Interfacial Separation Research Articles

Kinetics of electromigration mass transfer in micro- and nanoelectronics interface elements depending on the strength of thin-film junctions

The theoretical model proposed earlier by the authors, which describes the interrelation of strength and electromigration (diffusion) properties of interfaces formed by joined materials, has been perfected and extended. Within the framework of the developed model, a linear relationship between the values of the work of reversible interface separation Wa and the activation energy of electromigration in the interface HEM was established. The coefficients of the obtained relation are estimated and compared with experimental data on the study of electromigration in a copper conductors covered with protective dielectrics. Using also the model developed earlier by the authors, which describes the dependence of the value on the concentrations of non-equilibrium lattice defects in the volumes of joined materials, a number of effects due to the influence of such defects on the processes caused by electromigration have been predicted and investigated. In the paper we obtained that by introducing non-equilibrium lattice defects in the volumes of bonded materials in the form of atomic impurities of interstition or substitution it is possible to effectively influence the characteristics of electromigration instability of the shape of the interlayer interface. For the introduction impurities, quantitative analytical estimates of the impurity concentration necessary for a significant change (both increase and decrease) in the characteristic rise time of the instability of the shape of the initially flat interface have been obtained.

Copper porphyrin modified BiOBr/Bi19S27Br3 for efficient CO2 photoreduction

The insufficient solar light response ability of the photocatalyst, rapid recombination of interface charges, and lack of active sites significantly inhibit the efficiency of photocatalytic CO2 reduction. Addressing these challenges simultaneously is a very challenging task. Herein, an interface engineering coupled surface polarization strategy is proposed to optimize the CO2 photoreduction performance. The copper tetracarboxyphenylporphyrin (CuTCPP) modified BiOBr/Bi19S27Br3 (BBS) heterostructure was developed. The built-in electric field formed between BiOBr and Bi19S27Br3 interfaces induces the effective interfacial charge separation, while the surface polarization of CuTCPP induces the transfer of electrons from the conduction band (CB) of BBS to the CB of CuTCPP. Benefiting from this unique configuration and abundant active sites in CuTCPP, greatly improved photocatalytic CO2 reduction performance can be realized. Without adding cocatalysts and sacrificial agents, the optimized CO generation performance of CuTCPP-BiOBr/Bi19S27Br3 (BBS-CT) is 3.5 times higher than that of BBS. This work provides valuable insights of interface engineering coupled surface polarization strategy for collaborative improve the photocatalytic CO2 reduction performance.

Precise modulation of the debonding behaviours of ultra-thin wafers by laser-induced hot stamping effect and thermoelastic stress wave for advanced packaging of chips

Abstract Laser debonding technology has been widely used in advanced chip packaging, such as fan-out integration, 2.5D/3D ICs and MEMS devices. Typically, laser debonding of bonded pairs (R/R separation) is typically achieved by completely removing the material from the ablation region within the release material layer at high energy densities. However, this R/R separation method often results in a significant amount of release material and carbonized debris remaining on the surface of the device wafer, severely reducing product yields and cleaning efficiency for ultra-thin device wafers. Here, we propose an interfacial separation strategy based on laser-induced hot stamping effect and thermoelastic stress wave, which enables stress-free separation of wafer bonding pairs at the interface of the release layer and the adhesive layer (R/A separation). By comprehensively analyzing the micro-morphology and material composition of the release material, we elucidate the laser debonding behavior of bonded pairs under different separation modes. Additionally, we have calculated the ablation threshold of the release material in the case of wafer bonding and established the processing window for different separation methods. This work offers a fresh perspective on the development and application of laser debonding technology. The proposed R/A interface separation method is versatile, controllable and highly reliable, and does not leave release materials and carbonized debris on device wafers, demonstrating strong industrial adaptability, which greatly facilitates the application and development of advanced packaging for ultra-thin chips.

Lattice Match-Enabled Covalent Heterointerfaces with Built-in Electric Field for Efficient Hydrogen Peroxide Photosynthesis.

Crafting semiconducting heterojunctions represents an effective route to enhance photocatalysis by improving interfacial charge separation and transport. However, lattice mismatch (δ) between different semiconductors can significantly hinder charge dynamics. Here, meticulous lattice tailoring is reported to create a covalent heterointerface with a built-in electric field (BIEF), imparting markedly improved hydrogen peroxide (H2O2) photosynthesis. Specifically, an In2S3/CdS heterojunction with a coherent heterointerface, characterized by covalent In─S─Cd bridge and exceptionally low lattice mismatch of 0.27%, and a BIEF from In2S3 to CdS, is rationally designed. This heterojunction entails rapid charge separation and transfer, achieving an outstanding H2O2 production rate of 2.09 mmol g-1 h-1 without the need for scavengers and oxygen bubbling, and a high apparent quantum efficiency of 17.73% at 400 nm. Density functional theory (DFT) calculations further reveal that this Z-scheme heterojunction facilitates the adsorption of *O2 and the generation of *OOH intermediates during the 2e- oxygen reduction reaction, associated with a low Gibbs free energy. This study underscores the significance of fine-tuning interfacial lattices and integrating BIEF to accelerate photocatalysis. The simple yet robust strategy can be conveniently leveraged to enhance device performance in optoelectronics, electrocatalysis, photoelectrocatalysis, and sensing.

Vacuum laser zone refining of titanium towards lunar metallurgy: Experimental and numerical study

The development of in-situ utilisation technologies for lunar resources is crucial for future human deep-space exploration. This paper presents a novel vacuum laser zone refining technique aimed at in-situ separation of titanium and iron. The experimental and numerical simulation results indicate that increasing laser power while reducing the melting speed significantly increases the temperature gradient of the melt pool, thereby enhancing molten flow velocity. These factors effectively redistribute the elements at the solid-liquid interface, improving Fe and Ti separation efficiency. Additionally, increasing the number of refining passes can also significantly improve the separation efficiency of Fe and Ti. Under the conditions of 1000 W laser power, 0.05 mm/s melting speed, and 5 refining passes, the separation efficiency of Fe reached 76.5 %. Notably, the maximum molten flow velocity reached 0.157 m/s, which ensured a uniform distribution of Fe in the melting zone. Hence, the proposed vacuum laser zone refining technique is a promising approach for efficient separation of titanium and iron from titanium–iron alloys, providing potential support for deep-space exploration efforts.

Heterojunction Organic Solar Cells with Efficient Charge Mobility and Separation Capabilities Studied by DFT.

The properties of the active layer materials play a decisive role in determining the power conversion efficiency of organic solar cells (OSCs). Chlorophyll and its derivatives are abundant and environmentally friendly functional organic molecular materials. Using density functional theory (DFT) and time-dependent density functional theory (TD-DFT), we have calculated the absorption spectra and their excited state properties based on optimized ground state structures. It was found that bacteriochlorin exhibits superior structural properties, a smaller energy gap and hole reorganization energy, redshifted absorption spectra, and higher hole mobility compared to the donor D18. This suggests that bacteriochlorin exhibits superior donor properties. Comparative studies between o-AT-2Cl and m-AT-2Cl showed that o-AT-2Cl had superior acceptor properties, implying that differences in substitution positions can influence the physicochemical properties of non-fullerene acceptors (NFAs). Subsequently, six bulk heterojunctions (BHJs) were constructed by combining three donors with nonfused ring electron acceptors, o-AT-2Cl and m-AT-2Cl. The bacteriochlorin-based BHJs performed well among them, with BChl3/o-AT-2Cl and BChl4/o-AT-2Cl having the largest interfacial charge separation rate. The results suggested that BHJs composed of bacteriochlorin and NFAs can improve OSCs' photovoltaic performance, providing a feasible scheme for designing efficient OSCs.

Interface Synergy of Exposed Oxygen Vacancy and Pd Lewis Acid Sites Enabling Superior Cooperative Photoredox Synthesis.

Photo-driven cross-coupling of o-arylenediamines and alcohols has emerged as an alternative for the synthesis of bio-active benzimidazoles. However, tackling the key problem related to efficient adsorption and activation of both coupling partners over photocatalysts towards activity enhancement remains a challenge. Here, we demonstrate an efficient interface synergy strategy by coupling exposed oxygen vacancies (VO) and Pd Lewis acid sites for benzimidazole and hydrogen (H2) coproduction over Pd-loaded TiO2 nanospheres with the highest photoredox activity compared to previous works so far. The results show that the introduction of VO optimizes the energy band structure and supplies coordinatively unsaturated sites for adsorbing and activating ethanol molecules, affording acetaldehyde active intermediates. Pd acts as a Lewis acid site, enhancing the adsorption of alkaline amine molecules via Lewis acid-base pair interactions and driving the condensation process. Furthermore, VO and Pd synergistically promote interfacial charge transfer and separation. This work offers new insightful guidance for the rational design of semiconductor-based photocatalysts with interface synergy at the molecular level towards the high-performance coproduction of renewable fuels and value-added feedstocks.

Modulating stacking mode and molecular polarization in CTF/molecule heterojunction for meliorating photocatalytic CO2 conversion with nearly 100% CO selectivity

Herein, two conjugated molecules, i.e., D-π-A TAPT and non-D-A TAPB, are finely designed to incorporate with covalent triazine framework (CTF) in A-A and A-B stacking mode via π-π interaction, respectively. The transient photocurrent response of the generated AA-CTF/TAPT Z-Scheme heterostructure is 1.14 × 10-7 A, significantly higher than that of the other two metal-free heterostructures (AA-CTF/TAPB and AB-CTF/TAPT). The promoted photocarrier transportation is attributed to strong polarization (dipole moment = 2.634 D) imposed by the D-π-A effect in TAPT that motivates the interfacial charge separation, and the coexisting charge transfer channel built by the ordered A-A stacking mode in AA-CTF that expedites the charge delivery. The photocatalytic CO2 conversion conducted by AA-CTF/TAPT gives the optimal CO conversion rate as 7.47 μmol·g−1·h−1, and with nearly 100 % product selectivity obtained, which is attributable to the lower energy barrier of CO desorption barrier (−1.07 eV) rather than that of CHO* formation (1.52 eV) for generating CH4.

Needle growth of Nb2O5 nanoparticles on BiOCl nanosheets to fabricate S-scheme heterojunction with oxygen vacancies for enhanced photooxidation of cyclohexane

The exploration of cost-efficient, environmentally friendly, and high-efficacy photocatalysts for the enhanced selective photooxidation of cyclohexane to KA oil (cyclohexanone (CHA-one) and cyclohexanol (CHA-ol)) is a pivotal challenge in the industrial realm. Herein, the present study focuses on the synthesis of needle-like S-scheme heterojunction photocatalysts with oxygen vacancies, which are achieved by the needle growth integration of nano-sized Nb2O5 particles onto the BiOCl nanosheets. Remarkably, the 40 % Nb2O5/BiOCl composites exhibited superior performance in the solvent-free photooxidation of cyclohexane at room-temperature and under atmospheric pressure. The production yield of KA oil was 180.3 μmol (CHA-one/CHA-ol molar ratio = 3.5), and exceptional selectivity towards KA oil, reaching up to 99.3 %. The enhanced photocatalytic efficiency in cyclohexane oxidation can be attributed to the unique S-scheme heterogeneous interfaces with specific nanoneedle morphology, which result in the enhanced photonic absorption, effective charge carrier separation, a high density of oxygen vacancies, and the exposure of the highly reactive (001) plane of BiOCl. The excellent interfacial charge separation and transfer pathways of S-scheme heterojunction are disclosed by the in-depth EPR analysis and DFT calculations. These insights highlight the significant potential of the needle-like Bi-based S-scheme heterojunction photocatalysts for the efficient photooxidation of saturated alkanes.

Indium oxide layer dual functional modified bismuth vanadate photoanode promotes photoelectrochemical oxidation of water to hydrogen peroxide.

The photoelectrochemical (PEC) dual-electron pathway for water oxidation to produce hydrogen peroxide (H2O2) shows promising prospects. However, the dominance of the four-electron pathway leading to O2 evolution competes with this reaction, severely limiting the efficiency of H2O2 production. Here, we report a In2O3 passivator-coated BiVO4 (BVO) photoanode, which effectively enhances the selectivity and yield of H2O2 production via PEC water oxidation. Based on XPS spectra and DFT calculations, a heterojunction is formed between In2O3 and BVO, promoting the effective separation of interface and surface charges. More importantly, Mott-Schottky analysis and open-circuit potential measurements demonstrate that the In2O3 passivation layer on the BVO photoanode shifts the hole quasi-Fermi level towards the anodic direction, enhancing the oxidation level of holes. Additionally, the widening of the depletion layer and the flattening of the band bending on the In2O3-coated BVO photoanode favor the generation of H2O2 while suppressing the competitive O2 evolution reaction. In addition, the coating of In2O3 can also inhibit the decomposition of H2O2 and improve the stability of the photoanode. This work provides new perspectives on regulating PEC two/four-electron transfer for selective H2O2 production via water oxidation.

Bending of a piecewise homogeneous plate with a circular interfacial materials separation zone and radial crack considering the strip contact of its edges

Bending of a piecewise homogeneous plate with a circular interfacial materials separation zone and radial crack considering the strip contact of its edges

Dynamics of phase separation of metastable crystal surfaces by surface diffusion: A phase-field study.

A new phase-field approach is designed to model surface diffusion of crystals with strongly anisotropic surface energy. The model can be shown to asymptotically converge toward the sharp-interface equationfor surface diffusion in the limit of vanishing interface width. It is employed to investigate the dynamical evolution of a thermodynamically metastable crystal surface. We find that nucleation and growth by surface diffusion of the newly formed surface induce the formation of additional stable surfaces at its wake. This induced nucleation mechanism is found to produce domains composed of several stable surfaces of prescribed width. The domains propagate on the crystal surface and then coalesce to form a hill-and-valley structure. The resulting morphology is more regular than the typical hill-and-valley surface produced by random thermal nucleation, i.e., when motion-by-curvature controls the phase separation dynamics. Moreover, the induced nucleation mechanism is found to be peculiar to surface diffusion and to dominate the phase separation at high degree of metastability. Once the hill-and-valley structure is formed, coarsening operates by motion and elimination of facet junctions, points where two facets merge to form one and we find the following scaling law L∼t^{1/6}, for the growth in time t of the characteristic length scale L during this coarsening stage. The density of junctions is found to exhibit a t^{-2/3} regime. Our results elucidate the role of the induced nucleation mechanism on the dynamics of interfacial phase separation and corroborate surface faceting experiments on ceramics.

Connections between precast hollow concrete columns and foundations using UHPC and rebar lap splices

Hollow concrete columns (HCC) have been widely used in accelerated bridge construction worldwide. The column-foundation connections are vital in such precast systems to ensure seismic resilience. In this paper, a novel HCC-foundation connection using UHPC and rebar lap splices was proposed, which could facilitate the construction process. Cyclic tests were carried out on four specimens to examine their seismic performance. Test results showed that the proposed connections exhibited satisfying capacities, ductility, and energy dissipation comparable to monolithic connections under lateral cyclic loads. The use of a precast UHPC shell did not deteriorate the performance of the connection with no interface separation observed. The decrease in joint height would, however, bring about anchor rebar slippage and reduce energy dissipation. A validated fiber element model of the specimens was established for efficient seismic modeling of precast systems with the proposed connection in actual projects. Force transfer mechanisms and design methods for the connections were further deduced. The proposed connection has been verified to be comparable to cast-in-place connections and is thus suitable for use in precast column-foundation connections. Several design recommendations were derived for engineering reference.

Constructing type II heterojunction of 2D/1D Pg-C3N4/Ag3VO4 nanocomposite with high interfacial charge separation for boosting photocatalytic CO2 reduction under solar energy

The well-designed, template-free synthesis of 2D protonated g-C3N4 nanosheets (Pg-C3N4) coupled with novel 1D Ag3VO4 nanorods has been investigated to construct 2D/1D interface heterostructures with strong electrostatic interactions between the positively charged 2D Pg-C3N4 nanosheets and the negatively charged 1D Ag3VO4 nanorods. The coupling of Pg-C3N4 and Ag3VO4 with desirable characteristics resulted in a 2D/1D interface heterojunction with a type II charge carrier transfer mechanism, effectively maintaining and utilizing charge carriers. The 2D/1D Pg-C3N4/Ag3VO4 exhibited remarkable photocatalytic performance for CO2 conversion with H2O, resulting in maximum CH4 and dimethyl ether (DME) production of 352.3 and 130.9 µmol/g-cat, respectively. A quantum yield of 0.23 % for CH4 generation was achieved over the 2D/1D Pg-C3N4/Ag3VO4, which was 2.9 and 1.4 times higher than that of the Pg-C3N4 and Ag3VO4 samples, respectively. The improvement in photocatalytic performance primarily stems from the effective interaction between Pg-C3N4 and ternary Ag3VO4, leading to enhanced transfer and separation of photoinduced charge carriers through the creation of a type II heterojunction. The findings of this study are useful in designing template-free heterojunctions for photocatalytic CO2 conversion and other solar energy applications.

Electrochemical-mechanical coupled interfacial degradation model of Ternary polymer composite cathodes in all-solid-state batteries

Despite significant attention focused on the composite cathode composed of active particles, which is considered to increase the interfacial areas and satisfy high areal load, suffers from interfacial issues. In this article, we formulate an electrochemical-mechanical model of LiNixMnyCozO2 (NMC) composite cathode coupling the relations between interfacial degradation, charge transformation, diffusion transport, and mechanical deformation under cyclic loads. Based on the transition state theory, we regard the interfacial degradation as an energy barrier dependent on the interfacial debonding state. Physical mismatch due to chemical expansion results in interfacial current distinction, anisotropic Li diffusion and excessive local stress. Compared to single-crystal NMC particles, the effect of interfacial separation and internal cracks triggers an extremely nonuniformity of Li distribution within random orientation polycrystalline-type particles. The external pressure in the range of operation can cause mechanical deformation to fill in the interface vacancies, which effectively alleviates the rapid growth of damage and provides a better cyclic performance. Moreover, soft polymer-based solid electrolytes take advantage of their flexible property to deal with solid-solid contact, providing considerable maintenance of interface stability. This present framework reveals the failure mechanism with electrochemical-mechanical coupled relations for composite cathode materials and broadens the design guidance toward improving interfacial integrity.

Ultrasonic-induced amorphization and strengthening mechanisms of ultrasonic vibrations assisted friction stir Al/Ti welds

Integration of aluminum (Al) and titanium (Ti) alloys offers an effective approach to sustainable and high-quality development of the automotive and aviation industries. However, challenges arise when welding Al alloys to Ti alloys due to the formation of detrimental intermetallic compounds at the interface. With the implementation of ultrasonic vibrations, the temperature and strain rate were both increased during Al/Ti friction stir welding (FSW), leading to the formation of an amorphous interlayer, instead of intermetallic compound (IMC), at the interface. The interfacial microcracks were eliminated in the ultrasonic vibrations assisted friction stir welding (UVFSW). There were Ti particles separated from the Ti substrate and dispersed in the Al alloy, thereby resulting in a more gradual and moderate evolution of the interfacial microstructure. Due to the improved interfacial microstructure with ultrasonic vibrations, the lap shear strength was almost twice that of the conventional FSW welds within same welding conditions. Meanwhile, ultrasonic vibrations also improved the fabrication efficiency with a higher optimal traversing speed. The failure mode shifted from interface separation of FSW welds to a shear dimple fracture of the UVFSW welds, demonstrating the better plasticity and reliability of the UVFSW Al/Ti dissimilar joints.

Improved UV Photoresponse Performance of ZnO Nanowire Array Photodetector via Effective Pt Nanoparticle Coupling.

Ultraviolet (UV) photodetectors (PDs) based on nanowire (NW) hold significant promise for applications in fire detection, optical communication, and environmental monitoring. As optoelectronic devices evolve towards lower dimensionality, multifunctionality, and integrability, multicolor PDs have become a research hotspot in optics and electronic information. This study investigates the enhancement of detection capability in a light-trapping ZnO NW array through modification with Pt nanoparticles (NPs) via magnetron sputtering and hydrothermal synthesis. The optimized PD exhibits superior performance, achieving a responsivity of 12.49 A/W, detectivity of 4.07 × 1012 Jones, and external quantum efficiency (EQE) of 4.19 × 103%, respectively. In addition, the Pt NPs/ZnO NW/ZnO PD maintains spectral selectivity in the UV region. These findings show the pivotal role of Pt NPs in enhancing photodetection performance through their strong light absorption and scattering properties. This improvement is associated with localized surface plasmon resonance induced by the Pt NPs, leading to enhanced incident light and interfacial charge separation for the specialized configurations of the nanodevice. Utilizing metal NPs for device modification represents a breakthrough that positively affects the preparation of high-performance ZnO-based UV PDs.

Investigation of effects of environmental conditions on wear behaviors of glass fiber reinforced polyester composite materials

AbstractGlass fiber reinforced polymer (GFRP) composites can be subjected to different environmental conditions such as temperature, humidity, ultraviolet radiation, hydrothermal cycle, acidic and alkaline solution in environments where they operate. These environmental conditions cause different damage mechanisms in composites such as pore formation, micro‐cracks, delamination, fiber breakage, fiber/matrix interface separation, plasticization, swelling and surface color change. In this study, wear properties of hybrid glass fiber reinforced polymer composites exposed to various environmental conditions for constant load (60 N), speed (500 rpm) and 2 h were examined comprehensively, depending on material content and environmental conditions. In this experimental study, the service conditions in glass fiber reinforced composites were simulated using different artificial aging environments such as acidic environment, hydrothermal cycle and UV radiation. In addition to the material content, it appears that the environmental conditions to which composites are exposed has a significant effect on friction coefficient. Considering environmental conditions, it is seen that the acid environment and hydrothermal cycle have reduced wear resistance of GFRP composites, while UV radiation improved wear resistance of the composites. In C2 sample, the wear rates under different conditions are 1.87 × 10−14 m3/Nm in non‐treated sample, 6.05 × 10−14 m3/Nm in acid environment, 4.79 × 10−14 m3/Nm in hydrothermal cycle and 0.59 × 10−14 m3/Nm in UV radiation.Highlights Friction coefficient of glass fiber reinforced polyester (GFRP) is higher under aged condition compared to non‐treated. Glass fibers used in correct proportions can reduce friction coefficient in GFRP. GFRP exposed to environmental conditions has an important effect on wear. Acid environment and hydrothermal cycle has reduced wear resistance of GFRP. UV radiation improved wear resistance of GFRP composite.

SEARCH FOR METHODS TO INCREASE THE SEDIMENTATION RATE OF THE UPPER FLOATING LAYER OF OIL SLUDGE PITS

Traditionally, oil sludge with a liquid-viscous consistency is separated into petroleum product, water and solid mechanical impurities. A large number of technological devices, including separators, centrifuges, hydrocyclones of various designs, have been developed to carry out the operation of interfacial separation of liquid-viscous oil sludge.On the territory of every oil refinery that has been in operation for decades, there are oil sludge ponds — natural settling ponds in which large quantities of oil waste accumulate.The problem of processing barn oil sludge in the oil production and refining industry has not yet been completely solved. This is due to the high stability of barn emulsions, the peculiarities of their composition and properties, which are constantly changing under the influence of temperature and various processes occurring in them.The article presents the results of research aimed at identifying the possibility of destruction of a persistent oil-water emulsion taken from the upper floating layer of an oil sludge pit and its preparation without changing the technological scheme and technological parameters.The results of laboratory studies on the destruction of oily liquid during static sedimentation are considered. Simulation of the oily liquid preparation process was carried out in compliance with the temperature and time conditions of operation, with the use of demulsifiers, by analogy with the process of oily liquid preparation, as at the unit. The results of the simulation showed that at the dosage of the demulsifiers used at the unit, even with an increase in the dosage and an increase in the settling time to 5 days, the oil-water emulsion did not collapse at 60 0C. Further studies were carried out by testing eight brands of demulsifiers at different dosages and elevated temperatures. Based on the results of the research and the conclusions made, a scheme for the preparation of oil-containing liquid at static sludge with the existing set of equipment at the unit is proposed.Further studies were carried out to increase the depth and sedimentation rate of the persistent oil-water emulsion.

Identifying Root Origin of Insulating Polymer Mediated Solar Water Oxidation.

Rational construction of high-efficiency photoelectrodes with optimized carrier migration to the ideal active sites, is crucial for enhancing solar water oxidation. However, complexity in precisely modulating interface configuration and directional charge transfer pathways retards the design of robust and stable artificial photosystems. Herein, a straightforward yet effective strategy is developed for compact encapsulation of metal oxides (MOs) with an ultrathin non-conjugated polymer layer to modulate interfacial charge migration and separation. By periodically coating highly ordered TiO2 nanoarrays with oppositely charged polyelectrolyte of poly(dimethyl diallyl ammonium chloride) (PDDA), MOs/polymer composite photoanodes are readily fabricated under ambient conditions. It is verified that electrons photogenerated from the MOs substrate can be efficiently extracted by the ultrathin solid insulating PDDA layer, significantly boosting the carrier transport kinetics and enhancing charge separation of MOs, and thus triggering a remarkable enhancement in the solar water oxidation performance. The origins of the unexpected electron-withdrawing capability of such non-conjugated insulating polymer are unambiguously uncovered, and the scenario occurring at the interface of hybrid photoelectrodes is elucidated. The work would reinforce the fundamental understanding on the origins of generic charge transport capability of insulating polymer and benefit potential wide-spread utilization of insulating polymers as co-catalysts for solar energy conversion.