3D Copper Foam-Supported CuCo2O4 Nanosheet Arrays as Electrode for Enhanced Non-Enzymatic Glucose Sensing

CuCo2O4 anchored on Cu foam (CuCo2O4/CF) with polycrystalline features was fabricated by a mild process based on solvothermal reaction and subsequent calcination in this work. The structure and morphology of the obtained materials were thoroughly characterized by X-ray diffraction, X-ray photoelectron spectroscopy, field-emission scanning electron microscopy, and transmission electron microscopy. According to the above analysis, the morphology of the CuCo2O4 was nanosheet arrays. Meanwhile, the CuCo2O4 was grown on Cu foam successfully. The CuCo2O4/CF displayed good electrochemical properties for glucose detection at a linear range from 0 mM to 1.0 mM. Meanwhile, the detection limit was as low as 1 μM (S/N = 3), and the sensitivity was 20,981 μA·mM−1·cm−2. Moreover, the selectivity and the stability were tested with excellent results. This nanomaterial could show great potential application in electrochemical sensors.


Introduction
High-precision glucose detection is a growing demand for social development. It has been widely used in various fields such as biotechnology, food factories, and ecological environments [1]. Currently, many strategies are available to monitor glucose. Electrochemical sensor can transform the signals of chemical reaction on the electrode surface into electrical signals. These signals can be easily recorded and quantified. Therefore, this method is suitable for the rapid and precise monitoring of glucose [2]. In general, electrochemical sensor could be classified into electrochemical enzymatic sensor and electrochemical non-enzymatic sensor. To date, many studies reported that glucose oxidase-modified electrodes exhibit good sensitivity and high selectivity for glucose detection [3]. However, the development of electrochemical enzymatic sensor is limited because of the high price of the active enzyme. Moreover, the pH and temperature in the environment could easily exhibit a negative impact on the performance during detection. Thus, the research on non-enzymatic glucose sensors, which could reveal high stability, has drawn great attention.
CuCo 2 O 4 has attracted considerable attention in recent research on non-enzymatic glucose sensors. CuCo 2 O 4 has higher electrical conductivity and electrochemical activity than simple metal oxides because of a relatively low activation energy for electronic transmission between multiple transition-metal cations [4]. Consequently, the variety nanostructure of CuCo 2 O 4 , such as nanoflakes [5], nanowires [6], and nanoparticles [7], has been widely applied in Li-ion batteries [8], supercapacitors [4], and sensors [9]. In a recent study, hollow CuCo 2 O 4 -functionalized porous graphene composite was prepared successfully by Zhao et al. They used this composite as electrode materials to detect glucose with high sensitivity of 2426 µA·mM −1 ·cm −2 [10]. The performance of glucose sensors also significantly relied on the electrochemical properties of the electrodes in addition to the appropriate immediate constituents of active materials. In previous research, active nanomaterials directly growing on conductive substrates without polymer binders have become a great prospect because the "dead surface" from the direct contact with the electrolyte taking part in the Faradaic reactions could be decreased effectively [11]. Reliably, some works [12,13] demonstrated a remarkably improved detection sensitivity when the utilization of CuCo 2 O 4 nanosheets were grown on graphite paper and nanowires on carbon cloths in non-enzymatic glucose sensor. To fabricate a notable breakthrough, the electrochemical performance still needs to be further improved. Notably, copper foam is a popular material with three-dimensional network structure. Copper foam shows the advantages of high conductivity, cheap price, and convenient synthesis [14]. It can also be used as a conductive substrate to supply active sites, and the electrode preparation can be simplified. Herein, the copper foam is a potential material, which can be applied in the research of glucose sensor.
In this report, CuCo 2 O 4 nanosheet arrays on a copper foam substrate were synthesized by a simple solvothermal reaction and subsequent calcination. Then, they were used as electrode to detect glucose. Some of the drawbacks caused by the use of a binder were avoided because the copper foam-conductive substrate acted directly as an electrode. Moreover, the three-dimensional network of copper foam provided a large surface area for the loading of the material, resulting in several active site exposure on the electrode surfaces. Thus, the electrode material exhibited an excellent performance in glucose detection.

Chemicals
Cu foam was obtained from Jiangxi Chemical Reagent Factory (Nanchang, China). Co(NO 3 ) 2 , Cu(NO 3 ) 2 , hydrochloric acid, and NaOH were purchased from the Sinopharm Chemical Reagent Co., Ltd. (Shanghai, China). Ascorbic acid (AA), urea, uric acid (UA), and dopamine (DA) were bought from Guangzhou Chemical Reagent Factory (Guangzhou, China). Isopropanol and absolute ethanol were purchased from Guangdong Guanghua Sci.-Tech. Co. (Guangzhou, China). All chemical reagents used in the experiment were of analytical grade and without any further purification. All the aqueous solutions were prepared in deionized water.

Fabrication of CuCo 2 O 4 Nanosheets
Cu foam (CF) was cut into 2 cm × 3 cm slice and cleaned with the help of sonication in acetone, water, and 3.0 M HCl in sequence. Then, the cleaned Cu foam was washed quickly with ultrapure water and dried with pure nitrogen gas. The CuCo 2 O 4 nanosheet arrays on Cu foam substrate were fabricated via a hydrothermal reaction. In a typical process, 18.475 mg of Cu(NO 3 ) 2 ·6H 2 O and 36.375 mg of Co(NO 3 ) 2 ·6H 2 O were added into 40 mL isopropanol under magnetic stirring. In this case, a homogeneous apparent solution could be obtained. Subsequently, the solution was transferred into a Teflon-lined stainless steel autoclave, and the cleaned Cu foam was immersed into the solution. The autoclave was sealed and kept at 120 • C for 12 h in an electric oven. Finally, it was cooled naturally at room temperature. The Cu foam with precursor was removed from the autoclave. Then, it was washed with deionized water and absolute alcohol thoroughly before drying in air. Finally, the obtained samples were annealed at 350 • C for 2 h.

Electrochemical Measurements
All the electrochemical measurements were performed with a typical three-electrode system by using SP-200 Electrochemical Workstation (Bio-Logic Science Instruments, Paris, France). The CuCo 2 O 4 /CF was cut into a small pieces and directly served as the working electrode, and a platinum wire and a saturated Ag/AgCl electrode was utilized as counter and reference electrodes, respectively. All electrochemical measurements were tested in 0.1 M NaOH solution at room temperature (25 • C). The amperometric response tests were measured at an appropriate potential under stirring condition, and the analytes were added into the electrolyte after the background currents decay to a steady-state. X-ray photoelectron spectroscopy (XPS, TENSOR27, Karlsruhe, Germany) was tested to make a thorough inquiry about the chemical bonding status of the CuCo2O4 materials.

Electrochemical Measurements
All the electrochemical measurements were performed with a typical three-electrode system by using SP-200 Electrochemical Workstation (Bio-Logic Science Instruments, Paris, France). The CuCo2O4/CF was cut into a small pieces and directly served as the working electrode, and a platinum wire and a saturated Ag/AgCl electrode was utilized as counter and reference electrodes, respectively. All electrochemical measurements were tested in 0.1 M NaOH solution at room temperature (25 °C). The amperometric response tests were measured at an appropriate potential under stirring condition, and the analytes were added into the electrolyte after the background currents decay to a steady-state. Figure 1 schematically illustrates the synthesis of CuCo2O4 nanosheets on a foam copper as electrode materials. First, the copper foam was ultrasonically cleaned in water, alcohol, and 3.0 M HCl successively to remove some of the surface impurities. Then, CuCo2O4 nanosheet arrays were grown on a Cu foam substrate via a hydrothermal and calcination process. The Cu foam could be directly served as electrode because of its good electrical conductivity and lightweight.

Results and Discussion
. Confirming that the CuCo2O4 was successfully prepared on a copper foam. The structure was investigated by the field-emission SEM (FESEM). The surface of 3D Cu foam was deposited fully and uniformly, indicating that the CuCo2O4 was grown well on the substrate as shown in Figure 2b. The FESEM in Figure 2c,d further revealed the morphology of CuCo2O4. Figure 2c,d display that the CuCo2O4 morphology was nanosheets, and its thickness was approximately 50 nm. Thus, the thin nanosheets could provide several active sites for glucose oxidation. The TEM imaging was performed to further investigate the structure of CuCo2O4 nanosheets. As shown in Figure 2e, some porous structures were found in the nanosheets, possibly caused by the release of gas or water molecules during the annealing treatment [15].    Figure 2c,d display that the CuCo 2 O 4 morphology was nanosheets, and its thickness was approximately 50 nm. Thus, the thin nanosheets could provide several active sites for glucose oxidation. The TEM imaging was performed to further investigate the structure of CuCo 2 O 4 nanosheets. As shown in Figure 2e, some porous structures were found in the nanosheets, possibly caused by the release of gas or water molecules during the annealing treatment [15].  Additional data were obtained by XPS measurements to further determine the surface characteristics of these materials. The survey spectrum ( Figure 3a) showed the presence of Cu, Co, O, and C. In the Co 2p spectrum (Figure 3b), two main peaks located at binding energies of 780.0 and 794.4 eV could be assigned to Co 2p3/2 and Co 2p1/2, respectively, indicating the existence of both Co 3+ and Co 2+ [16]. Figure 3c shows the Cu 2p spectrum. Four peaks were observed at binding energies of 934.4, 942.7, 954.2, and 962.0 eV. The main peaks located at 934.4 and 954.2 eV could be assigned to Cu 2p3/2 and Cu 2p1/2, and the shakeup satellite peaks located at 942.8 and 962.0 eV could confirm the characteristic of the Cu 2+ oxidation state [17]. Three components (O1, O2, and O3) were present in the O 1s spectra (Figure 3d) 529.6, 531.4, and 532.4 eV, corresponding to the metal-oxygen bonds, large numbers of defect, and the multicity of physisorbed and chemisorbed water into and near the surface, respectively [18]. The XPS results above coincided with XRD results, confirming the successful formation of CuCo2O4 phase. Additional data were obtained by XPS measurements to further determine the surface characteristics of these materials. The survey spectrum (Figure 3a) showed the presence of Cu, Co, O, and C. In the Co 2p spectrum (Figure 3b), two main peaks located at binding energies of 780.0 and 794.4 eV could be assigned to Co 2p 3/2 and Co 2p 1/2 , respectively, indicating the existence of both Co 3+ and Co 2+ [16]. Figure 3c shows the Cu 2p spectrum. Four peaks were observed at binding energies of 934.4, 942.7, 954.2, and 962.0 eV. The main peaks located at 934.4 and 954.2 eV could be assigned to Cu 2p 3/2 and Cu 2p 1/2 , and the shakeup satellite peaks located at 942.8 and 962.0 eV could confirm the characteristic of the Cu 2+ oxidation state [17]. Three components (O1, O2, and O3) were present in the O 1s spectra (Figure 3d) 529.6, 531.4, and 532.4 eV, corresponding to the metal-oxygen bonds, large numbers of defect, and the multicity of physisorbed and chemisorbed water into and near the surface, respectively [18]. The XPS results above coincided with XRD results, confirming the successful formation of CuCo 2 O 4 phase. Cyclic voltammetry (CV) of the CuCo2O4/CF electrode was tested in the presence of 0.1 mol/L NaOH solution at different scan rates from 10 mV/s to 200 mV/s. Both the anodic and cathodic peak current densities increased with the increase of scan rate varying from 10 mV/s to 200 mV/s as shown in Figure 4a. Figure 4c shows the corresponding linear curves, indicating a good linear relationship with a correlation coefficient of 0.9995. This phenomenon indicated that the electrochemical reaction on the CuCo2O4/CF electrode was a diffusion-controlled process.
The electroactive surface area (A) was estimated to demonstrate the effective surface area of the CuCo2O4/CF electrode by using the Randles-Sevcik Equation [19] as follows: where A is the effective surface area (cm 2 ); Ip is the peak current of the redox reaction; n is the number of electrons transferred; D is the diffusion coefficient; v is the scan rate (V·s −1 ), and C is the reactant concentration. Figure 4b,d show the CV curves of bare Cu foam electrode at different scan rates and fitted curve. The slope of the fitted curve was lesser than that of the CuCo2O4/CF electrode. This result implied that the electrochemical active surface area of CuCo2O4/CF electrode was higher than that of Cu foam electrode according to the Randles-Sevcik equation.  Figure 4a. Figure 4c shows the corresponding linear curves, indicating a good linear relationship with a correlation coefficient of 0.9995. This phenomenon indicated that the electrochemical reaction on the CuCo 2 O 4 /CF electrode was a diffusion-controlled process.
The electroactive surface area (A) was estimated to demonstrate the effective surface area of the CuCo 2 O 4 /CF electrode by using the Randles-Sevcik Equation [19] as follows: where A is the effective surface area (cm 2 ); I p is the peak current of the redox reaction; n is the number of electrons transferred; D is the diffusion coefficient; v is the scan rate (V·s −1 ), and C is the reactant concentration. Figure 4b,d show the CV curves of bare Cu foam electrode at different scan rates and fitted curve. The slope of the fitted curve was lesser than that of the CuCo 2 O 4 /CF electrode. This result implied that the electrochemical active surface area of CuCo 2 O 4 /CF electrode was higher than that of Cu foam electrode according to the Randles-Sevcik equation. In this work, the prepared CuCo2O4/CF directly served as working electrode for glucose detection. The CV was recorded in 0.1 mol/L NaOH solution in the absence and presence of 0.1 mM glucose as shown in Figure 5. As a reference, the blank Cu foam electrode showed no obvious redox peak, implying a poor electrocatalytic activity. For the CuCo2O4/CF electrode, two sensitive oxidative peaks could be observed at 0.4 and 0.56 V in the CV curve. Similar to many other Cu-based glucose non-enzyme sensors, the oxidative current of Cu 2+ /Cu 3+ positioned at approximately 0.4 V was not obvious [13]. Therefore, the oxidative peaks at 0.4 V could be ascribed to the reversible transition between Co3O4 and CoOOH, whereas the oxidative peaks at 0.56 V could be ascribed to the reversible transition between and transition between CoOOH and CoO2 [20]. The reversible reaction mechanisms of CuCo2O4 species in the alkaline electrolyte could be expressed in Equations (2) and (3) [21]. The introduction of 0.1 mM glucose caused an obvious increase in the anodic peak currents. This phenomenon could be ascribed to the glucose oxidation to gluconolactone, which was accompanied by the conversion of CoO2 to CoOOH and M(Cu, Co)OOH to M(OH)2. The possible electro-oxidation mechanism of glucose could be expressed in Equations (4)-(6) [22]. The observed result demonstrated that the CuCo2O4/CF exhibited a high-efficient catalysis of glucose electrooxidation.
CuCo2O4 + OH − + H2O → CuOOH + 2CoOOH + e − CoOOH + OH − → CoO2 + H2O + e − 2CoO + C6H10O6 (glucose) → 2CoOOH + C6H10O6 (gluconolactone) CoOOH + C6H10O6 (glucose) → Co(OH)2 + C6H10O6 CuOOH + C6H10O6 (glucose) → Cu(OH)2 + C6H10O6 (6) In this work, the prepared CuCo 2 O 4 /CF directly served as working electrode for glucose detection. The CV was recorded in 0.1 mol/L NaOH solution in the absence and presence of 0.1 mM glucose as shown in Figure 5. As a reference, the blank Cu foam electrode showed no obvious redox peak, implying a poor electrocatalytic activity. For the CuCo 2 O 4 /CF electrode, two sensitive oxidative peaks could be observed at 0.4 and 0.56 V in the CV curve. Similar to many other Cu-based glucose non-enzyme sensors, the oxidative current of Cu 2+ /Cu 3+ positioned at approximately 0.4 V was not obvious [13]. Therefore, the oxidative peaks at 0.4 V could be ascribed to the reversible transition between Co 3 O 4 and CoOOH, whereas the oxidative peaks at 0.56 V could be ascribed to the reversible transition between and transition between CoOOH and CoO 2 [20]. The reversible reaction mechanisms of CuCo 2 O 4 species in the alkaline electrolyte could be expressed in Equations (2) and (3) [21]. The introduction of 0.1 mM glucose caused an obvious increase in the anodic peak currents. This phenomenon could be ascribed to the glucose oxidation to gluconolactone, which was accompanied by the conversion of CoO 2 to CoOOH and M(Cu, Co)OOH to M(OH) 2 . The possible electro-oxidation mechanism of glucose could be expressed in Equations (4)-(6) [22]. The observed result demonstrated that the CuCo 2 O 4 /CF exhibited a high-efficient catalysis of glucose electro-oxidation.
2CoO + C 6 H 10 O 6 (glucose) → 2CoOOH + C 6 H 10 O 6 (gluconolactone) CoOOH + C 6 H 10 O 6 (glucose) → Co(OH) 2 + C 6 H 10 O 6 (5) CuOOH + C 6 H 10 O 6 (glucose) → Cu(OH) 2 + C 6 H 10 O 6 (6) We selected a proper working potential for glucose determination. Figure 6a shows the amperometric response curves of CuCo2O4/CF to stepwise addition of 0.1 mM glucose into 0.1 M NaOH solution at different potentials between +0.45 V and +0.6 V. Figure 6b shows the corresponding Calibration curve. Obviously, the current response toward glucose improved with the increasing potential from 0.45 V to 0.55 V and then initially decreased from 0.55 V to 0.60 V, indicating that +0.55 V is the most appropriate potential for glucose sensing. Therefore, subsequent amperometric response to glucose was executed at the potential of +0.55 V.  Figure 7a shows the amperometric responses of the CuCo2O4/CF electrode to successive addition of glucose at the potential of +0.55 V vs. Ag/AgCl. The current was improved rapidly with the addition of glucose, indicating its stable and fast-response performance for glucose detection. At a glucose concentration of between 0.4 and 1.1 mM, the current response decreased gradually possibly be due to the faster consumption than the glucose diffusion, the local pH change, or the oxidized intermediate adsorption on active sites [23]. Figure 7b shows the corresponding calibration curve for glucose sensors, demonstrating a linear range from 0 mmol/L to 0.4 mmol/L glucose with a sensitivity of 20,981 μA·cm −2 ·mM −1 , a correlation coefficient of 0.9958, a linear concentration range from 0.4 mmol/L to 1.0 mmol/L glucose with a sensitivity of 7915 μA·cm −2 ·mM −1 , and a correlation coefficient of 0.9905. On the basis of the S/N = 3, the limit of detection (LOD) was calculated to reach 1.0 μM. The results suggested that the electrochemical behavior of the CuCo2O4/CF nanomaterial exhibited low detection limit, high sensitivity, and quick response time on glucose detection. The performance of the CuCo2O4/CF electrode was compared with other previously reported non-enzymatic glucose sensor based on Cu, Co, and self-supporting substrate as shown in Table 1. The CuCo2O4/CF electrode showed a low LOD, wide linear range, and ultrahigh sensitivity. The high performance could be We selected a proper working potential for glucose determination. Figure 6a shows the amperometric response curves of CuCo 2 O 4 /CF to stepwise addition of 0.1 mM glucose into 0.1 M NaOH solution at different potentials between +0.45 V and +0.6 V. Figure 6b shows the corresponding Calibration curve. Obviously, the current response toward glucose improved with the increasing potential from 0.45 V to 0.55 V and then initially decreased from 0.55 V to 0.60 V, indicating that +0.55 V is the most appropriate potential for glucose sensing. Therefore, subsequent amperometric response to glucose was executed at the potential of +0.55 V. We selected a proper working potential for glucose determination. Figure 6a shows the amperometric response curves of CuCo2O4/CF to stepwise addition of 0.1 mM glucose into 0.1 M NaOH solution at different potentials between +0.45 V and +0.6 V. Figure 6b shows the corresponding Calibration curve. Obviously, the current response toward glucose improved with the increasing potential from 0.45 V to 0.55 V and then initially decreased from 0.55 V to 0.60 V, indicating that +0.55 V is the most appropriate potential for glucose sensing. Therefore, subsequent amperometric response to glucose was executed at the potential of +0.55 V.  Figure 7a shows the amperometric responses of the CuCo2O4/CF electrode to successive addition of glucose at the potential of +0.55 V vs. Ag/AgCl. The current was improved rapidly with the addition of glucose, indicating its stable and fast-response performance for glucose detection. At a glucose concentration of between 0.4 and 1.1 mM, the current response decreased gradually possibly be due to the faster consumption than the glucose diffusion, the local pH change, or the oxidized intermediate adsorption on active sites [23]. Figure 7b shows the corresponding calibration curve for glucose sensors, demonstrating a linear range from 0 mmol/L to 0.4 mmol/L glucose with a sensitivity of 20,981 μA·cm −2 ·mM −1 , a correlation coefficient of 0.9958, a linear concentration range from 0.4 mmol/L to 1.0 mmol/L glucose with a sensitivity of 7915 μA·cm −2 ·mM −1 , and a correlation coefficient of 0.9905. On the basis of the S/N = 3, the limit of detection (LOD) was calculated to reach 1.0 μM. The results suggested that the electrochemical behavior of the CuCo2O4/CF nanomaterial exhibited low detection limit, high sensitivity, and quick response time on glucose detection. The performance of the CuCo2O4/CF electrode was compared with other previously reported non-enzymatic glucose sensor based on Cu, Co, and self-supporting substrate as shown in Table 1. The CuCo2O4/CF electrode showed a low LOD, wide linear range, and ultrahigh sensitivity. The high performance could be  Figure 7a shows the amperometric responses of the CuCo 2 O 4 /CF electrode to successive addition of glucose at the potential of +0.55 V vs. Ag/AgCl. The current was improved rapidly with the addition of glucose, indicating its stable and fast-response performance for glucose detection. At a glucose concentration of between 0.4 and 1.1 mM, the current response decreased gradually possibly be due to the faster consumption than the glucose diffusion, the local pH change, or the oxidized intermediate adsorption on active sites [23]. Figure 7b shows the corresponding calibration curve for glucose sensors, demonstrating a linear range from 0 mmol/L to 0.4 mmol/L glucose with a sensitivity of 20,981 µA·cm −2 ·mM −1 , a correlation coefficient of 0.9958, a linear concentration range from 0.4 mmol/L to 1.0 mmol/L glucose with a sensitivity of 7915 µA·cm −2 ·mM −1 , and a correlation coefficient of 0.9905. On the basis of the S/N = 3, the limit of detection (LOD) was calculated to reach 1.0 µM. The results suggested that the electrochemical behavior of the CuCo 2 O 4 /CF nanomaterial exhibited low detection limit, high sensitivity, and quick response time on glucose detection. The performance of the CuCo 2 O 4 /CF electrode was compared with other previously reported non-enzymatic glucose sensor based on Cu, Co, and self-supporting substrate as shown in Table 1. The CuCo 2 O 4 /CF electrode showed a low LOD, wide linear range, and ultrahigh sensitivity. The high performance could be attributed to that CuCo 2 O 4 possessed excellent electrochemical properties and high conductivity in the synergistic effect of copper and cobalt ions. Meanwhile, the morphology of ultrathin nanosheet arrays could improve the surface area and offer many catalytic sites for glucose oxidation. Moreover, 3D Cu foam as conductive substrate can provide several catalyst loadings and enhanced electron transport instead of the use of polymer binders [24].
Sensors 2018, 18, x FOR PEER REVIEW 8 of 11 attributed to that CuCo2O4 possessed excellent electrochemical properties and high conductivity in the synergistic effect of copper and cobalt ions. Meanwhile, the morphology of ultrathin nanosheet arrays could improve the surface area and offer many catalytic sites for glucose oxidation. Moreover, 3D Cu foam as conductive substrate can provide several catalyst loadings and enhanced electron transport instead of the use of polymer binders [24].  Selectivity is another important analysis parameter for glucose sensors. Therefore, to carry out anti-interference analysis is essential. AA, urea, UA, and DA would interfere the measurement results because they showed the analogous electrocatalysis behavior to the oxidation of glucose and usually existed together with glucose in human serum samples. Thus, the anti-interference performance of CuCo2O4/CF toward these interfering species was studied by amperometric method. Glucose aqueous solution of 50 μmol/L was added into 0.1 mol/L NaOH aqueous solution, and 5 μmol/L AA, 5 μmol/L urea, 5 μmol/L UA, 5 μmol/L DA, and 0.1 mmol/L NaCl were continuously added into 0.1 mol/L NaOH solution under stirring. The amperometric reaction is observed in Figure  8a. The current response caused by the interference was weak and almost negligible, indicating that the electrode exhibited good selectivity in glucose sensors.
Finally, the stability of CuCo2O4/CF was examined. Stability was performed through testing their steady-state current response over a period of 3000 s in a 0.1 mol/L NaOH with 100 μM glucose solution. As shown in Figure 8b, at the end of 3000 s, the deviation of current response was merely 1.70%. The result within a reasonable margin of error revealed good stability of glucose sensing.  Selectivity is another important analysis parameter for glucose sensors. Therefore, to carry out anti-interference analysis is essential. AA, urea, UA, and DA would interfere the measurement results because they showed the analogous electrocatalysis behavior to the oxidation of glucose and usually existed together with glucose in human serum samples. Thus, the anti-interference performance of CuCo 2 O 4 /CF toward these interfering species was studied by amperometric method. Glucose aqueous solution of 50 µmol/L was added into 0.1 mol/L NaOH aqueous solution, and 5 µmol/L AA, 5 µmol/L urea, 5 µmol/L UA, 5 µmol/L DA, and 0.1 mmol/L NaCl were continuously added into 0.1 mol/L NaOH solution under stirring. The amperometric reaction is observed in Figure 8a. The current response caused by the interference was weak and almost negligible, indicating that the electrode exhibited good selectivity in glucose sensors.
Finally, the stability of CuCo 2 O 4 /CF was examined. Stability was performed through testing their steady-state current response over a period of 3000 s in a 0.1 mol/L NaOH with 100 µM glucose solution. As shown in Figure 8b, at the end of 3000 s, the deviation of current response was merely 1.70%. The result within a reasonable margin of error revealed good stability of glucose sensing.

Conclusions
In summary, CuCo2O4 nanosheets grown on 3D Cu foam was successfully fabricated by solvothermal synthesis and subsequent calcined treatment. The structure and composition of materials were characterized by various instruments. CuCo2O4 as a binary metal oxide based on 3D Cu foam without binder was beneficial for mass electron transport and electrochemical oxidation of glucose. The electrochemical behavior was performed with high sensitivity (20,981 μA·cm −2 mM −1 ), low detection limit (1 μmol/L), and quick response times. In addition, the remarkable antiinterference made it possible in practical application. The superior glucose sensing properties should be attributed to the following reasons: The spinel structure of CuCo2O4 conducive to enhance the intrinsic catalytic activity and electronic transfer property, the morphology of nanosheet increase the specific surface area and provide more active sites, the in-situ growing hierarchical CuCo2O4 on 3D Cu foam helps to reduce the contact potential on the electrode and increase the electron collecting properties Furthermore, with the advantages of high sensitivity, good selectivity, and low cost, Cu foam was a great substrate material. Thus, Cu foam might be potential in other electrochemical studies.

Conclusions
In summary, CuCo 2 O 4 nanosheets grown on 3D Cu foam was successfully fabricated by solvothermal synthesis and subsequent calcined treatment. The structure and composition of materials were characterized by various instruments. CuCo 2 O 4 as a binary metal oxide based on 3D Cu foam without binder was beneficial for mass electron transport and electrochemical oxidation of glucose. The electrochemical behavior was performed with high sensitivity (20,981 µA·cm −2 mM −1 ), low detection limit (1 µmol/L), and quick response times. In addition, the remarkable anti-interference made it possible in practical application. The superior glucose sensing properties should be attributed to the following reasons: The spinel structure of CuCo 2 O 4 conducive to enhance the intrinsic catalytic activity and electronic transfer property, the morphology of nanosheet increase the specific surface area and provide more active sites, the in-situ growing hierarchical CuCo 2 O 4 on 3D Cu foam helps to reduce the contact potential on the electrode and increase the electron collecting properties Furthermore, with the advantages of high sensitivity, good selectivity, and low cost, Cu foam was a great substrate material. Thus, Cu foam might be potential in other electrochemical studies.