ABSTRACT
Electrochemical measurements are vital to a wide range of applications such as air quality monitoring, biological testing, food industry, and more. Integrated circuits have been used to implement miniaturized and low-power electrochemical potentiostats that are suitable for wearable devices. However, employing modern integrated circuit technologies with low supply voltage precludes the utilization of electrochemical reactions that require a higher potential window. In this paper, we present a novel circuit architecture that utilizes dynamic voltage at the working electrode of an electrochemical cell to effectively enhance the supported voltage range compared to traditional designs, increasing the cell voltage range by 46% and 88% for positive and negative cell voltages, respectively. In return, this facilitates a wider range of bias voltages in an electrochemical cell, and, therefore, opens integrated microsystems to a broader class of electrochemical reactions. The circuit was implemented in 180 nm technology and consumes 2.047 mW of power. It supports a bias potential range of 1.1 V to -2.12 V and cell potential range of 2.41 V to -3.11 V that is nearly double the range in conventional designs.
ABSTRACT
This paper introduces a novel compact low-power amperometric instrumentation design with current-to-digital output for electrochemical sensors. By incorporating the double layer capacitance of an electrochemical sensor's impedance model, our new design can maintain performance while dramatically reducing circuit complexity and size. Electrochemical experiments with potassium ferricyanide, show that the circuit output is in good agreement with results obtained using commercial amperometric instrumentation. A high level of linearity (R2 = 0.991) between the circuit output and the concentration of potassium ferricyanide was also demonstrated. Furthermore, we show that a CMOS implementation of the presented architecture could save 25.3% of area, and 47.6% of power compared to a traditional amperometric instrumentation structure. Thus, this new circuit structure is ideally suited for portable/wireless electrochemical sensing applications.
ABSTRACT
High-density on-chip electrochemical biosensor arrays are advancing toward a crucial role in health monitoring and development of new medicines and medical treatments. Nanopore and ion channel based sensors especially have great potential but present demanding resolution/speed/power/area requirements on instrumentation circuits. This paper presents a pixel-level current readout circuit and new group-cluster architecture to address the circuit challenges in high-performance biosensor arrays. Fabricated in 0.5 µm CMOS, this electrochemical voltammetry circuit achieves 7.2 pArms noise in an 11.5-kHz bandwidth and only consumes 21-µ W power and 0.06 mm2 area per readout channel. Cyclic voltammetry experiments in a potassium ferricyanide solution and patch-clamp whole-cell experiments were performed to validate the circuit's feasibility for electrochemical biosensor applications.
Subject(s)
Biosensing Techniques , Ferricyanides/analysis , Signal-To-Noise Ratio , Biosensing Techniques/instrumentation , Biosensing Techniques/methods , MicroelectrodesABSTRACT
In this paper employing double layer printed spiral coils (PSCs) is proposed for wireless power transmission in implantable biomedical applications. Detailed modeling of this type of PSCs is presented. Both calculations and measurements of fabricated double layer PSCs indicate that this structure can decrease the size of typical single layer PSCs without any change in the most important parameters of the coils, such as quality factor. Also, it is shown that with equal PSC dimensions and design parameters, double layer PSCs achieve significantly higher inductances and quality factors. Ultimately, a pair of double layer PSCs with a distance of 5 mm in air is used in an inductive link. The power transfer efficiency of this link is about 79.8% with a carrier frequency of 5 MHz and coupling coefficient of 0.189.