Change In Moment Research Articles

Adsorption of alkaline metals (Li, Na, K) on armchair silicene nanoribbons

The paper presents the results of studies of structural, electronic and magnetic properties of amrchair silicene nanoribbons (ASiNR) atomic systems adsorbing alkaline atoms (ASiNR-Li, ASiNR-Na, ASiNR-K). The results are calculated based on density function theory (DFT) and through a VASP simulation package. Some basic characteristics have been investigated such as: optimal adsorption position, electron band structures, density of states, charge density distribution, charge density difference, and spin density distribution. The results show that the hollow adsorption site is optimal. After adsorption, the system structure has changes in bond edge length and buckling. Adsorption systems do not exist band gap, exhibiting typical metallic properties. Alkaline adsorption leads to a redistribution of charge density; causes a strong charge shift compared to the pristine system, and also leads to a change in the magnetic moment of the structure.

Experimental and theoretical study of the Favipiravir association in water solvent

Favipiravir, also known as T-705, is an antiviral prodrug that was first developed against the influenza virus and was later found to be effective against other RNA viruses, including arenaviruses, bunyaviruses, Zika, Ebola, Lassa, and COVID-19 viruses, in addition to influenza A and B. Due to the global prevalence of SARS-COV-2 in 2019, Favipiravir was used as an antiviral drug for treating COVID-19, but the challenges facing it, including its solubility, tablet ability, and bioavailability, remain. It is critical and challenging to develop a drug with appropriate bioavailability, improved oral absorption, and increased solubility without interfering with other functions and preventing the consumption of high daily doses. For this purpose, in the present study, the interactions of Favipiravir-Favipiravir and Favipiravir-H2O and the association of the Favipiravir molecules were investigated experimentally and theoretically. The theoretical results showed that under normal conditions, all structures were stable, but the most stable structure based on calculations of electronic energy, Gibbs, and solvation Gibbs free energies (minimum value), both in the gas phase and in the aqueous phase, is related to the B-enol isomer. Also, the change in dipole moment in the solvation process for this isomer was less than others. Also, the intense intermolecular hydrogen bonds O-H…O and N-H…O between the Favipiravir and water molecules showed that Favipiravir…Favipiravir interactions are stronger than Favipiravir…H2O interactions in aqueous solutions. These interactions indicate that Favipiravir can participate in the aggregation phenomena in high concentrations. Also, Stokeʼs shift values slightly increased with the decreasing the drug concentration in water (intramolecular charge transfer phenomenon).

Analyzing the electronic and conductive characteristics of zigzag graphene nanoribbons upon NOx and N2O Adsorption: An ab-initio study

Achieving a cleaner and more sustainable environment relies on the precise identification and elimination of toxic gases. Addressing this imperative, our current study utilizes a symmetric zigzag graphene nanoribbon (ZGNR)-based sensor device to effectively detect gases from the NOx family at low concentrations. The ZGNR serves as the channel element within a simulated sensing device, with its electrodes connected to a variable direct voltage (d.c) source. The performance of the device is validated by monitoring changes in adsorption energy, charge transfer, dipole moment, recovery time and conductance. The manuscript utilizes non-equilibrium Green’s function (NEGF) theory and density functional theory (DFT). These theories serve as the foundation for electronic structure calculations, supplemented by the application of the Landauer-Büttiker equation for computing electrical characteristics.Three common gasses namely NO, NO2, and N2O have been taken into consideration for ZGNR-based sensor device detection. Notably, the suggested sensor device exhibits a higher sensor response (S= 4.63) and a selectivity of about 21% for NO gas. This is likely due to the high adsorption energy (-1.07 eV), and large dipole moment (4.86×10−30Cm) that substantiate larger charge transfer (-0.14e) as compared to NO2 and N2O.Meanwhile, the ZGNR sensor device shows great gas sensing performances, including excellent selectivity, repeatability (due to small recovery time of 103.00 and 0.01 microseconds), and stability. It can therefore be explored as a sensor device that is comparable as well as superior to various carbon-based chemical entities of both 1D and 2D nanomaterials.

The adsorption of CO and NO on (8,0) SWCNT decorated with transition metals: A DFT study as a possible gas sensor

The adsorption and sensing capabilities of CO and NO on pristine and metal-decorated (8,0) SWCNT were analyzed by DFT. Both gases cause a slight deformation of the nanotube curvature in the direction of molecular adsorption. The molecule's adsorption and sensing performance are enhanced with the transition metal (Sc, Cr, Fe, and Ni) decoration on SWCNT. Decorated nanotubes are suitable for high-temperature sensors. According to relative energies for NO, the operational range is 900–1200 K. For CO/Cr- and Sc-SWCNT between 100 and 200 K and close to 550 K in the cases of decoration with Fe and Ni. From the recovery time analysis, the metal-decorated materials exhibit better performance at high temperatures and low pressures for NO compared to CO. Changes in magnetic moment suggest that Cr-decorated SWCNT could serve as a magnetic sensor for both molecules.

A tight-binding model for illustrating exciton confinement in semiconductor nanocrystals.

The Brus equation describes the relation between the lowest energy of an electron-hole pair and the size of a semiconductor crystallite. However, taking the strong confinement regime as a starting point, the equation does not cover the transition from weak to strong confinement, the accompanying phenomenon of charge-carrier delocalization, or the change in the transition dipole moment of the electron-hole pair state. Here, we use a one-dimensional, two-particle Hubbard model for interacting electron-hole pairs that extends the well-known tight-binding approach through a point-like electron-hole interaction. On infinite chains, the resulting exciton states exhibit the known relation between the Bohr radius, the exciton binding energy, and the effective mass of the charge carriers. Moreover, by introducing infinite-well boundary conditions, the model enables the transition of the exciton states from weak to strong confinement to be tracked, while straightforward adaptations provide insights into the relation between defects, exciton localization, and confinement. In addition, by introducing the dipole operator, the variation of the transition dipole moment can be mapped when shifting from electron-hole pairs in strong confinement to delocalized and localized excitons in weak confinement. The proposed model system can be readily implemented and extended to different multi-carrier states, thus providing researchers a tool for exploring, understanding, and teaching confinement effects in semiconductor nanocrystals under different conditions.

Numerical Simulation of Double-row Piles in Deep Foundation Pit Excavation

This paper aims to investigate the stress and deformation characteristics of double-row piles in deep foundation pit excavation by selecting representative strata in the Changchun area. The changes in bending moment, displacement, and earth pressure of double-row piles during the excavation are established using the FALC 3D software. The findings indicate that the deformation of the front pile is larger than that of the back pile, and the earth pressure distribution of the fornt pile deviates from the conventional Rankine earth pressure theory. Moreover, there are noticeable variations in earth pressure at the soil layer interface of the rear pile.

Exploiting Hydrogen Interaction of Drugs and Biodegradable Scaffolds Using Nanoparticles Loaded Nanofibers

AbstractThis study presents a detailed investigation of the structural and surface modifications of Fe3O4 nanoparticles (NPs). Fourier Transform Infrared (FTIR) spectroscopy was utilized to analyze the distinct characteristic peaks of Fe3O4 NPs and their subsequent modifications with stearic acid (ST) layers. The FTIR analysis revealed characteristic peaks at 580 cm−1, and 441 cm−1, corresponding to the Fe‐O stretching vibrations of the bulk Fe3O4 NPs. The successful loading of stearic acid onto the Fe3O4 NPs was confirmed by the appearance of new peaks at 1413 cm−1 and 2908 cm−1, indicative of the asymmetric CH2 stretch and CH3 umbrella vibration modes of stearic acid. UV‐Vis spectroscopy further corroborated the efficient loading of tetracycline and ibuprofen onto Fe3O4/DST nanoparticles, as evidenced by changes in absorption spectra. N2 adsorption‐desorption isotherms illustrated the presence of micro and meso pores on the surface of Fe3O4 NPs, with alterations in pore volume and diameter post‐surface modification and drug loading. Evaluation of magnetic properties indicated a reduction in saturation magnetization after surface modification and drug loading, attributed to changes in homogeneity and surface moments. Differential Reflectance Spectroscopy (DRS) and Raman spectroscopy elucidated distinctive peaks and shifts in spectra, confirming the composition and structural changes in drug‐loaded nanofibers.

The study of electronic structure and magnetic properties of ferromagnetic Kondo-lattice CePd2P2 from the first-principles

The electronic structure of ferromagnetic CePd2P2 Kondo lattice crystallizing in the tetragonal ThCr2Si2-type structure is investigated by means of the Density Functional Theory (DFT) and Time-Depedent DFT (TDDFT) methods. The calculated electronic properties from DFT are presented and compared to those of the non-magnetic LaPd2P2 compound. The differences in the FS topologies upon changing magnetic states (paramagnetic → ferromagnetic) is also examined. Including the relativistic effects of without or with spin-orbit coupling, and Hubbard corrections in the calculations, ferromagnetic ground state with an ordered magnetic moment of ∼ 0.8-0.9 μB is corroborated. Meaningful changes in the magnetic moment and electronic properties of CePd2P2 are discussed in terms of effects brought by the Coulomb interaction (U), and the Hund coupling (J). In particular, the reduction in magnetic moment and simultaneously enhancement of DOS at the Fermi energy due to decreasing J are in quantitative concordance with the Kondo lattice characteristic. Furthermore, dynamical model used in TDDFT calculations exhibits that 4 f electrons in CePd2P2 tend to be delocalized. The frequency-temperature behavior of response function allows to estimate the Kondo temperature to amount 19 K.

Regulation Dipole Moments of N-Doped Graphene Coordinated with FePc Toward Highly Efficient Microwave Absorption Performance in C Band.

The development of composites with highly efficient microwave absorption (MA) performance deeply depends on polarization loss, which can be induced by charge redistribution. Considering the fact that polarization centers can be easily obtained in graphene, herein, iron phthalocyanine (FePc) is used as polarization site to coordinate with nitrogen-doped graphene (FePc/N-rGO) to optimize MA performance comprehensively. The factors influencing MA properties focus on the interaction between FePc and N-rGO, and the change of dipole moments. The density functional theory (DFT) results demonstrated that FePc has strong interaction with N defect sites in graphene. The charge loss for FePc and charge accumulation for N-rGO occurred, leading to great increase of dipole moment, and the increased dipole moment can be acted as a descriptor to evaluate the enhanced polarization loss. Due to high charge redistribution capacity of N defect sites and FePc polarization centers, the FePc/N-rGO showed excellent MA properties in C band, and the minimum reflection loss value can reach -49.3dB at 5.4GHz with thickness of 3.8mm. In addition, the fabric loaded with FePc/N-rGO showed good heat dissipation property. This work opens the door to the development of MA performance bound to polarization site with dipole moment.

Molecular Symmetry of Small-Molecule Passivating Agents Improves Crystal Quality of Perovskite Solar Cells.

Direct interaction with the defect sites of perovskite, functional groups have become the focal point of attention as passivating agents. However, the molecular parent nucleus determines the overall physical properties of the molecule, including the push-pull electronic characteristics of the functional groups, which poses significant challenges in terms of selectivity. Here, we discovered that the binary acid structure based on thiophene as the parent nucleus, due to changes in molecular symmetry, caused significant changes in the molecular dipole moment, resulting in significant changes in the passivation effects on under-coordinated Pb2+ in perovskite solar cells. For the axially symmetric thiophen-2,5-dicarboxylic acid (TPDC), the high dipole moment formed a concentrated surface negative potential on the carboxyl group, showing significant superiority over the centrally symmetric thieno[3,2-b] thiophene-2,5-dicarboxylic acid (TTDC) in forming high-quality perovskite crystals, suppressing charge recombination, enhancing effective charge transport, and raising internal electric fields. The power conversion efficiencies of the fully printable mesoscopic perovskite solar cells based on TPDC and TTDC were 17.15 % and 14.79 %, respectively, exhibiting important research value in the field of small molecule passivation mechanism research.

Probing Charge Transfer Character in Modern Donor/Acceptor Materials via Electroabsorption Spectroscopy.

We use electroabsorption (EA) spectroscopy to probe the charge transfer (CT) character in neat films and blends of donors and acceptors of interest for organic electronic applications. In particular, we compare the CT character in two polymer donor and non-fullerene acceptor blends, including 3,9-bis(2-methylene-((3-(1,1-dicyanomethylene)-6,7-difluoro)-indanone))-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3-d:2',3'-d']-s-indaceno[1,2-b:5,6-b']dithiophene (IT-4F) and 2,2'-((2Z,2'Z)-((12,13-bis(2-ethylhexyl)-3,9-diundecyl-12,13-dihydro-[1,2,5]thiadiazolo[3,4-e]thieno[2″,3″:4',5']thieno[2',3':4,5]pyrrolo[3,2-g]thieno[2',3':4,5]thieno[3,2-b]indole-2,10-diyl)bis(methanylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile (Y6). Like classic polymer/fullerene blends, the blend based on IT-4F exhibits primarily first derivative-like EA features, suggesting localized exciton formation upon photoexcitation. However, the Y6-based blend has an EA spectrum that is dominated by second derivative-like features, consistent with CT character. We show that this signal originates primarily from Y6. We find that Y6 exhibits the highest dipole moment change (7.5 ± 2.5 D) of the molecules that comprise this study, consistent with a high degree of the CT character, and a relatively large polarization volume of 361 ± 70 Å3, consistent with strong electron delocalization. These results point to the origins of exceptional performance of organic photovoltaics (OPVs) based on Y6.

Mapping the Intellectual Structure of Studies on Internationalization of the Curriculum: A Bibliometric Analysis From the Scopus Database

<p style="text-align:justify">The pervasive development and momentous changes of internationalization in higher education have led to the acceleration of research on its key component – the curriculum. However, there has not been any comprehensive analysis of the research status of the internationalization of the curriculum (IoC). To address the gap, this study employs the bibliometric method to construct an intellectual structure of research on the topic. The data, retrieved from the Scopus Database, consisted of 386 publications. The extracted data were then analyzed using citation, co-authorship, and keyword co-occurrence analysis. The results reveal a significant growth in research volume during the last ten years and the domination of Global North in the geographical distribution of publications. Besides, the most prominent authors include those who introduced fundamental knowledge on the topic. The most cited works and the most popular publishing sources focus on various aspects of internationalization of higher education. They also show a multidisciplinary interest in the topic. Finally, concerning newly emerged themes of studies on IoC, “cultural competence” and “internationalization at home” are outstanding keywords. The research findings emphasize IoC as a potential research matter. Hence, this study is recommended as a starting point for future researchers when examining related subjects.</p>

Sectors versus borders: interest group cleavages and struggles over corporate governance in the age of asset management

Abstract Universally invested asset managers like BlackRock have established a dominant position in equity markets around the globe. While extant contributions have explored their voting behaviour and role in shaping corporate governance at the firm level, less is known about their potential to build interest coalitions with other business groups, and their leverage over state-level corporate governance institutions. This article investigates conflict over a far-reaching reform to co-determination in Germany. Qualitative content analysis of over 100 stakeholder statements yields that asset managers forge coalitions with short-term-oriented investors to abolish key tenets of corporatist institutions. However, a domestic countercoalition of financial and non-financial firms prevented momentous institutional change. This article improves our understanding of international asset managers’ preferences and highlights coalition building as a key determinant of the political power of international finance. By aligning the costs of institutional change for incumbents, corporatist institutions continue to act as shields against financialization.

A Semi-Markov Approach to Study a Group of Kinesin Motors.

We propose a general mathematical and computational approach to study cellular transport driven by a group of kinesin motors. It is a framework for multi-scale modeling that integrates kinetic models of single kinesin motors, including detachment and reattachment events, to study group behaviors of several motors. By formulating the problem as a semi-Markov process and applying a central limit theorem, asymptotic velocity and diffusivity can be readily calculated, which offers considerable computational advantage over Monte Carlo simulations in tasks such as parameter sensitivity analysis and model selection. We demonstrate the method with some examples. The importance of incorporating the intrinsic microscopic-level dynamics of individual motors is illustrated by showing how changes at the microscopic level propagate to the motor-cargo complex at a mesoscopic level. Particularly, we showcase an example in which changes in the second moment of single-motor characteristics gives rise to different first moment characteristics of the motor group.

Sensing potential of C6N8 for ammonia (NH3) and nitrogen triflouride (NF3): A DFT study

The detection of toxic gases (NH3 and NF3) in regulating and monitoring air quality in the atmosphere has drawn a lot of attention. Herein, we explored a novel material (C6N8) for the detection of the important but toxic gases (NH3 and NF3). We investigated the interactions of the NH3 and NF3 with C6N8 through DFT at B3LYP, ωB97XD, and non-DFT M06-2X. Counterpoise interaction energy values (Eint. cp.) of NH3@C6N8 and NF3@C6N8 are −0.45 eV and −3.51 eV (for B3LYP), −0.42 eV and 2.11 eV (for ωB97XD) and −0.44 eV and −3.41eV (for M06-2X), respectively. Complexes having the most stable configurations were then subjected to further analyses including frontier molecular orbitals, H-L gap, and conductivity of complexes. An increase in the H-L gap in complexes (NH3@C6N8 and NF3@C6N8) is observed. The conductivity of NH3@C6N8 and NF3@C6N8 decreases as compared to C6N8. A considerable change in dipole moment was seen in C6N8 before and after complex formation. This is because of the shifting of charge between C6N8 and gases (NH3 and NF3). CHELPG and NBO charge analysis were used to evaluate the amount of charge transfer between C6N8 and gases. These analyses demonstrate that NH3 and NF3 withdraw electron density from C6N8. It was found that NH3 tends to be physically adsorbed on C6N8 while NF3 adsorbs chemically on C6N8. NCI and QTAIM analyses were performed to investigate the kind of interactions between the surface (C6N8) and gases (NH3 and NF3). Furthermore, the recovery time of NH3@C6N8 and NF3@C6N8 shows that C6N8 can be a better choice for sensing NH3 and NF3 gases.

Effect of alternating electric field induced by cold atmospheric plasma on conformation and function of interleukin-6

Cold atmospheric plasma (CAP) is considered to be a very promising cancer treatment method due to its “selective” killing effect on cancer cells. The CAP can inhibit tumor inflammatory responses and activate the immune system by reducing the expression of the key inflammatory factor Interleukin-6 (IL-6). However, the influence of the strong alternating electric field induced by CAP on the conformation and function of IL-6 remains unclear. In this study molecular dynamics simulation is used to investigate the effects of alternating electric fields with different frequencies and intensities on the conformation of IL-6. We statistically analyze the root mean square fluctuations, root mean square deviation, secondary structural alterations, and dipole moment changes of IL-6 under different electric field parameters. Furthermore, molecular docking is utilized to assess the influence on the receptor-binding process. The results show that when the electric field frequency is below 30 MHz and the intensity exceeds 0.5 V/nm, the average dipole moment of IL-6 increases, leading to changes in the rigid regions at the C-terminus which maintain structural stability. Specifically, the salt bridges that stabilize the long helices rupture, and the number of α-helices decreases. The docking outcomes reveal that the distance between the key binding residues of the conformationally altered IL-6 and its receptor increases, thereby disrupting the normal binding process and potentially impairing its normal biological functionality. This study explains the internal interaction mechanism of CAP-induced electric fields affecting IL-6-related biological effects at the micro level, and provides important theoretical basis for optimizing parameters in the practical application of CAP in tumor inflammation treatment and the development of effective cancer therapy strategies.

ON THE SUPPRESSION OF VIBRATIONS IN ELASTIC LINKS OF A THREEMASS ELECTRIC DRIVE SYSTEM

The main reason for failures of technological mechanisms is associated with the failure of elements of the electric drive system. One of the main reasons for the malfunction of electric drive elements is the presence of vibrations in the elastic links of the mechanical part of the electric drive. Such phenomena mainly occur during transient processes of starting and stopping an electric drive, as well as under the influence of a load that is variable in nature. From the above, it is obvious that suppression of vibrations in the elastic links of the mechanical part is of practical interest. The most promising studies aimed at studying and suppressing vibrations in the elastic links of a three-mass electric drive system are analyzed. A comparative analysis of these studies shows that they consider the operating features of individual specific electric drive systems, which cannot provide a complete understanding of a comprehensive solution to the problem of ensuring the suppression of vibrations, arising in the mechanical part for various reasons. That is why it is necessary to evaluate the possibilities of suppressing elastic vibrations of the electric drive system, taking into account all its links. The goal of this work is to propose an approach for suppressing vibrations in the elastic links of a three-mass electric drive system. The change in the elastic moment under various characteristics of the load created by the mechanism is considered, in particular, in cases of constant moment, exponential and step laws of change. The capabilities of proportional-integral (PI) and proportional-integral-derivative (PID) controllers for suppressing oscillations are analyzed. It is substantiated that although the system stabilizes with a PID controller in a short time, it does not provide the expected result and therefore it is recommended to use a controller with a fuzzy logic due to its simple control and rather high efficiency. The results obtained can be successfully used to improve the reliability of a three-mass electric drive system.

Predicting valence tautomerism in diverse cobalt-dioxolene complexes: elucidation of the role of ligands and solvent.

The ability of molecular switches to reversibly interconvert between different forms promises potential applications at the scale of single molecules up to bulk materials. One type of molecular switch comprises cobalt-dioxolene compounds that exhibit thermally-induced valence tautomerism (VT) interconversions between low spin Co(iii)-catecholate (LS-CoIII-cat) and high spin Co(ii)-semiquinonate (HS-CoII-sq) forms. Two families of these compounds have been investigated for decades but have generally been considered separately: neutral [Co(diox)(sq)(N2L)] and cationic [Co(diox)(N4L)]+ complexes (diox = generic dioxolene, N2L/N4L = bidentate/tetradentate N-donor ancillary ligand). Computational identification of promising new candidate compounds prior to experimental exploration is beneficial for environmental and cost considerations but requires a thorough understanding of the underlying thermochemical parameters that influence the switching. Herein, we report a robust approach for the analysis of both cobalt-dioxolene families, which involved a quantitative density functional theory-based study benchmarked with reliable quasi-experimental references. The best-performing M06L-D4/def2-TZVPP level of theory has subsequently been verified by the synthesis and experimental investigation of three new complexes, two of which exhibit thermally-induced VT, while the third remains in the LS-CoIII-cat form across all temperatures, in agreement with prediction. Valence tautomerism in solution is markedly solvent-dependent, but the origin of this has not been definitively established. We have extended our computational approach to elucidate the correlation of VT transition temperature with solvent stabilisation energy and change in dipole moment. This new understanding may inform the development of VT compounds for applications in soft materials including films, gels, and polymers.

Ultrafast excited state relaxation dynamics of pyran-based D-π-A systems: solvent polarity controls the triplet state.

The excited state relaxation dynamics of V-shaped D-π-A systems having 4H-pyranylidene appended barbituric acid as an acceptor and diphenylamine (TPAPBA) and diethyl amine (EAPBA) as donors were investigated using steady-state and time-resolved spectroscopy along with theoretical optimization. The steady-state photophysical characterization exhibited the bathochromic shift of the emission maximum (∼6400 cm-1) and large change in the dipole moment (∼24D) with an increase of solvent polarity, reflecting the occurrence of the intramolecular charge transfer state (ICT) in the excited state. The nanosecond and femtosecond transient absorption spectra of these derivatives in a non-polar solvent, toluene, reveal that the excited state relaxation pathway involving a local excited state (LE) decayed to ICT followed by the formation of a twisted ICT state by conformational relaxation, finally leading to the triplet state. The lack of observation of a triplet state in the polar solvent, acetonitrile, signifies that the relaxation dynamics of V-shaped triads in the excited state are influenced by the polarity of the solvent.

Boosting charge separation in organic photovoltaics: unveiling dipole moment variations in excited non-fullerene acceptor layers.

The power conversion efficiency (PCE) of organic photovoltaics (OPVs) has reached more than 19% due to the rapid development of non-fullerene acceptors (NFAs). To compete with the PCEs (26%) of commercialized silicon-based inorganic photovoltaics, the drawback of OPVs should be minimized. This drawback is the intrinsic large loss of open-circuit voltage; however, a general approach to this issue remains elusive. Here, we report a discovery regarding highly efficient NFAs, specifically ITIC. We found that charge-transfer (CT) and charge dissociation (CD) can occur even in a neat ITIC film without the donor layer. This is surprising, as these processes were previously believed to take place exclusively at donor/acceptor heterojunctions. Femtosecond time-resolved visible to mid-infrared measurements revealed that in the neat ITIC layers, the intermolecular CT immediately proceeds after photoirradiation (<0.1 ps) to form weakly-bound excitons with a binding energy of 0.3 eV, which are further dissociated into free electrons and holes with a time-constant of 56 ps. Theoretical calculations indicate that stacking faults in ITIC (i.e., V-type molecular stacking) induce instantaneous intermolecular CT and CD in the neat ITIC layer. In contrast, J-type stacking does not support such CT and CD. This previously unknown pathway is triggered by the larger dipole moment change on the excited state generated at the lower symmetric V-type molecular stacking of ITIC. This is in sharp contrast with the need of sufficient energy offset for CT and CD at the donor-acceptor heterojunction, leading to the significant voltage loss in conventional OPVs. These results demonstrate that the rational molecular design of NFAs can increase the local dipole moment change on the excited state within the NFA layer. This finding paves the way for a groundbreaking route toward the commercialization of OPVs.