Ultrafast Transient Absorption Spectroscopy Research Articles

Aromatic-bridged and meso-meso-linked BF2-smaragdyrin dimers exhibit fast decays in polar solvents by symmetry-breaking charge transfer

Symmetry-breaking charge transfer is one of the key process in photosynthetic reaction centers and specific artificial optoelectronic devices such as dye-sensitized solar cells. Here we report the synthesis of aromatic-bridged BF2-smaragdyrin dimers, meso-free BF2-smaragdyrin, and its meso-meso-linked BF2-smaragdyrin dimer. The decays of S1-states of these dimers are accelerated with an increase in solvent polarity and a decrease in the distance between the two BF2-smaragdyrin units, suggesting symmetry-breaking charge transfer. The fluorescence lifetimes of the dimers become shortened in polar solvents. However, ultrafast transient absorption spectroscopy do not detect charge-separated ion pairs. On the basis of these results, we conclude that the decays of the excited states of the BF2-smaragdyrin dimers are accelerated by solvation-induced symmetry-breaking charge transfer, depending on the degree of the electronic interaction between the smaragdryin units as a rare case for porphyrinoids. The degree of charge transfer is larger for dimers with larger electronic interactions.

Silver nanoparticle enhanced metal-organic matrix with interface-engineering for efficient photocatalytic hydrogen evolution

Integrating plasmonic nanoparticles into the photoactive metal-organic matrix is highly desirable due to the plasmonic near field enhancement, complementary light absorption, and accelerated separation of photogenerated charge carriers at the junction interface. The construction of a well-defined, intimate interface is vital for efficient charge carrier separation, however, it remains a challenge in synthesis. Here we synthesize a junction bearing intimate interface, composed of plasmonic Ag nanoparticles and matrix with silver node via a facile one-step approach. The plasmonic effect of Ag nanoparticles on the matrix is visualized through electron energy loss mapping. Moreover, charge carrier transfer from the plasmonic nanoparticles to the matrix is verified through ultrafast transient absorption spectroscopy and in-situ photoelectron spectroscopy. The system delivers highly efficient visible-light photocatalytic H2 generation, surpassing most reported metal-organic framework-based photocatalytic systems. This work sheds light on effective electronic and energy bridging between plasmonic nanoparticles and organic semiconductors.

Nanodiscs as a novel approach to resolve inter-protein energy transfer within the photosynthetic membrane of purple bacteria.

Photosynthetic purple bacteria capture sunlight and convert it to chemical energy with almost 100% quantum efficiency: almost every photon absorbed leads to charge separation. Such high efficiency is achieved through a series of ultrafast inter-protein energy transfer events within an antenna network of light-harvesting proteins located in the photosynthetic membrane. Understanding how the organization of proteins within the membrane leads to efficient energy transfer is imperative to designing efficient artificial solar harvesting techniques. Determining inter-protein energy transfer between light-harvesting complex 2 (LH2) proteins, the most common light-harvesting protein in vivo, has proven challenging due to the heterogeneous organization of proteins within the membrane environment. In this work, we introduce model membrane nanodiscs as a novel technique to reconstruct the complex membrane environment in a controlled manner. By forming nanodiscs large enough to incorporate two variants of LH2, we can directly resolve inter-protein energy transfer. By controlling nanodisc size, we can change the inter-protein distance and resolve the effect of membrane organization on energy transfer rate. Using a combination of ultrafast transient absorption spectroscopy, cryogenic electron microscopy, and quantum chemical calculations, we find that LH2 complexes prefer to associate closely in the membrane (25 Å), with an energy transfer rate of 5.7 ps. The results suggest that these tightly-packed LH2s are important for long-distance energy transfer, as the 25 Å distance is similar to the most common inter-protein distance in vivo. Overall, our work introduces nanodiscs as a platform to study complex energy transfer events and the effect of membrane organization on critical biological processes.

Investigation of third-order nonlinear optical properties in two novel ethyne-linked chromophores: Effect of donor-acceptor alternation

Two novel compounds of the alternating donor (D)/acceptor (A) system were designed and synthesized. In BSB (A-π-D-π-A) and SBS (D-π-A-π-D), thiophene, 2,1,3-benzothiadiazole (BTD) and ethylene act as donor, acceptor groups and π-bridge moiety, respectively. Z-scan experiments at 532 nm with various pulse durations show a transition from saturable absorption to reverse saturable absorption and self-defocusing effects in both compounds. The different alternating modes of D-A units lead to an order of magnitude increment in the second-order hyperpolarizability γ of SBS (4.4 × 10−28 esu) compared to BSB. Ultrafast transient absorption spectroscopy was carried out to analyze the enhancement of second-order hyperpolarizability. Results indicate that this enhancement originates from excited state absorption of the long-lived intramolecular charge transfer state. Using quantum chemical calculations, the stronger symmetrical intramolecular charge transfer in SBS can be demonstrated by the difference between the ground- and excited-state dipole moments Δμge. It is shown intuitively in the S0–S1 hole-electron analysis. All of the experimental and theoretical results suggest that changing the D-A alternation in organic molecules can effectively modulate the third-order nonlinear optical behavior, which may serve as a guide for future molecular design.

Elucidating Polaron Dynamics in Cs2AgBiBr6 Double Perovskite.

Lead-free Cs2AgBiBr6 double perovskites have recently emerged as a possible alternative to lead-based halide perovskites for photovoltaic and optoelectronic applications. Significant research efforts have been devoted toward device engineering to enhance the performance of Cs2AgBiBr6 double-perovskite-based photovoltaic and optoelectronic devices; however, less attention has been paid to address their intrinsic photophysical properties. In this work, we have shown that the small polaron formation under photoexcitation and polaron localization limits the carrier dynamics in Cs2AgBiBr6 double halide perovskites. Furthermore, temperature-dependent ac conductivity measurement reveals that single polaron hopping is the dominant conduction mechanism. Ultrafast transient absorption spectroscopy reveals that a deformed lattice under photoexcitation leads to the formation of small polarons which act as self-trapped states (STSs) and lead to the ultrafast trapping of charge carriers. Our findings provide an in-depth understanding of intrinsic limitations of Cs2AgBiBr6 perovskites, which can be applicable for other bismuth-based semiconductors.

Probing Bidirectional Plasmon-Plasmon Coupling-Induced Hot Charge Carriers in Dual Plasmonic Au/CuS Nanocrystals.

Heterostructured Au/CuS nanocrystals (NCs) exhibit localized surface plasmon resonance (LSPR) centered at two different wavelengths (551 and 1051nm) with a slight broadening compared to respective homostructured Au and CuS NC spectra. By applying ultrafast transient absorption spectroscopyweshow that a resonant excitation at the respective LSPR maxima of the heterostructured Au/CuS NCs leads to the characteristic hot charge carrier relaxation associated with both LSPRs in both cases. A comparison of the dual plasmonic heterostructure with a colloidal mixture of homostructured Au and CuS NCs shows that the coupled dual plasmonic interaction is only active in the heterostructured Au/CuS NCs. By investigating the charge carrier dynamics of the process,wefind that the observed interaction is faster than phononic or thermal processes (< 100fs). The relaxation of the generated hot charge carriers is faster for heterostructured nanocrystals and indicates that the interaction occurs as an energy transfer (we propose Landau damping or interaction via LSPR beat oscillations as possible mechanisms) or charge carrier transfer between both materials.Ourresults strengthen the understanding of multiplasmonic interactions in heterostructured Au/CuS NCs and will significantly advance applications where these interactions are essential, such as catalytic reactions.

Ultrafast X-ray Spectroscopy of Intersystem Crossing in Hexafluoroacetylacetone: Chromophore Photophysics and Spectral Changes in the Face of Electron-Withdrawing Groups.

Intersystem crossings between singlet and triplet states represent a crucial relaxation pathway in photochemical processes. Herein, we probe the intersystem crossing in hexafluoro-acetylacetone with ultrafast X-ray transient absorption spectroscopy at the carbon K-edge. We observe the excited state dynamics following excitation with 266 nm UV light to the 1ππ* (S2) state with element and site-specificity using a broadband soft X-ray pulse produced by high harmonic generation. These results are compared to X-ray spectra computed from orbital optimized density functional theory methods. It is found that the electron-withdrawing fluorine atoms decongest the X-ray absorption spectrum by enhancing separation between features originating from different carbon atoms. This facilitates the elucidation of structural and electronic dynamics at the chromophore. The evolution of the core-to-valence resonances at the carbon K-edge reveals an ultrafast population transfer between the 1nπ* (S1) and 3ππ* (T1) states on a 1.6 ± 0.4 ps time scale, which is similar to the 1.5 ps time scale earlier observed for acetylacetone [ J. Am. Chem. Soc. 2017, 139, 16576-16583, DOI: 10.1021/jacs.7b07532]. It therefore appears that terminal fluorination has little influence on the intersystem crossing rate of the acetylacetone chromophore. In addition, the significant role of hydrogen-bond opened and twisted rotational isomers is elucidated in the excited state dynamics by comparison of the experimental transient X-ray spectra with theory.

Topological effects in ultrafast photoinduced processes between flurbiprofen and tryptophan in linked dyads and within human serum albumin.

The interaction dynamics between flurbiprofen (FBP) and tryptophan (Trp) has been studied in covalently linked dyads and within human serum albumin (HSA) by means of fluorescence and ultrafast transient absorption spectroscopy. The dyads have proven to be excellent models to investigate photoinduced processes such as energy and/or electron transfer that may occur in proteins and other biological media. Since the relative spatial arrangement of the interacting units may affect the yield and kinetics of the photoinduced processes, two spacers consisting of amino and carboxylic groups separated by a cyclic or a long linear hydrocarbon chain (1 and 2, respectively) have been used to link the (S)- or (R)-FBP with the (S)-Trp moieties. The main feature observed in the dyads was a strong intramolecular quenching of the fluorescence, which was more important for the (S,S)- than for the (R,S)- diastereomer in dyads 1, whereas the reverse was true for dyads 2. This was consistent with the results obtained by simple molecular modelling (PM3). The observed stereodifferentiation in (S,S)-1 and (R,S)-1 arises from the deactivation of 1Trp*, while in (S,S)-2 and (R,S)-2 it is associated with 1FBP*. The mechanistic nature of 1FBP* quenching is ascribed to energy transfer, while for 1Trp* it is attributed to electron transfer and/or exciplex formation. These results are consistent with those obtained by ultrafast transient absorption spectroscopy, where 1FBP* was detected as a band with a maximum at ca. 425 nm and a shoulder at ∼375 nm, whereas Trp did not give rise to any noticeable transient. Interestingly, similar photoprocesses were observed in the dyads and in the supramolecular FBP@HSA complexes. Overall, these results may aid to gain a deeper understanding of the photoinduced processes occurring in protein-bound drugs, which may shed light on the mechanistic pathways involved in photobiological damage.

Electrocatalytic reduction of CO2 to CO by a series of organometallic Re(I)-tpy complexes.

A series of organometallic Re(I)(L)(CO)3Br complexes with 4'-substituted terpyridine ligands (L) has been synthesised as electrocatalysts for CO2 reduction. The complexes' spectroscopic characterisation and computationally optimised geometry demonstrate a facial geometry around Re(I) with three cis COs and the terpyridine ligand coordinating in a bidentate mode. The effect of substitution on the 4'-position of terpyridine (Re1-5) on CO2 electroreduction was investigated and compared with a known Lehn-type catalyst, Re(I)(bpy)(CO)3Br (Re7). All complexes catalyse CO evolution in homogeneous organic media at moderate overpotentials (0.75-0.95 V) with faradaic yields of 62-98%. The electrochemical catalytic activity was further evaluated in the presence of three Brønsted acids to demonstrate the influence of the pKa of the proton sources. The TDDFT and ultrafast transient absorption spectroscopy (TAS) studies showed combined charge transfer bands of ILCT and MLCT. Amongst the series, the Re-complex containing a ferrocenyl-substituted terpyridine ligand (Re5) shows an additional intra-ligand charge transfer band and was probed using UV-Vis spectroelectrochemistry.

Photoinduced asymmetric charge trapping in a symmetric tetraazapyrene-fused bis(tetrathiafulvalene) conjugate.

In fused donor-acceptor (D-A) ensembles, rapid charge recombination often occurs because the D and A units are spatially close and strongly coupled. To the best of our knowledge, a long-lived charge separated (CS) state is still elusive in such systems. The results presented here show that symmetric annulation of two tetrathiafulvalene (TTF) donors to a central tetraazapyrene (TAP) acceptor via two quinoxaline units leads to a CS state lifetime of a few ns. A detailed study of the electronic interactions between TTF and TAP units in the ground and excited states was performed and compared with the asymmetric counterpart by cyclic voltammetry, optical absorption and ultrafast transient absorption spectroscopy. The results demonstrate that the photoinduced asymmetric charge trapping between two TTFs significantly stabilizes the CS state, which is also verified theoretically.

Observation of Refractive Index Line Shape in Ultrafast XUV Transient Absorption Spectroscopy

Ultrafast extreme ultraviolet (XUV) transient absorption spectroscopy measures the time- and frequency-dependent light losses after light–matter interactions. In the linear region, the matter response to an XUV light field is usually determined by the complex refractive index n ˜ . The absorption signal is directly related to the imaginary part of n ˜ , namely, the absorption index. The real part of n ˜ refers to the real refractive index, which describes the chromatic dispersion of an optical material. However, the real refractive index information is usually not available in conventional absorption experiments. Here, we investigate the refractive index line shape in ultrafast XUV transient absorption spectroscopy by using a scheme that the XUV pulse traverses the target gas jet off-center. The jet has a density gradient in the direction perpendicular to the gas injection direction, which induces deflection on the XUV radiation. Our experimental and theoretical results show that the shape of the frequency-dependent XUV deflection spectra reproduces the refractive index line profile. A typical dispersive refractive index line shape is measured for a single-peak absorption; an additional shoulder structure appears for a doublet absorption. Moreover, the refractive index line shape is controlled by introducing a later-arrived near-infrared pulse to modify the phase of the XUV free induction decay, resulting in different XUV deflection spectra. The results promote our understanding of matter-induced absorption and deflection in ultrafast XUV spectroscopy.

Physical mechanisms on FRET and ICT for efficient Y6:PM6 as bulk heterojunction active layers.

Organic solar cells (OSCs) have emerged as a promising new energy technology because of their advantages of efficient light harvesting, comprehensive material sources, and flexible and translucent devices. In this study, fluorescence resonance energy transfer (FRET) and intermolecular charge transfer (ICT) in the donor-acceptor system for efficient OSCs of the Y6:PM6 heterostructure are investigated with ultrafast pump-probe transient absorption spectroscopy, time-resolved fluorescence spectroscopy, steady absorption, and fluorescence spectroscopy, which is significantly supported by theoretical results. The physical mechanisms of FRET and ICT in the donor-acceptor system for efficient OSCs of the Y6:PM6 heterostructure are investigated theoretically and experimentally. FRET can decrease the recombination of electron-hole in the donor's fluorescence and enhance the acceptor's fluorescence. Our study contributes to a better understanding of FRET and ICT and provides valuable references for the rational design of FRET- and ICT-based OSCs.

Broadband ultrafast photogenerated carrier dynamics induced by intrinsic defects in &lt;inline-formula&gt;&lt;tex-math id="Z-20231102113631"&gt;\begin{document}$\boldsymbol\beta$\end{document}&lt;/tex-math&gt;&lt;alternatives&gt;&lt;graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="21-20231173_Z-20231102113631.jpg"/&gt;&lt;graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="21-20231173_Z-20231102113631.png"/&gt;&lt;/alternatives&gt;&lt;/inline-formula&gt;-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;

The ultra-wide bandgap semiconductor gallium oxide &lt;i&gt;β&lt;/i&gt;-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; with enhanced resistance to the irradiation and temperature is favorable for high-power and high-temperature optoelectronic devices. &lt;i&gt;β&lt;/i&gt;-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; also exhibits great potential applications in the field of integrated photonics because of its compatibility with the CMOS technique. However, a variety of intrinsic and extrinsic defects and trap states coexist in &lt;i&gt;β&lt;/i&gt;-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;, including vacancies, interstitials, and impurity atoms. The defect-related carrier dynamics in &lt;i&gt;β&lt;/i&gt;-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; not only adversely affect the optical and electrical properties, but also directly limit the performance of &lt;i&gt;β&lt;/i&gt;-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; based devices. Therefore, a comprehensive understanding of the carrier transportation and relaxation dynamics induced by intrinsic defects is very important. Supercontinuum-probe spectroscopy can provide a fruitful information about the carrier relaxation processes in different recombination mechanisms, and thus becomes an effective way to study the defect dynamics. In this work, we study the dynamics of carrier trapping and recombination induced by intrinsic defects in pristine &lt;i&gt;β&lt;/i&gt;-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; crystal by using wavelength-tunable ultrafast transient absorption spectroscopy. The broadband absorption spectra induced by the intrinsic defects are strongly dependent on the polarization of pump pulse and probe pulse. Particularly, two absorption peaks induced by the two defect states can be extracted from the transient absorption spectra by subtracting the absorption transients under two probe polarizations. The observed defect-induced absorption features are attributed to the optical transitions from the valence band to the different charge states of the intrinsic defects (such as gallium vacancy). The data are well explained by a proposed carrier capture model based on multi-level energies. Moreover, the hole capture rate is found to be much greater than that of the electron, and the absorption cross-section of the defect state is at least 10 times larger than that of free carrier. Our findings not only clarify the relationship between intrinsic defects and photogenerated carrier dynamics, but also show the importance in the application of &lt;i&gt;β&lt;/i&gt;-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; crystals in ultrafast and broadband photonics.

Surface-plasmon-enhanced ethanol electrocatalysis and enhancement mechanism of nanoporous AuPd with wide-spectrum response characteristics under visible light irradiation

Localized surface plasmon resonance of Au enhanced catalytic performances of NP AuPd towards ethanol oxidation reaction. In situ-irradiated XPS and ultrafast transient absorption spectroscopy proved the hot electron transfer from Au to Pd.

Photoactivated plasmonic nanohybrid fibers with prolonged trapping of excited charge carriers for SERS analysis of biomolecules.

The quest to enhance Raman spectroscopic signals through the rational design of plasmonic substrates has enabled the detection and characterization of pharmaceutically important molecules with low scattering cross-sections, such as amino acids and proteins, and is helping in making forays into the diverse field of biomedical sciences. This work presents a simple strategy for synthesizing silver nanoparticles-incorporated alumina nanofibers (Ag-AlNFs) utilizing controlled microwave synthesis for enhancing the surface-enhanced Raman chemical enhancement factor through photo-induced charge accumulation at the plasmonic-dielectric interface. The plasmonic-dielectric fibers serve as excellent charge carrier trappers, as evident from the ultrafast transient absorption spectroscopy studies. Apart from chemical enhancement, the increase in electronic surface charge also enables the protein disulfide bonds to capture these electrons and form a transient disulfide electron adduct radical, which converts to free thiol radical on dissociation. This allows protein molecules to bind to the nanoparticle's surface with the favorable silver thiol bond leading to greater surface affinity and larger SERS enhancement. The proposed Ag-AlNFs represent a cost-effective material that can be potentially used to probe biological systems in a label-free manner by photoactivating the SERS substrate for obtaining higher enhancement factors.

Understanding the polaron behavior in Cs2CuSbCl6 halide double perovskite.

Lead-free halide double perovskites A2MM'X6 (A = Rb+, Cs+, etc.; M = Ag+, K+, Li+; M' = Sb3+, In3+ or Bi3+ and X = I-, Br- or Cl-) have recently been suggested as an alternative to lead-based halide perovskites for optoelectronic and photovoltaic applications. While a great deal of effort has been put into device engineering to improve the performance of photovoltaic and optoelectronic devices that are based on A2MM'X6 double perovskites, there has been relatively little attention given to their inherent photophysical properties. The current research demonstrates that small polaron formation under photoexcitation and polaron localization limit the carrier dynamics in the Cs2CuSbCl6 double halide perovskite. In addition, temperature-dependent AC conductivity measurements indicate that single polaron hopping is the primary conduction mechanism. The ultrafast transient absorption spectroscopy results revealed that the formation of small polarons, which function as self-trapped states (STSs) and result in the ultrafast trapping of charge carriers, are caused by a distorted lattice under photoexcitation. These findings provide a thorough understanding of the intrinsic restrictions of Cs2CuSbCl6 perovskite and could have relevance for other antimony-based semiconductors.

Effects of Proaromaticity on Excited-State Lifetimes and Charge Separation in Near-Infrared Sensitizer Dyes in Solution and on TiO2

The influence of proaromaticity on the excited state dynamics of near-infrared (NIR)-absorbing sensitizer dyes is explored using a combination of ultrafast transient absorption spectroscopy (TAS) and computational chemistry. The addition of a proaromatic π-bridge was found to stabilize the excited state and lead to lower excitation energies in solution and longer excited-state lifetimes, contrary to what is expected by the energy gap law. When studied under standard device conditions on TiO2, it was found that the dye structure plays a significant role in determining excited-state dynamics. Computational chemistry results confirm the proaromatic nature of the dyes through both bond length analyses and nucleus-independent chemical shift (NICS) calculations. Through incorporation of excited-state aromaticity, a 10× increase in excited-state lifetime was observed for dyes with a near 0.5 V lower energy excited state.

Triplets with a Twist: Ultrafast Intersystem Crossing in a Series of Electron Acceptor Materials Driven by Conformational Disorder.

Control over the populations of singlet and triplet excitons is key to organic semiconductor technologies. In different contexts, triplets can represent an energy loss pathway that must be managed (i.e., solar cells, light-emitting diodes, and lasers) or provide avenues to improve energy conversion (i.e., photon upconversion and multiplication systems). A key consideration in the interplay of singlet and triplet exciton populations in these systems is the rate of intersystem crossing (ISC). In this work, we design, measure, and model a series of new electron acceptor molecules and analyze them using a combination of ultrafast transient absorption and ultrafast broadband photoluminescence spectroscopies. We demonstrate that intramolecular triplet formation occurs within several hundred picoseconds in solution and is accelerated considerably in the solid state. Importantly, ISC occurs with sufficient rapidity to compete with charge formation in modern organic solar cells, implicating triplets in intrinsic exciton loss channels in addition to charge recombination. Density functional theory calculations reveal that ISC occurs in triplet excited states characterized by local deviations from orbital π-symmetry associated with rotationally flexible thiophene rings. In disordered films, structural distortions, therefore, result in significant increases in spin-orbit coupling, enabling rapid ISC. We demonstrate the generality of this proposal in an oligothiophene model system where ISC is symmetry-forbidden and show that conformational disorder introduced by the formation of a solvent glass accelerates ISC, outweighing the lower temperature and increased viscosity. This proposal sheds light on the factors responsible for facile ISC and provides a simple framework for molecular control over spin states.

InP/ZnSeS/ZnS Core–Shell Quantum Dots as Novel Saturable Absorbers in Mode‐Locked Fiber Lasers

AbstractIn this study, red light emitting InP/ZnSeS/ZnS quantum dots (QDs) are prepared by thermal injection method. The results show that the InP/ZnSeS/ZnS QDs saturable absorbers (SA) have good nonlinear saturable absorption properties with modulation depth of 24.2% and saturation intensity of 0.08 KW cm−2. Then the QD SAs are applied to the erbium‐doped fiber laser (EDFL) ring cavity system, and a mode‐locked laser pulse with a pulse width of 635 fs is generated. In addition, the pulse width is determined by the carrier recovery time, which is closely related to the defect density in the material. A large number of defects are eliminated in the QDs by hydrogen fluoride (HF) treatment, and the pulse width is reduced from 635 to 450 fs. Results of time‐resolved photoluminescence and ultrafast transient absorption spectroscopy (TAS) show that HF treatment indeed reduces defects in InP/ZnSeS/ZnS QDs, indicated by the decrease of the carrier recovery time. This is different from the reported 2D SA materials, which usually reduce the carrier recovery time by increasing the defect density. This study will inspire new applications of QDs in ultrafast photonics and nonlinear optics.

Vacancy Pair-Induced Charge Rebalancing with Surface and Interfacial Dual Polarization for CO2 Photoreduction

Poor charge kinetics greatly reduce the efficiency of photocatalytic CO2 reduction. Herein, a synchronous surface and interfacial dual polarization strategy was developed to promote charge separation. Bi–O vacancy pairs in Bi24O31Br10 atomic layers can trigger strong coupling between black phosphorus (BP) and Bi24O31Br10, forming a restructured closely contacted BP–Bi24O31Br10 configuration with a charge-redistributed interface via electronegativity-induced charge rebalancing. The Bi–O vacancy pairs on the surface of Bi24O31Br10 and restructured BP/Bi24O31Br10 interface enable synchronous surface and interfacial dual polarization, creating an electronic bridge from the interior of Bi24O31Br10 to the BP surface, as proven by ultrafast transient absorption spectroscopy. This configuration favors a low CO2 activation energy barrier, effectively stabilizes COOH* intermediates, and decreases the rate-determining step energy barrier. Benefiting from these features, the stable CO generation rate of optimized BP–Bi24O31Br10 reaches up to 39.8 μmol g–1 h–1 via CO2 photoreduction in water, which is 2.4 and 46.8 times higher than those of defective Bi24O31Br10 atomic layers and defect-poor Bi24O31Br10, respectively. This study provides insights into the synchronous design of surface defects and restructured interfaces for dual polarization.