Tantalum etch

AP Alexander P. M. Place
LR Lila V. H. Rodgers
PM Pranav Mundada
BS Basil M. Smitham
MF Mattias Fitzpatrick
ZL Zhaoqi Leng
AP Anjali Premkumar
JB Jacob Bryon
AV Andrei Vrajitoarea
SS Sara Sussman
GC Guangming Cheng
TM Trisha Madhavan
HB Harshvardhan K. Babla
XL Xuan Hoang Le
YG Youqi Gang
BJ Berthold Jäck
AG András Gyenis
NY Nan Yao
RC Robert J. Cava
NL Nathalie P. de Leon
AH Andrew A. Houck
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Initially we etched tantalum using a reactive-ion etch (8:3:2 CHF3:SF6:Ar chemistry at 50 mTorr, RF/ICP power of 100/100 W). However, scanning electron microscopy (SEM) images showed that reactive-ion etches can produce rough edges as well as small pillars and boulders near the sidewalls, likely due to micromasking (Supplementary Fig. 2a, b). The anomalous objects in Supplementary Fig. 2b remained after the device was cleaned in piranha solution and treated in an oxygen plasma. In order to avoid these fabrication problems, we employed a wet etch composed of 1:1:1 HF:HNO3:H2O. We found that several resists delaminated before the tantalum was etched through, leaving the sidewalls and nearby tantalum visibly rough in SEM (Supplementary Fig. 2c). This problem was circumvented by using thick AZ 1518 resist (~2-μm tall), which left cleaner sidewalls (Supplementary Fig. 2d). Comparing Devices 4–10 with Devices 11–18 in Supplementary Table 1, we note that the optimized wet etch likely improved T1.

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