Charge Transfer on the Surface-Enhanced Raman Scattering of Ag/4-MBA/PEDOT:PSS Syste: Intermolecular Hydrogen Bonding

: A sandwich-structured noble metal-probe molecule-organic semiconductor consisting of Ag nanoparticles (NPs), 4-mercaptobenzoic acid (4-MBA) and different concentrations of poly-(styrenesulfonate:poly(3,4-ethylenedioxythiophene) (PEDOT:PSS) was prepared by layer-by-layer assembly. Intermolecular hydrogen bonding was observed to have a signiﬁcant effect on the surface-enhanced Raman scattering (SERS) of Ag/4-MBA/PEDOT:PSS. Upon increasing the PEDOT:PSS concentration, the characteristic Raman band intensity of 4-MBA was enhanced. In addition, the selected b 2 vibration mode was signiﬁcantly enhanced due to the inﬂuence of the charge transfer (CT) mechanism. The CT degree ( ρ CT ) of the composite system was calculated before and after doping with PEDOT:PSS; when the concentration of PEDOT:PSS was 0.8%, the SERS intensity tended to be stable, and ρ CT reached a maximum. Compared with that of the undoped PEDOT:PSS system, ρ CT was signiﬁcantly enhanced after doping, which can be explained by the CT effect induced by hydrogen bonds. These results indicate that hydrogen bonding transfers a charge from the Fermi energy level of Ag to the lowest unoccupied molecular orbital (LUMO) of 4-MBA, and due to the resulting potential difference, the charge will continue to transfer to the LUMO of PEDOT:PSS. Therefore, the introduction of organic semiconductors into the ﬁeld of SERS not only expands the SERS substrate scope, but also provides a new idea for exploring the SERS mechanism. In addition, the introduction of hydrogen bonds has become an important guide for the study of CT and the structure of composite systems.


Introduction
Surface-enhanced Raman scattering (SERS) is a fast and nondestructive method with the advantages of high sensitivity, good selectivity, high accuracy, and fast response. It is extensively used in various fields for research on detection, environmental pollution, food safety [1,2], homeland security [3], and chemical reaction mechanisms. Although SERS has been the subject of considerable interest and has been extensively studied, there are still minor issues that have been neglected. These issues are due to the sensitivity of SERS to the local environment of molecules and the influence of the local environment on the SERS distribution of adsorbates, including H + concentration, sensing, potential, and other factors [4,5]. In fact, there are many factors that affect the performance of SERS, such as intermolecular forces, which often affect the self-assembly process of polymer molecules and liquid crystal molecules. By exploring intermolecular forces, we can better understand the properties of SERS and its influence on materials, allowing us to improve the properties of materials and broaden the substrate scope of SERS. Intermolecular forces usually include electrostatic interactions, van der Waals forces, dipole interactions, dispersion forces, and hydrogen bonding. Among them, the electrostatic effect was mainly affected by gravity or repulsion through positive and negative charges, affecting the SERS performance. Van der Waals forces hold matter together due to the asymmetric effects of electron clouds. Although the dipole-dipole interaction is weak, a large dipole moment still has a strong influence on the system. Dispersion force is the weakest intermolecular force, such as two molecules for the relative molecular mass of the material, and produces strong attraction. In particular, the study of hydrogen bonds, a kind of intermolecular force, provides some information on the internal structure of a molecule and interactions with other substances at the molecular level. Hydrogen bonding plays an important role in the study of molecular configuration, the identification of halogen bonding and the theoretical study of the transition from ground state to an excited state of a large number of chemicals and biological complex systems. Hydrogen bonds change the electronic structure of the nanocomposite system through the interaction between molecules, and then affects the SERS charge transfer process. Hydrogen bonds have been widely studied in recent years due to their directivity and saturation, which is very significant to the study of molecular structure and properties. We combined the research on hydrogen bonds with SERS according to the development status of SERS. Thus, the concentration-dependent Ag/4-MBA/PEDOT:PSS nanocomposite system was developed; however, the effect of hydrogen bonding on metal/semiconductor-molecule systems is still unclear and needs to be further improved. Therefore, studying hydrogen bonds via the SERS method can provide a better understanding of the SERS enhancement mechanism and allow further development of research on materials, chemical mechanisms, and environmental monitoring, biosensors, as well as research into other interdisciplinary fields.
The SERS enhancement mechanism is generally classified into two types: a chemical enhancement mechanism (CM) and an electromagnetic enhancement mechanism (EM). In the EM, the localized surface plasmon resonance (LSPR) excited by the rough surface of metal materials or the nanosized surface of a metal generates a strong electromagnetic field, resulting in Raman signal enhancement [6][7][8], and in the CM, an interaction between the target molecule and a metal surface forms a chemical bond, which enhances the SERS signal [9,10]. Among these mechanisms, the EM, which is a pure physical mechanism with a long-range effect that can produce a strong SERS signal without direct contact with a metal, is dominant. However, many phenomena in the experiment could not be fully explained by the electromagnetic field mechanism. For example, the distance between two nanoparticles (NPs) was not in the range of "hot spot". Besides, different molecules had different SERS enhancement effects on the same SERS substrate. In this case, the CM could make up for the deficiency of the EM. Unlike the enhancement mechanism of electromagnetic field, CM is a short-range effect with a "first-layer effect"; that is, it can only enhance molecules restricted in monolayer by surface adsorption and bonding [11,12], and requires direct contact with metal NPs. The charge transfer (CT) model is a widely accepted CM model. CT is closely related to the mutual effect between molecules attached to the surface of a composite system and atoms attached to the surface of a composite system. When the incident light distribution matches the potential barrier between the Fermi energy level of the metal and the electron affinity energy of a molecule [13], it will induce a better CT effect, which is mainly attributed to the electron resonance process and the CT between the empty orbital of the molecule and the Fermi energy level of the metal [14,15]. The EM and CM do not work alone. These two mechanisms often play a synergistic role, so it is of great significance to establish an integrated model of the two mechanisms to jointly explain the SERS phenomenon.
In recent years, the progress of SERS research has been closely related to the development of SERS-active substrates. To achieve an excellent SERS effect, substrates should be continuously improved. A strong SERS signal was first observed on rough silver (Ag) electrode surface-adsorbed pyridine and subsequently on the surfaces of Au, Ag, Cu and other coinage metals [16][17][18][19][20][21]. Then, it was discovered that transition metals can also produce excellent SERS effects as substrates [22]. Semiconductors have a controllable conductivity, universal structure, easily controlled synthesis [23], stable exciton formation and molecular structures with effective CT characteristics [24,25] and are gradually being applied with the development of flexible devices, trace detection, solar cells, and other new energy fields. In particular, organic semiconductors have been developed rapidly in recent years because they have the advantages of low cost, easy availability, good flexibility, few impurities, easy doping, energy level separation and recyclability.
Herein, a sandwich-structured noble metal-probe molecule-organic semiconductor was constructed via layer-by-layer assembly. Based on a study of the chain structure changes of PEDOT at different concentrations, the CT process was confirmed. We studied the SERS spectra of 4-mercaptobenzoic acid (4-MBA) induced by CT in different systems containing hydrogen bonding. Considering the influence of the CT degree (ρ CT ) on SERS intensity, we established a CT model, discussed the mechanism of CT, and further explained the role of hydrogen bonds. Therefore, the CT process between organic semiconductors and noble metals was explored to improve the theory that the CT process is an important factor to realize SERS enhancement.

Chemicals
PEDOT:PSS (1.5% in water) was obtained from Heraeus. Poly(diallyldimethylammonium chloride) (PDDA, numerator weight = 220,000-300,000, 20% in water) was obtained from J&K Chemical Co. 4-MBA (99%) and silver nitrate (AgNO 3 , 99.6%) was purchased from Sigma-Aldrich Co., Ltd. All the chemicals used in this study were purchased with the highest purity available and were used as received without further purification. Anhydrous ethanol (99.7%), hydrogen peroxide (H 2 O 2 , 30%), ammonia (NH 3 , 28%) and deionized water (18.25 MΩ·cm) were also used throughout this study. Ag NPs were prepared by the classic Lee method [26]. First, 0.036 g AgNO 3 was dissolved in 200 mL deionized water, and then the solution was stirred under reflux and heated to 90 • C. When the solution boiled slightly, 4 mL of 1% sodium citrate was added immediately, and the solution was heated to 85 • C for 45 min. During this process, the solution changed from colorless to light yellow, to brown, and finally, to a gray-green colloid with a maximum plasma absorption at approximately 430 nm. Ag NPs are spherical in distribution, and the average particle size was approximately 65 nm. A cleaned glass slide was placed in a mixed solution of H 2 O, 30% H 2 O 2 and 28% NH 3 ·H 2 O (28% NH 3 in H 2 O) at a volume ratio of 5:1:1. The solution was boiled until no bubbles were present and then cooled to room temperature, and the glass slide was washed several times with deionized water. A hydrophilic glass substrate rich in hydroxyl groups on the surface was obtained. The glass slide was immersed in 0.5% PDDA solution for 45 min, rinsed with deionized water, and allowed to dry naturally. The glass slide decorated with PDDA was soaked in a Ag sol for 8 h. Ag NPs were combined with the modified PDDA glass slide through electrostatic interaction, thereby obtaining Ag nanofilms with better particle dispersion.

Preparation of Ag/4-MBA System
Ag NPs were placed in a 4-MBA solution at a concentration of 10 −3 M for 1 h, and the 4-MBA molecules were bonded to the surface of Ag NPs by Ag-S covalent bonds to complete the assembly of the Ag/4-MBA system. Different concentrations of PEDOT:PSS (0.05%, 0.075%, 0.1%, 0.2%, 0.3%, 0.5%, 0.8%, and 1.0%) were dropped on the Ag/4-MBA-coated glass slide by titration method, and then naturally dried to complete the assembly, as shown in Scheme 1.

Preparation of Ag/4-MBA System
Ag NPs were placed in a 4-MBA solution at a concentration of 10 −3 M for 1 h, and the 4-MBA molecules were bonded to the surface of Ag NPs by Ag-S covalent bonds to complete the assembly of the Ag/4-MBA system.

Characterization and SERS Measurements
The appearance and particle diameter of Ag NPs were determined by scanning electron microscopy (SEM) at a 250 kV accelerating voltage with a JEOL 6500 F microscope. A Shimadzu UV-3600 Plus UV-Vis spectrometer was used to measure the UV-Vis absorption spectra of the Ag/4-MBA and Ag/4-MBA/PEDOT:PSS composite systems. Raman spectra of the composite systems were obtained with a 633 nm laser by using a Renishaw Raman system 2000 microscope. For the Raman experiments of the Ag/4-MBA/PE-DOT:PSS composite system, different concentrations (0.05%, 0.075%, 0.1%, 0.2%, 0.3%, 0.5%, 0.8%, and 1.0%) of PEDOT:PSS were titrated into the Ag/4-MBA composite system to form Ag/4-MBA/PEDOT:PSS systems.

Results
As shown in Scheme 1, first, the glass slide was coated with a positively changed polymer, PDDA. Second, the citrate ions stabilized Ag NPs was modified on the PDDAcoated glass slides based on the electrostatic adsorption interaction to form self-assembled Ag films. Third, 4-MBA was adsorbed on the Ag film to form the Ag/4-MBA system via Ag-S bonds. Finally, the Ag/4-MBA/PEDOT:PSS sandwich structure was formed by introducing the PEDOT: PSS to the Ag/4-MBA system via a hydrogen bond. Since the hydrogen is the electron acceptor, and oxygen is the electron donor, it is easy to form the hydrogen bond between the carboxyl of MBA and PEDOT or/and PSS. Herein, the oxygen on the carboxyl double bond of 4-MBA forms hydrogen bond with hydrogen on the sulfonic group of PSS, and the hydrogen on the carboxyl group of 4-MBA forms a hydrogen bond with oxygen on the sulfonic group [27]. Figure 1 displays SEM images of Ag NPs assembled on a PDDA-modified glass substrate and a Ag NP assembly system with different Scheme 1. Schematic of the layer-by-layer assembly of Ag/4-MBA/PEDOT:PSS films.

Characterization and SERS Measurements
The appearance and particle diameter of Ag NPs were determined by scanning electron microscopy (SEM) at a 250 kV accelerating voltage with a JEOL 6500 F microscope. A Shimadzu UV-3600 Plus UV-Vis spectrometer was used to measure the UV-Vis absorption spectra of the Ag/4-MBA and Ag/4-MBA/PEDOT:PSS composite systems. Raman spectra of the composite systems were obtained with a 633 nm laser by using a Renishaw Raman system 2000 microscope. For the Raman experiments of the Ag/4-MBA/PEDOT:PSS composite system, different concentrations (0.05%, 0.075%, 0.1%, 0.2%, 0.3%, 0.5%, 0.8%, and 1.0%) of PEDOT:PSS were titrated into the Ag/4-MBA composite system to form Ag/4-MBA/PEDOT:PSS systems.

Results
As shown in Scheme 1, first, the glass slide was coated with a positively changed polymer, PDDA. Second, the citrate ions stabilized Ag NPs was modified on the PDDAcoated glass slides based on the electrostatic adsorption interaction to form self-assembled Ag films. Third, 4-MBA was adsorbed on the Ag film to form the Ag/4-MBA system via Ag-S bonds. Finally, the Ag/4-MBA/PEDOT:PSS sandwich structure was formed by introducing the PEDOT: PSS to the Ag/4-MBA system via a hydrogen bond. Since the hydrogen is the electron acceptor, and oxygen is the electron donor, it is easy to form the hydrogen bond between the carboxyl of MBA and PEDOT or/and PSS. Herein, the oxygen on the carboxyl double bond of 4-MBA forms hydrogen bond with hydrogen on the sulfonic group of PSS, and the hydrogen on the carboxyl group of 4-MBA forms a hydrogen bond with oxygen on the sulfonic group [27]. Figure 1 displays SEM images of Ag NPs assembled on a PDDA-modified glass substrate and a Ag NP assembly system with different concentrations of PEDOT:PSS. According to the statistical distribution of particle size of Ag NPs in Figure 2, we found that most particle sizes of Ag NPs was obtained about 60-70 nm. As shown in Figure 1, before the introduction of PEDOT:PSS, Ag NPs were spherical distributed on the surface of glass substrate. After PEDOT:PSS coating, the morphology of Ag NPs self-assemble film was aggregated, and the aggregation degree increased gradually with the increase of the PEDOT:PSS. concentrations of PEDOT:PSS. According to the statistical distribution of particle size of Ag NPs in Figure 2, we found that most particle sizes of Ag NPs was obtained about 60-70 nm. As shown in Figure 1, before the introduction of PEDOT:PSS, Ag NPs were spherical distributed on the surface of glass substrate. After PEDOT:PSS coating, the morphology of Ag NPs self-assemble film was aggregated, and the aggregation degree increased gradually with the increase of the PEDOT:PSS.  The compositions, contents and structures of different systems can be determined and analyzed by UV-Vis spectroscopy. Figure 3 shows the UV-Vis absorption spectra of Ag NPs, Ag/4-MBA, and Ag/4-MBA/PEDOT:PSS composite systems (PEDOT:PSS concentrations were 0.05%, 0.075%, 0.1%, 0.2%, 0.3%, 0.5%, 0.8%, and 1.0%, respectively). The Ag NPs were deposited on the PDDA-decorated glass slide by employing the self-assemble method. After deposition of the Ag NPs on the PDDA-decorated glass slide, the distance of Ag NPs decreased and the aggregation occurred, which induced wide absorbance bands located at 400-700 nm. The strong interactions and coupling may have also contributed to the plasmon resonance red shift if the LSPR existed between neighboring Ag NPs. The dipole-dipole interaction assigned to Ag NP were blue shifted by 22 nm more than the silver sol. After different concentrations of PEDOT:PSS were added, the SPR peak of concentrations of PEDOT:PSS. According to the statistical distribution of particle size of Ag NPs in Figure 2, we found that most particle sizes of Ag NPs was obtained about 60-70 nm. As shown in Figure 1, before the introduction of PEDOT:PSS, Ag NPs were spherical distributed on the surface of glass substrate. After PEDOT:PSS coating, the morphology of Ag NPs self-assemble film was aggregated, and the aggregation degree increased gradually with the increase of the PEDOT:PSS.  The compositions, contents and structures of different systems can be determined and analyzed by UV-Vis spectroscopy. Figure 3 shows the UV-Vis absorption spectra of Ag NPs, Ag/4-MBA, and Ag/4-MBA/PEDOT:PSS composite systems (PEDOT:PSS concentrations were 0.05%, 0.075%, 0.1%, 0.2%, 0.3%, 0.5%, 0.8%, and 1.0%, respectively). The Ag NPs were deposited on the PDDA-decorated glass slide by employing the self-assemble method. After deposition of the Ag NPs on the PDDA-decorated glass slide, the distance of Ag NPs decreased and the aggregation occurred, which induced wide absorbance bands located at 400-700 nm. The strong interactions and coupling may have also contributed to the plasmon resonance red shift if the LSPR existed between neighboring Ag NPs. The dipole-dipole interaction assigned to Ag NP were blue shifted by 22 nm more than the silver sol. After different concentrations of PEDOT:PSS were added, the SPR peak of The compositions, contents and structures of different systems can be determined and analyzed by UV-Vis spectroscopy. Figure 3 shows the UV-Vis absorption spectra of Ag NPs, Ag/4-MBA, and Ag/4-MBA/PEDOT:PSS composite systems (PEDOT:PSS concentrations were 0.05%, 0.075%, 0.1%, 0.2%, 0.3%, 0.5%, 0.8%, and 1.0%, respectively). The Ag NPs were deposited on the PDDA-decorated glass slide by employing the self-assemble method. After deposition of the Ag NPs on the PDDA-decorated glass slide, the distance of Ag NPs decreased and the aggregation occurred, which induced wide absorbance bands located at 400-700 nm. The strong interactions and coupling may have also contributed to the plasmon resonance red shift if the LSPR existed between neighboring Ag NPs. The dipoledipole interaction assigned to Ag NP were blue shifted by 22 nm more than the silver sol. After different concentrations of PEDOT:PSS were added, the SPR peak of Ag NPs continued to shift to longer wavelengths, and as the concentration increased, the redshift phenomenon became more obvious, and the peak gradually widened. After introduction of the polymer, layers of Ag, 4-MBA and PEDOT:PSS interacted to form a new CT state [28].
Ag NPs continued to shift to longer wavelengths, and as the concentration increased, the redshift phenomenon became more obvious, and the peak gradually widened. After introduction of the polymer, layers of Ag, 4-MBA and PEDOT:PSS interacted to form a new CT state [28].   [29][30][31]. In turn, it affected the electronic structure of the Ag/4-MBA complex, and the intensity of the 4-MBA band also changed. With increasing PEDOT:PSS concentration, the number of carboxyl groups combined with PSS increased, and the effect on the system increased. When the concentration of PEDOT:PSS increased to a certain extent, the number of carboxyl groups bound to PSS in the system became saturated, and the influence on the system became stable [32].  Figure 5B. Compared with the original 0.8% PEDOT:PSS system, the Ag/4-MBA/0.8% PEDOT:PSS composite system exhibited a larger blueshift at 1395~1437 cm −1 because Ag and sulfhydryl groups combined through Ag-S bonds to form a structure with C2v symmetry. 4-MBA is a derivative containing sulfhydryl and carboxyl groups [33][34][35][36]. It has two hydrogen bond donors, namely, the oxygen atoms on the sulfhydryl and carboxyl groups, and five potential hydrogen bond acceptors, namely, π electrons on the benzene ring and the lone pair electrons of the oxygen and sulfur atoms.
When PSS bound to 4-MBA, the three lone pairs of electrons on the oxygen atom of the sulfonic group of PSS served as donors, and the hydrogen on the carboxyl group of 4-MBA served as an acceptor. With the combination of the two forms of hydrogen bonds, the conjugation degree of the whole system increased, the density of the electron cloud increased, and the vibration signal shifted to higher wavenumbers, corresponding to a blueshift. This phenomenon shows that hydrogen bonding in the molecule led to charge redistribution of the Ag/4-MBA complex. According to the ρCT formula proposed by Lombardi, the contribution of the hydrogen bond to CT resonance was estimated [37,38].    [29][30][31]. In turn, it affected the electronic structure of the Ag/4-MBA complex, and the intensity of the 4-MBA band also changed. With increasing PEDOT:PSS concentration, the number of carboxyl groups combined with PSS increased, and the effect on the system increased. When the concentration of PEDOT:PSS increased to a certain extent, the number of carboxyl groups bound to PSS in the system became saturated, and the influence on the system became stable [32].  Figure 5B. Compared with the original 0.8% PEDOT:PSS system, the Ag/4-MBA/0.8% PEDOT:PSS composite system exhibited a larger blueshift at 1395~1437 cm −1 because Ag and sulfhydryl groups combined through Ag-S bonds to form a structure with C 2v symmetry. 4-MBA is a derivative containing sulfhydryl and carboxyl groups [33][34][35][36]. It has two hydrogen bond donors, namely, the oxygen atoms on the sulfhydryl and carboxyl groups, and five potential hydrogen bond acceptors, namely, π electrons on the benzene ring and the lone pair electrons of the oxygen and sulfur atoms. membrane, and when the I k (SPR) value is extremely small or close to 0, the SERS spectral intensity mainly comes from the contribution of CT. The formula can be approximated as follows: ρ CT (κ)= I k CT I k CT +I 0 (SPR) (2)   Table 2 and Figure 6A. This band corresponds to an in-plane circulatory breathing mode, which is coupled to the νC-S circulatory breathing mode (b2 mode) of 4-MBA at 1014 cm −1 . At present, it is only slightly affected by SPR, mainly due to the contribution of CT. By calculating the ρCT of 4-MBA and the ratio of b2 to a1, the relationship between these values and the PEDOT:PSS concentration was obtained. When ρCT (κ) = 0.5, the contributions of SPR and CT to SERS enhancement were the same; when ρCT(κ) = 0, the mainly SPR effect affected SERS enhancement. When ρCT(κ) was about 1, the mainly CT effect affected the SERS enhancement. As shown in Figure 6B, ρCT(κ) = 0.395 and 0.650 for the Ag/4-MBA composite system and Ag/4-MBA/PEDOT:PSS (0.8%) composite system, respectively. Therefore, for the Ag/4-MBA/PEDOT:PSS (0.8%) composite system, ρCT(κ) > 0.5 was due to the CT process of the system. Figure 6A shows a column chart of the ρCT values of the Ag/4-MBA/PEDOT:PSS composite system with different concentrations of PE-DOT:PSS (0.05%, 0.075%, 0.1%, 0.2%, 0.3%, 0.5%, 0.8%, and 1.0%). There is a positive correlation between ρCT and PEDOT:PSS concentration, indicating that the formation of hydrogen bonds is beneficial to the CT process [40,41]. As the number of hydrogen bonds increased, the CT process of Ag/4-MBA was further distributed to form a CT state, forming a CT state more matched to the incident light. When the PEDOT:PSS concentration was 0.8%, the CT distribution was stable. When PSS bound to 4-MBA, the three lone pairs of electrons on the oxygen atom of the sulfonic group of PSS served as donors, and the hydrogen on the carboxyl group of 4-MBA served as an acceptor. With the combination of the two forms of hydrogen bonds, the conjugation degree of the whole system increased, the density of the electron cloud increased, and the vibration signal shifted to higher wavenumbers, corresponding to a blueshift. This phenomenon shows that hydrogen bonding in the molecule led to charge redistribution of the Ag/4-MBA complex. According to the ρ CT formula proposed by Lombardi, the contribution of the hydrogen bond to CT resonance was estimated [37,38].
The calculation formula is as follows [39]: The exponent k represents the line of the Raman spectrum when the molecule has CT resonance. When I 0 (SPR) = I k (SPR), spectral line k belongs to a completely symmetric membrane, and when the I k (SPR) value is extremely small or close to 0, the SERS spectral Chemosensors 2021, 9, 111 8 of 11 intensity mainly comes from the contribution of CT. The formula can be approximated as follows: Here, the band at 1184 cm −1 attributed to C-H deformation mode (a 1 mode) and 1395−1437 cm −1 (b 2 mode) were selected to calculate ρ CT . The ρ CT values of the Ag/ 4-MBA/PEDOT:PSS composite systems with different concentrations of PEDOT:PSS are shown in Table 2 and Figure 6A. This band corresponds to an in-plane circulatory breathing mode, which is coupled to the νC-S circulatory breathing mode (b 2 mode) of 4-MBA at 1014 cm −1 . At present, it is only slightly affected by SPR, mainly due to the contribution of CT. By calculating the ρ CT of 4-MBA and the ratio of b 2 to a 1 , the relationship between these values and the PEDOT:PSS concentration was obtained. When ρ CT (κ) = 0.5, the contributions of SPR and CT to SERS enhancement were the same; when ρ CT (κ) = 0, the mainly SPR effect affected SERS enhancement. When ρ CT (κ) was about 1, the mainly CT effect affected the SERS enhancement. As shown in Figure 6B, ρ CT (κ) = 0.395 and 0.650 for the Ag/4-MBA composite system and Ag/4-MBA/PEDOT:PSS (0.8%) composite system, respectively. Therefore, for the Ag/4-MBA/PEDOT:PSS (0.8%) composite system, ρ CT (κ) > 0.5 was due to the CT process of the system. Figure 6A shows a column chart of the ρ CT values of the Ag/4-MBA/PEDOT:PSS composite system with different concentrations of PEDOT:PSS (0.05%, 0.075%, 0.1%, 0.2%, 0.3%, 0.5%, 0.8%, and 1.0%). There is a positive correlation between ρ CT and PEDOT:PSS concentration, indicating that the formation of hydrogen bonds is beneficial to the CT process [40,41]. As the number of hydrogen bonds increased, the CT process of Ag/4-MBA was further distributed to form a CT state, forming a CT state more matched to the incident light. When the PEDOT:PSS concentration was 0.8%, the CT distribution was stable.  When Ag, 4-MBA and PEDOT:PSS contacted each other, a new CT process occurred at the contact interface, and a new CT state formed. The Fermi energy level of Ag NPs in vacuum is −4.84 eV [42], and the highest occupied molecular orbital (HOMO) and lowest When Ag, 4-MBA and PEDOT:PSS contacted each other, a new CT process occurred at the contact interface, and a new CT state formed. The Fermi energy level of Ag NPs in vacuum is −4.84 eV [42], and the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of 4-MBA have energies of −8.48 eV and −3.21 eV, respectively [43]. The HOMO and LUMO of PEDOT:PSS are −6.20 eV and −5.50 eV [44], respectively, and the band gap (E g ) is 1.80 eV. Figure 7 shows the CT process in the Ag/4-MBA/PEDOT:PSS composite system. Under 633 nm excitation, the incident light energy is 1.96 eV, the Fermi level of Ag is full of electrons, the electrons are excited to the LUMO level of the 4-MBA molecule, and the electrons will continue to transfer to the LUMO level of PEDOT:PSS because of the potential difference. An electron in the HOMO level of PEDOT:PSS is excited to the LUMO level of PEDOT:PSS and then transferred to the LUMO level of the 4-MBA molecule. When the LUMO level of PEDOT:PSS is full of electrons, the LUMO level of PEDOT:PSS will increase, while the Fermi energy level of Ag will decrease until the Fermi levels of both sides are equal. In this case, the CT velocity in both directions is equal, and the SERS signal is stable [45]. For the Ag/4-MBA system, ρ CT (κ) is 0.395, which means that the EM is still dominant in the Ag/4-MBA system. By introducing PEDOT:PSS, the electron continues to transfer from the LUMO level of 4-MBA to the LUMO level of PEDOT:PSS, and the electron is excited from the HOMO level of PEDOT:PSS to the LUMO level of PEDOT:PSS and the LUMO level of 4-MBA, resulting in an increase in ρ CT (κ) from 0.395 to 0.650, which indicates a new CT process. The CT process has considerable effects on SERS enhancement, thus increasing the SERS intensity. Compared with the Ag/4-MBA system, the Ag/4-MBA/PEDOT:PSS composite system exhibits better SERS activity because PEDOT:PSS increases the contributions of CT. When Ag, 4-MBA and PEDOT:PSS contacted each other, a new CT process occurred at the contact interface, and a new CT state formed. The Fermi energy level of Ag NPs in vacuum is −4.84 eV [42], and the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of 4-MBA have energies of −8.48 eV and −3.21 eV, respectively [43]. The HOMO and LUMO of PEDOT:PSS are −6.20 eV and −5.50 eV [44], respectively, and the band gap (Eg) is 1.80 eV. Figure 7 shows the CT process in the Ag/4-MBA/PEDOT:PSS composite system. Under 633 nm excitation, the incident light energy is 1.96 eV, the Fermi level of Ag is full of electrons, the electrons are excited to the LUMO level of the 4-MBA molecule, and the electrons will continue to transfer to the LUMO level of PEDOT:PSS because of the potential difference. An electron in the HOMO level of PE-DOT:PSS is excited to the LUMO level of PEDOT:PSS and then transferred to the LUMO level of the 4-MBA molecule. When the LUMO level of PEDOT:PSS is full of electrons, the LUMO level of PEDOT:PSS will increase, while the Fermi energy level of Ag will decrease until the Fermi levels of both sides are equal. In this case, the CT velocity in both directions is equal, and the SERS signal is stable [45]. For the Ag/4-MBA system, ρCT(κ) is 0.395, which means that the EM is still dominant in the Ag/4-MBA system. By introducing PEDOT:PSS, the electron continues to transfer from the LUMO level of 4-MBA to the LUMO level of PEDOT:PSS, and the electron is excited from the HOMO level of PEDOT:PSS to the LUMO level of PEDOT:PSS and the LUMO level of 4-MBA, resulting in an increase in ρCT(κ) from 0.395 to 0.650, which indicates a new CT process. The CT process has considerable effects on SERS enhancement, thus increasing the SERS intensity. Compared with the Ag/4-MBA system, the Ag/4-MBA/PEDOT:PSS composite system exhibits better SERS activity because PEDOT:PSS increases the contributions of CT.

Conclusions
Ag/4-MBA/PEDOT:PSS composite systems with different concentrations of PE-DOT:PSS (0, 0.05%, 0.075%, 0.1%, 0.2%, 0.3%, 0.5%, 0.8%, and 1.0%) were successfully constructed by the layer-by-layer assembly method. The hydrogen bonds between the probe molecule 4-MBA and the polymer PEDOT:PSS were studied by SERS. Ag/4-MBA/ PEDOT:PSS composite systems with different concentrations of PEDOT:PSS were studied, and their ρ CT values were calculated. When the PEDOT:PSS concentration was 0.8%, the intensity increase tended to be stable, and ρ CT reached a maximum. Compared with that of the undoped system, the ρ CT value of the doped system increased, which was attributed to the CT process. In terms of the mechanism, the formation of hydrogen bonds promotes charge excitation from the Fermi level of Ag to the LUMO level of the 4-MBA molecule, and the electrons will continue to transfer to the LUMO level of PEDOT:PSS under the action of a potential difference. This distinctly shows that the change in SERS intensity can be attributed to the molecular hydrogen bond formed by PEDOT:PSS and 4-MBA. The addition of organic semiconductors greatly improved the study of SERS and provided new ideas for research on flexible device development, biosensors, trace analysis, food safety, and environmental protection.