Experimental techniques to monitor and visualize the behaviors of single nanoparticles have not only revealed the significant spatial and temporal heterogeneity of those individuals, which are hidden in ensemble methods, but more importantly, they have also enabled researchers to elucidate the origin of such heterogeneity. In pursuing the intrinsic structure-function relations of single nanoparticles, the recently developed stochastic collision approach demonstrated some early promise. However, it was later realized that the appropriate sizing of a single nanoparticle by an electrochemical method could be far more challenging than initially expected owing to the dynamic motion of nanoparticles in electrolytes and complex charge-transfer characteristics at electrode surfaces. This clearly indicates a strong necessity to integrate single nanoparticle electrochemistry with high-resolution optical microscopy. Hence, this review aims to give a timely update of the latest progress for both electrochemically sensing and seeing single nanoparticles. A major focus is on collision-based measurements, where nanoparticles or single entities in solution impact on a collector electrode and the electrochemical response is recorded. These measurements are further enhanced with optical measurements in parallel. For completeness, advances in other related methods for single nanoparticle electrochemistry are also included.
Inspired by the addition-elimination catalytic mechanism of natural pyrroloquinoline quinone (PQQ) containing proteins, PQQ-modified hybrid nanomaterials have been increasingly developed recently as biomimetic heterogeneous electrocatalysts. However, up until now, no existing electrochemical approach was able to assess the intrinsic catalytic activity of PQQ sites, impeding the design of efficient PQQ-based electrocatalysts. Herein, in this work, we introduced a new method to calculate the turnover frequency (TOF) of any individual PQQ functional group for electrocatalytic oxidation of tris(2-carboxyethyl)phosphine (TCEP), through the study of single PQQ-decorated carbon nanotube (CNT) collisions at a carbon fiber ultramicroelectrode by chronoamperometry. The core advantage of this approach is being able to resolve the number of PQQ catalytic sites grafted on each individual CNT, so that the charge of any CNT collision event can be accurately translated into the intrinsic activity of the respective PQQ functional groups. The resulting collision-induced current responses clearly showed that the functionalization of CNTs with PQQ could indeed enhance its catalytic performance by 3 times, reaching a TOF value of 133 s at 1.0 V vs Ag/AgCl. Such a single CNT collision technique, which is proposed for the first time in this work, can open up a new avenue for studying the intrinsic (electro)catalytic performance at a molecular level.
Tyrosinase (TYR) which can catalyze the oxidation of catechol is recognized as a significant biomarker of melanocytic lesions, thus developing powerful methods for the determination of TYR activity is highly desirable for the early diagnosis of melanin-related diseases, including melanoma. Herein, we develop a novel portable and recyclable surface-enhanced Raman scattering (SERS) sensor, prepared by assembling gold nanoparticles and p-thiol catechol (p-TC) on an ITO electrode, for detecting TYR activity via the SERS spectral variation caused by the conversion of p-TC into its corresponding quinone under TYR catalysis. The developed SERS sensor has a rapid response to TYR within 1 min under the optimized conditions and shows high selectivity for TYR with the detection limit at 0.07 U/mL. Importantly, this SERS sensor can be easily regulated by applying negative voltage to achieve circular utilization, favoring the automation of SERS detection. Furthermore, the presented recyclable SERS sensor can perform well on both the determination of TYR activity in serum and the assessment of TYR inhibitor, demonstrating huge potential in the sensitive, selective, and facile detection of TYR activity for disease diagnosis and drug screening related with TYR.
Collision at a single molecule level was achieved based on the nanoimpact of an individual pyrroloquinoline quinone (PQQ) modified multiwalled carbon nanotube (MWCNT) at the carbon fiber ultramicroelectrode (C UME). Electrocatalytic amplification of the current responses was observed when the PQQ-modified MWCNT collided with C UME in the presence of hydrazine (N2H4) in a Tris-HCl buffer solution, which was also supported by the conventional cyclic voltammetry and chronoamperometry techniques. The enhanced catalytic oxidation of N2H4 was due to the “addition-elimination” redox cycling mechanism of PQQ/PQQH2, where the oxidation of N2H4 occurred together with the reduction of PQQ under an external bias, and the formed PQQH2 intermediate would be reoxidized back to PQQ simultaneously. The average collision current, duration, and charge for PQQ-modified MWCNT at 1.0 V vs Ag/AgCl were 105 pA, 0.45 ms, and 49 fC, respectively. As a result, the turnover frequency of electrocatalytic oxidation of N2H4 by PQQ was calculated to be 54 s–1. In this regard, the proposed individual carbon nanotube collision method can not only serve as a promising sensing technique to detect biochemical species, but more importantly provide a robust approach to determine the intrinsic catalytic activity as well.
The rapid and precise measurement of dopamine (DA) levels is of great benefit to unveil physiological and pathological processes. The electrochemical detection approaches feature fast DA response, but remain challenging at the moment to realize ultra-high sensitivity and selectivity to the trace amount of DA, especially in the presence of highly concentrated ascorbic acid (AA, the most common interferent in the human body). To address this issue, a negatively charged hybrid bilayer membrane (HBM) modified gold electrode was designed, which was only attractive to the positive DA but not the negative AA. As a result, this work managed to achieve an ultra-low detection limit of 0.41 pM DA under the interference of AA of 10 9 times higher concentration. Such an excellent performance is over three orders of magnitude better than previously reported electrochemical sensing methods, suggesting the promise of applying HBM functionalization in electrochemical and bio-sensing applications.
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