Cobalt Phosphide (Co₂P) with Notable Electrocatalytic Activity Designed for Sensitive and Selective Enzymeless Bioanalysis of Hydrogen Peroxide

Abstract

In this work, cobalt phosphide nanoparticles (Co₂P NPs) were prepared by simple and mild hydrothermal method without the use of harmful phosphorous source. The morphological structure and surface component of Co₂P were characterized by transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy measurements. Considering the excellent electrocatalytic reduction activity and good electrical conductivity of transition-metal phosphide, we fabricated Co₂P NPs on indium tin oxide (ITO) substrate (Co₂P/ITO) for H₂O₂ detection. The Co₂P/ITO transducer displayed a rapid amperometric response less than 5 s, a broader response range from 0.001 to 10.0 mM and a low detection limit of 0.65 μM. In addition, the non-enzymatic Co₂P/ITO sensor showed outstanding selectivity, reproducibility, repeatability and stability, all of which qualified the Co₂P/ITO electrode for quite a reliable and promising biosensor for H₂O₂ sensing.

Introduction

Hydrogen peroxide (H₂O₂) is a representative reactive oxygen species in living organisms, and it plays a critical role in normal physiologic function [1]. The concentration of H₂O₂ in living cells is related closely with the cell physiological balance [2]. Numerous studies have also been reported that cancer, Alzheimer’s diseases, Parkinson’s diseases and some severe diseases may be caused by abnormal concentration of H₂O₂ [3–5]. Developing accurate, sensitive, rapid and selective methods to detect the concentration of H₂O₂, a normal oxidative stress biomarker, will be undoubtedly beneficial to the early diagnosis. Up to now, a host of analytical methods such as spectroscopy [6], colorimetry [7], fluorescence [8, 9] and electrochemical methods [10–12] have been applied in H₂O₂ determination. Electrochemical method, especially amperometric test is gradually becoming one of the most simple and effective detection methods for H₂O₂ biological analysis among diverse sensing methods due to its advantages such as high sensitivity, outstanding selectivity and low cost.

Enzymatic electrochemical sensors have been proved to be effective instruments for detecting H₂O₂. However, the large-scale practical application of enzyme-based sensors is limited by complicated immobilization, environmental instability and low reproducibility. Therefore, developing non-enzymatic electrochemical H₂O₂ sensors is highly indispensable.

In recent years, a growing number of sensors based on noble metal [13–15], non-noble metal and their corresponding compounds [16–19] or carbon materials [20, 21] have been used for electrochemical H₂O₂ detection. As electrochemical active materials for fabricating non-enzymatic biosensors, transition metal compounds have been received increasing interests. Transition-metal phosphides (TMPs) are a class of newly developed materials with excellent electrocatalytic activity, good electrical conductivity and a plenty of outstanding properties. Thus, they have been extensively studied for applications in water splitting [22, 23], hydrodesulfurization [24], and supercapacitor electrodes [25]. Recent research indicates that CoP, Ni₂P and Cu₃P [26–28] can also be used as efficient electrocatalyst for non-enzymatic H₂O₂ detection. However, the number of researches about the application of TMPs in bioanalysis is still limited nowadays. Besides, the use of triphenylphosphine [29, 30], white phosphorous [31, 32] or other environmental hazardous phosphorous source [33] can increase the operational risk in the preparation of TMPs. Therefore, some research work for developing green method in TMP preparation is worth being supplemented in this area.

In this work, cobalt phosphide nanoparticles (Co₂P NPs) were prepared by one-step hydrothermal method utilizing cobalt acetate and red phosphorous as raw materials. Herein, we fabricated Co₂P NPs on indium tin oxide (ITO) substrate by drop-casting method for H₂O₂ detection. Co₂P displayed excellent electrocatalytic activity toward H₂O₂ reduction. Moreover, it revealed favorable selectivity, excellent reproducibility and good stability, which therefore exhibited its potential application as a sensitive platform for H₂O₂ detection.

Experimental Section

Reagents and Materials

All reagents were analytical grade and used without further purification. Cobalt (II) acetate tetrahydrate (Co(Ac)₂·4H₂O), cobalt chloride hexahydrate (CoCl₂·6H₂O), D-(+)-glucose, L-Glycine (L-Gly), ascorbic acid (AA), uric acid (UA), urea, NaCl, KCl, NaH₂PO₄, Na₂HPO₄, hydrogen peroxide (30% H₂O₂), ethanol and acetone were purchased from Sinopharm Chemical Reagent Co., Ltd. China. D-(–)-fructose, L-arginine (L-Arg), L-lysine (L-Lys), dopamine (DA), acetaminophen (APAP), amino trimethylene phosphonic acid (ATMP, 50 wt%) were purchased from Aladdin Ltd. Commercial red phosphorous (98.5%, 100 mesh) were purchased from Energy Chemical Technology (Shanghai) Co., Ltd. Nafion PFSA polymer dispersion (5%) were purchased from Beijing Honghaitian technology Co., Ltd. Deionized water was used in all the experiments. The indium tin oxide (ITO) glass (10 × 20 × 1.1 mm with an ITO film of 185 ± 2 nm and a sheet resistance of 6.6 ± 0.1 Ω) was supplied from Shenzhen South Xiangcheng Technology Co., Ltd.

Synthesis of Co₂P Nanoparticles

Commercial red phosphorous (2 g) was dispersed in 15 mL H₂O under sonification and hydrothermally treated at 200 °C for 12 h in a 50 mL Teflon-lined stainless autoclave to clear oxide layers [34]. Then, the hydrothermal treated red phosphorous was dried in a vacuum oven. After finishing the pretreatment of red phosphorous, 1 mmol Co(Ac)₂·4H₂O was dissolved in 30 mL distilled water to obtain an aqueous solution. Then, the hydrothermal treated red phosphorous was added into the solution under ultrasonication for 15 min with the molar ratio of Co/P 1/10. The prepared suspension was rapidly poured into a 50 mL Teflon-lined autoclave. Then, the autoclave was placed in an electronic oven and hydrothermally treated at 160, 200, 240 °C for 12 h, respectively. Then, the product was collected by centrifugation and washed three times with distilled water and ethanol, respectively. Finally, Co₂P NPs were dried at 60 °C for 3 h in air.

Synthesis of Co(PO₃)₂

The preparation method of Co(PO₃)₂ was referred to the previous report [35]. 0.1 M CoCl₂·6H₂O methanol solution was prepared firstly. Then, 2 mL ATMP (50 wt%) was added dropwise into 20 mL the above purple solution and stirred for 30 min. The insoluble cobalt-metaphosphate coordination polymer formed in the solution subsequently. The obtained pink powder was further heated to 900 °C under Ar flow with a heating rate of 5 °C·min⁻¹ and then held for 2 h. After cooling down to room temperature, the black product was collected and reheated at 650 °C for 4 h in air to remove the carbonized organic ligand. Finally, the light-purple powder of Co(PO₃)₂ was obtained.

Fabrication of Co₂P/ITO Electrode

Firstly, the ITO glass (1 cm × 2 cm) was cleaned in acetone, ethanol and deionized water for 10 min, respectively, by sonication. After that, the treated ITO was dried under nitrogen sweeping. For the modification of the electrode, 5 mg of the Co₂P NPs was dispersed in 1 mL deionized water to form 5 mg mL⁻¹ Co₂P suspension. Then, 5 μL 5% Nafion solution was added into the suspension and the mixture was ultrasonicated for 15 min to obtain uniform ink-like suspension. The Co₂P/ITO electrode was prepared by drop-casting 100 μL of Co₂P suspension on the ITO surface, and dried in air as working electrode. The schematic preparation process of Co₂P/ITO electrode is shown in Scheme 1.

Scheme 1.

Schematic preparation of Co₂P/ITO electrode and H₂O₂ sensing

Characterizations

The X-ray diffraction (XRD) data were analyzed by a D8 ADVANCE diffractometer with Cu Kα radiation. The transmission electron microscopy (TEM) measurement was conducted using a Tecnai G2 F20 with energy dispersed spectrum detector. X-ray photoelectron spectroscopy (XPS) spectra were measured on a Thermo ESCALAB 250XI spectrometer.

Electrochemical Measurements

Voltammetry measurements were accomplished by CHI 660E electrochemical workstation in a three-electrode system, employing Co₂P/ITO electrode as working electrode, a platinum foil (1 cm × 1 cm) as counter electrode and Ag/AgCl with 3 M KCl solution as reference electrode to study the electrochemical activities of the synthesized samples for H₂O₂ detection. Phosphate buffer saline (PBS; 0.1 M, pH 7.4) was used as the electrolyte to simulate the physiological medium in human body. The sensing performances of Co₂P/ITO electrode toward H₂O₂ detection were investigated by cyclic voltammetry (CV) and amperometry (I-t). All the detection experiments were performed under 100 rpm stirring at room temperature. Electrochemical impedance tests were performed on VersaSTAT 3F electrochemical workstation and ferricyanide solution was used as the electrolyte for impedance measurement.

Results and Discussion

Characterization of Co₂P NPs

The crystal structure of Co₂P NPs was confirmed by XRD measurement. Figure 1a shows the XRD patterns of Co₂P samples prepared at 160, 200 and 240 °C for 12 h. The Co₂P sample prepared at 200 °C shows diffraction peaks at around 40.7°, 40.9°, 52.0° and 56.2° which correspond to the characteristic diffraction planes at (121), (201), (002) and (320) for the orthorhombic phase of Co₂P (JCPDS no. 32-0306). When temperature varied from 160 to 200 °C, the intensities of diffraction peaks increased and the peaks became narrower and sharper, indicating that the products had a higher crystallinity at 200 °C. However, when temperature reached 240 °C, some impurities were formed and the diffraction peaks at 29.7° was attributed to the diffraction plane at (-222) of Co(PO₃)₂ (JCPDS no. 27-1120). The influence of synthetic time on the preparation of Co₂P under 200 °C is shown in Additional file 1: Fig. S1. When the time duration was controlled within 12 h, the obtained Co₂P NPs displayed the lowest value of full width at half maximum of (121) peak, suggesting better crystallinity. Besides, none of impurities existed in the sample when the reaction time varied from 6 to 24 h. According to the Scherrer formula, the calculated grain size of Co₂P NPs prepared at 200 °C for 12 h was 14.2 nm.

Fig. 1.

a XRD patterns of Co₂P NPs prepared at different temperatures for 12 h. b Transmission electron microscopic image and high-resolution transmission electron microscopic image (inset) of Co₂P NPs. XPS spectra of Co₂P in the c Co 2p region and d P 2p region

The morphology of Co₂P NPs was assessed by TEM measurements. As shown in Fig. 1b, the product prepared at 200 °C is composed of irregular nanoparticles with the diameter around 10–20 nm and two lattice fringes can be clearly seen in the high-resolution TEM (HRTEM) image (inset in Fig. 1b). The distance between the neighboring planes is 0.22 nm, corresponding to the (121) facets of Co₂P, which further confirms that the formation of TMP is Co₂P.

The XPS technique was employed in analyzing the chemical compositions on the surface of the Co₂P. Additional file 1: Fig. S2 shows the XPS survey spectrum of Co₂P. Co, P and O elements are detected in the sample, confirming the existence of Co₂P and some oxidized products. Energy-dispersive X-ray spectroscopy (EDX) spectra of Co₂P (Additional file 1: Fig. S3) further confirms the co-existence of three elements (Co, P, O) in the sample. The high-resolution XPS spectra of Co 2p and P 2p are shown in Fig. 1c, d, respectively. In Co 2p spectrum, the peaks at 781.1 and 797.6 eV can be ascribed to the binding energies (BEs) of Co²⁺ 2p_3/2 and Co²⁺ 2p_1/2, respectively [26, 36]. The peaks at 786.0 and 803.1 eV are two apparent shake-up satellite peaks. The Co 2p BE of 778.2 eV shifts positively from that of metallic Co (777.9 eV), which suggests that Co in Co₂P has a partial positive charge (δ⁺) with a small value (0 < δ < 2) [37]. On the contrary, the P 2p BE of 129.4 eV shifts negatively from that of elemental P (130.2 eV) so that the P has a partial negative charge (δ⁻) in Co₂P. The changes of BE in Co and P element compared with their elementary substance, respectively, reveal that the transfer direction of electron density in Co₂P is from Co to P [38]. Superficial oxidation of Co₂P generates a few of oxidized P species in the sample. Therefore, the peaks at 133.2 eV in high BE range are assigned to the oxides [39].

Electrochemical Detection of H₂O₂ at Co₂P/ITO Electrode

To investigate the electrocatalytic activity of Co₂P NPs in H₂O₂ reduction, we designed a non-enzymatic H₂O₂ electrode by drop-casting Co₂P NPs suspension on a bare ITO surface. Figure 2a shows the CV curves of bare ITO and Co₂P/ITO in 0.1 M PBS at pH 7.4 with and without 5.0 mM H₂O₂, respectively. The dash lines indicate that the response of bare ITO to H₂O₂ reduction is negligible. However, the Co₂P/ITO electrode exhibits a remarkable reduction peak at − 0.5 V in the presence of H₂O₂, which demonstrates the prominent electrocatalytic activity of Co₂P NPs toward H₂O₂ reduction. Figure 2b presents the CV curves of Co₂P/ITO at different scan rates (from 30 to 100 mV s⁻¹) with 2.5 mM H₂O₂. When increasing the scan rate, the reduction peak current increased and the peak potential shifted to the more negative potential side, indicating the reduction in H₂O₂ on Co₂P/ITO was an irreversible reaction. The corresponding calibration curve (inset, Fig. 2b) shows that the reduction peak current densities increase linearly proportional to the scan rate, suggesting that the electrochemical reduction of H₂O₂ on the surface of Co₂P/ITO electrode is a surface-controlled process [40].

Fig. 2.

a CV curves of bare ITO and Co₂P/ITO electrode in 0.1 M PBS with and without 5.0 mM H₂O₂ at a scan rate of 100 mV s⁻¹. b CV curves of Co₂P/ITO electrode in 2.5 mM H₂O₂ at scan rates from 30 to 100 mV s⁻¹. Inset: The corresponding plot of current versus the scan rate. c Amperometric responses of Co₂P/ITO electrode with successive addition of H₂O₂ in 0.1 M PBS. d The calibration curve of steady current versus the concentration of H₂O₂

Figure 2c, d show the amperometric response and the calibration curve of Co₂P/ITO electrode upon the successive addition of H₂O₂ into the 0.1 M PBS at − 0.5 V with stirring. The Co₂P/ITO electrode exhibited quick response to the addition of H₂O₂ and achieved the steady-state current within 5 s. The calibration curve in Fig. 2d shows that the transducer displays a multi-linear range of H₂O₂ concentration from 0.001 to 1.0 mM, 1.0–5.0 mM and 5.0–10.0 mM. The sensitivity of the sensor alters with the increasing concentration of H₂O₂, due to the change of electrocatalytic reduction kinetics of H₂O₂ on the electrode surface. According to previous reports, the rate-determining step of H₂O₂ reduction is dominated by H₂O₂ adsorption at low concentration, whereas the activation of H₂O₂ is the major determinant at high concentration. In the middle region, the reduction kinetics of H₂O₂ is controlled by adsorption and activation at the same time [10]. A multitude of analysts will adsorb on the surface of Co₂P and cover the active sites in the high concentration, which lead to the decrease in sensitivity [41].

The comparison on H₂O₂ sensing performances of the prepared Co₂P sample at various reaction temperature and time is shown in Additional file 1: Fig. S4, S5 and Table S1, indicating that the Co₂P sample prepared at 200 °C for 12 h displays the best H₂O₂ sensing performances. When reaction temperature raised to 240 °C, the formed Co(PO₃)₂ in Co₂P could be regarded as impurity. To further clarify the influence of Co(PO₃)₂ on H₂O₂ detection, the electrochemical properties of Co(PO₃)₂ were investigated. As shown in Additional file 1: Fig. S6, Co(PO₃)₂ displays negligible electrochemical response toward H₂O₂ and its conductivity is inferior to Co₂P, which declines the current signal of Co₂P/ITO in amperometric test. Therefore, the higher purity and better crystallinity of Co₂P sample may contribute to the improvement of sensing performances. Thus, we choose the Co₂P sample prepared at 200 °C and 12 h as the best H₂O₂ sensing material. The calibration I–t curve also presents a good linear relationship in the concentration of 1.0–50 μM, the physiological range of H₂O₂ concentration in biosystem (Fig. S7) [28], which could be helpful to improve the possibility of practical applications of this sensor. In addition, the limit of detection (LOD) of the H₂O₂ sensor can be calculated to be 0.65 μM at a signal-to-noise ratio of 3. Compared with the previously reported H₂O₂ sensor, the comprehensive electrochemical performances of our Co₂P/ITO transducer are superior to those with favorable sensitivity, linear range and LOD, as shown in Table 1.

Table 1.

Sensing performances on comparison of Co₂P/ITO with other cobalt-based non-enzymatic H₂O₂ sensors

Materials	Linear range	Sensitivity (μA mM−1 cm−2)	Detection limit (μM)	References
Co3O4–rGO	15–675 μM	1140	2.4	[42]
Co3O4 nanowire/N-carbon foam	0.01–1.4 mM	230	1.4	[16]
Co3O4/MWCNTs	0.02–0.43 mM	1000	2.46	[43]
Co3O4/rGO	1–18.5 mM	–	0.5	[44]
CoS	0.005–14.82 mM	459	1.5	[45]
CoP NWs	0.001–12 mM	–	0.48	[26]
Hb/CoP-CC (carbon cloth)	2.0–2670 μM	56.2	0.67	[40]
Co2P/ITO	0.0001–1.0 mM	668.6	0.65	This work
	1.0–5.0 mM	339.0
	5.0–10.0 mM	102.3

After detecting 1.0 mM H₂O₂ repeatedly for 35 times (Fig. 3a, b), the XPS spectra in Co 2p and P 2p region of Co₂P are analyzed to further investigate the sensing mechanism. There is no significant change in the position of the peaks in P 2p region before and after H₂O₂ detection. However, the peaks at 778.2 and 793.0 eV in Co 2p spectrum disappeared after multiple measurements. As the peak at 778.2 eV indicates the existence of reduced Co species in Co₂P sample [37], the disappearance of these two peaks demonstrates that the reduced Co species with low valence in Co₂P may be oxidized by H₂O₂ during the detection process, especially with high concentration of H₂O₂. The remnant peaks in Co 2p region (782.1 and 798.3 eV) are attributed to Co²⁺ 2p_3/2 and Co²⁺ 2p_1/2, respectively, suggesting the exclusive existence of Co(II) species in Co₂P after multiple measurements. According to previous reports about the utilization of cobalt-based electrocatalyst in H₂O₂ detection, Co²⁺ species are demonstrated as the catalytic active sites for H₂O₂ reduction [46–48]. Generally, the electrochemical reduction in H₂O₂ goes through two steps in PBS [49, 50], as shown below.

$${\text{H}}_2{\text{O}}_2+{\text{e}}^{-}\to {\text{OH}}_{\text{ad}}+{\text{OH}}^{-}$$ 1

$${\text{OH}}_{\text{ad}}+{\text{e}}^{-}\to {\text{OH}}^{-}$$ 2

$${\text{2OH}}^{-}+{\text{2H}}^{+}\to {\text{2H}}_2\text{O}$$ 3

Fig. 3.

The comparison of XPS spectra in a Co 2p region and b P 2p region of Co₂P before and after detection

In the first step, H₂O₂ obtains an electron to form adsorbed OH⁻ (OH_ad). When the intermediate OH_ad obtains an additional electron, the final reduction product of H₂O₂, H₂O, is generated. As the redox potential of H₂O₂/H₂O is higher than Co³⁺/Co²⁺, the Co(II) species in Co₂P can be oxidized to Co(III) in the electron transfer process and H₂O₂ is reduced to H₂O irreversibly. During the amperometric test, the applied bias is − 0.5 V versus Ag/AgCl (equals to 0.14 V vs. NHE), which is lower than the standard redox potential of Co³⁺/Co²⁺. As a result, the oxidized Co(III) can be reduced to Co(II) and theses catalytic active sites of Co(II) are regenerated again. Therefore, it can be concluded that the catalytic cycle of Co (II) species takes place during electrochemical detection of H₂O₂ and the reduced Co species with low valence are oxidized by H₂O₂ after repetitive measurements.

Selectivity, Stability, Reproducibility and Repeatability of Co₂P/ITO Electrode

Anti-interference performance is another important property of biosensor. High purity nitrogen was utilized to avoid the influence by dissolved oxygen in solution because oxygen could be reduced at similar potential which was applied in amperometric test [51]. Comparing the CV curves of Co₂P/ITO in 0.1 M PBS with or without nitrogen purging, the reduction potential and the current response of 2.5 mM H₂O₂ are similar, as shown in Fig. S8, which therefore suggests that the interference of dissolved oxygen can be neglected. Selectivity of Co₂P/ITO was also tested with common substances and other small molecules in body fluid, such as some inorganic salts, saccharides, amino acids and reductive biomolecules. As shown in Fig. 4a, the current response after adding the above interferents can be neglected compared with the response of 1.0 mM H₂O₂. As both two O atoms of H₂O₂ could be bonded with one or two Co atoms [52], the H₂O₂ molecule would chemically adsorb on Co(II) species in Co₂P specifically. In addition, the interference from indiscriminate oxidation of some reductive compounds in real biological samples at high potential can be also reduced significantly at lower bias potential [53]. Therefore, the favorable selectivity of Co₂P toward H₂O₂ mainly benefits from the Co(II) species as specific adsorption sites and the applied negative bias potential during sensing process.

Fig. 4.

a Amperometric responses of Co₂P/ITO electrode with the addition of 1 mM H₂O₂ and other interfering species (10 mM NaCl, KCl, Glu, Fru, urea, L-Gly, L-Arg, L-Lys, AA; 1 mM DA, UA; 0.5 mM APAP) in 0.1 M PBS. b The cathodic peak currents of ten successive scanning CV curves in 50 μM H₂O₂. c Reproducibility of six Co₂P/ITO electrodes for detecting 1.0 mM H₂O₂. d Repeatability of Co₂P/ITO electrode for detecting 1.0 mM H₂O₂ eight times

Moreover, the stability, reproducibility and repeatability of the Co₂P/ITO transducer were also evaluated. The reduction peak currents of ten successive scanning CV curves in 50 μM H₂O₂ is shown in Fig. 4b. After ten cycles, the peak current of the electrode only fell by 2.7%. In addition, the sensor remained about 98.2% of its initial current response after being stored in air for one month (Fig. S9), demonstrating ideal detecting stability and outstanding long-term durability. The electrode-to-electrode reproducibility is investigated by calculating the relative standard deviation (RSD) of H₂O₂ current responses. To eliminate the potential error from electrode fabrication as far as possible, the steady current density in the presence of H₂O₂ is subtracted by the initial background signal of individual electrode and the obtained difference value is regarded as the electrochemical response of each electrode. Six Co₂P/ITO electrodes were fabricated under the same conditions for controlled experiments and the RSD of current responses was 1.24%, as shown in Fig. 4c, indicating the relatively excellent reproducibility of Co₂P/ITO. Meanwhile, repeatability was measured in one electrode by detecting 1.0 mM H₂O₂ eight times, and the RSD of 1.14% was achieved (Fig. 4d). The above results illustrate the satisfactory stability, reproducibility and repeatability of the electrode for non-enzymatic electrochemical detection of H₂O₂.

Conclusion

In summary, Co₂P NPs were successfully synthesized by hydrothermal method. Furthermore, the Co₂P NPs prepared at 200 °C for 12 h have been proved as an efficient catalyst toward electrochemical reduction of H₂O₂ in pH 7.4 PBS. As a non-enzymatic H₂O₂ sensor, the Co₂P/ITO electrode displayed a rapid amperometric response less than 5 s, a broader response range from 0.001 to 10.0 mM and a low detection limit of 0.65 μM, as well as satisfactory selectivity, reproducibility and stability. This work aims to broaden the research about the application of transition metal phosphide in electrochemical detection of small biomolecules and our Co₂P/ITO sensor could be designed as a new non-enzymatic platform for H₂O₂ detection.

Abbreviations

NPs

Nanoparticles

ITO

Indium tin oxide

TEM

Transmission electron microscopy

HRTEM

High-resolution transmission electron microscopy

XRD

X-ray diffraction

XPS

X-ray photoelectron spectroscopy

EDX

Energy-dispersive X-ray spectroscopy

CV

Cyclic voltammetry

I-t

Amperometry

Gly

Glycine

AA

Ascorbic acid

UA

Uric acid

Arg

Arginine

Lys

Lysine

DA

Dopamine

APAP

Acetaminophen

ATMP

Trimethylene phosphonic acid

PBS

Phosphate buffer

LOD

Detection limit

RSD

Relative standard deviation

Authors' contributions

The manuscript was written through contributions of all authors. DHY, JYT and RBB designed and performed the experiments. JYT and SYY analyzed the experiment data and wrote the manuscript. MNJ and HML assisted with interpretation of the data from electrochemical test. ZGK, FW and CLL helped to check the manuscript before submission. CLL conceived of the study and all authors read and approved the final version of the manuscript.

Funding

We appreciate the financial support by the National Natural Science Foundation of China (81660708), National Key Research and Development Project (2019YFC0312602), Science and Technology Support Program of Jiangsu Province (BE2018389) and the Key Project of Tibetan Medical Administration of Tibet (2017005). The work is also supported by “Double First-Class” University Project (CPU2018GY25), the Qinglan Project of Young Academic Leaders of Jiangsu Province and Fundamental Research Funds for the Central Universities (2632019YX01).

Availability of data and materials

All data and materials are fully available without restriction.

Competing interests

The authors declare that they have no competing interests.

Supplementary information

The online version contains supplementary material available at 10.1186/s11671-020-03469-9.