Recent Advances in Functionalization Strategies for Biosensor Interfaces, Especially the Emerging Electro-Click: A Review

: The functionalization of biosensor interfaces constitutes a crucial aspect of biosensing systems, as it directly governs key characteristics, including sensitivity, selectivity, accuracy, and rapidity. Among the diverse range of functionalization strategies available for biosensor interfaces, the click reaction has emerged as an exceptionally straightforward and stable approach for modifying electrodes and sensing ﬁlms. Notably, the electro-click reaction enables the reagent-free functionalization of the biosensing interface, offering signiﬁcant advantages, such as high speed, selectivity


Introduction
Biosensors represent a distinct branch within the broader domain of analytical sensors, with a specific emphasis on incorporating biometric entities into the detection mode [1]. These remarkable devices house miniature analytical sensing systems that seamlessly integrate biometric components, thereby showcasing micro-level analyte specificity. By leveraging this capability, biosensors can proficiently identify a diverse array of analytes, including proteins, cells, and viruses within living organisms, as well as track heavy-metal pollutants and biochemical waste within the environment encompassing air, water, and soil [2,3]. The accurate detection of these analytes assumes paramount importance in disease surveillance and treatment and environmental monitoring [4]. Typical biosensors contain two basic functional units: recognition elements and signal transducers [5]. The selectivity of a biosensor hinges upon the inherent properties of the recognition element, while its sensitivity relies upon the signal transducer. The fusion of these two components facilitates the attainment of stringent requirements for both high selectivity and sensitivity. The analysis process of a biosensor is usually carried out on the sensor interface. It is at this interface that the core functionality and defining characteristics of the biosensor, such as the sensitivity, selectivity, accuracy, and speed, are directly determined. Accordingly, the development of innovative interfaces stands as the foundational approach for enhancing the biosensor performance. Hence, the functionalization of biosensor interfaces assumes a vital role within the biosensing system. On addition of GO without the presence of the target DNA (path A′), HP1 and HP2 are adsorbed onto the GO surface, giving rise to a low background signal (path B′). Upon the addition of the target DNA (path A), it hybridizes and forms a duplex structure with HP1 (a). The HP1-target DNA complex in cycle I allows Exo III to digest HP1 from the 3′ blunt end (b) to free the part of HP1 complementary to HP2, release the fluorophore, and regenerate the target DNA (c). In cycle II, the released fragment of HP1 binds with HP2 (d) and activates the enzyme again (e) to digest HP2, free the fluorophore, and release a fragment of HP1 to repeat the cycle (f). The subsequent addition of GO (path B) cannot quench the fluorescence of FAM, leading to the production of a strong fluorescence signal Reprinted with permission from [28], copyright 2019, Microchimica Acta. (b) Schematic representation of the fabrication of DNA impedimetric biosensor and its detection through enzyme-assisted target recycling. After the target DNA binds to the probe DNA on the electrode (path 1), exonuclease III is added to selectively hydrolyze the DNA probe in the double-stranded structure (path 2), and the released target DNA will bind to another probe to initiate another round of exonuclease III digestion (path 3). Reprinted with permission from [34], copyright 2019, Analyst.

Porous Carbon
Porous carbon possesses notable advantages, including a high specific surface area and superior electron-transfer performance, making it a promising candidate for biosensor applications [36]. In recent years, there has been significant interest in porous carbon derived from biomaterials due to its ease of preparation through low-cost precursor On addition of GO without the presence of the target DNA (path A ), HP1 and HP2 are adsorbed onto the GO surface, giving rise to a low background signal (path B ). Upon the addition of the target DNA (path A), it hybridizes and forms a duplex structure with HP1 (a). The HP1-target DNA complex in cycle I allows Exo III to digest HP1 from the 3 blunt end (b) to free the part of HP1 complementary to HP2, release the fluorophore, and regenerate the target DNA (c). In cycle II, the released fragment of HP1 binds with HP2 (d) and activates the enzyme again (e) to digest HP2, free the fluorophore, and release a fragment of HP1 to repeat the cycle (f). The subsequent addition of GO (path B) cannot quench the fluorescence of FAM, leading to the production of a strong fluorescence signal Reprinted with permission from [28], copyright 2019, Microchimica Acta. (b) Schematic representation of the fabrication of DNA impedimetric biosensor and its detection through enzyme-assisted target recycling. After the target DNA binds to the probe DNA on the electrode (path 1), exonuclease III is added to selectively hydrolyze the DNA probe in the double-stranded structure (path 2), and the released target DNA will bind to another probe to initiate another round of exonuclease III digestion (path 3). Reprinted with permission from [34], copyright 2019, Analyst.

Porous Carbon
Porous carbon possesses notable advantages, including a high specific surface area and superior electron-transfer performance, making it a promising candidate for biosensor applications [36]. In recent years, there has been significant interest in porous carbon derived from biomaterials due to its ease of preparation through low-cost precursor carbonization. Guan et al. [37] prepared a self-powered biosensor using lactate oxidase-modified porouscarbon film. This porous-carbon film exhibits the ability to absorb sweat and generate Chemosensors 2023, 11, 481 5 of 32 electricity by harnessing the heat from natural sweat evaporation. The output voltage of the biosensor increases in proportion to the concentration of lactic acid present in sweat. Furthermore, the surface enzymatic reaction alters the zeta potential of the carbon, thereby influencing the output voltage. Gao et al. [38] utilized a luminescent reagent, luminol, for the in situ reduction in chloroauric acid on the nanopores of porous carbon. By combining this approach with an enzyme-cycle and chain-replacement mechanism, they achieved the ultra-sensitive detection of mucin1, an important tumor biomarker. The incorporation of Au-Lum nanoparticles (NPs) within the pores and hollow interiors of porous-carbonaccelerated electron transfer, resulting in excellent luminescence properties of the composite (Figure 2a). Tian et al. [39] designed an accurate biosensor based on n-doped porous-carboncontaining Fe (Fe/N-C) nanocomposites for the detection of H 2 O 2 in real water samples and renal epithelial 293T cells. The Fe/N-C nanocomposites substantially enhanced the electron-transfer process and catalytic activity of the sensor, enabling the detection of trace amounts of H 2 O 2 . This development holds significance for various applications, such as monitoring H 2 O 2 levels in water samples and studying its impact on renal epithelial cells.
Chemosensors 2023, 11, x FOR PEER REVIEW 5 of 32 carbonization. Guan et al. [37] prepared a self-powered biosensor using lactate oxidasemodified porous-carbon film. This porous-carbon film exhibits the ability to absorb sweat and generate electricity by harnessing the heat from natural sweat evaporation. The output voltage of the biosensor increases in proportion to the concentration of lactic acid present in sweat. Furthermore, the surface enzymatic reaction alters the zeta potential of the carbon, thereby influencing the output voltage. Gao et al. [38] utilized a luminescent reagent, luminol, for the in situ reduction in chloroauric acid on the nanopores of porous carbon. By combining this approach with an enzyme-cycle and chain-replacement mechanism, they achieved the ultra-sensitive detection of mucin1, an important tumor biomarker. The incorporation of Au-Lum nanoparticles (NPs) within the pores and hollow interiors of porous-carbon-accelerated electron transfer, resulting in excellent luminescence properties of the composite (Figure 2a). Tian et al. [39] designed an accurate biosensor based on n-doped porous-carbon-containing Fe (Fe/N-C) nanocomposites for the detection of H2O2 in real water samples and renal epithelial 293T cells. The Fe/N-C nanocomposites substantially enhanced the electron-transfer process and catalytic activity of the sensor, enabling the detection of trace amounts of H2O2. This development holds significance for various applications, such as monitoring H2O2 levels in water samples and studying its impact on renal epithelial cells.  After further integrating with proximity-initiated secondary target DNA strand displacement (a), the ECL signal quality was significantly higher than that before replacement (b). Reprinted with permission from [38], copyright 2019, Nanoscale. (b) Nanosensor preparation via probe-tip sonicating SWCNTs in the presence of ssDNA followed by ultracentrifugation of the resultant dispersion. Reprinted with permission from [40], copyright 2021, Advanced Functional Materials. Carbon Nanotubes Carbon nanotubes, resembling rolled-up graphene cylinders, exhibit remarkable tensile strength, high conductivity, and excellent electrocatalytic abilities [41]. Single-walled carbon nanotubes (SWCNTs) consist of a single graphene cylinder, while multi-walled carbon nanotubes (MWCNTs) are composed of multiple layers [42,43]. Notably, through a comprehensive analysis of the existing literature, Gooding et al. [44] observed that SWCNTs outperformed their MWCNT counterparts in terms of electroanalytical performance. Although SWCNT-based electrodes expose a larger number of surface oxides to reactants and facilitate faster electron transfer, the reaction primarily occurs in a non-oriented manner, with the sidewalls predominantly immersed in the solution. This arrangement hampers the transmission and detection of the charge [36]. Consequently, current research predominantly focuses on SWCNTs. Exploiting the excellent light stability and fluorescence properties of SWCNTs in the near-infrared (NIR) range, which lies outside the autofluorescence region of chlorophyll, Lew et al. [45] developed a detection platform utilizing a pair of DNA-coated SWCNT probes. This ratio measurement platform enabled the in vivo detection of endogenous hydrogen peroxide in plants. The functionalized biosensing interface not only holds potential for monitoring H 2 O 2 levels in human tumors, but also finds application in monitoring the therapeutic response of pancreatic ductal adenocarcinoma (PDAC) cells to tumors in vitro and in vivo, as well as in evaluating the efficacy of chemotherapy drugs (Figure 2b), as demonstrated by Bhattacharya et al. [46]. Safaee et al. [40] employed optical core-shell microfiber textiles incorporating SWCNTs for the real-time optical monitoring of the hydrogen peroxide concentration in in vitro wounds, enabling the tracking of the wound-healing progress. The versatility of the SWCNT biosensor extends to other applications depending on the utilization of wrapped single-stranded DNA. For instance, Harvey et al. [47] selected this implantable optical biosensor to swiftly quantify the exposure of doxorubicin in living tissues. Furthermore, Salem et al. [48] devised a sensor capable of distinguishing Cu(II), Cd(II), Hg(II), and Pb(II) at a concentration of 100 µM.

Polymer and Bio-Nanomaterials
Conducting polymers possessing favorable electrochemical properties, nanostructural morphology, and biological-coupling functionality play a crucial role in polymer biosensor systems. To reduce reliance on traditional nanomaterials, Meng et al. [49] employed tetrabutylammonium perchlorate as a soft template to fabricate a bifunctional poly(3,4-ethylenedioxythiophene) (PEDOT) interface with an adjustable 3D nanofiber network and carboxylic acid groups. This was achieved by controlling the copolymerization of 3,4-ethylenedioxythiophene(EDOT) and EDOT-COOH monomers ( Figure 3a). The newly developed Bio-Nano-PEDOT-COOH interface allows for the coupling of various biorecognition molecules through the carboxylic acid groups, enabling the development of advanced all-polymer biosensors. Expanding on this work, Zhao et al. [50] demonstrated the sensitive and specific monitoring of 17β-estradiol (E2) by modifying electrodeposited PEDOT-graphene oxide (GO) with Au@Pt nanocrystals (Au@Pt). The PEDOT-GO nanocomposite film was polymerized in situ on a glassy carbon electrode using cyclic voltammetry, followed by the synthesis of Au@Pt on the conductive polymer. This provided a platform for aptamer immobilization. With the addition of E2, the differential pulse voltammetry signal gradually decreased due to hindered electron transfer at the E2-aptamer complex interface. Additionally, Zhu et al. [51] investigated the self-assembly of size-controlled tetrahedral framework nucleic acids (FNAs) on a microfluidic microchannel interface, allowing the elevation of DNA probes from the interface to construct a nanoscale threedimensional reaction space. The highly ordered orientation, configuration, and density of the DNA probes within this three-dimensional reaction space optimize the reaction kinetics in molecular recognition processes. The FNA-designed interface was successfully applied to the one-stop detection of Escherichia coli O157:H7 (E. coli O157:H7), achieving a bacterial detection efficiency of 10 CFU/mL with excellent selectivity and precision. In recent advancements, the design and development of polymer-based biosensing platforms for detection have been realized through novel analytical and scientific methodologies.

Other Nanomaterials
Besides the graphene nanomaterials and polymer and bio-nanomaterials mentioned earlier, various other nanomaterials, such as metal nanomaterials and metal oxide nanomaterials, have also been explored [52,53]. Zhou et al. [54] introduced a novel class of chameleon DNA-template silver nanoclusters (AgNCs) capable of switching fluorescence colors among red, orange, and yellow in response to Mg 2+ , non-fluorescent auxiliary AgNC and complementary DNA. Based on this principle, a ratiometric fluorescence analysis platform was developed for the detection of target DNA. The yellow fluorescence of the probe increased, and the red fluorescence weakened as the amount of target DNA decreased. Regarding metal oxide nanomaterials, Fan et al. [55] discovered that MnO 2 nanosheets (NSs) can effectively quench the fluorescence of highly fluorescent Scopoletin (SC) while enhancing the fluorescence of non-fluorescent Amplex Red (AR) through an oxidation reaction. Upon the addition of glutathione (GSH), MnO 2 was reduced to Mn 2+ and lost the oxide properties (Figure 3b). At this stage, the fluorescence of the SC intensified, and the AR was quenched. The biosensor system monitors GSH levels by detecting changes in the fluorescence signals of SC and AR.
Another commonly employed nanomaterial is MoS 2 , a layered 2D transition metal dihalide exhibiting unique structural, physicochemical, optical, and biological properties [56]. Yan et al. [57] developed an aptasensor using hierarchical MoS 2 nanostructuring and SiO 2 nano-signal amplification. In this approach, hierarchical MoS 2 nanostructures served as functional interfaces, enhancing the accessibility between molecules and improving the efficiency of DNA hybridization. Simultaneously, the SiO 2 nanoprobes, combined with electroactive labels and DNA probes, amplified the electrochemical signal. This biosensing system enabled the simultaneous detection of prostate-specific antigen (PSA) and sarcosine, two prostate cancer (PCa) biomarkers.
Overall, nanomaterials play a pivotal role in the functionalization strategies of biosensing interfaces. Table 1 provides a comparison of nanostructure-functionalized biosensor interfaces. ity and precision. In recent advancements, the design and development of polymer-based biosensing platforms for detection have been realized through novel analytical and scientific methodologies.

Other Nanomaterials
Besides the graphene nanomaterials and polymer and bio-nanomaterials mentioned earlier, various other nanomaterials, such as metal nanomaterials and metal oxide nanomaterials, have also been explored [52,53]. Zhou et al. [54] introduced a novel class of chameleon DNA-template silver nanoclusters (AgNCs) capable of switching fluorescence colors among red, orange, and yellow in response to Mg 2+ , non-fluorescent auxiliary AgNC and complementary DNA. Based on this principle, a ratiometric fluorescence analysis platform was developed for the detection of target DNA. The yellow fluorescence of the probe increased, and the red fluorescence weakened as the amount of target DNA decreased. Regarding metal oxide nanomaterials, Fan et al. [55] discovered that MnO2 nanosheets (NSs) can effectively quench the fluorescence of highly fluorescent Scopoletin (SC) while enhancing the fluorescence of non-fluorescent Amplex Red (AR) through an oxidation reaction. Upon the addition of glutathione (GSH), MnO2 was reduced to Mn 2+ and lost the oxide properties (Figure 3b). At this stage, the fluorescence of the SC intensified, and the AR was quenched. The biosensor system monitors GSH levels by detecting changes in the fluorescence signals of SC and AR.
Another commonly employed nanomaterial is MoS2, a layered 2D transition metal dihalide exhibiting unique structural, physicochemical, optical, and biological properties [56]. Yan et al. [57] developed an aptasensor using hierarchical MoS2 nanostructuring and SiO2 nano-signal amplification. In this approach, hierarchical MoS2 nanostructures served as functional interfaces, enhancing the accessibility between molecules and improving the efficiency of DNA hybridization. Simultaneously, the SiO2 nanoprobes, combined with electroactive labels and DNA probes, amplified the electrochemical signal. This biosensing system enabled the simultaneous detection of prostate-specific antigen (PSA) and sarcosine, two prostate cancer (PCa) biomarkers.
Overall, nanomaterials play a pivotal role in the functionalization strategies of biosensing interfaces. Table 1 provides a comparison of nanostructure-functionalized biosensor interfaces.

Small-Molecule-Mediated Interfacial Regulation
Small molecules offer several advantages, including good biocompatibility, clear structures, and easy modification, making them versatile for biosensor functionalization [58]. For instance, Cui et al. [59] utilized dopamine as a functional monomer to synthesize graphdiyne (GDY) with high biocompatibility and conductivity through hydrogen bonding and multipoint electrostatic attraction. They incorporated GDY into C-reactive molecularimprinted polymers (C-MIPs), achieving high sensitivity and selective recognition of human C-reactive protein ( Figure 4a). Salimian et al. [60] employed polyethylene glycol to modify the sensing interface, effectively preventing non-specific protein adsorption and enabling the sensitive and specific detection of cancer biomarkers in serum. Similarly, Zhang et al. [61] employed 6-mercapto-1-hexanol to modify DNA probes and immobilized them on the gold-nanoparticle interface to analyze DNA methylation through current changes.
Fluorescent probes based on small molecules have also found widespread application in the detection of crucial biological analyses [62]. These probes undergo changes in luminescence intensity or emission wavelength through various sensing mechanisms. Among them, electrochemiluminescence (ECL), also known as electrogenerated chemiluminescence, stands out as a superior method for biosensing compared to other photoexcitation spectroscopy techniques. ECL involves the generation of free radicals on the electrode surface, which undergo high-energy electron-transfer reactions to form excited states and emit light [63]. Consequently, ECL does not require excitation light and exhibits minimal background signals [64]. Currently, luminol serves as the most commonly used organicsmall-molecule ECL emitter. Zhao et al. [65] developed a paper-based dual-mode detection platform to detect Pb 2+ based on the oxidation reaction initiated by horseradish peroxidase (HRP) in the presence of H 2 O 2 . Upon the addition of Pb 2+ to the interface, cleaved oligonucleotide fragments linked to HRP-functionalized Au nanocubes penetrated into the cellulose, quenching the ECL signals of CDs and quantum dots via resonance energy transfer [63] while enhancing the ECL intensity generated by luminol catalyzed by H 2 O 2 ( Figure 4b). On this basis, Guo et al. [66] further advanced the field by using reactive oxygen species (ROS) instead of H 2 O 2 to develop a new luminol-ROS ECL system for GSH detection. The dissolved oxygen was reduced to superoxide radicals (O 2 − ) by atomized gold-loaded 2D VO 2 nanobelts (Au/VO 2 ), which combined with the loaded luminol to promote the ECL. The ECL resonance energy transfer (ECL-RET) between the hollow SiO 2 nanospheres and luminol resulted in a significant decrease in the ECL-signal response.
In the presence of GSH, the effective redox reaction between SiO 2 and GSH restored the ECL signal.
Due to distinct luminescence mechanisms and low electroluminescence efficiency in the aqueous phase, most small organic molecules are unsuitable for recognition and response analysis, limiting their application in biosensing [67]. Therefore, further research is needed to explore the interfacial regulation mediated by organic electroluminescent small molecules. Table 2 shows a comparison of small-molecule-functionalized biosensor interfaces. penetrated into the cellulose, quenching the ECL signals of CDs and quantum dots v resonance energy transfer [63] while enhancing the ECL intensity generated by lumin catalyzed by H2O2 (Figure 4b). On this basis, Guo et al. [66] further advanced the field using reactive oxygen species (ROS) instead of H2O2 to develop a new luminol-ROS E system for GSH detection. The dissolved oxygen was reduced to superoxide radicals (O by atomized gold-loaded 2D VO2 nanobelts (Au/VO2), which combined with the load luminol to promote the ECL. The ECL resonance energy transfer (ECL-RET) between t hollow SiO2 nanospheres and luminol resulted in a significant decrease in the ECL-sign response. In the presence of GSH, the effective redox reaction between SiO2 and GSH stored the ECL signal.
Due to distinct luminescence mechanisms and low electroluminescence efficiency the aqueous phase, most small organic molecules are unsuitable for recognition and sponse analysis, limiting their application in biosensing [67]. Therefore, further resear is needed to explore the interfacial regulation mediated by organic electroluminesce small molecules. Table 2 shows a comparison of small-molecule-functionalized biosens interfaces.   [59], copyright 2022, Chemical Engineering Journal. (b) Illustration of assembly and operating process of the dual-mode lab-on-paper device. Reprinted with permission from [65], copyright 2020, Anal. Chem.

Biomacromolecule-Mediated Interfacial Regulation
In response to the growing demand for biosensing, the development of biomacromoleculemediated sensing interfaces with precise molecular recognition, controllable signal amplification, and enhanced sensing performance has become imperative. Various biomacromolecules, including enzymes, DNA, proteins, and cells, have been employed to modify the sensing interface, enabling the creation of highly sensitive and selective biosensors [32].

Enzyme-Based Interfaces
Enzymes, in particular, are widely utilized components in biosensor interfaces, leveraging their ability to detect targets with high specificity through the catalytic conversion of the analyte or enzyme inhibition [7]. To achieve a superior sensing performance, it is crucial to immobilize efficient biological enzymes onto the sensing interface while preserving their biological properties. Consequently, numerous immobilization methods have been developed, ranging from membrane encapsulation and physical adsorption to covalent binding [75].
For example, Gu et al. [76] employed a membrane encapsulation method to modify the electrode surface with glucose oxidase (GOx) for glucose sensing (Figure 5a). They utilized a 3D porous Ti 3 C 2 T x ·Mxene-graphene (MG) hybrid film with an adjustable porous structure, which provided a highly hydrophilic microenvironment for GOx immobilization. Dhanjai et al. [77] employed chitosan (CHI) as a binder for the physical adsorption of glucose oxidase (GOx) onto a cobalt oxide-loaded mesoporous carbon framework (Co 3 O 4 @ MCF), enabling highly selective glucose detection upon the modification of a glassy carbon electrode. Levien et al. [7] covalently linked GO x and acetylcholinesterase (AChE) onto the surface of plasma-polymerized (pp) hydrogels to fabricate an electrochemical biosensor interface. They utilized glucose as the substrate for GOx and eserine as the AChE inhibitor to validate the practicality of the biosensing approach.

DNA-Based Interfaces
DNA, a genetic biological macromolecule, plays a crucial role in regulating life activities with remarkable accuracy. Additionally, DNA possesses the unique attribute of sequence programmability, allowing for the incorporation of desired functions through well-designed sequences [78]. Currently, DNA modifications can be broadly categorized into chain DNA, DNA nanomaterials, and framework DNA (FDNA) [79][80][81]. For instance, Su et al. [80] investigated the impact of probe DNA on the detection performance of adenosine triphosphate aptamer (ATPA) and adenosine triphosphate (ATP) in the presence of hairpin DNA and double-stranded DNA (DsDNA). Subsequently, Zhu et al. [82] separated the two and developed two aptamer sensors based on hairpin DNA (HDNA) and linear single-stranded DNA (ssDNA) for the detection of aflatoxin B1 and diethyl phthalate.
In the DNA/nano-functionalized electrochemical sensing interface, thiol-modified DNA is immobilized on the gold-electrode surface through strong gold-thiol interactions [81]. Miao et al. [83] proposed an electrochemical biosensor utilizing DNAmodified Fe 3 O 4 @ Au magnetic NPs (Figure 5b). The three DNA probes contain specific mismatched base pairs, and the presence of different heavy-metal ions promotes hybridization with distinct DNA probes, enabling the detection of corresponding electrochemical species on the magnetic nanoparticle surface. Han et al. [84] anchored methylene bluelabeled polyadenine DNA onto a gold electrode to construct an electrochemical biosensor interface for the detection of the COVID-19 virus.
Comparatively, FDNA offers a higher probe density on the electrode surface compared to DNA nanomaterials [79]. Su et al. [85] covalently coupled DNA tetrahedrons to the carbon surface and applied them for the detection of various bioactive molecules. Furthermore, Mao et al. [86] developed a three-dimensional pure DNA hydrogel serving as a scaffold for electron transfer. The DNA hydrogel incorporates an embedded electron mediator through binding, while DNAzyme is introduced at the hydrogel scaffold nodes to enable the long-range acquisition of DNAzyme catalytic signals. pairs, and the presence of different heavy-metal ions promotes hybridization with distinct DNA probes, enabling the detection of corresponding electrochemical species on the magnetic nanoparticle surface. Han et al. [84] anchored methylene blue-labeled polyadenine DNA onto a gold electrode to construct an electrochemical biosensor interface for the detection of the COVID-19 virus.
Comparatively, FDNA offers a higher probe density on the electrode surface compared to DNA nanomaterials [79]. Su et al. [85] covalently coupled DNA tetrahedrons to the carbon surface and applied them for the detection of various bioactive molecules. Furthermore, Mao et al. [86] developed a three-dimensional pure DNA hydrogel serving as a scaffold for electron transfer. The DNA hydrogel incorporates an embedded electron mediator through binding, while DNAzyme is introduced at the hydrogel scaffold nodes to enable the long-range acquisition of DNAzyme catalytic signals.

Protein-Based Interfaces
Proteins, as quintessential biological macromolecules, exhibit distinct binding affinities and sequence specificities towards DNA and RNA, as elucidated by Berezovski et al.

Protein-Based Interfaces
Proteins, as quintessential biological macromolecules, exhibit distinct binding affinities and sequence specificities towards DNA and RNA, as elucidated by Berezovski et al. [88].
For instance, Campuzano et al. [89] demonstrated that Tombusviral p19 protein forms dimers and selectively binds to short dsRNA, making it a valuable tool for identifying miRNAs upon hybridization with specific RNA probes. Rubio et al. [90] harnessed the concept of de novo-designed protein switches to create protein-based biosensors, enabling the reversal of information flow. Applying this approach, they developed a biosensor for the SARS-CoV-2 spike protein, incorporating a de novo-designed spike receptor-binding domain (RBD) binder4, with a remarkable limit of detection of 15 pM. Innovative techniques involving the combination of proteins and molecular-imprinting technology (MIT) have led to the development of protein-imprinted hydrogels (MIHs) [91]. Extensive efforts have been made in this area. Utilizing free-radical polymerization, a new type of protein-imprinting hydrogel was created by combining N,N -methylenebis(acrylamide) cross-linkers, N,Ndimethylaminoethyl methacrylate gas-sensitive monomers, and human serum albumin (HSA) as the template protein. This hydrogel exhibited unique self-recognition properties towards HSA protein [92]. Furthermore, Cui et al. [87] synthesized a protein-imprinted hydrogel using acrylamide as a functional monomer through free-radical polymerization. This hydrogel demonstrated high sensitivity and selectivity for detecting target immunoglobulins in complex biological samples (Figure 5c).

Cell-Based Interfaces
Cell-mediated biosensing interfaces have emerged as promising tools in biomedicine [93]. For example, Qi et al. [94] utilized marine-pathogen sulfate-reducing bacteria (SRB) to facilitate the synthesis of bio-imprinted membranes, leading to the formation of a biosensing interface. The electrochemical impedance method enabled the direct measurement of the bacterial concentration. Building upon this work, Jiang et al. [95] employed electropolymerization to create a Salmonella-imprinted membrane, resulting in the development of a biosensor interface capable of detecting Salmonella within a short span of 20 min. In addition to molecular-imprinting technology (MIT), red blood cell (RBC)-mediated biosensing interfaces have also witnessed significant advancements. Shete et al. [96] employed a reversible membrane-opening/resealing method to incorporate a designed nanosensor into RBCs, facilitating the detection of exchangeable Pb 2+ concentrations over time and space. Furthermore, Chen et al. [97] immobilized gold-coated Fe 3 O 4 core-shell nanocomposites on RBCs, enabling the use of RBCs as cell biosensors for detecting H 2 O 2 . As technology continues to progress, cell-mediated interface regulation strategies are becoming increasingly sophisticated. In 2018, Liu et al. [98] combined red cell membrane vesicles with near-infrared persistent luminescent nanophosphors (PLNPs) and employed mesoporous SiO 2 as a carrier to fabricate a biosensor interface for the in situ monitoring of tumor-growth inhibition. Although there are relatively fewer examples of cell-mediated biosensing interfaces compared to nanomaterials and other biomolecules, their development prospects remain highly promising. This is attributed to the superior biocompatibility of cells, which allows biosensors to play a crucial role in human medicine. Table 3 shows a comparison of biomacromolecule-functionalized biosensor interfaces.

Electro-Click Chemistry for the Functionalization of Biosensor Interfaces
In 2001, Sharpless et al. [8] first proposed the concept of connecting small units with heteroatom connections (C-X-C) to generate matter. They hope to develop a set of powerful and selective "modules" that can work reliably in both large and small applications. The basis of this method is named "click chemistry". In simple terms, click chemistry is a selective assembly of two molecular building blocks under mild reaction conditions. It has the characteristics of high yield, harmless by-products, and easy separation via nonchromatographic methods [14].
For click chemistry, carbon-heteroatom-bond-formation reactions are the most common examples, including cycloadditions of unsaturated species, nucleophilic substitution chemistry, carbonyl chemistry of the "non-aldol" type, and additions to carbon-carbon multiple bonds [8]. Then, researchers from the same group reported that the reaction rate and regioselectivity can be improved by using Cu(I) to catalyze the Huisgen dipolar cycloaddition in 2002 [99]. A few years later, Sharpless et al. [100] and Rodionov et al. [101] further found that Cu(I)-catalyzed alkyne-azide cycloaddition (CuAAC) can effectively form 1-4-disubstituted 1,2,3-triazole bonds in water and organic solvents ( Figure 6). Today, CuAAC has become the most representative cycloaddition reaction, compatible with a wide range of solvents, pH values, and temperatures [102]. Of course, there are also the thiol-ene reaction, Michael addition reaction, imine and oxime reaction, and Diels-Alder cycloaddition reaction [103]. Click chemistry is considered an effective strategy to immobilize biomolecules while maintaining their biological activities [104][105][106]. This review will take the CuAAC click reaction as an example to introduce the development in recent years. The basis of this method is named "click chemistry". In simple terms, click chemistry is a selective assembly of two molecular building blocks under mild reaction conditions. It has the characteristics of high yield, harmless by-products, and easy separation via non-chromatographic methods [14].
For click chemistry, carbon-heteroatom-bond-formation reactions are the most common examples, including cycloadditions of unsaturated species, nucleophilic substitution chemistry, carbonyl chemistry of the "non-aldol" type, and additions to carbon-carbon multiple bonds [8]. Then, researchers from the same group reported that the reaction rate and regioselectivity can be improved by using Cu(I) to catalyze the Huisgen dipolar cycloaddition in 2002 [99]. A few years later, Sharpless et al. [100] and Rodionov et al. [101] further found that Cu(I)-catalyzed alkyne-azide cycloaddition (CuAAC) can effectively form 1-4-disubstituted 1,2,3-triazole bonds in water and organic solvents ( Figure 6). Today, CuAAC has become the most representative cycloaddition reaction, compatible with a wide range of solvents, pH values, and temperatures [102]. Of course, there are also the thiol-ene reaction, Michael addition reaction, imine and oxime reaction, and Diels-Alder cycloaddition reaction [103]. Click chemistry is considered an effective strategy to immobilize biomolecules while maintaining their biological activities [104][105][106]. This review will take the CuAAC click reaction as an example to introduce the development in recent years.

Traditional Click Technology
Because CuAAC is an addition reaction of azides and alkynes catalyzed by Cu(I), Cu(I) can be directly added to the reaction environment or in situ generated by the reaction of Cu(II) with reducing agents [9]. Although Cu(I) can be directly added to the reaction system, the development of stable Cu(I) catalysts is of great significance for the application of CuAAc due to the poor stability of Cu(I). Yang et al. [108] prepared Cu2−xSySe1−y nanoparticles, which have a large number of Cu vacancies, and Cu(II) and Cu(I) coexist, to catalyze the click chemistry of CuAAC (Figure 7a). Because glutathione can stabilize Cu(I), Zhang et al. [104] successfully prepared a novel nanocatalyst containing abundant and stable Cu (I). Therefore, the reduction in Cu(II) by a reducing agent is also a common method of the CuAAC click reaction. Guerrero et al. [105] reported the first electrochemical immunosensor for the detection of CXCL7 (chemokine (C-X-C motif) ligand 7) as an autoimmune marker via the click reaction of azide-functionalized MWCNTs and ethynyl-IgG on screen-printed carbon electrodes using ascorbic acid to reduce the Cu(II) ( Figure  7b). Then, Xue et al. [109] used specific antigen-antibody recognition to trigger the in situ reduction in Cu MOF, thereby generating a powerful click catalyst for the CuAAC click reaction.

Traditional Click Technology
Because CuAAC is an addition reaction of azides and alkynes catalyzed by Cu(I), Cu(I) can be directly added to the reaction environment or in situ generated by the reaction of Cu(II) with reducing agents [9]. Although Cu(I) can be directly added to the reaction system, the development of stable Cu(I) catalysts is of great significance for the application of CuAAc due to the poor stability of Cu(I). Yang et al. [108] prepared Cu 2−x S y Se 1−y nanoparticles, which have a large number of Cu vacancies, and Cu(II) and Cu(I) coexist, to catalyze the click chemistry of CuAAC (Figure 7a). Because glutathione can stabilize Cu(I), Zhang et al. [104] successfully prepared a novel nanocatalyst containing abundant and stable Cu (I). Therefore, the reduction in Cu(II) by a reducing agent is also a common method of the CuAAC click reaction. Guerrero et al. [105] reported the first electrochemical immunosensor for the detection of CXCL7 (chemokine (C-X-C motif) ligand 7) as an autoimmune marker via the click reaction of azide-functionalized MWCNTs and ethynyl-IgG on screen-printed carbon electrodes using ascorbic acid to reduce the Cu(II) (Figure 7b). Then, Xue et al. [109] used specific antigen-antibody recognition to trigger the in situ reduction in Cu MOF, thereby generating a powerful click catalyst for the CuAAC click reaction.
However, as a catalyst, Cu(I) has certain toxicity, and some Cu-catalyzed fixed viruses or oligonucleotide chains will degrade [111]. Bertozzi et al. [112] first proposed copper-free click chemistry, which eliminates the adverse effects of Cu(I), simplifies the experimental steps, and becomes an alternative CuAAC click reaction. This is an alternative method to activate alkynes for the catalyst-free [3+2] cycloaddition reaction with azides. Then, Xiang et al. [110] reported a biosensor system based on azide-co-functionalized graphene oxide (GO-N 3 ) and carbon dots (CDs). Carbon-dot-labeled DNA (CD-DNA) binds to GO-N 3 by copper-free click chemistry and quenches the fluorescence of CDs by fluorescence resonance energy transfer (FRET) (Figure 7c). After adding carcinoembryonic antigen (CEA), CEA binds to the aptamer and fluorescence recovers. The latest research progress was proposed by Yang et al. [113]. They designed and constructed a nanopore complex containing unnatural amino acid, which is a conical rigid complex formed by octameric Mycobacterium smegmatis porin A (MspA). Through the strain-promoted azide-alkyne cycloaddition reaction, single-stranded DNA composed of 40 thymines (poly-T(40)) and lysozyme molecules with dibenzocyclooctyne (DBCO) were successfully connected to the functionalized nanopore interface, and it was found that it exhibited a new signal distribution pattern and the signal was significantly enhanced. When combined with different oligosaccharide substrates, the corresponding signals will change significantly. The prepared functionalized interface provides a new direction for single-molecule sensing. We can see that click chemistry is also an attractive technique in the biomedical field. However, there are only a few papers on the latest application of click chemistry in the biomedical field [15]. However, as a catalyst, Cu(I) has certain toxicity, and some Cu-catalyzed fixed viruses or oligonucleotide chains will degrade [111]. Bertozzi et al. [112] first proposed copper-free click chemistry, which eliminates the adverse effects of Cu(I), simplifies the experimental steps, and becomes an alternative CuAAC click reaction. This is an alternative method to activate alkynes for the catalyst-free [3+2] cycloaddition reaction with azides. Then, Xiang et al. [110] reported a biosensor system based on azide-co-functionalized graphene oxide (GO-N3) and carbon dots (CDs). Carbon-dot-labeled DNA (CD-DNA) binds to GO-N3 by copper-free click chemistry and quenches the fluorescence of CDs by fluorescence resonance energy transfer (FRET) (Figure 7c). After adding carcinoembryonic antigen (CEA), CEA binds to the aptamer and fluorescence recovers. The latest research progress was proposed by Yang et al. [113]. They designed and constructed a nanopore complex containing unnatural amino acid, which is a conical rigid complex formed by octameric Mycobacterium smegmatis porin A (MspA). Through the strain-promoted azide-al- (c) Schematic illustration of CEA detection system based on click chemistry and FRET between GO-N 3 and CD -DNA. Reprinted with permission from [110], copyright 2020, Anal Chim Acta.

Electro-Click Technology
In the CuAAC click reaction, Cu(I) salts or the in situ reduction in Cu(II) are commonly employed to introduce a catalytic amount of Cu(I). Various methods can be used to generate the required Cu(I) ions, including microwave [114], ultrasound [115], UV irradiation [116], and electrochemical reactions [117]. The electrochemical approach enables the reagent-free functionalization of biosensing interfaces, known as electro-click [16]. Devaraj et al. [118] demonstrated that catalytic Cu(I) ions can be generated by applying a mild reduction potential (−300 mV vs. Ag/AgCls) at the interface in contact with the Cu(II) solution. For example, Lesniewski et al. [119] deposited gold nanoparticles modified with terminal alkynyl groups onto azide-functionalized glassy carbon surfaces. The generation of the Cu catalyst can be precisely controlled by adjusting the treatment time, allowing control over the surface coverage by altering the deposition time. Villalba et al. [120] achieved the catalytic assembly of multilayers through the covalent bonding of poly(acrylic acid) (PAA) multilayers with alkynyl (PAAalk) and azide (PAAaz) groups. Recently, Yamamoto et al. [121] utilized electro-click chemistry to modify boron-doped diamond (BDD) electrodes. The electro-click strategy enables precise control over the amount of Cu(I) catalyst and the loading of azide-terminated ferrocene on alkyne-terminated BDD electrodes. Compared with the chemical synthesis method, the electro-click approach offers advantages such as faster reaction kinetics, environmental friendliness, and the absence of chemical residues. Furthermore, the assessment technique inherent to electro-click chemistry is inherently uncomplicated, affording the direct interpretation of the reaction through the analysis of the cyclic voltammetry profile.
These reasons contribute to the ongoing popularity of the electro-click strategy.

Electro-Click Strategies for the Functionalization of Biosensor Interfaces
Before constructing biosensors, careful attention must be given to the functionalization strategies of the biosensor interfaces in order to meet diverse sensing requirements. The resulting interface should not only immobilize the biometric element in a stable manner, but also offer a selective and sensitive response. In this section, we will discuss the functionalization strategies for electrochemical biosensor interfaces and optical biosensor interfaces.

Electro-Click Strategies for the Functionalization of Electrochemical Biosensor Interfaces
Electrochemical biosensors have long been extensively utilized across various fields. These biosensors can generate sensing signals by monitoring changes in impedance, current, and dielectric properties when the target analyte is formed on the electrode surface. Numerous strategies exist for the modification of interfaces in electrochemical biosensors, encompassing approaches such as self-assembled monolayers, covalent immobilization, and electro-click methodologies, among others [122,123]. Concurrently, a diverse array of electrochemical biosensor variants is available. Notably, owing to its electrochemically mediated modifications and notable versatility, the electro-click strategy finds predominant utility within the domain of electrochemical biosensors. The functional modification strategies based on electro-click for electrochemical biosensor electrodes can be categorized into four parts: electrografting, electropolymerization, electrodeposition, and bipolar electrode methods.

Electrografting
The most commonly employed approach for modifying biosensing interfaces is electrografting [124,125]. Electro-click-mediated electrografting plays a crucial role in preparing controllable nanostructures, enhancing the sensor performance, and expanding the sensor functionalities [126]. In simple terms, azide and alkyne are grafted onto the biosensing interface and modifier, respectively, and then connected by the CuAAC electro-click reaction. For instance, Sciortino et al. [127] achieved a network structure of organic/inorganic hybrid products containing alkynes and polyethylene glycol azides with bifunctional groups through the electro-click reaction on an F-SnO 2 electrode. The composition and loading of these hybrid films can be adjusted, demonstrating the versatility of such hybrid coatings. Fenoy et al. [126] reported the synthesis of azide-derived organic electrochemical transistor monomers and applied them in a CuAAC reaction with a dibenzocyclooctynegrafted thrombin-specific HD22 aptamer to achieve specific thrombin recognition. Also, Guerrero et al. [128] utilized ethynylated IgG bonded to azide-modified multi-walled carbon nanotube (MWCNT) electrodes to construct an electrochemical immunosensor for the cytokine interleukin 1b (IL-1b). The detection limit of this immunosensor was significantly improved to 5.2 pg/mL compared to the commercial kit. Effective coupling methods between interfaces are vital for achieving both sensitivity and selectivity. Therefore, we employed cucurbituril-and azide-grafted graphene oxide to develop a novel functional nanomaterial as a biosensor interface for the detection of VEGF165 protein (Figure 8a) [129]. This interface demonstrated the simultaneous acquisition of sensitivity and selectivity, with a dynamic detection range of from 10 fg/mL to 1 ng/mL and a detection limit of 8 fg/mL. Electro-click-mediated electrografting enables the preparation of multipoint-specific electrode functionalization for multi-target biosensors on various materials. The examples discussed above clearly illustrate the potential of electro-click-mediated electrografting in expanding the capabilities of biosensor interfaces [130].
Electropolymerization Electropolymerization (EP) refers to the network polymerization of solution components into a film when applying electrical stimulation through cyclic voltammetry (CV) [131]. This unique film structure enables the immobilization of functional molecules on or within the coating, making it suitable for combining with electro-click chemistry to create new functional biosensing interfaces. Rydzek et al. [131] developed self-assembled functional polymer films based on aniline and naphthalene using a one-pot method that involved simultaneous EP and electro-click functionalization. CV facilitated the oxidation of 4-azidoaniline and the reduction in Cu(II) ions, allowing for the simultaneous polymerization of the former and the CuAAC click reaction. For electropolymerization on conductive substrates, electrochemically mediated surface-initiated atom-transfer radical polymerization (SI-eATRP) offers a convenient approach to control polymer growth with low catalyst concentrations [132]. Wu et al. [133] achieved the fixation of sparse monomolecular membranes of ethynylphenyl on a carbon matrix through the electroreduction in aryldiazonium ions. They subsequently polymerized Poly(N-isopropylacrylamide) (PNIPAM) from the substrate in a one-pot solution containing an azide-derived initiator, PNIPAM, and a Cu catalyst (Figure 8b). The electro-reduction from Cu(II) to Cu(I) facilitated both the click reaction and SI-eATRP on the surface of the ethynylphenyl. This method is simple, convenient, and combines the advantages of electro-click chemistry and SI-eATRP.

Electrodeposition
Electrodeposition, as an electrochemical synthesis method based on solution-based synthesis, allows for the synthesis of different material types and the manipulation of various synthetic variables affecting morphology. It also enables the fabrication of uniform and tightly joined multi-junction electrodes through continuous multilayer deposition [134]. This feature proves particularly beneficial for synthesizing and functionalizing biosensing interfaces.
Conductive hydrogels, among various synthetic materials, have garnered attention from researchers. These hydrogels consist of conductive polymer networks formed by combining hydrogels with inherently conductive polymers. They offer a combination of biocompatibility, flexibility, high diffusivity, and conductivity [135,136]. Hydrogels can be prepared in specific forms on various substrates to suit the desired purpose. Hu et al. [137] described a method for coating chitosan hydrogel on a conductive surface using the electro-click-mediated electrodeposition technique. Chitosan was functionalized with azide or alkynyl groups, and a cathodic potential was applied to a gold chip to reduce Cu(II) ions to Cu(I) ions, catalyzing the CuAAC click reaction between the alkynyl chitosan and azide chitosan to form a conjugated chitosan hydrogel attached to the gold surface (Figure 8c). Experiments demonstrated the encapsulation of biomolecules within this hydrogel for biosensing purposes. Similarly, Choi et al. [138] electrodeposited PVA-based hydrogel on an indium tin oxide glass electrode using a Cu(I)-catalyzed CuAAC reaction with the reduction in Cu(II) ions. They found that embedding carbon nanotubes within the hydrogel enabled the deposition of thicker films due to the larger electrochemically active area provided by the carbon nanotubes. face (Figure 8c). Experiments demonstrated the encapsulation of biomolecules within this hydrogel for biosensing purposes. Similarly, Choi et al. [138] electrodeposited PVA-based hydrogel on an indium tin oxide glass electrode using a Cu(I)-catalyzed CuAAC reaction with the reduction in Cu(II) ions. They found that embedding carbon nanotubes within the hydrogel enabled the deposition of thicker films due to the larger electrochemically active area provided by the carbon nanotubes.

Bipolar Electrodes
Bipolar electrodes (BPEs) can simultaneously perform anodic and cathodic reactions, making them a versatile electrochemical-reaction-driving mode and suitable as radio electrodes [139]. BPEs do not require electrical connection and can accommodate conductive materials of any shape and size, and even multiple materials at once (Figure 9a) [140]. These characteristics align well with electro-click chemistry (Figure 9b). The potential gradient at the BPE interface has been successfully utilized as a controllable template for forming molecular-or polymer-gradient materials, making it suitable for biomimetic materials or biosensor analysis equipment [141]. A study was conducted on the gradient modification of azide-functionalized conductive-polymer film using electrogenerated Cu(I) species on a bipolar electrode through an electroshock reaction in the presence of terminal alkyne [142]. This allowed the introduction of various gradient functions, such  [133], copyright 2019, ChemElectroChem. (c) Schematic illustrating the "electro-click" chitosan hydrogel on a gold chip triggered by a negative potential that reduces Cu 2+ to Cu + . Reprinted with permission from [137], copyright 2014, RSC Advances.

Bipolar Electrodes
Bipolar electrodes (BPEs) can simultaneously perform anodic and cathodic reactions, making them a versatile electrochemical-reaction-driving mode and suitable as radio electrodes [139]. BPEs do not require electrical connection and can accommodate conductive materials of any shape and size, and even multiple materials at once (Figure 9a) [140]. These characteristics align well with electro-click chemistry (Figure 9b). The potential gradient at the BPE interface has been successfully utilized as a controllable template for forming molecular-or polymer-gradient materials, making it suitable for biomimetic materials or biosensor analysis equipment [141]. A study was conducted on the gradient modification of azide-functionalized conductive-polymer film using electrogenerated Cu(I) species on a bipolar electrode through an electroshock reaction in the presence of terminal alkyne [142]. This allowed the introduction of various gradient functions, such as gradient hydrophobicity/hydrophilicity and visible labeling, on the poly(3,4-ethylenedioxythiophene) (PEDOT) film to prepare the biosensing interface. In subsequent work, Zhou et al. [143] introduced a bipolar electrolytic micelle disruption (BEMD) system for shaping organic films. They created a U-shaped bipolar electrolysis system with an S-shaped potential gradient on the BPE, enabling the formation of a gradient film containing various organic compounds. This approach provided a novel idea and method for modifying organic membranes using the CuAAC electro-click reaction.
as gradient hydrophobicity/hydrophilicity and visible labeling, on the poly(3,4-ethylenedioxythiophene) (PEDOT) film to prepare the biosensing interface. In subsequent work, Zhou et al. [143] introduced a bipolar electrolytic micelle disruption (BEMD) system for shaping organic films. They created a U-shaped bipolar electrolysis system with an Sshaped potential gradient on the BPE, enabling the formation of a gradient film containing various organic compounds. This approach provided a novel idea and method for modifying organic membranes using the CuAAC electro-click reaction.

Applications of Electro-Click Strategies in Electrochemical Biosensor Functionalization with Submicron Resolution
Numerous techniques are available for effecting functional alterations in biosensing interfaces, including single-molecule modification/deposition [144]. However, these methods seldom permit intricate modifications at the micron scale. Furthermore, they often exhibit constrained control over interface surfaces or necessitate costly equipment [145]. In stark contrast, a notable facet of electro-click chemistry, which entails electrochemical reactions, is its spatial selectivity. This distinctive attribute facilitates the precise functionalization of nanogaps, gradients, and microelectrodes, all achieved with submicron precision.
The utilization of NPs as fundamental building blocks has catalyzed the emergence of a novel category of nano-building materials, thereby illuminating a promising avenue for nano-gap functionalization. In a pioneering endeavor, Rydezk et al. [146] orchestrated a nanodevice with a high aspect ratio, selectively focused through covalent self-assembly via spatially arranged Cu(I)-catalyzed electro-click reactions. Employing dendritic iron oxide nanoparticles endowed with azide and alkyne functionalities as building blocks, they achieved a spatially orchestrated electro-click network structure. This method of NP functionalization proves highly adaptable and can be extrapolated to diverse nanoparticle varieties featuring clickable moieties. As such, the electro-click approach emerges as a sanguine instrument for seamlessly integrating covalent NPs into nanodevices, thereby beckoning forth prospects for biosensors and granular electronic devices [147].
The manipulation of physicochemical property gradients-marked by gradual spatial and temporal transitions-can substantially amplify the efficacy of catalyst and drug

Applications of Electro-Click Strategies in Electrochemical Biosensor Functionalization with Submicron Resolution
Numerous techniques are available for effecting functional alterations in biosensing interfaces, including single-molecule modification/deposition [144]. However, these methods seldom permit intricate modifications at the micron scale. Furthermore, they often exhibit constrained control over interface surfaces or necessitate costly equipment [145]. In stark contrast, a notable facet of electro-click chemistry, which entails electrochemical reactions, is its spatial selectivity. This distinctive attribute facilitates the precise functionalization of nanogaps, gradients, and microelectrodes, all achieved with submicron precision.
The utilization of NPs as fundamental building blocks has catalyzed the emergence of a novel category of nano-building materials, thereby illuminating a promising avenue for nano-gap functionalization. In a pioneering endeavor, Rydezk et al. [146] orchestrated a nanodevice with a high aspect ratio, selectively focused through covalent self-assembly via spatially arranged Cu(I)-catalyzed electro-click reactions. Employing dendritic iron oxide nanoparticles endowed with azide and alkyne functionalities as building blocks, they achieved a spatially orchestrated electro-click network structure. This method of NP functionalization proves highly adaptable and can be extrapolated to diverse nanoparticle varieties featuring clickable moieties. As such, the electro-click approach emerges as a sanguine instrument for seamlessly integrating covalent NPs into nanodevices, thereby beckoning forth prospects for biosensors and granular electronic devices [147].
The manipulation of physicochemical property gradients-marked by gradual spatial and temporal transitions-can substantially amplify the efficacy of catalyst and drug design, introducing novel analytical avenues of considerable import in solution and interface functionalization. Krabbenborg et al. [148] harnessed electro-click chemistry to fabricate a solution gradient, thereby enabling the high-throughput control and monitoring of the surface reactivity across spatial and temporal dimensions. By virtue of the solution gradient, finely adjustable and inherently predictable variations in the spatial concentration of chemically active species are achieved, engendering micron-scale surface gradients. In analogous fashion, Nicosia et al. [149] harnessed the CuAAC reaction to generate a monolayer on a glass surface flanked by platinum electrodes, effectively manipulating the gradient of the Cu(I) solution to effect microelectrode interface functionalization.
Beyond gradient-driven surface modification, the repertoire of electro-click chemistry extends to the direct functionalization of microelectrodes. Hansen et al. [150] directly functionalized microelectrodes with PEDOT-N 3 , showcasing a universally applicable and convenient strategy for diverse conductive-polymer functionalization. Notwithstanding the aforementioned applications, numerous prospects for submicron-resolution applications await exploration.

Electro-Click Strategies for the Functionalization of Optical Biosensor Interfaces
In recent times, the augmentation of optical biosensors using the electro-click approach has gained prominence. This development is attributed to the understanding that electron dynamics can arise not exclusively from direct electrochemical processes, but also from alternative energy excitations [151]. Consequently, as investigations into the interplay between photons and electrons advance, the electro-click strategy has found application within the realm of optical sensing [142,152]. Optical biosensors rely on measuring changes in the optical properties of the transducer surface when the analyte and recognition element form a complex [153]. They can be categorized as direct optical biosensors or indirect optical biosensors. While there are limited examples of optical biosensing interfaces prepared using electro-click chemistry, luminescent products prepared through electro-click have been identified. It is expected that similar functionalization strategies will be applied in the near future to prepare corresponding optical biosensors.
Direct optical biosensor signals depend on the complex formation on the biosensor interface. Shida et al. [142] used rhodamine-based acetylene as a visible indicator. After electroshock reaction on the bipolar electrode (Figure 10a), the polymer film was uniformly oxidized to the doped state, reducing the background absorption of PEDOT in the visible-light region. Consequently, the cathode part turned purple, allowing for naked-eye detection (Figure 10b). In addition to the existing direct optical sensor, Goll et al. [152] blended EDOT and branched 2,2 :3 ,2 -terthiophene (3T) to form an EDOT-N 3 film that facilitated functional modification through an electro-click reaction. By altering the mixing ratio of the two materials, the optical properties exhibited significant changes that could be detected via infrared spectroscopy (Figure 10c). Indirect optical biosensors commonly employ various labels, such as fluorophores, to detect and amplify signals. As early as 2008, Ku et al. [107] introduced the use of electroclick reactions to attach non-reactive fluorescent molecular patterns onto azide glass substrates (Figure 11a). This approach can be extended to enable the growth of any fluorescent molecule on an insulating substrate, forming a direct covalent bond beneath the mi- Indirect optical biosensors commonly employ various labels, such as fluorophores, to detect and amplify signals. As early as 2008, Ku et al. [107] introduced the use of electro-click reactions to attach non-reactive fluorescent molecular patterns onto azide glass substrates (Figure 11a). This approach can be extended to enable the growth of any fluorescent molecule on an insulating substrate, forming a direct covalent bond beneath the microelectrode. The F-SnO 2 coating developed by Sciortino et al. [127] using the aforementioned electro-click reaction exhibited notable differences in fluorescence spectra when loaded with 4,4-Difluoro-8-(4-trimethylsilylethynylphenyl)-1,3,5,7-tetramethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacene(BODIPY) (Figure 11b). This method also proves to be a viable approach for indirect optical biosensors. Coceancigh et al. [154] employed electrochemically assisted CuAAC to precisely control the inner surface of poly(ethylene terephthalate) (PET) track-etched pores. In this process, the ethynyl groups within the etched holes were first modified via the amidation of the surface-COOH groups. Subsequently, a solution containing copper (II) and azide-labeled fluorescent dye was introduced and sandwiched between gold electrodes (Figure 11c). Rydzek et al. [155] harnessed the electro-click reaction methodology to fabricate a thin film atop a gold electrode. Variations in the pH induced distinct electrostatic-repulsion patterns between PAA-Alk moieties, thereby governing the structural attributes of the resultant film. These disparities in the film structure were anticipated to manifest as discernible divergences in fluorescence responses. As a result, the fluorescent group could be directly immobilized onto the membrane. Furthermore, materials such as CNTs, CDs, and luminol exhibit light-specific properties [45,63,110]. If they can be utilized for modification, then a broader range of functional optical biosensor interfaces could be developed to meet diverse requirements. Electro-click chemistry offers an expedient, versatile, and facile approach to biose ing interface functionalization; nevertheless, it is not without its imperfections. Seve challenges persist, warranting researchers dedicated efforts. Within the realm of bios Reprinted with permission from [154], copyright 2017, Langmuir.

Limits of Electro-Click Strategies for the Functionalization of Biosensor Interfaces
Electro-click chemistry offers an expedient, versatile, and facile approach to biosensing interface functionalization; nevertheless, it is not without its imperfections. Several challenges persist, warranting researchers' dedicated efforts. Within the realm of biosensors, a paramount concern in the electro-click methodology is the retention of copper ions (Cu(II)/Cu(I)) during functionalization, which could potentially impede biomolecular activity. Cu(II) might catalyze the production of reactive oxygen species at the biosensing interface, engendering lipid peroxidation, protein oxidation, and DNA degradation [156]. Cu(I) is highly thiophilic and can directly damage the Fe-S-cluster-containing enzyme modifiers in the biosensing interface [157]. Schaaf et al. [158] ventured to ameliorate the Cu(II) influence via EDTA, yielding commendable outcomes. Contemporary endeavors, such as those by Cheng et al. [159], persist in deploying EDTA overdosing to tackle this conundrum. Beyond chemical mitigation, physical adsorption emerges as an effective countermeasure against Cu(II). In this vein, Liu et al. [160] prepared triethanolamine-GO nanosheets to robustly adsorb Cu(II), displaying an elevated equilibrium capacity even at higher initial Cu(II) concentrations.
The widespread adoption of the electro-click reaction rests on its attributes of expeditious reaction kinetics, ecological benignity, and minimal pollution. However, investigations into the recycling and reutilization of electro-click-functionalized biosensing interfaces have remained relatively sparse, casting a spotlight on a nascent concern for future inquiry. Encouragingly, select researchers have delved into recycling experiments concerning electroclick-functionalized biosensors. For instance, Fomo et al. [106] demonstrated the potential for electrode reuse by washing it with deionized water after sample detection, subsequently reemploying the electrode with negligible alteration in DPSV voltammograms, attesting to the sensor viability. Likewise, Qi et al. [117] exhibited a stable immunosensor retention for 15 days, with the subsequent detection revealing a commendable 88% retention of the initial steady-state current. These instances provide inspiring precedents. Thus, within the domain of electro-click-functionalized biosensing interfaces, the focus must expand beyond novel modification methodologies, encompassing heightened attention toward interface recyclability and, building upon this foundation, the exploration of straightforward recovery protocols. In general, the journey toward electro-click-modified-functionalized biosensing interfaces stretches ahead, necessitating persistent exploration and innovation.

Conclusions
In summary, we have comprehensively examined the different strategies for functionalizing biosensing interfaces, encompassing nanomaterials, small molecules, biomacromolecules, and cell-mediated interfacial regulations. We have also delved into the process of transforming identified elements into signals, imparting functionality to the sensor, and enhancing its performance.
Among the various functionalization strategies for biosensing interfaces, click chemistry stands out due to its advantages of rapidity, selectivity, and low pollution. We have elucidated the origins and principles of click chemistry, with CuAAC serving as an exem-plar, highlighting its advantages. In the realm of electrochemical biosensors, the use of click-chemistry-based modifications on the sensing interface offers improved stability and convenience, leading to more discernible electrochemical signals. For optical biosensors, the modified sensing interface not only generates optical signals in response to the target analyte, but also amplifies the signal through the incorporated materials, thereby bolstering the reliability of the sensing outcomes. Within this domain, electro-click chemistry emerges as an environmentally friendly, swift, and convenient approach, surpassing traditional click chemistry in terms of functionalizing biosensing interfaces. We have summarized the research and application progress of electro-click chemistry in functionalizing electrochemical biosensors and optical sensors. While there may be fewer corresponding examples in optical biosensors, drawing from related literature, this review has identified potential examples that can be utilized for constructing optical biosensor interfaces.
This review provides a fresh perspective for the development of novel functional biosensing interface strategies. Moreover, the expansion of biosensing systems based on electro-click chemistry will contribute to the selection of materials and the advancement of strategies. Ultimately, this will broaden the applications of biosensors across diverse fields, such as chemistry, agriculture, food science, clinical diagnostics, pharmaceuticals, and environmental analysis.