1. Introduction
In the biomedical field, applications that monitor vital signs have experienced significant growth in recent years. These advances aim to understand the physiological phenomena of the human body and their impact on daily life [
1,
2]. Consequently, the research and development of devices capable of detecting a wide range of biopotential signals has become essential to assess patient health [
3,
4].
Most electrophysiological interfaces are designed to operate in a typical frequency range of
to several kilohertz [
5,
6,
7]. However, relevant biological signals are present at low frequencies in the range of hundreds of millihertz (mHz), which are often ignored by such systems. This limitation restricts the ability to detect essential biopotentials, providing better disease prevention, detection, and treatment.
Recent studies show that there are components of clinical interest in the tens of mHz range, which are usually attenuated by conventional techniques. These signals are known as DC-biosignals. They can complement the diagnosis and prevention of multiple diseases and conditions. The recording of DC-biosignals focuses on preserving the very low-frequency components of biopotentials, which are often attenuated by the bandwidth of conventional front ends. For this reason, it is necessary to have acquisition systems with wider bandwidths that include very low frequencies, while maintaining low noise levels and power consumption.
Electroencephalography (EEG) is a fundamental technique for monitoring brain activity and detecting bioelectric changes associated with cognitive processes. DC-EEG enables the readout of ultra-low-frequency components below
[
8]. These signals reflect slow fluctuations in ionic currents and voltage oscillations, providing critical information to understand neuronal activity. The results of this information help diagnose and monitor conditions such as epilepsy [
9].
Electrogastrography (EGG) is a non-invasive technique that detects electrical signals generated by the coordinated contractions of the stomach muscles, which helps identify gastric disorders [
10,
11]. It can also detect gastric arrhythmias, consisting of fast-frequency waves (tachygastrias) and slow-frequency waves (bradygastrias). In the presence of abnormal gastric bioelectric potentials, the frequency range of the EGG can range from
to
[
5,
12].
Capacitively coupled instrumentation amplifiers (CCIA) are widely used in biomedical applications in integrated circuits due to their well-defined gain, high DC rejection, and simple design [
13]. CCIAs’ amplifiers use only one operational transconductance amplifier (OTA), and their gain depends on the ratio of the capacitors. That makes them advantageous because the capacitive mismatch is minimal compared to the resistive mismatch generated by process variations [
2].
In CCIA amplifiers, the low-frequency corner is determined by the constant of the feedback network. In conventional biomedical applications, a low-frequency corner in the order of hundreds of mHz is required. To achieve this, high-value capacitors and resistors are needed, which is challenging due to area restrictions in technological processes. For DC-biosignal applications, the low-frequency corner requires a lower value than in conventional techniques, which increases complexity. A practical alternative is to increase , since increasing usually consumes a significant amount of die area for a few pF. However, polysilicon resistors also consume a significant amount of die area, even to achieve a few megaohms (M). Therefore, the development of techniques that provide equivalent resistances on the order of tens or hundreds of teraohms (T) is essential to ensure adequate bandwidth for detecting very low-frequency signals.
Several recent works employ CCIAs to develop low-power, portable systems for biosignal acquisition in very low-frequency ranges, achieving a low-frequency corner (
) below 100 mHz while maintaining high gain. In [
14], a DC-Servo Loop (DSL) achieves
. However, the feedback transconductance design can be complex and is affected by process, voltage, and temperature (PVT) variations. Similarly, in [
15], an
is achieved using a fully symmetric ring pseudo-resistor structure, reaching an equivalent pseudo-resistance on the order of gigaohms (G
). However, this technique remains sensitive to variations in PVT. In [
16], the Bootstrapped-PR technique is used to achieve an
, however, chopping must be implemented to achieve good input-referred noise (IRN) performance, and the equivalent effective pseudo-resistance is not high enough. In [
5], a non-continuous sampling mode called sample-level duty-cycling (SLDC) is used in a direct digitization ADC, capable of detecting signals down to
through short sampling periods followed by oversampling and digital processing. However, this requires additional complex control logic, and information from fast or transient events can be lost since the circuit is mostly inactive. Finally, in [
17], an
is obtained by implementing a switched-capacitor-resistor-pseudo-resistor, which is a hybrid feedback resistor using switch-capacitor resistor (SCR) and pseudo-resistor (PR) techniques. This approach is robust to PVT variations. However, it requires precise control of multiple switching frequencies, and the resulting equivalent effective pseudo-resistance is insufficient for emerging biosignal applications.
The commonly used pseudo-resistors in CCIA feedback structures offer high resistance, a small size, and a low noise contribution [
13,
18]. However, they are susceptible to PVT and voltage non-linearities, resulting in variable bandwidth [
19]. To solve this problem, techniques that are robust to these variations have been developed, such as the segmented duty-cycle resistor (SDR) [
20]. This technique is based on single-rate-switched resistors, which are robust to PVT variations, and utilizes complementary linear switches to achieve resistances in the
range. The use of SDR enables high resistance with a switching frequency that is outside the bandwidth of the signal of interest. Other techniques, such as switched capacitor resistors or duty-cycle resistors, require a switching frequency within or below the bandwidth of the signal of interest to achieve high equivalent resistance [
20]. Another technique that has been proposed to achieve high feedback resistance in CCIAs is the Complementary Transimpedance Boosting (CTB) [
21]. By combining positive and negative feedback, this technique can increase the effective feedback resistance to hundreds of
. However, positive feedback can induce instability under mismatch variations [
22].
The goal of the proposed work is to demonstrate a technique that pushes the low-frequency corner of CCIAs to the sub-mHz domain. This is achieved by the joint implementation of CTB and SDR techniques. We chose a standard folded-cascode OTA as a test amplifier to ensure objectivity and provide generality. The folded-cascode OTA has been implemented in real-world biomedical instrumentation applications [
23]. Additionally, we used the recently proposed SDR in order to provide tunability in case of instability, which is inherent in the CTB technique [
22].
This paper is organized as follows.
Section 2 introduces the principles of CCIA and amplifier design.
Section 3 presents the performance of the Complementary Transimpedance Boosting implementation using the cascaded pseudo-resistor technique.
Section 4 details the implementation of Complementary Transimpedance Boosting using the Segmented Duty-Cycled Resistor technique,
Section 5 presents the results, and the conclusions are given in
Section 6.
5. Results
The open-loop gain obtained for the test folded-cascode OTA is approximately
, with a variation of
across PVT.
Figure 6 shows the open-loop frequency-gain results of the test folded-cascode OTA. The PVT verification was performed considering the following process (TT, SS, FF, SF, FS), voltage (
), and temperature (−20 °C, 27 °C, 60 °C) variations. The temperature variation is in agreement with the standards of biomedical integrated circuits [
20].
The frequency response of the CCIA with CTB-CPR technique is shown in
Figure 7a. With an
size of
we achieve an equivalent effective pseudo-resistance of 368.4
. This enables a low-frequency corner of 960
and a high-frequency corner of 479.7 Hz, providing an ideal bandwidth for detecting a wide range of DC-biosignals.
Figure 7b shows the post-layout frequency response of the SDR and CTB-SDR techniques implemented in the CCIA. The conventional SDR technique achieves an equivalent effective pseudo-resistance of 1.5
, resulting in a low-frequency corner of 232 mHz, which is suitable for conventional biomedical applications. However, this equivalent effective pseudo-resistance is not enough for applications that require the detection of very low frequencies. Combining the CTB technique with the SDR technique, an increase of 543.3
is achieved, reaching an equivalent effective pseudo-resistance of 535.8
, which allows for a low-frequency corner of 660
while maintaining a high-frequency corner of 170.7 Hz. This provides an optimal bandwidth for detecting very low-frequency biosignals.
Table 3 shows the noise contributions and noise-related parameters obtained from the implementation of the CTB-CPR and CTB-SDR techniques. Both configurations achieve low noise contributions.
For the test folded-cascode OTA, the noise contribution of each transistor can be seen as the sum of the thermal noise contribution and flicker noise, as shown in Equation (
6). Where
k is the Boltzmann constant,
is the white-noise factor, and
is a process-dependent constant.
The noise contribution to the output of transistors
and
, in the following associated as (
) = (
), i.e.,
,
, and
, is given by Equation (
7).
Dividing by
of the amplifier, using the value shown in Equation (
8).
The input-referred noise is obtained, which is shown in Equation (
9).
where the main noise contribution comes from transistors
, because by design
, where the current of
is greater than that of
and
. The noise of the cascode
and
is negligible at low frequencies because the gain of the noise voltage source at the output is much lower than the gain of the amplifier [
31].
The total input-referred noise considering the entire bandwidth (
Hz–479.7 Hz) is
as shown in
Figure 8a, and for the CTB-SDR technique, the total noise referred to the input considering the entire bandwidth (
–
) is
as shown in
Figure 8b.
PVT verification evaluates amplifier performance using CTB-CPR and CTB-SDR feedback techniques under process variations (TT, SS, FF, SF, FS), voltage (), and temperature conditions (−20 °C, 27 °C, 60 °C).
Using the CTB–CPR technique, a very high equivalent effective pseudo-resistance was achieved, enabling a low-frequency corner in the sub-mHz range, which is ideal for detecting very low-frequency biosignals. However, using pseudo-resistors generates variations in equivalent resistances , , and , which affect the equivalent effective pseudo-resistance obtained using the CTB technique. This occurs because the CPR implementation exhibits low robustness against PVT variations. As a consequence, the likelihood of instability increases, or the equivalent resistance is reduced, resulting in a low-frequency corner that is insufficient to meet the bandwidth requirements for DC-biosignal detection. In the proposed design, the low-frequency corner obtained with the CTB–CPR technique ranged from 17.8 mHz to 0.34 mHz.
The CTB–SDR technique provides greater robustness than CTB–CPR while maintaining a low-frequency corner in the sub-mHz range. This improvement is due to the robustness of the SDR technique against PVT variations. The nominal condition is TT corner, with
and
°C. The variation in the low-frequency corner for supply voltage is 20.7
for
. Temperature variation is 168
for
°C to 60 °C. Finally, process variation is 2.13 mHz for TT, SS, FF, SF, and FS corners. The total variation is 2.4 mHz, as shown in
Figure 9.
Table 4 compares the low-frequency corner and gain parameters obtained with the CTB–CPR and CTB–SDR techniques. In both cases, the gain shows minimal variation. However, the low-frequency corner variation is significantly reduced, from a maximum of 17.8 mHz with the CTB–CPR technique to 2.4 mHz with the CTB–SDR technique, demonstrating improved performance and high robustness against PVT variations.
The Monte Carlo analysis was performed under nominal conditions with
and a temperature of
for a run of 400 samples, to evaluate the performance of the CTB-SDR technique under mismatch variations.
Table 5 shows the parameters obtained.
Using the CTB-CPR technique, the low-frequency corner showed an average value of 7.79 mHz with a standard deviation of 4.68 mHz according to JESD91 standards [
32], where 99% of the cases remain below 16 mHz. However, this value is not sufficiently low to ensure the detection of a wide range of DC-biosignals. On the other hand with the CTB-SDR technique, the low-frequency corner achieved an average value of 0.73 mHz with a standard deviation of 0.19 mHz, and 99% of the cases remain below 1.3 mHz. This allows for greater bandwidth, which is ideal for detecting DC-biosignals.
Figure 10a,b show the histograms of the low-frequency corner using the CTB–CPR and CTB–SDR techniques, respectively. The average value decreased from 7.79 to 0.73 mHz, representing a 90.6% reduction, which demonstrates the improved robustness and precision of the CTB–SDR technique. Using the CTB–CPR technique, an average gain of 36.24 dB with a standard deviation of 3.7 dB was obtained, with 99% of cases maintaining a gain above 26 dB. With the CTB–SDR technique, the average gain increased to 40.12 dB with a standard deviation of 3.2 dB, and 99% of cases maintained a gain above 34 dB, demonstrating improved performance under mismatch.
Monte Carlo analysis revealed variations in gain with both methods that deviate significantly from the design specifications. This can be attributed to the inherent instabilities of the CTB technique caused by mismatch, which affects the system response. Compared to CPR, the SDR technique is more robust against PVT and allows tuning of the equivalent effective pseudo-resistance through duty-cycling. This enables the low-frequency corner to be adjusted and compensates for variations caused by mismatch, thereby restoring stability to the design.
In the CTB–SDR technique, the resistive segments implemented with polysilicon have relatively large dimensions, making them less susceptible to mismatch variations. On the other hand, the elements that have the greatest impact on this technique are the complementary switches. Mismatch variations can modify their resistances,
and
. As a result, the equivalent resistances of
,
, and
change, which can compromise stability when
and
become too close in value. This issue can be mitigated by adjusting the duty-cycle, as the equivalent values of
,
, and
depend on the duty-cycle, as shown in Equation (
4). By tuning the duty-cycle, the ratio between
and
can be adjusted so that the stability condition described in Equation (
3) is satisfied. This tuning helps compensate for voltage and temperature variations, as well as mitigate mismatch variations introduced by the manufacturing process.
To demonstrate this, we force an unstable situation in the amplifier using the CTB–SDR technique, as shown in
Figure 5a. The instability is introduced by varying the sizing of the complementary switches in the resistor branches. Each resistor branch is implemented with five complementary switches, whose widths are summarized in
Table 6. These asymmetric width assignments intentionally break the symmetry of the CTB–SDR network and increase its sensitivity to mismatch. The idea is to restore the circuit to a stable state via duty-cycling tuning.
Figure 11 illustrates this for three switching frequencies of 300 Hz, 600 Hz and 900 Hz. The operating point is recovered by tuning the duty cycle. This procedure provides enhanced control and represents a significant advantage over the inherent limitations of the CTB technique.
Finally,
Figure 12 presents a Monte Carlo analysis with 400 samples of the low-frequency corner. Two values are compared for the segmentation of resistor
, while resistor
is kept constant with 13 fingers. In the more stable case, 7 fingers are used in the
segments, resulting in a larger resistance difference between
and
. In the less stable case, 11 fingers are used in the
segments, which reduces this resistance difference to only two fingers. For 7 fingers, the low-frequency corner remained above 1 mHz. For 11 fingers, it shifted below 1 mHz, but with more unstable cases. This confirms the trade-off of the CTB–SDR technique, where higher equivalent resistances increase sensitivity to mismatch and the risk of instability. Therefore, it is crucial to choose appropriate values for
and
to minimize instabilities caused by mismatch, and to use duty-cycle tuning to compensate for the remaining instabilities.
Table 7 shows the performance comparison of the proposed design in relation to the parameters reported in the state-of-the-art of the amplifiers used to acquire DC-biosignals. A higher bandwidth is observed as a result of the increased equivalent resistance by implementing the CTB technique. Moreover, the design provides tunability, allowing the bandwidth to be adjusted for better accuracy and adaptability to specific application requirements, which is ideal for detecting DC-biosignals and portable systems.
6. Conclusions
This work introduces the integration of two techniques to achieve equivalent feedback resistances in the order of hundreds of in a CCIA, enabling a low-frequency corner in the microhertz range for DC-biosignal detection.
The CTB technique provides high equivalent resistance with minimal area overhead and can be implemented using multiple techniques. Using cascaded pseudo-resistors, resistances of up to 368.4 were achieved, corresponding to = 960 Hz. However, this approach is vulnerable to process, voltage, and temperature (PVT) variations.
The Segmented Duty-Cycled Resistor technique was implemented to overcome this limitation, enabling tunable pseudo-resistances robust to PVT variations. In combination, the CTB-SDR approach achieved a resistance of 535.8 with = 660 Hz, maintaining tunability and PVT robustness, while ensuring low noise, and reducing the instability associated with the CTB technique.
Finally, adjusting the low-pass corner using duty-cycling enables the bandwidth to be adapted to various bio-applications, such as EEG and DC-EEG, while tuning compensates for instabilities generated by mismatches, ensuring reliable performance in acquisition systems.