydroxide traces that cannot be removed in ammonia-containing solutions such as RCA1. These include Al(OH)<sub>3</sub>, Fe(OH)<sub>3</sub>, Mg(OH)<sub>2</sub> and Zn(OH)<sub>2</sub>. It is important that the chemicals used are very clean. RCA mixtures are therefore only used shortly after mixing and for a limited number of samples.<br>


Since RCA1 can oxidize silicon to silicon dioxide, an HF dip is sometimes used between RCA1 and RCA2. This will also remove contaminants that can be trapped in the formed oxide. This step can also be omitted, since RCA1 removes the native oxide and then re-oxidizes the surface. This in itself has a cleaning action. It is generally not advised to do an HF dip after RCA-2 if the samples will be processed by wet chemical processes afterwards. This is because the hydrogenated surface will be extremely reactive and therefore attract contaminants from both the air and processing liquids. In this case it is better to continue processing with the passivated oxide surface. For furnace processes, an HF dip after RCA-2 makes more sense (but ideally the wafers should be transferred to the furnace processes immediately).<br>


The RCA clean is used for cleaning wafers before taking them into the furnaces and a few other equipments (check the cross contamination sheet). As mentioned above a crucial part of the RCA cleaning procedure is the oxidation by H<sub>2</sub>O<sub>2</sub> at elevated temperatures. Therefore, the lifetime of RCA1 and RCA2 solutions is limited to about 1 hour after preparation and heating to 70<sup>o</sup>C because H<sub>2</sub>O<sub>2</sub> decomposes at this temperature.
As mentioned above a crucial part of the RCA cleaning procedure is the oxidation by H<sub>2</sub>O<sub>2</sub> at elevated temperatures. Therefore, the lifetime of RCA1 and RCA2 solutions is limited to about 1 hour after preparation since heating to 70<sup>o</sup>C because H<sub>2</sub>O<sub>2</sub> decomposes at this temperature.


*RCA1 contains: H<sub>2</sub>O, NH<sub>4</sub>OH and H<sub>2</sub>O<sub>2</sub> (5:1:1). It is used for removal of light organics, particles and metals.<br>
*RCA1 contains: H<sub>2</sub>O, NH<sub>4</sub>OH and H<sub>2</sub>O<sub>2</sub> (5:1:1). It is used for removal of light organics, particles and metals.<br>
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*'''RCA1: 10 min'''
*'''RCA1: 10 min'''
*DI water rinsing (dumping three times)
*DI water rinsing (dumping three times)
*HF: 30 sec (you may avoid this step in case of a very thin oxide (0-200 Å) as the top layer)
*Optional: HF: 30 sec (you may avoid this step in case of a very thin oxide (0-200 Å) as the top layer)
*DI water rinsing (bubbler)<br>
*DI water rinsing (bubbler)<br>
*'''RCA2: 10 min'''
*'''RCA2: 10 min'''

Revision as of 12:22, 15 May 2019

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RCA cleaning

RCA bench: positioned in cleanroom B1.
RCA1 - RCA2 - HF - BHF(pre-dep wafers)

The RCA cleaning procedure was originally developed by the Radio Corporation of America (RCA) as part of manufacturing electron tube components. This process has since been adapted to silicon semiconductor processing. RCA is a two-step process (RCA1 and RCA2, sometimes referred to as SC-1 and SC-2 (Standard Clean)), and RCA1 should always be made before RCA2 because removing organic contaminants is a requirement before metal contaminants can be removed effectively.

RCA1 is a powerful oxidizer and will thus remove organic contaminants. The ammonium hydroxide in RCA1 also has good solvating power as it can complex metals such as Cu, Ag, Ni, Co and Cd into solution. RCA2 forms soluble complexes with heavy metals and also shows cleaning action similar to that of piranha solutions. Furthermore, solutions of hydrochloric acid, which is a major constituent of RCA2, has proven effective at removing alkali metal ions. RCA2 is effective at removing metal hydroxide traces that cannot be removed in ammonia-containing solutions such as RCA1. These include Al(OH)3, Fe(OH)3, Mg(OH)2 and Zn(OH)2. It is important that the chemicals used are very clean. RCA mixtures are therefore only used shortly after mixing and for a limited number of samples.

Since RCA1 can oxidize silicon to silicon dioxide, an HF dip is sometimes used between RCA1 and RCA2. This will also remove contaminants that can be trapped in the formed oxide. This step can also be omitted, since RCA1 removes the native oxide and then re-oxidizes the surface. This in itself has a cleaning action. It is generally not advised to do an HF dip after RCA-2 if the samples will be processed by wet chemical processes afterwards. This is because the hydrogenated surface will be extremely reactive and therefore attract contaminants from both the air and processing liquids. In this case it is better to continue processing with the passivated oxide surface. For furnace processes, an HF dip after RCA-2 makes more sense (but ideally the wafers should be transferred to the furnace processes immediately).

As mentioned above a crucial part of the RCA cleaning procedure is the oxidation by H2O2 at elevated temperatures. Therefore, the lifetime of RCA1 and RCA2 solutions is limited to about 1 hour after preparation since heating to 70oC because H2O2 decomposes at this temperature.

  • RCA1 contains: H2O, NH4OH and H2O2 (5:1:1). It is used for removal of light organics, particles and metals.
  • RCA2 contains: H2O, HCl and H2O2 (5:1:1). It is used for removal of heavy metals, metal hydroxides, and residual metals including alkali metals.

You can find the APV for the RCA bench here

RCA procedure

  • RCA1: 10 min
  • DI water rinsing (dumping three times)
  • Optional: HF: 30 sec (you may avoid this step in case of a very thin oxide (0-200 Å) as the top layer)
  • DI water rinsing (bubbler)
  • RCA2: 10 min
  • DI water rinsing (dumping three times)
  • Optional: HF: 30 sec (avoid it if you have a very thin oxide (0-200 Å) as the top layer)
  • DI water rinsing (bubbler)

For procedure details please look in the user manual in LabManager.


The user manual, user APV and contact information can be found in LabManager: RCA info page in LabManager

Overview of RCA process data

RCA1 RCA2 HF
General description

Used for removal of light organics, particles and desorption of trace metals (Au, Ag, Ni, Cd, Zn, Co, Cr, etc).

Used for removal of alkali ions, metal hydroxides (of Al, Fe, Mg, Zn) and residual trace metals (e.g. Cu and Au).

Used for removal of oxide generated in RCA1 and RCA2

Chemical solution H2O, NH4OH(25-29%) and H2O2(30%) (5:1:1) H2O, HCl(37%) and H2O2(30%) (5:1:1) 5% HF
Process temperature 70-80 oC 70-80 oC Room temperature
Process time

10 min.

10 min.

30 sec.

Life time of the chemical solutions Can only be heated one time. When hot: it lasts for ~1h Can only be heated one time. When hot: it lasts for ~1h ~2 months
Allowed materials
  • Silicon
  • Silicon oxide
  • Silicon nitride
  • Quartz wafers/fused silica
  • Silicon
  • Silicon oxide
  • Silicon nitride
  • Quartz wafers/fused silica
  • Silicon
  • Silicon oxide
  • Silicon nitride
Batch size

1-25 2",4" or 6" wafers at a time

1-25 2",4" or 6" wafers at a time

1-25 2",4" or 6" wafers at a time

Size of substrate

4"-6" wafers
For 2" wafers please contact Danchip staff

4"-6" wafers
For 2" wafers please contact Danchip staff

4"-6" wafers
For 2" wafers please contact Danchip staff