Page 421 - Microsensors, MEMS and Smart Devices - Gardner Varadhan and Awadelkarim
P. 421

FABRICATION  OF A MEMS-IDT  ACCELEROMETER     401

    3.  The  sacrificial  layer  is  then  etched  with  hydrofluoric  acid  (HF)  to  release  the
       seismic mass.
    4.  The  seismic  mass  is now ready to be flip-chip bonded to  the SAW substrate.

    These  steps are only  one  of  the  many  possible methods of realising these structures.
       After  the  sacrificial  oxide is removed in  HF,  the  wafers  are  rinsed  in  deionised (DI)
    water and dried. The surface tension of the water under the structures tends to pull them
    down  to the  surface  of the  wafer,  and  in  some cases, causes them to stick permanently.
    This problem  can  be  avoided by  using  thick structural and  sacrificial  layers and short
    structures. There are several other methods of adhesion prevention that rely on avoiding
    the problem of  surface  tension. These include  the  following:
     •  Freeze drying  (sublimation)  of the final rinsing solution  (DI water, t-butyl alcohol)
     •  Using an integrated polymer support structure during release etching and then ashing
       in  oxygen
     •  Gradually replacing acetone with photoresist, then  spinning  and ashing the resist
     •  Electrically fusing  (vaporising) micromechanical support structures




  14.3.1  Fabrication  of  the  SAW Device

  The  SAW device  consists  of  a piezoelectric  substrate  on  which  IDTs  are  deposited.  The
  IDTs can be sputtered through a mask  or they can be etched  using the lift-off  technique as
  described  in Chapter  12. The  choice  of the  method  is dependent  on the minimum feature
  size  to  be  fabricated  and  adhesion  of  the  electrode  metal  to  the  piezoelectric  substrate.
  The fabrication  of  the  IDTs  is  essentially  a  single  mask  process.
    For  example,  in  the  lift-off  technique,  fabrication  begins  with  standard  photolitho-
  graphy  using  standard  equipment  such  as  a  wet  bench,  resist  spinner,  hot  plates,  and
  an  evaporator.  The  lithium  niobate  wafers  are  cleaned  using  acetone,  isopropanol,  and
  trichloroethylene  (in  turn)  at  about  60°C  for  about  10 minutes.  The  wafers  are  then
  thoroughly  rinsed  in  DI  water  for  about  5 minutes  and  subsequently  heated  at  125°C
  (on  a  hot  plate)  for  about  10 minutes  to  remove  surface  moisture.  Upon  cooling  the
  wafer  on  a  heat  sinking  plate,  Shipley  1813  photoresist  is  spin-coated  (at  4000  rpm
  for  55  seconds)  on  the  wafer  after  soaking  the  top  face  with  an  adhesion  agent  called
  hexamethyl  disilazane  (HMDS).  The  wafer  is  then  heated  at  125°C  for  2 minutes  in
  what  is  commonly  referred  to  as  the  soft-bake.  The  wafer  is  then  exposed  to  ultravio-
                           2
  let  (UV)  light  (of  15 mW/cm )  for  1.2 seconds  such  that  the  regions  of  the  resist  that
  are  exposed  become  soluble  to  the  developer  (DI  water  and  MF3 12 in  a  1:1  ratio).  A
  negative  mask,  whereby  the  patterns  are  glass  set  against  a  background  of  chrome,  is
  used for this purpose.  The wafer  is developed  until the sections  that have been  exposed  to
  UV  light and  therefore  soluble  are  etched  away. The  wafer is  then  hard-baked  at  125 °C
  for  1 minute  30  seconds.  The  patterned  wafer  is  coated  with  20 nm  of  chromium  using
  electron  gun  evaporation,  which  is  deposited  to  improve  the  adhesion  of  the  subsequent
  thermally  evaporated  120 nm  gold  layer.  The  wafer  is  then  submerged  into  acetone  to
  facilitate  the  lift-off  process.
   416   417   418   419   420   421   422   423   424   425   426