Ag Bond Research Articles

Adsorption of Ag, Au, Cu, and Ni on MoS2: theory and experiment

Here, we present results of a computational and experimental study of adsorption of various metals on MoS2. In particular, we analyzed the binding mechanism of four metallic elements (Ag, Au, Cu, Ni) on MoS2. Among these elements, Ni exhibits the strongest binding and lowest mobility on the surface of MoS2. On the other hand, Au and Ag bond very weakly to the surface and have very high mobilities. Our calculations for Cu show that its bonding and surface mobility are between these two groups. Experimentally, Ni films exhibit a composition characterized by randomly oriented nanoscale clusters. This is consistent with the larger cohesive energy of Ni atoms as compared with their binding energy with MoS2, which is expected to result in 3D clusters. In contrast, Au and Ag tend to form atomically flat plateaued structures on MoS2, which is contrary to their larger cohesive energy as compared to their weak binding with MoS2. Cu displays a surface morphology somewhat similar to Ni, featuring larger nanoscale clusters. However, unlike Ni, in many cases Cu exhibits small plateaued surfaces on these clusters. This suggests that Cu likely has two competing mechanisms that cause it to span the behaviors seen in the Ni and Au/Ag film morphologies. These results indicate that calculations of the initial binding conditions could be useful for predicting film morphologies. In addition, out calculations show that the adsorption of adatoms with odd electron number like Ag, Au, and Cu results in 100% spin-polarization and integer magnetic moment of the system. Adsorption of Ni adatoms, with even electron number, does not induce a magnetic transition.

The effect of co-modification of ultrathin g-C3N4 nanosheets with Ag and S on photocatalytic hydrogen production

The technology of photocatalytic water splitting holds immense potential for hydrogen (H2) generation. However, its development is hindered by a lack of active sites and low efficiency of photogenerated carriers. In this study, Ag-S-CN ultrathin nanosheets were successfully fabricated by co-modification of graphitic carbon nitride (CN) with silver (Ag) and sulfur (S). S doping within the CN layers broadened light absorption and provided additional reaction sites, while the incorporation of Ag into the CN interlayers enhanced the migration rate of photogenerated carriers between adjacent layers via Ag-S bonds. Consequently, the 0.05 Ag-S-CN photocatalyst achieved a high H2 yield of 0.93 mmol g-1 h-1 without requiring any additional cocatalyst, which is approximately 23.25 and 10.33 times higher than that of CN and S-CN, respectively. This work presents an effective strategy for developing highly efficient photocatalysts.

Design of silver nanoparticle-embedded nano zirconium-based metal-organic frameworks for highly sensitive detection of chlorpyrifos in real samples.

Chlorpyrifos (CPS) is widely found in food and water sources due to agricultural use, posing health and environmental risks. Therefore, this work introduces a fluorescent sensor design of silver nanoparticle-embedded nano zirconium-based metal-organic frameworks (UiO-66-NH2@AgNPs) for accurate examination of CPS. Briefly, UiO-66-NH2 was synthesized hydrothermally, exhibiting weak luminescence owed to ligand-to-metal charge transfer (LMCT). Here, it limits its direct utility in fluorescence-based detection. To address this limitation, silver nanoparticles (AgNPs) were introduced into UiO-66-NH2, enhancing fluorescence via the metal-enhanced fluorescence (MEF) effect. Briefly, a comprehensive spectral analysis such as XPS, SEM, TEM, PXRD, etc., was performed to validate the synthesis of UiO-66-NH2@AgNPs. Subsequent evaluation revealed that CPS effectively quenched the luminescence intensity of UiO-66-NH2@AgNPs through a static quenching mechanism. The fluorescence intensity exhibited good linearity with CPS concentration in the span of 10 to 1,000 ng/mL, with a recognition limit of 191.5ng/mL(S/N = 3). The interaction involved Ag-S bond formation and electrostatic interactions, reducing fluorescence intensity. The method was confirmed through successful CPS detection in fruit samples. The UiO-66-NH2@AgNPs nanoprobe offers a simple, sensitive, and accurate platform for CPS sensing, with potential for future use in detecting CPS in fruits and vegetables.

Excellent performance of BiOI/AgEuW2O8 S-Scheme heterojunction for photocatalytic degradation of contaminants under visible light: Experimental and computational studies

A series of xBiOI/AgEuW2O8 (BIAEW-x, x = 1, 2, 3) photocatalysts were prepared by hydrothermal method, further applied for photocatalytic degradation of organic contaminants under the visible light irradiation. The microstructure and photocatalytic properties of the as-synthesized samples were determined by various techniques such as XRD, SEM, TG-DTG, XPS, UV–Vis, ESR, and N2-adsorption. Heterojunction was formed within transition area between BiOI and AgEuW2O8, and the special structure was further validated by the results of XRD and XPS. It was found the composite with 2:1 ratio of BiOI/AgEuW2O8 possessed the highest activity of 99.48 % rhodamine B (RhB) photodegradation which was observed under the optimized conditions (3 h, pH = 5, 60 mg, 30 mg/L). This may be due to the maximum existence of BiOI/AgEuW2O8 heterojunction within the solid, which promotes the generation of the active species during the photocatalytic process. Besides, the newly-formed O–Ag bonds bridging the interface between BiOI (1 0 2) and AgEuW2O8 (0 0 4) were also confirmed according to the DFT calculations, and the electrons and holes increased largely for the interface structure. Moreover, the photodegradation process of RhB promoted by xBiOI/AgEuW2O8 follows first-order kinetic law. Furthermore, the trapping experiments were respectively conducted via addition of different trapping reagents, of which the holes were confirmed as the key active species on photodegradation of RhB over BIAEW-2 under visible light irradiation.

A Three-Dimensional AgNPs/TiO2/Ti3C2Tx Composite for Label-Free Thrombin Aptamer Sensor

A one-step hydrothermal method was employed to synthesize a three-dimensional (3D) AgNPs/TiO2/Ti3C2Tx composite. Hydrothermal conditions were used to promote the growth of TiO2 nanorods on the Ti3C2Tx sheet, resulting in the formation of a three-dimensional composite nanomaterial. Glutamic acid served as both a reducing agent and a stabilizer to load Ag nanoparticles (AgNPs) onto the 3D composite nanomaterial. The structure of the composite material provided a large accessible surface area, facilitating the anchoring of Ag NPs. Thrombin aptamers were then linked to Ag NPs through Ag-S bonds, establishing a sensitive and label-free aptasensor for thrombin detection. The proposed aptasensor demonstrated excellent electrochemical performance, with a broad linearity range of 5.0 fM to 500 nM and a relatively low detection limit of 2.0 fM (S/N = 3). These findings indicate the potential of Ag NPs/TiO2/Ti3C2Tx in the development of promising electrochemical biosensors.

Relativistic effect influencing the diverse bonding character of the interfacial Ag staple motifs in thiolate-protected nanoclusters.

Thiolate-protected noble-metal nanoclusters have recently attracted extensive attention due to their appealing properties in optics, catalysis, etc. Within the same group element, experiments indicate that Ag staples exhibit di-, tri-, or even tetra-coordination, in contrast to the di-coordination observed in Au staples, rendering the structures of Ag nanoclusters more intricate. However, the underlying chemical insight of the bonding feature of multiple-coordinated Ag staples remains unclear. In this study, we employed density functional theory coupled with all-electron scalar relativistic calculations to elucidate the critical role of relativistic effect in determining the conformational complexity of Ag staples. Unlike Au, the relatively weaker relativistic effect induces fewer contributions of d orbitals in bonding for the Ag atom, showing an extreme sensitivity to the structural architecture in liganded clusters. A relatively higher d orbital percentage favors di-coordination with a shortened Ag-S bond, while a relatively lower d orbital percentage favors tri- and tetra-coordinations with an elongated Ag-S bond. The Lewis structures of the multi-coordinated Ag motifs were also unveiled. In addition, two AgNCs, including the [Ag29(SCH3)18]3- cluster with tri-coordinated Ag motifs and [Ag29(SCH3)18(PCH3)6]3- with tetra-coordinated Ag motifs, were predicted after clarifying the bonding characters of the multiple-coordinated Ag motifs. This work not only deepens the understanding of the bonding characteristics of the Ag staple motif in AgNCs and AuAg alloy clusters but also provides a new perspective to understand the relativistic effect in the thiolate-protected noble-metal nanocluster.

Silver Bonding Wire - an Alternative for Mechanical Sensitive Chip Configurations in Automotive Electronics Packaging

Silver (Ag) bond wires are mainly used in consumer products as a reliable low-cost alternative to gold (Au) bond wires. In previous investigations, we have shown that silver wires also have potential for use in the automotive sector (1, 2, 3, 4], where the materials are exposed to particularly harsh environmental conditions. In order to understand thc intluence of these conditions in the electronic package on the silver-aluminum material system, we carried out extensive studies on test packages built on laboratory level. For the future development of challenging automotive devices, it will be important to have a cooperation between semiconductor package developer and material supplier with an assist of characterization spccialists. In this project, we formed a threeparty project in which characterization specialists, package developer, and wire manufacturer collectivcly conduct a feasibility study of a new Ag wire material for automotive application. Two wire types (standard Ag wire and new type of Ag wire GX2s) were chosen for the investigation in direct comparison regarding long-term reliability. Samples were built under mass production conditions and then subjected to various reliability tests following AEC-Q006 requirements. Subsequently, mechanical characterizations by means of ball shear and pull tests as weil as high resolution SEM microstructure analyses on cross-section samples are applied. In the paper, results of the different tests will be summarized, but a more in-depth analysis will be given to the temperature cycle test (TCT), where the most significant differences between the sample variations occurred. Overall, the results show the importance of the knowledge for the material reliability upfront a device qualification process (robustness validation) and give further guidance for material selection.

Metal Nanoparticles Assisted Ultrafast Laser Plasmonic Microwelding of Oxide-Semiconductor Interconnects.

Integration of wafer-scale oxide and semiconductor materials meets the difficulties of residual stress and materials incompatibility. In this work, Ag NPs thin film is contributed as an energy confinement layer between oxide (Sapphire) and semiconductor (Si) wafers to localize the materials interaction during ultrafast laser irradiation. Due to the plasmonic effects generated within constructed dielectric-metal-dielectric structures (i.e., Sapphire-Ag-Si), thermal diffusion and chemical reaction between Ag and its neighboring materials facilitate the microwelding of Sapphire and Si wafers. Ag NPs can be totally sintered within the junction area to bridge oxide and semiconductor, while Al─O─Ag bond and Ag─Si bond are formed at Ag-Sapphire and Ag─Si interfaces, respectively. As-received heterogeneous joint exhibits a high shear strength up to 5.4MPa, with the fracture occurring inside Si wafer. Meanwhile, insertion of metal nanolayer can greatly relieve the residual stress-induced microcracking inside the brittle materials. Such wafer-scale Sapphire and Si interconnects thus show robust strength and excellent impermeability even after thermal shocking (-40 °C to 120 °C) for 200 cycles. This metal NPs layer-assisted plasmonic microwelding technology can extend to broad materials integration, which is promising for high-performance microdevices development in MEMS, MOEMS, or microfluidics.

Ultralow thermal conductivity and thermally-deactivated electrical transport in a 1D silver array with alternating δ-bonds.

We report the synthesis of a (TMA)AgBr2 (TMA = tetramethylammonium) crystal, which comprises inorganic anionic chains of -(AgBr2)∝- stabilized by columnar stacks of organic TMA cations with a periodic arrangement of shorter and longer Ag(i)⋯Ag(i) bonds, even though all the Ag(i) ions are chemically equivalent. The presence of two chemically non-equivalent bridging Br ions is attributed to the primary cause of such an unusual arrangement, as clearly visualized in the charge density plot of (TMA)AgBr2 extracted from the theoretical calculations based on density functional theory. Remarkably, we identified from the orbital-projected density of states the existence of alternate δ-like bonding involving d xy orbitals of 4d10 Ag(i), which was attributed to the cause for ultralow thermal conductivity and thermally-deactivated electrical transport in (TMA)AgBr2. Barring the energetics, our observations on the existence of a δ-bond will shed new light in understanding the nature of metal-metal chemical bonding and its unprecedented implications.

On‐Surface Ullmann‐Type Coupling: Reaction Intermediates and Organometallic Polymer Growth

AbstractUllmann‐type coupling is the most widely used on‐surface reaction to form rationally designed bottom‐up molecular nanoarchitectures. A commonly observed reaction product in this reaction is an organometallic phase, however little is known about the formation of this phase. The on‐surface polymerization of the prochiral precursor 6,12‐dibromochrysene (DBCh) on Ag(111) is studied. Upon annealing of DBCh on Ag(111), a linear organometallic polymer forms. However, the delicate energy balance involved in the polymerization of DBCh is such that, at room temperature, several reaction intermediates, which eventually lead to the formation of the organometallic polymer, can be observed experimentally. Organometallic monomers, dimers, and trimers are finds, that self‐assemble into distinct networks. The experimental availability of these reaction intermediates provides key insights into the formation of the organometallic polymer. Comparing the chirality of the intermediates and the polymer sheds additional light on the reaction mechanism leading to the formation of the polymer. The main finding is that the organometallic polymer is not formed by a simple coupling of the reaction intermediates, but rather requires the breaking and re‐establishing of the C─Ag bonds. Additionally, a Br‐enhanced growth mode is observed, where the split‐off halogens align the polymers, which results in an increased polymer length.

A novel core-shell heterostructure of zinc oxide/metal-organic frameworks anchored silver nanoparticles for enhanced SERS and photocatalytic performance

Here, a novel well-ordered ZnO rod-flower/zeolitic imidazolate framework-M (ZIF-M, using 5-mercapto-1-methyltetrazole as ligand) core-shell heterostructure (Al/ZnO/ZIF-M, AZZ*) is induced by aluminum (Al) sheet. Subsequently, Ag nanoparticles (AgNPs) are tightly attached to the ZIF-M layer in AZZ* through the strong Ag-N and Ag-S bonds, and a portable bifunctional substrate of Al/ZnO/ZIF-M/Ag (AZZ*Ag) is constructed. The finite difference time domain (FDTD) analysis shows that the AZZ*Ag substrate generates the stronger electromagnetic field intensity than the AZAg. Also, there is a strong synergistic effect among Al, ZnO, ZIF-M and Ag which can effectively facilitate the electron transfer. Importantly, the AZZ*Ag substrate exhibits outstanding SERS response with high sensitivity and selectivity for crystal violet (CV) molecules. The low detection limit (LOD) of CV molecule is 2.81 × 10−11 mol·L−1 with high analysis enhancement factor (AEF) of 1.93 × 106. In addition, AZZ*Ag substrate shows good photocatalytic performance for CV molecules with high degradation efficiency of 97.35% within 105 min, which is 4.72 times that of AZAg. Importantly, the SERS and photocatalytic performance of AZZ*Ag are 4.4 times and 3.09 times those of the Al/ZnO/ZIF-8/Ag (AZZ#Ag, using 2-methylimidazole as ligand), respectively. Moreover, the AZZ*Ag substrate displays excellent stability, good reproducibility, recyclability and uniformity. Thus, the designed portable bifunctional composite exhibits great potential for SERS detection and photocatalytic degradation of other pollutants in environmental wastewater.

Insight into Scattering Mechanisms and Transport Properties of AgCuS for Flexible Thermoelectric Applications.

The development of flexible thermoelectric devices requires materials possessing ductility and high thermoelectric performance at room temperature. However, only a few existing materials meet both criteria. In this study, the ductile properties, electronic structure, and transport properties of the low-temperature phase α-AgCuS were elucidated using first-principles calculations combined with Boltzmann transport theory. With a layered zigzag structure similar to the well-known ductile semiconductor Ag2S, AgCuS is determined to have good metal-like ductility. Through consideration of various intrinsic scattering mechanisms, we found that electron-polar optical phonon interactions have the most significant impact on the transport behavior of AgCuS. The predominance of this type of interaction is also disclosed by the covalent-ionic bonding nature of the Ag-S and Cu-S bonds. Therefore, weakening this interaction via doping or alloying could optimize the thermoelectric performance of the system. At room temperature, a maximum dimensionless figure of merit ZT of up to 0.592 could be achieved under a tuning of hole concentration to 2 × 1019 cm-3, suggesting that α-AgCuS could be a promising p-type candidate for flexible thermoelectric applications.

An environmentally friendly bifunctional composite mediated by metal organic frameworks for dramatically enhanced SERS and photocatalytic performances

The portable materials with excellent bi-functionality used in monitoring and photocatalytic degradation of organic contaminants are significant in light energy utilization and sustainability. Herein, a plug and play and cost-efficient Ti-TiO2-ZIF-8-Ag (ET-Z8-Ag) composite was facilely fabricated. It showed that the etched titanium sheet was conducive to the growths of the zeolitic imidazolate framework-8 (ZIF-8) and Ag with good dispersion. Furthermore, the SERS and photocatalytic performances of the ET-Z8-Ag were studied with p-aminothiophenol (p-ATP, a harmful pesticide intermediate) as the analyte. It showed that more p-ATP molecules can be adsorbed as a result of the π-π interaction and Ag-S bond between p-ATP and the ET-Z8-Ag. Moreover, the large and special heterogeneous interface in the ET-Z8-Ag was advantageous to promoting charge transfer, and thus SERS response and photocatalytic degradation of p-ATP were improved. Compared with some materials reported, the ET-Z8-Ag with a smaller amount of Ag showed higher sensitivity and faster degradation rate towards p-ATP. Especially, almost 100% p-ATP in river water can be rapidly removed within 5 min with the help of the ET-Z8-Ag, and its efficiency was still remained after six cycles. The cost-efficient and portable composite will be potential in the detection and removal of organic pollutants in wastewater.

First-principles calculation of electronic structure, chemical bonding and optical properties of β-AgBiS2

We investigated the structural, electronic, chemical bonding, and optical properties of β-AgBiS2 crystal by using the Perdew-Burke-Ernzerhof (PBE) functional and the hybrid functional Heyd Scuseria Ernzerhof (HSE) within the DFT formalism. The electronic band structures obtained by both methods indicate that β-AgBiS2 is an indirect band gap semiconductor with band gap of 0.571 and 1.025 eV, respectively. The electron density difference and Mulliken overlap population show that the Ag-S bonds and Bi-S bonds are both ionic bonds. The calculated optical absorption spectrum prove that β-AgBiS2 is a promising material for solar photovoltaic conversion

Study on Synthesis of Silver Nanoparticles Using dsDNA as Template and Detection of GSH

AbstractIn this work, silver nanoparticles are synthesized using a simple and sensitive method by using double‐stranded DNA (dsDNA‐Ag NPs) as a template. The prepared dsDNA‐Ag NPs are characterized by fluorescence spectroscopy analysis, X‐ray photoelectron spectroscopy analysis, and transmission electron microscopy analysis. The excitation wavelength of the prepared silver nanoparticles is 295 nm, the emission wavelength is 377 nm, the average particle size is 11.2 nm, and the dispersion is uniform with pleasurable stability. The nanomaterials are used as fluorescent probes to detect glutathione (GSH). After adding glutathione to the dsDNA‐Ag NPs fluorescent probes, the fluorescence of dsDNA‐Ag NPs is burst due to electron transfer and SAg bond generation, and the linear range of detection concentration is 0–90 mm with a detection limit of 0.37 mm.

Etching triangular silver nanoparticles to initiate the fluorescent response of Ru@SiO2 for sensitive detection of glutathione

Fluorescent probes usually face the issue of photobleaching and premature leakage when they are directly exposed to exterior environment, causing poor photostability and low sensitivity. In this paper, Ru(bpy)32+ encapsulated fluorescent SiO2 nanoparticles (Ru@SiO2 NPs) were synthesized and used as fluorescent probe. The SiO2 nanoparticles were used as carriers to prevent the leakage of the probe. Triangular Ag nanoparticles (T-Ag NPs) were prepared as quenchers to construct a quenching system (Ru@SiO2-T-Ag NPs) with Ru@SiO2 NPs through inner filter effect (IFE). In this quenching system, T-Ag NPs were also designed as recognize units for glutathione (GSH) detection. When GSH existed, the GSH bond with T-Ag NPs to form Ag-S bonds, making the T-Ag NPs etched. In this case, the fluorescent signal of Ru@SiO2 NPs quenched by T-Ag NPs restored. The fluorescence recovery of the Ru@SiO2 NPs depended on GSH concentrations and thus it could realize the quantitative analysis of GSH. Under optimized conditions, the proposed assay had good analytical performance for the detection of GSH in the concentration range of 0.01–1 µM with a limit of detection (LOD) as low as 2.8 nM. This assay was also used to measure GSH levels in human serum samples. This work provides a new way for the fluorescent analysis of thiol biomolecules.

Highly Sensitive Fluorescence Detection of Three Organophosphorus Pesticides Based on Highly Bright DNA-Templated Silver Nanoclusters

It is still challenging to achieve simultaneous and sensitive detection of multiple organophosphorus pesticides (OPs). Herein, we optimized the ssDNA templates for the synthesis of silver nanoclusters (Ag NCs). For the first time, we found that the fluorescence intensity of T base-extended DNA-templated Ag NCs was over three times higher than the original C-riched DNA-templated Ag NCs. Moreover, a "turn-off" fluorescence sensor based on the brightest DNA-Ag NCs was constructed for the sensitive detection of dimethoate, ethion and phorate. Under strong alkaline conditions, the P-S bonds in three pesticides were broken, and the corresponding hydrolysates were obtained. The sulfhydryl groups in the hydrolyzed products formed Ag-S bonds with the silver atoms on the surface of Ag NCs, which resulted in the aggregation of Ag NCs, following the fluorescence quenching. The fluorescence sensor showed that the linear ranges were 0.1-4 ng/mL for dimethoate with a limit of detection (LOD) of 0.05 ng/mL, 0.3-2 µg/mL for ethion with a LOD of 30 ng/mL, and 0.03-0.25 µg/mL for phorate with a LOD of 3 ng/mL. Moreover, the developed method was successfully applied to the detection of dimethoate, ethion and phorate in lake water samples, indicating a potential application in OP detection.

Influence of the Steric/Electronic Properties of N-Aryl Substituents in Cycloplatinated Guanidinate(1−) Complexes on the Formation of Discrete Pt → Ag Complexes and One-Dimensional Coordination Polymer

The reactions of cycloplatinated guanidinate(1-) complexes 1-6 with AgTFA (TFA = OC(O)CF3) in 1:1 and 1:2 PtII/AgI molar ratios afforded complexes containing three types of Pt2Ag2 skeletons (7-10, 11, and 13), one 1D CP containing Pt2Ag3 skeleton (16), and a Pt2Ag4 complex (17) in 91-95% (method 1), 73-82% (method 2) (7-10), and 54-79% (11, 13, 16, and 17) yields. The reactions of 11 with 2,6-XylNC (2,6-Xyl = 2,6-Me2C6H3) and 4-DMAP (4-dimethylaminopyridine) gave a neutral complex 18 and an ionic complex 19, respectively. Molecular structures of 12 complexes were unambiguously determined by single-crystal X-ray diffraction. Ten complexes contain unprecedented PtAg skeletons and are shown to contain multiple number of dative Pt → Ag bonds supported by the TFA ligand, platinated carbon of the TAG ligand, or both these ligands in conjunction with the Ag-Ag contacts stabilized by argentophilic interaction. Further, the new complexes were characterized by analytical, IR, and multinuclear NMR (19F, 1H, 13C{1H}, and 195Pt) spectroscopies, powder X-ray diffraction, and TGA/DTA. In solution, 9 and 19 exist in more than one form as identified by multinuclear NMR, and this behavior is ascribed to the restricted (N2)C-N(H)Ar single-bond rotation of the TAG ligand. The photophysical properties of 9 and 11 are reported.

Insulated, Passivated & Adhesively-Promoted Bond Wire Using All-in-One Al2O3 Coating

Insulated, Passivated & Adhesively-Promoted Bond Wire Using All-in-One Al2O3 Coating

Effect of Water on the Rearrangement of Hydrogen-Bonded Structures of 4-Aminobenzoic Acid on Au(111) and Ag(111) Surfaces

Water plays a very important role in promoting the biological self-assembly process, while our understanding is limited about how water affects and reshapes the assembly structure. Herein, the water-induced assembly structures of 4-aminobenzoic acid (PABA) on Au(111) and Ag(111) are investigated by scanning tunneling microscopy and density functional theory calculations. Water molecules could break the weak-hydrogen-bonded Kagomé structure on Au(111) and the consequent four-leaf clover structure formed by intermediate hydrogen bonds between the functional groups of PABA molecules and spontaneous release of water molecules. Upon water exposure, the four-leaf clover structure remains intact on the Au(111) surface, while the water molecules can break selectively the weak hydrogen bonds connecting the four-leaf clovers on Ag(111) and form preferential hydrogen bonds with the functional groups of PABA molecules, resulting in the generation of the water-involved structure. The adsorption energy of this hydrated structure on Ag(111) is significantly lower than that on Au(111), which may be the reason that the water-involved structure only appears on Ag(111). The result provides the real-space evidence of the interaction between water and organofunctional groups related to the type of the metal surface.