RESUMO
Organic photoelectrochemical transistor (OPECT) has shown substantial potential in the development of next-generation bioanalysis yet is limited by the either-or situation between the photoelectrode types and the channel types. Inspired by the dual-photoelectrode systems, we propose a new architecture of dual-engine OPECT for enhanced signal modulation and its biosensing application. Exemplified by incorporating the CdS/Bi2S3 photoanode and Cu2O photocathode within the gate-source circuit of Ag/AgCl-gated poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) channel, the device shows enhanced modulation capability and larger transconductance (gm) against the single-photoelectrode ones. Moreover, the light irritation upon the device effectively shifts the peak value of gm to zero gate voltage without degradation and generates larger current steps that are advantageous for the sensitive bioanalysis. Based on the as-developed dual-photoelectrode OPECT, target-mediated recycling and etching reactions are designed upon the CdS/Bi2S3, which could result in dual signal amplification and realize the sensitive microRNA-155 biodetection with a linear range from 1 fM to 100 pM and a lower detection limit of 0.12 fM.
Assuntos
Cobre , Técnicas Eletroquímicas , Sulfetos , Tiofenos , Técnicas Eletroquímicas/instrumentação , Cobre/química , Sulfetos/química , Compostos de Cádmio/química , Técnicas Biossensoriais/instrumentação , Bismuto/química , Transistores Eletrônicos , Processos Fotoquímicos , Poliestirenos/química , MicroRNAs/análise , Eletrodos , Polímeros/químicaRESUMO
The organic photoelectrochemical transistor (OPECT) has been proven to be a promising platform to study the rich light-matter-bio interplay toward advanced biomolecular detection, yet current OPECT is highly restrained to its intrinsic electronic amplification. Herein, this work first combines chemical amplification with electronic amplification in OPECT for dual-amplified bioanalytics with high current gain, which is exemplified by human immunoglobulin G (HIgG)-dependent sandwich immunorecognition and subsequent alkaline phosphatase (ALP)-mediated chemical redox cycling (CRC) on a metal-organic framework (MOF)-derived BiVO4/WO3 gate. The target-dependent redox cycling of ascorbic acid (AA) acting as an effective electron donor could lead to an amplified modulation against the polymer channel, as indicated by the channel current. The as-developed bioanalysis could achieve sensitive HIgG detection with a good analytical performance. This work features the dual chemical and electronic amplification for OPECT bioanalysis and is expected to stimulate further interest in the design of CRC-assisted OPECT bioassays.
Assuntos
Técnicas Biossensoriais , Estruturas Metalorgânicas , Humanos , Técnicas Eletroquímicas , Oxirredução , Polímeros , Limite de DetecçãoRESUMO
Herein we present a proof-of-concept study of target-dependent gating of nanopores for general photoelectrochemical (PEC) bioanalysis in an H-cell. The model system was constructed upon a left chamber containing ascorbic acid (AA), the antibody modified porous anodic alumina (AAO) membrane separator, and a right chamber placed with the three-electrode system. The sandwich immunocomplexation and the associated enzymatic generation of biocatalytic precipitation (BCP) in the AAO nanopores would regulate the diffusion of AA from the left cell to the right cell, leading to a varied photocurrent response of the ZnInS nanoflakes photoelectrode. Exemplified by fatty-acid-banding protein (FABP) as the target, the as-developed protocol achieved good performance in terms of sensitivity, selectivity, reproducibility, as well as efficient reutilization of the working electrode. On the basis of an H-cell, this work features a new protocol of target-dependent gating-based PEC bioanalysis, which can serve as a general PEC analytical platform for various other targets of interest.
Assuntos
Técnicas Biossensoriais , Nanoporos , Técnicas Eletroquímicas , Eletrodos , Processos Fotoquímicos , Reprodutibilidade dos TestesRESUMO
The design and development of a 3D hierarchical CdS/NiO heterojunction and its application in a self-powered cathodic photoelectrochemical (PEC) bioanalysis is introduced. Specifically, NiO nanoflakes (NFs) were in situ formed on carbon fibers via a facile liquid-phase deposition method followed by an annealing step and subsequent integration with CdS quantum dots (QDs). The glucose oxidase (GOx) was then coated on the photocathode to allow the determination of glucose. Under 5 W 410 nm LED light and at a working voltage of 0.0 V (vs. Ag/AgCl), this method can assay glucose concentrations down to 1.77×10-9 M. The linear range was 5×10-7 M to 1×10-3 M, and the relative standard deviation (RSD) was below 5%. The photocathodic biosensor achieved target detection with high sensitivity and selectivity. This work is expected to stimulate more passion in the development of innovative hierarchical heterostructures for advanced self-powered photocathodic bioanalysis. Design of 3D hierarchical CdS/NiO heterojunction and its application in a self-powered cathodic photoelectrochemical (PEC) bioanalysis.
Assuntos
Compostos de Cádmio/química , Glucose Oxidase/metabolismo , Glucose/análise , Nanocompostos/química , Níquel/química , Sulfetos/química , Técnicas Biossensoriais , Fibra de Carbono , Técnicas Eletroquímicas , Limite de Detecção , Processos Fotoquímicos , Pontos QuânticosRESUMO
This Letter reports a novel synthetic methodology for the fabrication of three-dimensional (3D) nanostructured CdS@carbon fiber (CF) networks and the validation of its feasibility for applications as a general platform for photoelectrochemical (PEC) bioanalysis. Specifically, 3D architectures are currently attracting increasing attention in various fields due to their intriguing properties, while CdS has been most widely utilized for PEC bioanalysis applications because of its narrow band gap, proper conduction band, and stable photocurrent generation. Using CdS as a representative material, this work realized the innovative synthesis of 3D CdS@CF networks via a simple solvothermal process. Exemplified by the sandwich immunoassay of fatty-acid-binding protein (FABP), the as-fabricated 3D CdS@CF networks exhibited superior properties, and the assay demonstrated good performance in terms of sensitivity and selectivity. This work features a novel fabrication of 3D CdS@CF networks that can serve as a general platform for PEC bioanalysis. The methodology reported here is expected to inspire new interest for the fabrication of other 3D nanostructured Cd-chalcogenide (S, Se, Te)@CF networks for wide applications in biomolecular detection and beyond.
Assuntos
Compostos de Cádmio/síntese química , Fibra de Carbono/química , Técnicas Eletroquímicas/instrumentação , Processos Fotoquímicos , Sulfatos/síntese química , Compostos de Cádmio/química , Fibra de Carbono/ultraestrutura , Nanoestruturas , Sulfatos/químicaRESUMO
This work reports the first synthesis and characterization of a ferroelectric perovskite oxide-based heterostructure as well as its application for photoelectrochemical (PEC) bioanalytical purposes. Specifically, exemplified by [KNbO3]1- x[BaNi1/2Nb1/2O3-δ] x (KBNNO), the ferroelectric perovskite oxides were prepared by solid-state synthesis, while the TiO2 nanorod (NR) arrays were obtained via a hydrothermal method. Using the technique of pulsed laser deposition (PLD), KBNNO were then deposited on TiO2 NRs to form KBNNO@TiO2 NR heterostructures. Various characterization techniques were applied to reveal compositional and structural information on the as-fabricated sample, and favorable alignment existed between the two components as displayed by the PEC test. In the detection of l-cysteine, the as-fabricated KBNNO@TiO2 NRs demonstrated good performance in terms of sensitivity and selectivity. This work revealed the potential of ferroelectric perovskite oxide and its heterostructures for innovative PEC bioanalytical applications, and we hope it will generate more interest in the development of various ferroelectrics-based heterostructures for advanced PEC bioanalysis.
Assuntos
Compostos de Cálcio/química , Técnicas Eletroquímicas/métodos , Compostos Ferrosos/química , Nanotubos/química , Óxidos/química , Processos Fotoquímicos , Titânio/química , Microscopia Eletrônica de Varredura , Microscopia Eletrônica de Transmissão , Análise Espectral Raman , Difração de Raios XRESUMO
This work reports the synthesis, characterization, and application of bifunctional semiconducting CuO nanotubes (NTs) electrode for innovative synergized cathodic photoelectrochemical (PEC) enzymatic bioanalysis. Specifically, CuO NTs electrode was fabricated by surface oxidation of the copper foil in an alkaline aqueous solution with (NH4)2S2O8 and then annealed in air at 200 °C. After the subsequent coupling with the model enzyme of xanthine oxidase (XOD), the resulted photocathodic enzyme biosensor exhibited good analytical performance of rapid response, high stability, and good sensitivity. Especially, due to the unique catalytic property of CuO toward H2O2, a novel enzymatic cascade design between biological catalyst (XOD as natural enzyme) and biomimetic catalyst (CuO as the peroxidase mimetics) was constructed, and the dual-catalyst system with special synergy effect could achieve the cathodic PEC guanine bioanalysis with enhanced efficiency. In the determination, the cathodic photocurrent was found to be proportional to the guanine concentration, which was different from the commonly observed O2-dependent suppression of the photocurrent. In all, such a bifunctional CuO NTs-based PEC bioassay format has not been reported. The success of this work can offer great chances for further development and implementation of novel CuO-based PEC bioanalytical systems. More importantly, the strategy proposed here could contribute to the development of an original prototype for general PEC enzymatic bioanalysis.
Assuntos
Técnicas Biossensoriais , Cobre/química , Técnicas Eletroquímicas , Nanotubos/química , Xantina Oxidase/análise , Eletrodos , Processos Fotoquímicos , Semicondutores , Xantina Oxidase/metabolismoRESUMO
This work reports the development of three-dimensional (3D) semiconducting polymer/graphene (SP/G) networks toward sensitive photocathodic enzymatic bioanalysis. Specifically, the porous 3D graphene was first synthesized via the hydrothermal and freeze-dry processes and then mixed with semiconducting polymer to obtain the designed hierarchical structure with unique porosity and large surface area. Afterward, the as-prepared hybrid was immobilized onto the indium tin oxide (ITO) for further characterizations. Exemplified by sarcosine oxidase (SOx) as a model biocatalyst, an innovative 3D SP/G-based photocathodic bioanalysis capable of sensitive and specific sarcosine detection was achieved. The suppression of cathodic photocurrent was observed in the as-developed photocathodic enzymatic biosystem due to the competition of oxygen consumption between the enzyme-biocatalyst process and O2-dependent photocathodic electrode. This work not only presented a unique protocol for 3D SP/G-based photocathodic enzymatic bioanalysis but also provided a new horizon for the design, development, and utilization of numerous 3D platforms in the broad field of general photoelectrochemical (PEC) bioanalysis.
Assuntos
Fluorenos/química , Grafite/química , Maleatos/química , Polímeros/química , Poliestirenos/química , Sarcosina Oxidase/química , Sarcosina/análise , Técnicas Biossensoriais/métodos , Técnicas Eletroquímicas/métodos , Eletrodos , Enzimas Imobilizadas/química , Fluorenos/efeitos da radiação , Grafite/síntese química , Luz , Maleatos/efeitos da radiação , Processos Fotoquímicos , Polímeros/efeitos da radiação , Poliestirenos/efeitos da radiação , Porosidade , Compostos de Estanho/químicaRESUMO
We have developed sensitive photoelectrochemical (PEC) detection of cysteine using the gold nanoparticles (Au NPs) equipped perovskite Bi4NbO8Cl heterostructure. The Bi4NbO8Cl was prepared by a solid-state reaction, and the Au NPs/Bi4NbO8Cl electrode was made through the electrostatic layer-by-layer self-assembly technique. The Au NPs/Bi4NbO8Cl electrode provided much enhanced photocurrent with a great increase compared to the bare Bi4NbO8Cl electrode and allowed for the plasmon-enhanced PEC detection of cysteine with good performance. It demonstrated rapid response, high stability, wide linear detection range and certain selectivity, implying its great promise in its application. Therefore, the Au NPs/Bi4NbO8Cl heterostructure has provided a promising platform for the development of PEC bioanalysis. More generally, these findings offered an insight into the exploitation of perovskite materials for PEC bioanalytical purposes.
Assuntos
Compostos de Cálcio/química , Cisteína/análise , Técnicas Eletroquímicas/métodos , Ouro/química , Nanopartículas Metálicas/química , Óxidos/química , Titânio/química , Eletrodos , Glutationa/química , Reprodutibilidade dos Testes , Compostos de Estanho/químicaRESUMO
Anion recognitions between common anions and a novel pincer-like receptor (N,N'-bis(5-fluorobenzoyloxyethyl)urea, BFUR) were theoretically explored, particularly on geometric features of the BFUR@X (X = F-, Cl-, Br-, I-, CO32-, NO3-, and SO42-) systems at a molecular level in this work. Complex structures show that two N-H groups as a claw and two -C6F5 rings on BFUR as a pair of tweezers simultaneously interact with captured anions through cooperative double-dentate hydrogen bond and double-side anion-π interactions. The binding energies and thermodynamic information indicate that the recognitions of the seven anions by BFUR in vacuum are enthalpy-driven and entropy-opposed, which occur spontaneously. Although the binding energy ΔEcp between F- and BFUR is relatively high (289.30 kJ·mol-1), ΔEcp, ΔG, and ΔH of the recognition for CO32- and SO42- are much larger than the cases of F-, Cl-, Br-, I-, and NO3-, suggesting that BFUR is an ideal selective anion receptor for CO32- and SO42-. Additionally, energy decomposition analysis based on localized molecular orbital energy decomposition analysis (LMO-EDA) was performed; electronic properties and behaviors of the present systems were further discussed according to calculations on frontier molecular orbital, UV-vis spectra, total electrostatic potential, and visualized weak interaction regions. The present theoretical exploration of BFUR@X (X = F-, Cl-, Br-, I-, CO32-, NO3-, and SO42-) systems is fundamentally crucial to establish an anion recognition structure-property relationship upon combination of different noncovalent interactions, that is, double-dentate hydrogen bond and double-side anion-π interactions.
RESUMO
This work reports a plasmonic strategy capable of label-free yet amplified photoelectrochemical (PEC) immunoassay for the sensitive and specific detection of model protein p53, an important transcription factor that regulates the cell cycle and functions as a tumor suppressor. Specifically, on the basis of Au nanoparticles (NPs) deposited on hierarchically ordered TiO2 nanotubes (NTs), a protein G molecular membrane was used for immobilization of alkaline phosphatase (ALP) conjugated anti-p53 (ALP-a-p53). Due to the immunological recognition between the receptor and target, the plasmonic charge separation from Au NPs to the conduction band of TiO2 NTs could be influenced greatly that originated from multiple factors. The degree of signal suppression is directly associated with the target concentration, so by monitoring the changes of the plasmonic photocurrent responding after the specific binding, a new plasmonic PEC immunoassay could be tailored for label-free and amplified detection. The operating principle of this study could be extended as a general protocol for numerous other targets of interest.
Assuntos
Fosfatase Alcalina/química , Técnicas Eletroquímicas , Ouro/química , Imunoensaio , Nanopartículas/química , Titânio/química , Proteína Supressora de Tumor p53/análise , Fosfatase Alcalina/metabolismo , Eletrodos , Tamanho da Partícula , Processos Fotoquímicos , Propriedades de SuperfícieRESUMO
Photoelectrochemical (PEC) immunoassay is an attractive methodology as it allows for an elegant and sensitive protein assay. However, advanced PEC immunoassay remains challenging and the established amplifications rely almost exclusively on the labeling of various enzymes, which usually suffer the inferior stabilities. Here we report the development and validation of the DNA labeling that leads to a unique amplification probe for the sensitive PEC immunoassay of HIV-1 capsid protein, p24 antigen, an important biomarker of human immune deficiency virus (HIV). Following the sandwich immunobinding, the DNA tags could be released and the subsequent dipurinization of the oligonucleotide strands enables the easy oxidation of free nucleobases at a CdTe quantum dots (QDs) modified ITO transducer. Such DNA tags induced PEC amplification and readout permits the exquisite assay of HIV-1 p24 antigen with high sensitivity. As compared to the existing method of enzymatic labeling, the easy preparation and stability of these labels make them very suitable for PEC amplification. Another merit of this method is that it separates the immunobinding from the PEC transducer, which eliminates the commonly existing affection during the biorecognition processes. This work paves a new route for the PEC immunoassay of HIV-1 p24 antigen and provides a general format for the PEC biomolecular detection by means of the DNA labeling.
Assuntos
Proteína do Núcleo p24 do HIV/metabolismo , HIV-1/metabolismo , Imunoensaio/métodos , Humanos , Imunoensaio/normas , Limite de Detecção , Técnicas de Amplificação de Ácido Nucleico , FotoquímicaRESUMO
In this Feature, electrochemiluminescent (ECL) and photoelectrochemical (PEC) properties and mechanisms of semiconductor quantum dots (QDs) are reviewed, with emphasis on their specific fundamentals and concise comparison on their similarities and differences. With recent illustrative examples of bioanalytical applications, the main signaling strategies for QDs-based ECL and PEC bioanalysis are then highlighted. The future prospects in this field are also discussed.
Assuntos
Bioensaio , Técnicas Eletroquímicas , Luminescência , Processos Fotoquímicos , Pontos QuânticosRESUMO
The nanoscale host-guest interactions between [n]cycloparaphenylene ([n]CPP; n = 10, 8 and 9) nano-ring and fullerene C60 were explored theoretically. It is found that relatively small variations in the sizes of the [n]CPP host lead to very significant changes in encapsulation property toward the fullerene C60 guest. Expectedly, one stable inclusion-configuration of [10]CPPâC60 and one floating-configuration of [8]CPPâC60 are located on the potential surfaces of the two complexes, respectively. Unexpectedly, besides a floating-configuration (F-[9]CPPâC60), another stable inclusion-configuration (I-[9]CPPâC60) is also located on the potential surface of [9]CPPâC60 host-guest complex. Interaction energies and natural steric analysis show that these complexes are stabilized by balancing concave-convex π-π attractive and steric repulsive host-guest interactions. In contrast, the steric repulsive energy (Es) between host and guest of I-[9]CPPâC60 is as high as 233.12 kJ mol(-1), which is much larger than those in other complexes. The movements of C60 guest through the cavities of [n]CPP host (n = 10, 8 and 9) are simulated by calculating the energy profile, and the results interestingly reveal that the encapsulation of C60 by [10]CPP is in the manner of a single-potential well, by [8]CPP in the manner of a double-potential well, and by [9]CPP in the special manner of a three-potential well. We predict that the movement of C60 guest through the cavity of [9]CPP host should be experimentally observable owing to the relatively low energy barrier (<50 kJ mol(-1), M06-2X/6-31G(d)). Charge population analysis shows that an obvious charge transfer between host and guest takes place during the formation of I-[9]CPPâC60, which is different from those during the formation of [8]CPPâC60, [10]CPPâC60 and F-[9]CPPâC60. Additionally, the host-guest interaction regions were detected and visualized in real space based on the electron density and reduced density gradient.
Assuntos
Fulerenos/química , Nanoestruturas/química , Modelos Moleculares , Teoria Quântica , TermodinâmicaRESUMO
A novel urea-based anion receptor with an electron-deficient aromatic structural unit, N-p-nitrophenyl-N-(4-vinyl-2-five-fluoro-benzoic acid benzyl ester)-phenyl-urea (FUR), was designed to probe the potential for halide-anion recognition through the cooperation of two distinct noncovalent interactions including hydrogen bonds and anion-π in this work. The nature of the recognition interactions between halide-anion and the designed receptor was theoretically investigated at the molecular level. The geometric features of the hydrogen bond and anion-π of the FUR@X(-) (X = F, Cl, Br, and I) systems were thoroughly investigated. The binding energies and thermodynamic information on the halide-anion recognitions show that the presently designed FUR might selectively recognize anion F(-) based on the cooperation of the N-H···F(-) hydrogen bond and anion-π interactions both in vacuum and in solvents. IR and UV-visible spectra of free FUR and FUR@F(-) have been simulated and discussed qualitatively, which may be helpful for further experimental investigations in the future. Additionally, the electronic properties and behaviors of the FUR@X(-) systems were discussed according to the calculations on the natural bond orbital (NBO) data, molecular electrostatic potential (MEP), and weak interaction regions.
Assuntos
Teoria Quântica , Ureia/química , Ânions/química , Ligação de Hidrogênio , Conformação Molecular , Eletricidade Estática , Termodinâmica , Ureia/análogos & derivados , Ureia/síntese químicaRESUMO
Organic photoelectrochemical transistor (OPECT) biosensing represents a new platform interfacing optoelectronics and biological systems with essential amplification, which, nevertheless, are concentrated on depletion-type operation to date. Here, a polymer dot (Pdot)-gated accumulation-type OPECT biosensor is devised and applied for sensitive urea detection. In such a device, the as-designed Pdot/poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA) is validated as a superior gating module against the diethylenetriamine (DETA) de-doped poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) channel, and the urea-dependent status of Pdots has been shown to be sensitively correlated with the device's response. High-performance urea detection is thus realized with a wide linear range of 1 µM-50 mM and a low detection limit of 195 nM. Given the diversity of the Pdot family and its immense interactions with other species, this work represents a generic platform for developing advanced accumulation-type OPECT and beyond.
Assuntos
Técnicas Biossensoriais , Polímeros , Ureia , Estireno , OuroRESUMO
Three-dimensional (3D) nanostructured materials have recently attracted intensive research interest in various fields. For the photoelectrochemical (PEC) bioanalysis, unique 3D nanostructured semiconductors are also of special appeal because they allow direct mass transport and offer large surface areas for biomolecular immobilization. Currently, two-dimensional and 3D metal-sulfide semiconductor materials have drawn tremendous interest because of their different chemophysical features. This work presents the innovative fabrication of 3D ZnInS nanoflakes (NFs)@carbon fiber (CF) frameworks and its validation as a unique 3D platform for the biocatalytic precipitation (BCP)-based PEC immunoassay. Experimental results revealed that the as-developed 3D framework photoelectrode was advantageous for the accommodation of biomolecules and in situ deposition of BCP. The corresponding BCP growth process on the photoelectrode was also systematically characterized. Exemplified by lipoprotein-associated phosPhohPaseA2 (LpPLA2), the as-derived PEC immunoassay exhibits good analytical performance. This study features the first fabrication of 3D ZnInS NFs@CF frameworks for advanced BCP-based PEC bioanalysis and is expected to inspire more interest in the development of 3D nanoframework photoelectrodes for future PEC bioanalysis development.
RESUMO
This work reports a customized methodology for the fabrication of 3D CdS nanosheet (NS)-enwrapped carbon fiber framework (CFF) and its utilization for sensitive split-type CuO-mediated PEC immunoassay. Specifically, the 3D CdS NS-CFF was fabricated via a solvothermal process, while the sandwich immunocomplexing was allowed in a 96 well plate with CuO nanoparticles (NPs) as the signaling labels. The subsequent release of the Cu2+ ions was directed to interact with the CdS NS, generating trapping sites and thus inhibiting its photocurrent generation. In such a protocol, the 3D CdS NS-CFF photoelectrode could not only guarantee its sufficient contact with the Cu2+-containing solution but also supply plenty CdS surface for the Cu2+ ions. Because of the target-dependent release of the Cu2+ ions and its proper coupling with the 3D CdS NS-CFF photoelectrode, a sensitive split-type PEC immunoassay was achieved for the detection of brain natriuretic peptide (BNP). This proposed system exhibited good stability and selectivity, and its applicability for real sample analysis was also demonstrated via comparison with the commercial BNP enzyme-linked immunosorbent assay (ELISA) kit. We expect this work could stimulate more interest in the design and utilization of 3D photoelectrodes for novel PEC bioanalysis.
Assuntos
Anticorpos Imobilizados/química , Técnicas Biossensoriais/métodos , Compostos de Cádmio/química , Fibra de Carbono/química , Cobre/química , Peptídeo Natriurético Encefálico/sangue , Sulfetos/química , Técnicas Eletroquímicas/métodos , Humanos , Imunoensaio/métodos , Limite de Detecção , Nanoestruturas/química , Peptídeo Natriurético Encefálico/análise , Processos FotoquímicosRESUMO
The prediction and characterization of the single-electron sodium bond complexes Y-C...Na-H [Y = H(3), H(3)CH(2), (H(3)C)(2)H and (H(3)C)(3)] have been investigated for the first time by using MP2/6-311++G(d,p), MP2/6-311++G(2d,2p) and MP2/aug-cc-pVDZ methods. The strength of the interactions in H(3)C...Na-H, H(3)CH(2)C...Na-H, (H(3)C)(2)HC...Na-H, and (H(3)C)(3)C...Na-H complexes has been analyzed. It is shown that the (H(3)C)(3)C radical with Na-H forms the strongest single-electron sodium bond, followed by the (H(3)C)(2)HC radical and then the H(3)CH(2)C radical. H(3)C radical forms the weakest single-electron sodium bond. NBO and AIM analyses have also been used to estimate such conclusions. Furthermore, there are few linear/nonlinear relationships among the several parameters in system and the interaction mode of single-electron Na bond is LP(1)(C) --> LP(1)*(Na), which is different from the single-electron H bond and single electron halogen bond. By comparisons with some related systems, it is concluded that the strength of single-electron bond is increased in the order: hydrogen bond < sodium bond < bromine bond < lithium bond.
Assuntos
Hidrogênio/química , Sódio/química , Elétrons , Ligação de Hidrogênio , Teoria Quântica , TermodinâmicaRESUMO
Previously reported copper oxide-based cathodic photoelectrochemical bioanalysis of cysteine had attributed the decrease of the photocurrents to the binding of cysteine onto the CuO surface. However, our latest investigation found that the previous explanation was not correct. This Letter presents the in-depth study of such phenomena and a new insight into the underlying mechanism. Specifically, the unique redox reaction between the CuO photocathode and cysteine produced [Cys-Cu(I)] and cystine, and the insoluble complex blocked the partial contact between the photoelectrode and the dissolved O2-containing electrolyte and reduced the effective working area of the photocathode, leading to the decrease of photocurrent.