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fully edited. Content may change prior to final publication. Citation information: DOI 10.1109/TBCAS.2019.2924416, IEEE
Transactions on Biomedical Circuits and Systems
8 First Author et al.: Title

A 2.55 NEF 76dB CMRR DC-Coupled Fully Differential Difference


Amplifier Based Analog Front-end for Wearable Biomedical Sensors

Yang Zhao, Student Member, IEEE, Zhongxia Shang, and Yong Lian, Fellow, IEEE

Abstract— High input impedance, low noise, high common mode


rejection ratio (CMRR), and ultralow power are the most
important performance indicators in the design of analog front-end
(AFE) for wearable biomedical sensors. This paper presents a fully
differential difference amplifier (FDDA) based AFE that employs
DC-coupled input stage to increase the input impedance and
improve CMRR. A parasitic capacitor reuse technique is proposed
to improve the noise/area efficiency and CMRR. An on-body DC Fig. 1. A typical topology of AFE for wearable biomedical sensors.
bias scheme is introduced to deal with the input DC offset.
Implemented in 0.35µm CMOS process with an area of 0.405mm2,
ratio (CMRR), etc. For wearable biomedical sensors, the design
the proposed AFE consumes 0.9µW at 1.8V and shows excellent
noise effective factor of 2.55, and CMRR of 76dB. Experiment of AFE faces more challenges for two reasons. First, the motion
shows the proposed AFE not only picks up clean ECG signal with artifact due to body movements in daily life introduces severe
electrodes placed as close as 2cm under both resting and walking interferences which could saturate the AFE output. Second, the
conditions, but also obtain the distinct α-wave after eye blink from wearable biomedical sensors need low power solution for long
EEG recording. battery life and small sensor size. To deal with motion artifacts,
it is necessary to increase the AFE input impedance as
Index Terms—DC-coupled analog front-end (AFE), fully demonstrated by [6]. It is also important to achieve high CMRR
differential difference amplifier (FDDA), common mode rejection to minimize ambient noise. For low power implementation, we
ratio (CMRR), parasitic capacitance reuse, on-body DC bias,
should keep the circuits as simple as possible.
ultralow power, wearable biomedical sensor.
For wearable biomedical sensors, a typical AFE is composed
of low noise instrumentation amplifier (IA) and the
programmable gain amplifier (PGA) [7] as shown in Fig. 1.
Assume the gain of IA is G1, CMRR of IA and PGA are
I. INTRODUCTION
respectively CMRR1 and CMRR2, the input referred noise of IA

C ARDIOVASCULAR diseases (CVDs) is the number 1


cause of death globally according to World Health
Organization. An estimated 17.9 million people died from
and PGA are vn1 and vn2. Then, the CMRR of the AFE is the
product of CMRR1 and CMRR2. CMMR2 is determined by the
mismatch of the gain ratio of the capacitors in the
CVDs in 2016, representing 31% of all global deaths [1]. The capacitive-coupled PGA, i.e., CMRR2 is restricted by the
direct and indirect costs of CVDs between 2014 and 2015 were maximum allowable capacitor area. While, CMRR1 is affected
$351.2 billion in USA according to American Heart by the chosen IA topology and its components.
Association 2019 Statistics [2]. Early detection and prevention The input referred noise of the AFE, vnoise, is given by:
would save life of many CVD patients. Recent research shows
that the use of home monitoring system effectively lowered ⁄ . (1)
heart failure hospitalization rates [3]. Thus, wearable
electrocardiogram (ECG) sensors such as ECG patches, ECG The impact of is negligible when G1 is sufficiently large.
belts, and flexible ECG bandage [4] are cost effective tools for Thus, IA stage generally consumes the most of power in the
managing CVDs. AFE to minimize the noise. In other words, the noise
Analog front-end (AFE) is one of the critical components in performance of IA determines the overall noise performance of
biomedical sensors. A medical grade AFE should follow the AFE when the gain of PGA is sufficiently large. The AFE can
medical equipment standard, such as IEC 60601-2-47 for be roughly classified into AC-coupled and DC-coupled. Most
ambulatory electrocardiographic (ECG) systems [5] that of existing AFEs use AC-coupled approach [7]-[20] while
defines the requirements of AFE in terms of gain, bandwidth, several AFEs with high input impedance are based on
noise, input offset, input impedance, common mode rejection DC-coupled structure [6], [21]-[24].
Fully integrated AC-coupled AFE can be designed with
This paper was received on March 15, 2019 for review. The research is
supported by NSERC Discovery Grant. We would like to acknowledge CMC
some degree of programmability [7]-[10]. It can handle
Microsystems for the provision of products and services that facilitated this skin-electrode DC offset but is vulnerable to motion artifact due
research. to its relatively low input impedance. CMRR1 of AC-coupled
The authors are with the Electrical Engineering and Computer Science AFE is determined by the mismatch of gain ratio capacitors of
Department, Lassonde School of York University, Toronto, ON M3J1L4
Canada (e-mail: yangzhao@eecs.yorku.ca).
the IA stage. For better CMRR performance, the input coupling
capacitor is made large resulting large chip area and low input

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This article has been accepted for publication in a future issue of this journal, but has not been fully edited. Content may change prior to final publication. Citation information: DOI 10.1109/TBCAS.2019.2924416, IEEE
Transactions on Biomedical Circuits and Systems
8 First Author et al.: Title

IA with complicated analog-digital mixed feedback loops are


used for the improvement of CMRR and noise performance,
which presents 75dB CMRR. However, the complex
compensation scheme consumes more power. In terms of
CMRR, differential difference amplifier (DDA) is a favorable
choice. In [25], a chopper stabilized DDA AFE with CMRR of
85dB is proposed for bio-potential acquisition. The rail-to-rail
DDA reported in [26] achieves 137dB CMRR for biosensor. As
high as 150dB CMRR is possible as shown by the simulation
result in [27] by using DDA. These results prompt us to design
a simple yet acceptable AFE to address the CMRR issue in the
three-amplifier DC-coupled ones.
Since bioelectrical signals have extremely weak drive
capability, the input DC bias for the DC-coupled AFE is
commonly provided by Giga-ohm level resistors R2 as shown in
Fig. 2. R2 can be implemented by a pseudo resistor [22] or in
series diode-connected transistors [23]. It is worth noting that
the bias provided by the pseudo resistors is unpredictable due to
the leakage. Furthermore, the leakage of input transistor is not
Fig. 2. Topology of three-amplifier DC-coupled AFE. negligible if its size is made large for better noise performance.
This leakage reduces the input impedance to the level close to
impedance. Several techniques have been proposed to boost the the bias resistors. In such case, the unpredictable bias resistance
input impedance such as passive input impedance boosting would produce uncontrollable input DC-offset.
network [11], impedance boosting with positive feedback In this paper, several techniques are proposed to address the
[12]-[14], and the combination of positive feedback with active issues in the DC-coupled AFE. The proposed AFE uses fully
electrode [15], [16]. The passive network merely provides differential difference amplifier (FDDA) to replace the
hundred MΩ input impedance and requires off-chip three-amplifier topology for the improvement of CMRR. An
components, thus not widely adopted. Positive feedback boosts on-body common mode DC voltage is introduced to provide the
the input impedance to GΩ level but requires off-chip tunable on-body DC bias voltage to the bioelectrical signal in order to
components or complicated on-chip auto calibration technique handle uncontrollable input DC offset. To reduce the flicker
to maintain the stability. The auxiliary impedance boosting noise, large-size input transistors are often used. We propose to
circuits need extra power which is not preferred by wearable reuse the parasitic capacitance in the large input transistors to
biomedical sensors. To save area and cost, chopper improve noise performance and area efficiency. We also use
stabilization circuits [17], [18] are proposed to improve the the current mirror load in the first stage of FDDA to replace the
noise, CMRR and anti-offset performance by modulating the common mode feedback (CMFB) for better power efficiency.
noise, offset and common mode signal to out-band frequency at Implemented in 0.35µm CMOS technology, the proposed AFE
the price of clocking and power. DC-serve loop, integrator, and attains the best NEF of 2.55.
clock staggering are often employed to compensate the The rest of paper is organized as follows. Details of the
interferences due to chopper clocking [19], [20]. However, the proposed FDDA DC-coupled AFE and design considerations
modulator before the instrumentation amplifier (IA) are presented in Section II. Measurement results as well as the
deteriorates the input impedance. In summary, AC-coupled performance summary are provided in Section III. Conclusion
AFE with auxiliary impedance boosting as well as chopper remarks are drawn in Section IV.
stabilization techniques may not be the best candidate for
ultra-low power wearable ExG sensors. II. FDDA DC-COUPLED AFE
DC-coupled AFE presents inherent Giga-ohm level input
impedance by connecting the input directly to the transistor A. Proposed FDDA IA
gate instead of the input capacitor used in AC-coupled circuits. The conventional three-amplifier DC-coupled IA has two
There are several attempts for DC-coupled AFE in recent years amplification branches. The input DC bias is provided by Vcm
[6], [21]-[24]. IA with two amplification branches is the via pseudo resistors [6]. The CMRR is mainly determined by
conventional topology in DC-coupled AFE which is well the mismatch of gain ratio capacitors. Due to the limited chip
known as three-amplifier AFE, as shown in Fig. 2. The two area, the feedback ratio capacitors are commonly selected as
branches amplify both common mode and differential signal at one or few times of minimum allowable MIM capacitor,
the same gain. CMRR is determined by the mismatch of the otherwise the gain ratio capacitors would be unacceptable large.
gain ratio capacitors in both IA and PGA stages assuming the Hence, this topology generally presents poor CMRR.
mismatch of the capacitor is much higher than then mismatch The proposed IA, as shown in Fig. 3, isolates the
of the transistor. Since the three-amplifier topology requires an common-mode input from the amplification branches by
extra LNA in the IA stage comparing with AC-coupled utilizing a FDDA, where only differential signal is amplified.
approach, the area left for ratio capacitors is smaller than that of The inputs of FDDA are defined by:
AC-coupled one if area constraint is the same, resulting larger
mismatch and worse CMRR. In [24], open-loop DC-coupled

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This article has been accepted for publication in a future issue of this journal, but has not been fully edited. Content may change prior to final publication. Citation information: DOI 10.1109/TBCAS.2019.2924416, IEEE
Transactions on Biomedical Circuits and Systems
8 First Author et al.: Title

Fig. 4. On-body DC bias for EEG and ECG monitoring.

proposed FDDA. The parasitic capacitance, (CGS+CGB) referred


as C5 in Fig. 3, contributes to better gain consistency among
different chips without extra area cost. That is because the unit
size of transistor is much smaller than the MIM capacitor, i.e.,
many more symmetrically placed units are allowable for
Fig. 3. Topology of proposed FDDA DC-coupled IA. transistors than capacitors with same area. For a single MOS
and MIM capacitor, the precision of absolute value from MOS
is worse than MIM. In this process, the minimum size of MIM
[ ] [ ][ ]. (2) capacitor is 5μm×5μm. The area taken by 100 minimum MIM
capacitors can be used to symmetrically place over 800
transistors with size of W/L=0.5μm/2μm, i.e., the match of
MOS capacitor is better than MIM capacitor. In addition to the
where, , , , and are respectively defined as the much more units for reduction of geometry mismatch, the
differential input signal, the none inverting common mode on-body bias relaxes the input DC offset to reduce the non-ideal
signal, the inverting common mode signal, and the differential effect. Thus, gain variation from chip to chip by using MOS
common mode signal. The linear model of the FDDA is given capacitor is smaller than using MIM capacitors. Furthermore,
by: the capacitor area of C2 can be reduced since part of capacitance
is provided by C5, i.e., we can transfer part of capacitance from
( ), (3) input transistor to ratio capacitor. In this design, 4 large size
input transistors with size of 5mm/2μm are used to improve the
where represents the differential gain, is the common noise performance and offset. From the simulation, the
mode signal. The second term in the parentheses can be parasitic capacitance contributes about 1/3 of the gain, i.e., the
rewritten as [28] ratio of C5 and C2 is around 1/2. This helps to reduce the chip
area. Although the reuse of C5 improves the area utilization in
. (4) terms of the CMRR and noise performance, MIM capacitors
are not totally replaced by C5 for two reasons. The first is area
budget. With same capacitance, C5 occupies roughly 7/3 area of
In (4), all the CMRRs are in dB; the CMRRp and CMRRn are
C2. The second is the increased gate leakage. The impedance at
only related to the mismatch of input pair; CMRRd is
DC is targeted at over 1GΩ in this design, so C5 cannot be too
determined by both the input pair mismatch ( ) and tail
large.
current mismatch ( ) as given by (5) and (6) [28], Assume the two Gm cell of the FDDA is matched, and
respectively. ignoring the CMRR term in (3). Then we have

( √ ) (5) (( ) ( )). (7)


. /
(6) According to the circuit in Fig. 3, (7) can be transformed to:

In (5), and are geometry-dependent amplification factor (( ) (


( )
separately for inverting and non-inverting pairs. In (6), and
are expected ideal values, while and are respectively the )), (8)
tail current of the practical inverting and non-inverting
branches. The impact of tail current mismatch can be easily
suppressed by increasing the impedance of the tail current via Simplify (8) with assumption that is very large (designed
cascaded current mirror or increasing the transistor length to value is 70dB), transfer function for the FDDA IA is given by:
several times (e.g. 4×) of default length. To relax the mismatch
( )
of input transistor, large size and symmetrical layout are ( ) . (9)
necessary for these transistors. The large size transistor
provides extra benefits in additional to better CMRR in the
That is, FDDA IA has unit DC gain, a high-pass cut-off

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This article has been accepted for publication in a future issue of this journal, but has not been fully edited. Content may change prior to final publication. Citation information: DOI 10.1109/TBCAS.2019.2924416, IEEE
Transactions on Biomedical Circuits and Systems
8 First Author et al.: Title

Fig. 5. Schematic of proposed FDDA.

frequency of ( ), and midband gain of (C2+C5+C1)/C1. more modifications are made to the conventional FDDA for
R1 is back-to-back connected pseudo resistor [6] which is better power efficiency and circuit stability as shown in Fig. 5
hundreds GΩ. The high-pass cut-off is meant to be sub-Hertz, by red dash boxes. Firstly, the CMFB module to supply the MP1
of which the precise value is obtained from the chip and MP2 bias is replaced by the current mirror load connection
measurement. The low-pass cut-off frequency is determined by as denoted by the top box. If using CMFB, the loop is from VP
the FDDA bandwidth and the load ( , miller capacitor in and VN to the gate of MP1 and MP2, where there are two main
FDDA, and the input capacitor of PGA). poles. One is at the point VP (or VN) and the other is at the gate
of MP1 and MP2. Assume it employs the same CMFB structure
B. On-body DC biasing with the output stage as shown by the right side of the red
Employing large size input transistor increases the leakage dotted line in Fig. 5, the two poles can be approximated by
current, making the leakage resistance comparable with the
pseudo resistor. In this case, the inaccurate pseudo resistor bias, , (10)
such as the bias via R2 in Fig. 2, results uncontrollable input ( )[( ) ]

offset. We introduce an extra DC electrode, as shown in Fig. 4,


to deal with the DC offset. The DC electrode is placed away , (11)
( )[( ) ( )]
from the two input electrodes, to provide the DC bias Vcm for
the bioelectrical signal.
Two examples for electrode placement are individually where, is the gain for output stage. Due to the Miller effect
illustrated in Fig. 4 for EEG and ECG monitoring. For ECG, as and the large-size input transistor, the capacitance in (10) is
the DC-coupled input impedance is high enough, the distance much larger than (11), but the resistance part of (11) is over ten
between two input electrodes placed on chest can be as close as times of that in (10) because of the bias current for the CMFB
2cm. The Vcm electrode is placed on the left upper arm to (10nA) is much smaller than that in the first stage of the core
provide the DC bias voltage via the path constitute of body circuit (150nA). That is, the two poles are very close to each
tissue (Rbody) and input electrodes (10nF in parallel with 1MΩ other and appear at relative low frequency. Thus, the phase
for dry electrode [29]). The equivalent resistance, Rbody in series margin quickly degrades with the decrease of the loop gain.
with 1MΩ, is significantly smaller than the pseudo resistor and With one feedback amplifier, it’s hard to maintain sufficient
the equivalent input resistance of the gate leakage, presenting loop phase. Extra isolated feedback amplifier is required to
negligible DC offset. The position of the Vcm electrode is not achieve the required loop phase and gain [30], which needs
limited to left upper arm. It can be placed any point that is at extra current. Using the current mirror connection, the CMFB
least 5cm away from the input electrodes, e.g., the point for loop stability issue is mitigated. Moreover, this configuration
driven right leg (DRL) electrode. For EEG acquisition, the wastes no power on the CMFB. The proposed asymmetrical
electrode connected to the non-inverting terminal Vinp is placed connection deteriorates the CMRR of the FDDA. Even with
on the forehead, and the other input electrode is on earlobe. As extremely large size input transistor size and well-matched
amplitude of EEG signal is much smaller than ECG, the layout design, the CMRR does not match with the conventional
distance of the two input electrodes cannot be too close as for FDDA topology of higher than 80dB [25]-[27]. Nevertheless, it
the ECG. The Vcm electrode, is tagged on the other earlobe for is still better than the conventional three-amplifier DC-coupled
biasing. topology, and meets the requirements in ECG standard.
The insertion of MN3 and MN4 at the output stage stabilizes
C. Design Considerations of Proposed FDDA the biasing current. Without MN3 and MN4, the current in the
Besides the large-size input transistor (MN7-MN10), two conventional FDDA output stage is determined by the feedback

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Transactions on Biomedical Circuits and Systems
8 First Author et al.: Title

Fig. 7. Topology of PGA.

Considering both thermal and flicker noises, the equivalent


voltage noise source seen from the transistor gate is defined by
Fig. 6. Simulated integrated input referred noise at different transistor size and
bias current. ( )
. / , (15)
voltage VFB generated from the output of CMFB which is the
classic one-stage amplifier (the five-transistor cell at the right where B is flicker noise constant and purely decided by process,
side). This bias is sensitive to process variation. The adoption η is determined by the body coefficient, the surface potential,
of MN3 and MN4 makes the bias current independent on the and the source-body potential.
fixed VB rather than the unpredictable VFB. In this way, the VFB If the design is ideal, then the current in MP1 is twice of MN7.
just modulates the output common mode voltage to VCM but has Assuming η and has no relation with the transistor size, from
no effect on bias current. (12), (14), and (15), the equivalent input referred noise is
The input referred noise of the FDDA can be written as obtained as

( )
⁄ ( ) , (16)
( ) ( )
To achieve good noise performance, the bias current and the
. . || || / / transistor size of MN7-MN10 and MP1, MP2 should be large
( ⁄ ) enough. The simulated integrated input referred noise at
different currents and transistor sizes are provided in Fig. 6. It is
⁄( ) ( ⁄ ) obvious that the noise drops quickly before 10000μm2 while
( ⁄( )) keeps steady or even slightly higher after that point, where the
flicker noise is much lower than thermal noise. Thus, in this
( ⁄ ) , (12) design, the size of MN7-MN10 is 5mm/2μm, and the size of
MP1 and MP2 is 800μm /10μm. Furthermore, the noise level
where is the output equivalent resistance of the output drops with the increasing of the bias current. However, in ECG
stage, and is the output equivalent resistance of the first and EEG applications, low bias current is preferred to achieve
stage. In (12), we assume MN9 is the same as MN7. Note that the narrow low-pass cut-off frequency.
the 2nd and 4th terms contain the ( ) attenuation (over The load of IA is composed of feedback ratio capacitor, C1
100 according to the simulation) leading to the final (as in Fig. 3), the Miller capacitor, CM, and the input ratio
approximation. When transistors in subthreshold region, the capacitor in PGA, C4. If the gain of IA is G1, then the low-pass
relation between ID and VGS is given by [31] cut-off frequency of the IA can be derived as

⁄( )
. (13) ⁄* ,( ) -+. (17)

As is purely proportional to bias current, thus, to achieve


In which represents the thermal voltage, stands for the
characteristic current, and the parameter n is slope factor, both around 100Hz, the area used for capacitors are extremely
large if the current is set to hundreds of nano-ampere. Also, the
and n are process dependent. Then, the transconductance of
increase of the current is not preferable for wearable sensors.
the transistor in subthreshold region can be expressed as
Thus, the bias current for non-inverting branch and inverting
⁄( )
branch is kept as 150nA.
. (14) In summary, the large-size input transistor and the load
transistor improve the CMRR, gain consistence, and noise. As

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Transactions on Biomedical Circuits and Systems
8 First Author et al.: Title

Fig. 8. Chip micrograph.

Fig. 11. Measured input referred noise.

Fig. 9. Measured frequency response at three different gain settings.

Fig. 12. Analysis of harmonic distortion.

budget, rather it helps in improving performance. The increased


leakage current due to the larger transistor size degrades the
impedance, for which the pseudo resistor biasing is not suitable.
The on-body DC biasing is thus proposed to mitigate the
deteriorated DC-offset.
D. PGA
PGA has 4 gain settings controlled by two digital control bits
as shown in Fig. 7. The default gain is set as the maximum
value which is determined by C4/C3. The tunable capacitor can
be changed among C3, 2C3, and 3C3, i.e., when switch S is
Fig. 10. Tested CMRR at three different gain settings.
closed, the gain can be set as 1/2, 1/3, and 1/4 of the default gain.
TABLE I Different gain setting presents different load for the amplifier
MEASURED GAIN FOR 9 CHIPS OP2. Thus, minimum low-pass cut-off frequency in PGA stage
Chip 1 2 3 4 5 6 7 8 9 should higher than that of IA stage to avoid the bandwidth
55.6 56.0 56.8 57.0 56.4 56.0 56.3 57.0 56.1 changing when tuning gain, i.e., the low-pass cut-off frequency
Gain of PGA at minimum gain setting should larger than that in IA.
58.1 58.8 58.5 58.6 58.1 58.6 59.1 58.7 58.6
(dB) As AFE is the cascade of IA and PGA. The gain of IA stage
61.8 62.1 63.2 62.3 61.8 62.1 62.4 63.4 62.2
is generally higher than the gain in PGA to relax the design of
OP2. In this design, the gain of IA and maximum gain of PGA
the parasitic capacitance of the input transistor is reused for
are 75 and 36, respectively. As part of the gain of IA is
gain ratio capacitors as discussed early, thus the increase of
contributed by the parasitic capacitance of the input transistor,
transistor size helps to reduce the ratio capacitor in IA. In other
the gain of IA stage is estimated by simulation. Although the
words, the large-size transistor doesn’t post as thread to the area

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Transactions on Biomedical Circuits and Systems
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TABLE II
PERFORMANCE COMPARISON WITH RELATED WORKS
JSSC JSSC JSSC JSSC TBioCAS TBioCAS TBioCAS TBioCAS This
2016 [6] 2018 [15] 2011[14] 2015 [20] 2018 [7] 2017 [22] 2019 [16] 2011 [13] Work
Current 1.19µA 0.361µA 5.3µA 31nA 160nA 8.25µA 18µA 50µA 499nA
VDD 1.2V 0.8V 2V 0.6V 2V 1.2V 5V 1.8V 1.8V
Gain 38-55dB 26-52dB 50-62dB 51-96dB 40dB 52dB 0-20dB 9.5-40dB 56-68dB
Bandwidth 0.5-150Hz 1-400Hz 0-170Hz 0.1-250Hz 0.2-200Hz 1Hz-6.5KHz 0.26-100Hz N/A 0.4-120Hz
Input Noise 3.06µV 8.26µV 1.7µV 6.52µV 2.05µV 5µV 3.7µV 0.8µV 1.02µV
CMRR 64.9dB 66dB 105dB 55dB 65dB 65dB 70dB 82dB 76dB
THD N/A N/A N/A 2.87% 1% 0.95% N/A N/A 1%
Area (mm2) 0.35* 0.86* 5.2* 1.1* 0.18 0.018 1.23 6.48 0.405
Input Impedance 3.6GΩ 200GΩ N/A 110MΩ 20MΩ N/A 400GΩ 2GΩ 1GΩ
Process 0.13µm 0.18µm 0.5µm 65nm 0.35µm 0.13µm 0.18µm 0.18µm 0.35µm
NEF 10.6 8.43 11.7 2.64 2.26 7 N/A 12.3 2.55, 1.98
* The area is approximated from the chip micrograph

absolute gain is not able to be precisely calculated in design


stage, the gain variation is smaller than one using pure MIM
capacitor as discussed before. By such gain distribution, the
classic differential input, single-end output two-stage amplifier
with Miller compensation is adopted for OP2 as in the right side
of Fig. 7.
To drive the on-chip module, generally ADC with capacitive
coupling with several pico-farad, 20nA biasing is good enough
in the output stage of the PGA. In this design, for testing
purpose, extra 100nA is added to drive the probe of the
oscilloscope, which is 10MΩ || 4pF, to avoid the use of extra
buffer.
Fig. 13. Monitored ECG signal.
III. MEASUREMENT RESULTS
The design is fabricated in 0.35µm CMOS process with core
area of 450µm×900µm. The chip micrograph is shown in Fig. 8.
The current consumed by the entire AFE is 499nA, of which
350nA is taken by IA, and 120nA is used for the output stage of
the PGA to drive the oscilloscope probe with 10MΩ and 4pF
load. Except the maximum gain, other three gain settings are
verified during the measurement of frequency response, CMRR,
and gain variation as illustrated in Fig. 9, Fig. 10, and Table I,
respectively. It can be seen that different gain settings have
fixed bandwidth from 0.4Hz to 120Hz and 76dB CMRR. The
gain variation based on the measurement from 9 chips is within
3%, which is much smaller than the required 10% by the
standard [5]. The input referred noise is 1.02µVrms integrated
over the pass-band as shown in Fig. 11. Two distortion peaks
occurs at 50Hz and 150Hz due to the power line interferences
as given in Fig. 12. The total harmonic distortion (THD) is
smaller than 1% excluding the components caused by the
power line interference.
Noise efficiency factor (NEF) was first introduce by [31] to
quantify the trade-off between the noise and power, which is
defined by
Fig. 14. Acquired EEG with distinct α component after eye blink.
√ , (18) Compare with the state-of-the-art works, this design presents
the best NEF, and best CMRR among the designs without
where is the input referred RMS noise voltage; is
chopper stabilization. Thanks to the DC-coupling, input
the total current supplied to the OTA; is the thermal voltage impedance 1GΩ at DC is achieved. The chip area is as small as
kT/q and BW is the OTA bandwidth in Hertz. The NEF of the 0.405mm2 benefiting from the reuse of the parasitic capacitance
proposed FDDA DC-coupled IA is 1.98, and 2.55 for entire
even with almost the highest gain setting.
AFE counting the current to drive oscilloscope probe.
To demonstrate the capability of the chip in acquiring ECG

1932-4545 (c) 2019 IEEE. Personal use is permitted, but republication/redistribution requires IEEE permission. See http://www.ieee.org/publications_standards/publications/rights/index.html for more information.
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Transactions on Biomedical Circuits and Systems
8 First Author et al.: Title

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1932-4545 (c) 2019 IEEE. Personal use is permitted, but republication/redistribution requires IEEE permission. See http://www.ieee.org/publications_standards/publications/rights/index.html for more information.
This article has been accepted for publication in a future issue of this journal, but has not been fully edited. Content may change prior to final publication. Citation information: DOI 10.1109/TBCAS.2019.2924416, IEEE
Transactions on Biomedical Circuits and Systems
8 First Author et al.: Title

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Yang Zhao (M’18) received the B.S. and


M.S. degree in electrical engineering from
Xi’an Jiaotong University, Xi’an, Shaanxi,
China, in 2012 and 2015, respectively. He
is currently pursuing the Ph.D. degree in
electrical engineering at York University,
Toronto, Ontario, Canada. His research
interests include ultralow power circuits
and system for next generation wearable biomedical sensors.

Zhongxia Shang received the B.S. and


M.S. degree in electrical engineering from
Xi’an Jiaotong University, Xi’an, Shaanxi,
China, in 2013 and 2016, respectively.
From 2011 to 2013, he studied in
SUPELEC, Gif-sur-Yvette, France. He is
currently pursuing the Ph.D. degree in
electrical engineering at York University,
Toronto, Ontario, Canada. His research interests include
ultralow power circuits and system for next generation
wearable biomedical sensors, including the design of PMU,
transceiver, PLL, etc.

Yong Lian (M’90–SM’99–F’09) Dr.


Lian's research interests include
biomedical circuits and systems and signal
processing. He has published more than
300 papers and received more than 15
awards including IEEE Circuits and
Systems Society’s Guillemin-Cauer Award,
IEEE Communications Society
Multimedia Communications Best Paper
Award, Institution of Engineers Singapore Prestigious
Engineering Achievement Award, Winner of the Design
Contest Award in ISLPED2015.

Dr. Lian is the President of the IEEE Circuits and Systems


(CAS) Society, Chair of the IEEE Periodicals Partnership
Opportunities Committee, Member of the IEEE Periodicals
Committee, Member of the IEEE Biomedical Engineering

1932-4545 (c) 2019 IEEE. Personal use is permitted, but republication/redistribution requires IEEE permission. See http://www.ieee.org/publications_standards/publications/rights/index.html for more information.

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