Thermal Annealing Treatment Research Articles

Triazine derivative as volatile solid additive for non‐halogenated solvent and thermal annealing‐free processed organic solar cells with over 18% efficiency

AbstractVolatile solid additive (VSA) has been demonstrated to be an effective strategy to optimize the morphology of the active layer for high‐performance organic solar cells (OSCs). Most of the reported OSCs with VSA are processed by chloroform (CF) and relies on thermal annealing (TA) posttreatment. However, the CF solvent problems of low boiling point, toxicity, and environmental‐unfriendly as well as increasing cost from TA restricted the large‐scale production. Here, a simple‐structured and low‐cost triazine derivative 2,4,6‐trichloro‐1,3,5‐triazine (TCT) as a VSA was introduced into PM6:BTP‐eC9‐based OSCs. Employing the TCT additive, the nonhalogenated solvent (o‐xylene) processed OSCs without TA treatment and delivered higher power conversion efficiencies (PCEs) in comparison to the TA‐treated counterpart. Benefiting from the intermolecular interactions between TCT and the active layer materials, the TCT‐treated blend films exhibited optimized morphology and enhanced crystallinity. As a result, the PM6:BTP‐eC9 OSCs achieved a champion PCE of 18.18% and fill factor (78.5%), which is among one of the most advanced nonhalogenated solvent‐processed and annealing‐free OSCs. Meanwhile, the TCT‐treated blend films also demonstrated the better photo‐stability compared to the control device. This work provides a guideline of triazine derivatives as VSA for high‐performance OSCs with TA‐free and nonhalogenated solvent‐processing treatment.

Ethanol Processable Inorganic-Organic Hybrid Hole Transporting Layers Enabled 20.12 % Efficiency Organic Solar Cells.

In this study, a high-performance inorganic-organic hybrid hole transporting layer (HTL) was developed using ethanol-soluble alkoxide precursors and a self-assembled monolayer (SAM). Three metal oxides-vanadium oxide (VOx), niobium oxide (Nb2O5), and tantalum oxide (Ta2O5)-were synthesized through successive low-temperature (100 °C) thermal annealing (TA) and UV-ozone (UVO) treatments of their respective precursors: vanadium oxytriethoxide (EtO-V), niobium ethoxide (EtO-Nb), and tantalum ethoxide (EtO-Ta). Among these, the Nb2O5 film exhibited excellent transmittance, a high work function, and good conductivity, along with a more compact and uniform structure featuring fewer interfacial defects, which facilitated efficient charge extraction and transport. Furthermore, the deposition of a SAM of (2-(9H-carbazol-9-yl)ethyl)phosphonic acid (2PACz) on top of Nb2O5 further passivated defects, enhancing interfacial contact with the photoactive layer. The resulting inorganic-organic hybrid HTL of Nb2O5/2PACz demonstrated excellent compatibility with various photoactive blends, achieving impressive power conversion efficiencies of 19.44 %, 19.18 %, and 20.12 % for the PM6:L8-BO, PM6:BTP-eC9, and D18:BTP-eC9 based organic solar cells, respectively. 20.12 % is the best performance for bulk heterojunction organic solar cells with binary components as the photoactive layer.

Gradual Optimization of Molecular Aggregation and Stacking Enables Over 19% Efficiency in Binary Organic Solar Cells.

Volatile solid additive is an effective and simple strategy for morphology control in organic solar cells (OSCs). The development of environmentally friendly new additives which can also be easily removed without high-temperature thermal annealing treatment is currently a trend, and the working mechanism needs to be further studied. Herein, a highly volatile and non-halogenated solid additive 1-benzothiophene (BBT) is reported to regulate molecular aggregation and stacking of active layer components. According to the film-forming kinetics process, a momentary intermediate phase is formed during spin-coating, which slows down the film-forming process and leads to more ordered molecular stacking in the solid film after introducing solid additive BBT. Subsequently, after solvent vapor annealing (SVA) further treatment, the resultant blend films exhibit a tighter and more ordered molecular stacking. Consequently, the synergistic effect of solid additive BBT and SVA treatment can effectively control morphology of active layer and improve carrier transport characteristics, thereby enhancing the performance of OSCs. Finally, in D18-Cl:N3 system, an impressive power conversion efficiency of 19.53% is achieved. The work demonstrates that the combination of highly volatile solid additives and SVA treatment is an effective morphology control strategy, guiding the development of efficient OSCs.

Morphological improvement of a novel & non-toxic double perovskite MA2NaBiCl6 by thermal annealing treatment: Enhanced the PCE of solar cell device

Morphological improvement of a novel & non-toxic double perovskite MA2NaBiCl6 by thermal annealing treatment: Enhanced the PCE of solar cell device

Effect of post-annealing treatment on structural, optical and photocatalytic properties of TiO2 nanoparticles prepared via pulsed laser ablation in liquid

Ultrasmall TiO2 nanoparticles were synthesized through pulsed laser ablation of a metal titanium target in liquid followed by thermal annealing treatment. The impact of post-annealing treatment on the structural, morphological, optical properties, and the photocatalytic activity of the synthesized TiO2 nanoparticles have been investigated through a variety of analytical techniques, including X-Ray diffraction, transmission electron microscopy, ultraviolet-visible diffusion reflectance spectra, X-ray photoelectron spectroscopy. The results reveal that annealing temperature significantly improved the crystallinity of laser ablated TiO2 nanoparticles and modified the chemical states of surface elements. Defects introduced by laser ablation, which serve as electron traps, combined with enhanced crystallinity resulting from thermal annealing, have improved the photocatalytic degradation performance of TiO2 nanoparticles. Specifically, TiO2 nanoparticles annealed at 300 ℃ exhibited optimal photocatalytic performance in decomposition of model dye under the irradiation from xenon lamp, demonstrating the critical role of annealing in improving photocatalytic properties. This study not only broadens the comprehension of the impact of post-treatment on the characteristics of laser-ablated TiO2 nanoparticles nanoparticles but also highlights their potential for effective wastewater remediation.

Enhanced Performance of Polymer Solar Cells by Ultraviolet-Ozone Treatment of MoOX Films with non-Thermal Annealing Treatment of MoOX Films

Molybdenum oxide (MoOX) is a commonly used hole extraction material (HEL) in polymer solar cells (PSCs). Here, we perform ultraviolet ozone treatment (UVO, non-thermal annealing treatment) on MoOX film (by spin-coated (NH4)6Mo7O24-4H2O solution on the ITO top) prepared by solution processing to develop hole extraction materials for efficient PSC. After UVO treatment of MoOX films (US-MoOX), the (NH4)6Mo7O24-4H2O molecules decompose to form a denser and higher energy levels MoOX film. Compared with E-MoOX films (vacuum evaporated MoO3 powder), US-MoOX films have similar square resistance and electrical conductivity to E-MoOX films, and the photovoltaic performance of US-MoOX-based PSCs is comparable to that of E-MoOX-based PSCs and higher than that of PEDOT:PSS-based PSCs. Therefore, US-MoOX-based PSCs show the advantages of combining high photovoltaic performance with solution processing. In addition, US-MoOX-based PSCs have the advantage of not requiring thermal annealing treatment. The results indicate that US-MoOX films are promising HEL materials for the practical production of PSCs.

Thermoluminescence and ATR-FTIR study of UVC-irradiated low-density polyethylene (LDPE) food packaging

This research aims to study the effects of ultraviolet C (UVC) radiation on low-density polyethylene (LDPE) food packaging. Main objectives include evaluating LDPE degradation and detecting UVC radiation using thermoluminescent dosimeters (TLDs) placed under LDPE samples. Results confirm accurate UVC detection after one hour of exposure, providing a useful tool for optimize food treatment procedures.ATR-FTIR spectroscopy analysis revealed subtle alterations (<8 % transmittance relative) in UVC-irradiated LDPE samples, including possible CH breakage (2910 and 2848 cm−1) and potential CC bond vibrations (1470 cm−1), among others. However, observed variations may stem from LDPE properties rather than entirely from UVC radiation. A comparative study of UVC-induced thermoluminescence (TL) emissions provided insights into various TLDs materials. TL kinetic analysis, using computerised glow curve deconvolution (CGCD) method, unveiled trap charge activation due to UVC exposure, including partial ionization, bleaching effect and photo-transfer (PTTL) processes. LDPE samples amplified UVC-TL responses, revealing intensity differences between the TLDs attributed to the PTTL process, accentuated by the lack of an annealing treatment. Additionally, chemical composition of the TL detectors such as, type, concentration, number, oxidation states and ionic radii of their dopants may influence UVC-TL response. Consequently, TL intensity ratios follow as: GR-200 (LiF: Mg, Cu, P) > TLD-100 (LiF: Ti, Mg) > TLD-400 (CaF2: Mn) > TLD-200 (CaF2: Dy). Thus, GR-200 detects ionizing radiation but cannot distinguish between ionizing and non-ionizing UVC radiation, while TLD-100 has limited effectiveness as a UVC radiation detector. In contrast, TLD-400 is suitable for detecting UVC radiation and TLD-200 emerges as the most favorable UVC detector, showing consistent response levels and minimal PTTL effect placed under the LDPE samples without the need of a thermal annealing treatment that makes the TLD-200 to be reusable in a low-cost measurement protocol.

Self-Assembled Chiral Polymers Exhibiting Amplified Circularly Polarized Electroluminescence.

Circularly polarized electroluminescence (CPEL) is highly promising in realm of 3D display and optical data storage. However, designing a groundbreaking chiral material with high comprehensive CPEL performance remains a formidable challenge. In this work, a pair of chiral polymers with self-assembled behavior is designed by integrating a chiral BN-moiety into polyfluorene backbone, named R-PBN and S-PBN, respectively. The chiral polymers show narrowband emission centered at 490 nm with full-width half maximum (FWHM) of 29 nm and high photoluminescence quantum yield (PLQY) of 79 %. After thermal annealing treatment, the chiral polymers undergo self-assembly, exhibiting amplified circularly polarized luminescence (CPL) with asymmetry factor (|glum|) of up to 0.11. Moreover, the solution-processed nondoped CP-OLEDs based on the chiral polymers as emitting layers exhibit maximum external quantum efficiency (EQEmax) of 9.8 %, intense CPEL activities with |gEL| of up to 0.07, and small FWHM of 36 nm, simultaneously. This represents the first case of self-assembled chiral polymers that combines high EQE, large gEL value and narrowband emission.

Self‐Assembled Chiral Polymers Exhibiting Amplified Circularly Polarized Electroluminescence

Circularly polarized electroluminescence (CPEL) is highly promising in realm of 3D display and optical data storage. However, designing a groundbreaking chiral material with high comprehensive CPEL performance remains a formidable challenge. In this work, a pair of chiral polymers with self‐assembled behavior is designed by integrating a chiral BN‐moiety into polyfluorene backbone, named R‐PBN and S‐PBN, respectively. The chiral polymers show narrowband emission centered at 490 nm with full‐width half maximum (FWHM) of 29 nm and high photoluminescence quantum yield (PLQY) of 79%. After thermal annealing treatment, the chiral polymers undergo self‐assembly, exhibiting amplified circularly polarized luminescence (CPL) with asymmetry factor (|glum|) of up to 0.11. Moreover, the solution‐processed nondoped CP‐OLEDs based on the chiral polymers as emitting layers exhibit maximum external quantum efficiency (EQEmax) of 9.8%, intense CPEL activities with |gEL| of up to 0.07, and small FWHM of 36 nm, simultaneously. This represents the first case of self‐assembled chiral polymers that combines high EQE, large gEL value and narrowband emission.

Phase Transformation on Multilayer 2M-WS2 for Improved Surface-enhanced Raman Scattering.

In recent years, two-dimensional (2D) transition metal dichalcogenides (TMDCs) have been widely recognized as an ideal platform for surface-enhanced Raman scattering (SERS). Given their rich structural phases, phase transformation in 2D TMDCs is an efficient strategy to tailor their SERS performance. In this paper, we present the great SERS performance of multilayer 2M-WS2 and then investigate the effect of its phase transformation on SERS performance. It is observed that multilayer 2M-WS2 nanosheets undergo a thermally induced single-crystal phase transition from 2M-WS2 to 2H-WS2 upon thermal annealing or laser treatment. Distinguishing from the commercially available pure 2H-WS2 (P-2H-WS2), 2H-WS2 obtained by annealing and laser treatment still retain SERS properties comparable to those of 2M-WS2, among which the detection limits for CV molecules (10-8 M) are 3 orders of magnitude lower than that of P-2H-WS2 and the Raman intensity enhancements are ∼10-37 times higher. In contrast to the charge transfer (CT) mechanism governed by the Fermi level in metallic-phase 2M-WS2, 2H-WS2 obtained by phase transition exhibits accelerated CT facilitated by the bandgap reduction and reorganization resulting from the abundance of vacancies. This study introduces an interesting perspective and potential avenue for enhancing SERS through metal-to-semiconductor phase transitions in 2D TMDCs materials.

Spin coating high‐k multicomponent (Al,Ti,V,Zr,Hf)Ox films with sub‐nm EOT for MOS‐based electronic devices

AbstractThe facile spin coating fabrication of high‐dielectric‐constant (high‐k) multicomponent (Al,Ti,V,Zr,Hf)Ox films with an equivalent oxide thickness of ≈0.95 nm and the investigation of their thermal stability and dielectric and electrical properties of the resulting advanced metal–oxide–semiconductor (MOS)‐based electronic devices are reported in this study. Various heating conditions, including drying following spin coating, annealing after drying, and forming gas annealing, were investigated to optimize the quality of the films and reduce film defects. The favorable film‐based MOS devices exhibited robust capacitance–voltage (C–V) and current–voltage (I–V) characteristics with a remarkable k value of approximately 62 at 1 kHz. The thermal stability of the films was affirmed through a rapid thermal annealing treatment at 900°C for 5 s and observation of nondegraded C–V and I–V curves. The electrical performance of the resulting MOS field‐effect transistors (MOSFETs), including a threshold voltage of 0.4 V, an on/off ratio of 106, a saturated mobility of 40.1 cm2 V−1 s−1, and a subthreshold swing of 66.7 mV dec−1, was obtained. Moreover, hole‐ and electron‐trapping measurements through negative and positive gate bias stress instabilities, respectively, indicate the reliable performance of our MOSFETs. Our results imply that solution‐based processes are promising for fabricating fundamental semiconductor devices.

Understanding the impact of thiazole unit sequence in π-bridge on the performance of small molecule donor materials

Energy level regulation and crystallization optimization of materials are the key ideas to improve the performance of organic solar cells. In this work, based on clarifying small molecule structure, we introduce thiazole into different positions of π-bridge and investigate its effect on the properties of small molecule donors (SMDs) and related device performance. As thiazole gradually moves towards BDT, the electron clouds of these three SMDs (BTTTzR, BTTzTR and BTzTTR) tend to be divided on the framework, gradually deepened the energy level, and enlarged band gaps. In terms of device performance, the BTTzTR:Y6 device shows good inhibition of charge recombination and phase separation performance, and the efficiency of the related OSCs is 7.87 %. Morphological analysis shows that BTTTzR is prone to form nanoscale microcrystals after thermal annealing treatment, with slightly decreased performance of 6.79 %. BTzTTR is affected by difficult intramolecular charge transfer and weak intermolecular interactions, shows the worst performance of 5.77 %. This work is conducive to a deeper understanding of the electron-deficient substitution of the π-bridge in SMDs.

Amplified Circularly Polarized Luminescence Behavior in Chiral Co-assembled Liquid Crystal Polymer Films via the Strategic Manipulation of Chiral Inducers.

One of the most important factors for the future application of circularly polarized luminescence (CPL) materials is their high dissymmetry factors (gem), and more and more studies are working tirelessly to focus on increasing the gem value. Herein, we chose an achiral liquid crystal polymer (LC-P) and two chiral binaphthyl-based inducers (R/S-3 and R/S-6) with different substitution positions (3,3' positions for R/S-3 and 6,6' positions for R/S-6) to construct chiral co-assemblies and explored their induced amplification CPL behaviors. Interestingly, after the thermal annealing treatment, this kind of chiral co-assembly (R/S-3)0.05-(LC-P)0.95 can emit a superior CPL signal (|gem| = 0.31 and λem = 424 nm), which achieves about 13-fold signal amplification in the spin-coated film, compared to (R/S-6)0.1-(LC-P)0.9 (|gem| = 0.023 and λem = 424 nm). This is because (R/S-3)0.05-(LC-P)0.95 could further co-assemble to form a more ordered arrangement LC state and generate regular helix nanofibers than that of (R/S-6)0.1-(LC-P)0.9. This work provides an efficient method for synthesizing high-quality CPL-active materials through the strategic manipulation of the structure of chiral binaphthyl-based inducers in chiral co-assembled LCP systems.

Optimization of p-type contact for electrical injection and light extraction for 365 nm UV-A LEDs

This paper demonstrates low-resistance and high-transparency p-type contact materials for ultraviolet (UV) micro-light-emitting diodes (LEDs) at 365 nm. As a commonly used p-type LED contact, indium tin oxide (ITO) and nickel/ITO (Ni/ITO) contacts were studied before and after rapid thermal annealing (RTA) treatments. The transmittance at 365 nm wavelength of 200 nm thick ITO films increased from approximately 57%–90% after RTA at a temperature exceeding 400 °C, while the Ni/ITO film had a transmittance of about 73% after annealing. Micron-sized UV-LEDs with Ni/ITO p-contact were fabricated. Electrical characterization shows that Ni/ITO films annealed at 600 °C demonstrated good ohmic contact behavior and the highest on-wafer external quantum efficiency, despite slightly lower transmittance. This paper shows the potential of annealed Ni/ITO films as promising p-contact materials for high-performance 365 nm UV-LEDs.

Vertically Concentrated Quantum Wells Enabling Highly Efficient Deep‐Blue Perovskite Light‐Emitting Diodes

AbstractDeep‐blue perovskite light‐emitting diodes (PeLEDs) based on quasi‐two‐dimensional (quasi‐2D) systems exist heightened sensitivity to the domain distribution. The top‐down crystallization mode will lead to a vertical gradient distribution of quantum well (QW) structure, which is unfavorable for deep‐blue emission. Herein, a thermal gradient annealing treatment is proposed to address the polydispersity issue of vertical QWs in quasi‐2D perovskites. The formation of large‐n domains at the upper interface of the perovskite film can be effectively inhibited by introducing a low‐temperature source in the annealing process. Combined with the utilization of NaBr to inhibit the undesirable n=1 domain, a vertically concentrated QW structure is ultimately attained. As a result, the fabricated device delivers a narrow and stable deep‐blue emission at 458 nm with an impressive external quantum efficiency (EQE) of 5.82 %. Green and sky‐blue PeLEDs with remarkable EQE of 21.83 % and 17.51 % are also successfully achieved, respectively, by using the same strategy. The findings provide a universal strategy across the entire quasi‐2D perovskites, paving the way for future practical application of PeLEDs.

Vertically Concentrated Quantum Wells Enabling Highly Efficient Deep-Blue Perovskite Light-Emitting Diodes.

Deep-blue perovskite light-emitting diodes (PeLEDs) based on quasi-two-dimensional (quasi-2D) systems exist heightened sensitivity to the domain distribution. The top-down crystallization mode will lead to a vertical gradient distribution of quantum well (QW) structure, which is unfavorable for deep-blue emission. Herein, a thermal gradient annealing treatment is proposed to address the polydispersity issue of vertical QWs in quasi-2D perovskites. The formation of large-n domains at the upper interface of the perovskite film can be effectively inhibited by introducing a low-temperature source in the annealing process. Combined with the utilization of NaBr to inhibit the undesirable n=1 domain, a vertically concentrated QW structure is ultimately attained. As a result, the fabricated device delivers a narrow and stable deep-blue emission at 458 nm with an impressive external quantum efficiency (EQE) of 5.82 %. Green and sky-blue PeLEDs with remarkable EQE of 21.83 % and 17.51 % are also successfully achieved, respectively, by using the same strategy. The findings provide a universal strategy across the entire quasi-2D perovskites, paving the way for future practical application of PeLEDs.

Synergistic strategies to unveil the dual influence of additive and annealing treatment on the morphology of isatin-derived low bandgap small molecule donor in solution-processed organic solar cells

A novel organic small molecule, 5-(4-(diphenylamino)phenyl)-1-octylindoline-2,3-dione (TPI) containing an alkyl chain substituted electron accepting isatin (indoline-2,3-dione) and strong electron withdrawing N, N-diphenylaniline units have been synthesized through Suzuki coupling reaction. The molecular structure of TPI is confirmed by NMR, FT-IR, and Mass spectroscopy techniques. The TPI molecule exhibits a low band gap of approximately ∼ 2.03 eV which is also supported by the DFT results. The influence of additive and heat treatment on the electronic, morphological, and photovoltaic performance of organic solar cells was investigated meticulously. The TPI donor exhibits complementary light absorption with fullerene acceptor in combination with DIO and TA which efficiently absorb the photon in the 300–730 nm range. The TPI was later used as an electron donor material for the fabrication of organic solar cells. Remarkably, the morphology-dependent optimized TPI:PC71BM (1:3.0) exposed excellent power conversion efficiency (PCE) of about ∼ 5.56 % with enhanced VOC of ∼ 0.811 V, JSC of 11.81 mA cm−2 and FF of 55.3 % fabricated in addition with DIO and thermal annealing treatment. Most importantly, the unencapsulated devices maintained > 96 % of the initial PCE value after 240 h under ambient temperature. Our findings indicate that isatin-derived small molecules with simple architecture propose great potential for promising BHJ-OSCs material.

Optimization of transparent conductive properties of magnetron sputtered Sb-doped SnO2 films by RF power: Towards application in polymer-dispersed liquid crystal (PDLC) films

Sb-doped SnO2 (ATO) films were prepared with different RF powers (PRF) under two O2 flow rates (FO2) by magnetron sputtering, and then subjected to rapid thermal annealing (RTA) treatment. The effects of PRF, FO2, and RTA on the crystallinity, stress, surface morphology, conductive properties, transmittance in visible-light range (TVis), and energy gap (Eg) of the films were investigated. As the PRF increases, the film crystallinity improves or first improves and then slightly degrades, and the compressive stress decreases. With increasing PRF, the surface changes from textured to granular morphology and from granular to honeycomb-like morphology under two FO2, respectively. Meanwhile, the conductive properties first enhance and then degrade, and the TVis and Eg tend to decrease, especially at higher PRF. Basically, the films prepared with higher FO2 have lower compressive stress, inferior conductive properties, and larger TVis and Eg compared with the films prepared with lower FO2. After RTA, the film crystallinity obviously improves, the compressive stress transforms into tensile stress, and the surface morphology has not undergone significant changes. Meanwhile, the conductive properties significantly enhance and Eg obviously increases. The TVis of the films prepared with lower FO2 can be increased by RTA. The influence mechanisms of the above factors on the structure and optoelectronic properties of the ATO films were explored, and ultimately, the ATO films have the TVis of 76.35–80.86%, sheet resistance of 51.7–91.9 Ω/sq., and quality factor of 1.03–1.67 × 10−3 Ω−1 within the optimized PRF range. Polymer-dispersed liquid crystal (PDLC) films were fabricated using optimized performance ATO films as electrodes, and their on-state transmittance, off-state transmittance, threshold electric field, and saturation electric field were 2.08–4.61%, 61.69–68.56%, 0.656–0.796 V/μm, and 1.68–2.108 V/μm, respectively. The current results indicate the potential application of ATO films in PDLC films as electrode.

Vanadyl Sulfate Based Hole‐Transporting Layer Enables Efficient Organic Solar Cells

Comprehensive SummaryIt remains an urgent task to develop alternative hole‐transporting layer (HTL) materials beyond commonly used PEDOT:PSS to increase the shelf‐life of organic solar cells (OSCs). Inorganic metal oxide type materials, such as NiOx, CoOx and VOx, with suitable work functions have attracted numerous research attention recently. In this work, more abundant and easily accessible oxygenated salt, vanadyl sulfate (VOSO4) has been demonstrated to be excellent choice as HTL for OSCs. The VOSO4‐based HTL can be readily processed by spin‐coating from the precursor solution with subsequent thermal annealing and UVO treatment. As a consequence, a high power conversion efficiency (PCE) of 18.72% can be achieved for PM8:L8‐BO based OSCs with the VOSO4‐based HTL. High transmittance, smooth film surface, suitable energy level and high conductivity were revealed to contribute to the high OSC performance. More importantly, compared to device with PEDOT:PSS, VOSO4‐based OSCs exhibit improved stability when stored in the N2 filled glove box. After being stored for 600 h, VOSO4‐based device can retain 89% of its initial efficiency. Notably, VOSO4 can be used as general HTL in PM6:BTP‐BO‐4Cl and PM6:IT‐4F based OSCs, yielding high PCEs of 17.87% and 13.85%, respectively.

Efficient all-small-molecule organic solar cells processed with non-halogen solvent

All-small-molecule organic solar cells with good batch-to-batch reproducibility combined with non-halogen solvent processing show great potential for commercialization. However, non-halogen solvent processing of all-small-molecule organic solar cells are rarely reported and its power conversion efficiencies are very difficult to improve. Herein, we designed and synthesized a small molecule donor BM-ClEH that can take advantage of strong aggregation property induced by intramolecular chlorine-sulfur non-covalent interaction to improve molecular pre-aggregation in tetrahydrofuran and corresponding micromorphology after film formation. Tetrahydrofuran-fabricated all-small-molecule organic solar cells based on BM-ClEH:BO-4Cl achieved high power conversion efficiencies of 15.0% in binary device and 16.1% in ternary device under thermal annealing treatment. In contrast, weakly aggregated BM-HEH without chlorine-sulfur non-covalent bond is almost inefficient under same processing conditions due to poor pre-aggregation induced disordered π-π stacking, indistinct phase separation and exciton dissociation. This work promotes the development of non-halogen solvent processing of all-small-molecule organic solar cells and provides further guidance.