Small Molecular Materials Research Articles

Non-Aqueous Calcium-Based Dual-Ion Batteries with an Organic Electrode of High-Rate Performance

Energy issues have become one of the most critical topics in human society to maintain sustainable development. More specifically, the increasing demand for energy speeds up the evolution of energy storage devices, such as batteries and supercapacitors. Accordingly, lithium-ion batteries became the mainstream energy storage device because of the high demands of electric vehicles and diverse electronic devices. However, the subsequent concerns regarding the abundance, safety, cost, efficiency, and sustainability issues behind the vast daily energy demands initiate the research on the post-lithium-ion batteries in the recent decade. Among them, multivalent batteries based on calcium ions draws lots of attention as a promising energy storage system due to its high earth abundance and improved ionic mobility compared to magnesium ions. Nevertheless, the critical challenge is to solve the incompatibility between the metallic calcium electrode and conventional electrolytes as well as the scarcity of high-rate performance electrode materials for hosting calcium ions simultaneously to construct a practical energy storage device.Herein, we firstly investigate a small molecular organic material, 3,4,9,10-perylenetetracarboxylic diimide (PTCDI), as the calcium-ion host for calcium-ion batteries (CIBs) in the non-aqueous electrolyte. Spectroscopic, structural, and computational studies reveal that PTCDI with an enhanced Ca2+-storage degree can increase the solubility of reduced PTCDI due to the reduced π-π interaction, suppressed by the saturated electrolyte owing to the high redeposition rate to form a PTCDI film with strengthened hydrogen bonds, which facilitates a fast enolization reaction for Ca2+ storage. Furthermore, the compatibility issue among the metallic Ca, conventional calcium-based electrolyte, and PTCDI was unraveled by employing graphite type material, namely mesocarbon microbead (MCMB), as the positive electrodes for facilitating anion intercalation, as opposed to the utilization of calcium metal negative electrode for Ca2+ plating/stripping. Consequently, a cell assembled with the PTCDI negative electrode and carbon-based positive electrode, as illustrated in Figure 1, exhibits a high-power density >3000 W kg-1, a high energy density of ~150 Wh kg-1, and superior reversible capacity of 80 mAh g-1 at 5 A g-1. The assembled CIB even demonstrates the high-rate performance (90 mAh g-1 at 1 A g-1) and ultra-stable cyclability over 4000 cycles with negligible decay at -10 °C, suggesting the promising future as low-temperature batteries. Figure 1

Integrating Molecular Motions in Ternary Cocrystals for NIR‐II Photothermal Conversion

Organic photothermal conversion materials hold immense promise for various applications owing to their structural flexibility. Recent research has focused on enhancing near‐infrared (NIR) absorption and mitigating radiative transition processes. In this study, we have developed a viable approach to the design of photothermal conversion materials through the construction of ternary organic cocrystals, by introducing a third component as a molecular blocker and motion unit into a binary donor–acceptor system. Superstructural and photophysical properties of the ternary cocrystals were characterized using various spectroscopic techniques. The role of the molecular blocker in radical stabilization and photothermal conversion were demonstrated. Intriguingly, the motions of the entire pyrene molecules in the cocrystal have been observed by variable temperature single‐crystal X‐ray diffraction results. The excellent performance of ternary cocrystal as a photothermal material was validated through efficient NIR‐II photothermal and solar‐driven water evaporation experiments. The efficiency of water evaporation reached 88.7 %, with a corresponding evaporation rate of 1.29 kg m−2 h−1, representing excellent performance among pure organic small molecular photothermal conversion materials. Our research underscores the introduction of molecular blockers and motion units to stabilize radicals and produce outstanding photothermal conversion materials, offering new pathways for developing efficient and stable photothermal conversion materials.

Integrating Molecular Motions in Ternary Cocrystals for NIR-II Photothermal Conversion.

Organic photothermal conversion materials hold immense promise for various applications owing to their structural flexibility. Recent research has focused on enhancing near-infrared (NIR) absorption and mitigating radiative transition processes. In this study, we have developed a viable approach to the design of photothermal conversion materials through the construction of ternary organic cocrystals, by introducing a third component as a molecular blocker and motion unit into a binary donor-acceptor system. Superstructural and photophysical properties of the ternary cocrystals were characterized using various spectroscopic techniques. The role of the molecular blocker in radical stabilization and photothermal conversion was demonstrated. Intriguingly, the motions of the entire pyrene molecules in the cocrystal have been observed by the results of variable temperature single-crystal X-ray diffraction. The excellent performance of the ternary cocrystal as a photothermal material was validated through efficient NIR-II photothermal and solar-driven water evaporation experiments. The efficiency of water evaporation reached 88.7 %, with a corresponding evaporation rate of 1.29 kg m-2 h-1, representing excellent performance among pure organic small molecular photothermal conversion materials. Our research underscores the introduction of molecular blockers and motion units to stabilize radicals and produce outstanding photothermal conversion materials, offering new pathways for developing efficient and stable photothermal conversion materials.

Double-bridged N–B←N bipyridyl-based airfoil-shaped small molecule dyes: π-bridge regulation on photovoltaic performance

The double-bridged N–B←N bipyridine unit (BNBP) with boron-nitrogen covalent bond and coordination bond can reduce the electronic energy level of the π-conjugated system, resulting in a reduction of band gap and a red shift in the absorption spectrum. Embedding the BNBP building block into organic optoelectronic materials provides a novel possibility in molecule design. In this paper, under the guidance of density functional theory (DFT) calculations, a series of 3D “airfoil-shaped” small molecule donors (SMDs) have been designed and successfully synthesized through Sonogashira, Suzuki and Stille coupling reactions. BNBP is adopted as the central electron-withdrawing unit and strong electron-rich triphenylamine (TPA) as the terminal group. The novel “airfoil-shaped” structure plays a supporting role in reducing the carrier recombination in the active layer. It reveals that molecular design engineering can achieve the expected results by the following steps: Firstly, the introduction of electron-rich alkoxy groups into the end of TPA through side chain engineering helps to improve the solubility and film-forming properties of the materials. Then, the π-bridge regulation not only extends the conjugate structure, but also plays a crucial role in the regulation of photovoltaic properties. It is worth noting that the compound BNBP(3TTPA)2 was synthesized by introducing thiophene oligomer into BNBP-based SMDs for the first time. Finally, the compound BNBP(EDPPTPA)2 was constructed by combining BNBP with DPP dye unit. Its narrow band gap is only 1.36 eV, which is one of the narrowest band gaps in small molecular organic-boron materials. In particular, compared with the starting compound BNBP(ETPA)2, the synergistic effects of DPP and BNBP broaden the edge absorption wavelength to 814 nm, resulting in a red shift of 170 nm. The power conversion efficiency (PCE) of 4.48 % is obtained in BNBP(EDPPTPA)2-based bulk heterojunction (BHJ) organic solar cells (OSCs), which is more than twice that of reference compound BNBP(ETPA)2. This work provides important references for the future development of 3D BNBP-based organic-boron SMDs and the structural regulation of materials through molecular engineering.

Carrier mobility in organic semiconductors with an exponential density of states under the framework of admittance spectroscopy

The carrier transport in amorphous organic semiconductors with an exponential density of states is systematically studied under the framework of admittance spectroscopy. Due to the exponential distribution, the slope of the double logarithmic curve of current density versus voltage is expressed as b+2, where b relates to the width of the density of states. And the mobility is proportional to nb, where n is the density of carrier. In this case, the peak frequencies of the negative differential susceptance and imaginary part of impedance turn out to be functions of parameter b. Therefore, the relation between transit time and mobility will be a linear function of parameter b. Applying our model to interpret experimental data of both small molecular and polymeric materials are illustrated. The contributions of electric field and of carrier density to mobility are discussed.

Small molecular donor materials based on β-β-bridged BODIPY dimers with a triphenylamine or carbazole unit for efficient organic solar cells.

Herein, we have designed and synthesized two novel BODIPY dimer-based small molecules, denoted as ZMH-1 and ZMH-2, covalently linked and functionalized with triphenylamine (TPA) (ZMH-1) and carbazole (CZ) (ZMH-2) units as the electron donor at the 3- and 5-positions of the BODIPY core, respectively. Their optical and electrochemical properties were investigated. We have fabricated all small molecule bulk heterojunction organic solar cells using these BODIPY-based small molecules as electron donors along with fullerene derivative (PC71BM) and medium bandgap non-fullerene acceptor IDT-TC as electron acceptors. The optimized OSCs based on ZMH-1:PC71BM, ZMH-2:PC71BM, ZMH-1:IDT-IC, and ZMH-2:IDT-IC attain overall PCEs of 8.91%, 6.61%, 11.28%, and 5.48%, respectively. Moreover, when a small amount of PC71BM as guest acceptor is added to the binary host ZMH-1:IDT-TC and ZMH-2:IDT-TC, the ternary OSCs based on ZMH-1 and ZMH-2 reach PCEs of 13.70% and 12.71%, respectively.

A new type pyranthrene-based copolymer as a promising hole-transport material for perovskite solar cells

Perovskite solar cells (PSCs) with n-i-p configuration demonstrated rapid progress in the past few years, though the most efficient devices were made using doped small molecular hole-transport material, spiro-OMeTAD, which...

Recent advances in circularly polarized luminescence of planar chiral organic compounds.

Circularly polarized luminescence (CPL), as an important chiroptical phenomenon, can not only directly characterize excited-state structural information about chiroptical materials but also has great application prospects in 3D optical displays, information storage, biological probes, CPL lasers and so forth. Recently, chiral organic small molecules with CPL have attracted a lot of research interest because of their excellent luminescence efficiency, clear molecular structures, unique flexibility and easy functionalization. Planar chiral organic compounds make up an important class of chiral organic small molecular materials and often have rigid macrocyclic skeletons, which have important research value in the field of chiral supramolecular chemistry (e.g., chiral self-assembly and chiral host-guest chemistry). Therefore, research into planar chiral organic compounds has become a hotspot for CPL. It is time to summarize the recent developments in CPL-active compounds based on planar chirality. In this feature article, we summarize various types of CPL-active compounds based on planar chirality. Meanwhile, we overview recent research in the field of planar chiral CPL-active compounds in terms of optoelectronic devices, asymmetric catalysis, and chiroptical sensing. Finally, we discuss their future research prospects in the field of CPL-active materials. We hope that this review will be helpful to research work related to planar chiral luminescent materials and promote the development of chiral macrocyclic chemistry.

Self-assembled molecular network with waterwheel-like architecture: experimental and theoretical evaluation toward electron transport capabilities for optoelectronic devices.

In recent times, self-assembled electron transport materials for optoelectronic devices, both solar cells and organic light-emitting diodes (OLEDs), have been gaining much interest as they help in fabricating high-efficiency devices. However, designing organic small molecular materials with star-shaped self-assembled networks is a challenge. To achieve this sort of target, we chose triazine and benzene-1,3,5-tricarbonyl cores for developing such architecture, and we developed four molecular systems, vizTCpCN, TCmCN, TmCN, and TpCN. Successful isolation of single crystals followed by structural analysis of TmCN revealed interesting molecular arrangements in the solid state resulting in the formation of a waterwheel type architecture with an extended network bearing characteristic voids. Theoretical calculations was carried out to check their electron transportability. The natural transition orbital calculation helped in understanding the locally excited and charge transfer excited states. The low electron reorganization energies of these molecules indicated that these materials may have potential to be used in electron transport layers of optoelectronic devices, particularly in OLEDs. Moreover, the assembled networks have a relatively wide surface area and linked structures, which are advantageous for the conduction of carriers with poor electron recombination inside the ETL, and these may offer a straightforward channel for electron conduction to the emissive layer. Finally, the fabricated electron-only device indicated that the synthesized materials may be used as ETMs in the electron transport layer of optoelectronic devices.

Long Cycle Life for Rechargeable Lithium Battery using Organic Small Molecule Dihydrodibenzo[c,h][2,6]naphthyridine-5,11-dione as a Cathode after Isoindigo Pigment Isomerization.

Sustainability and adaptability in structural design of the organic cathodes present promises for applications in alkali metal ion batteries. Nevertheless, a formidable challenge lies in their high solubility in organic electrolytes, particularly for small molecular materials, impeding cycling stability and high capacity. This study focuses on the design and synthesis of organic small molecules, the isomers of (E)-5,5'-difluoro-[3,3'-biindolinylidene]-2,2'-dione (EFID) and 3,9-difluoro-6,12-dihydrodibenzo [c, h][2,6]naphthyridine-5,11-dione (FBND). While EFID, characterized by a less π-conjugated structure, exhibits subpar cycling stability in lithium-ion batteries (LIBs), intriguingly, another isomer, FBND, demonstrates exceptional capacity and cycling stability in LIBs. FBND delivers a remarkable capacity of 175mAhg-1 at a current density of 0.05Ag-1 and maintains excellent cycling stability over 2000 cycles, retaining 90% of its initial capacity. Furthermore, an in-depth examination of redox reactions and storage mechanisms of FBND are conducted. The potential of FBND is also explored as an anode in lithium-ion batteries (LIBs) and as a cathode in sodium-ion batteries (SIBs). The FBND framework, featuring extended π-conjugated molecules with an imide structure compared to EFID, proves to be an excellent material template to develop advanced organic small molecular cathode materials for sustainable batteries.

Evolution of the characterization of horizontally aligned organic light‐emitting molecules and their recent progress of molecular design

AbstractThis review article surveys the organic small molecular materials, light‐emitting for most of them, being studied for the molecular alignment or orientation in thin films. Following a chronicle order, three practical characterization techniques, variable angle spectroscopic ellipsometry (VASE), angle‐dependent photoluminescence (ADPL), and grazing incidence wide‐angle x‐ray scattering (GIWAXS) have been used to probe phosphorescence, thermally activated delayed fluorescence (TADF) materials, as well as those of non‐phosphorescence and non‐TADF materials.

Non-aqueous calcium-based dual-ion batteries with an organic electrode of high-rate performance

Calcium-based batteries are considered a promising candidate for the sustainable energy storage system of the next generation because of the abundance of Ca. However, the development of Ca-based batteries is hindered by the incompatibility between metallic Ca and common electrolytes as well as the absence of calcium-ion-hosted materials with good performance and cycling stability. Herein, we firstly investigate a small molecular organic material, 3,4,9,10-perylenetetracarboxylic diimide (PTCDI), as the calcium-ion host for calcium-ion batteries (CIBs) in the non-aqueous electrolyte. Spectroscopic, structural, and computational studies reveal that PTCDI with an enhanced Ca2+-storage degree can increase the solubility of reduced PTCDI due to the reduced π-π interaction, suppressed by the saturated electrolyte owing to the high redeposition rate to form a PTCDI film with strengthened hydrogen bonds, which facilitates a fast enolization reaction for Ca2+ storage. A cell assembled with the PTCDI negative electrode and carbon-based positive electrode exhibits a high-power density >3000 W kg−1, a high energy density of ∼150 Wh kg−1, and superior reversible capacity of 80 mAh g−1 at 5 A g−1. The assembled CIB even demonstrates the high-rate performance (90 mAh g−1 at 1 A g−1) and ultra-stable cyclability over 4000 cycles with negligible decay at -10 °C, suggesting the promising future as low-temperature batteries.

New Mechanism Insights on Ca-Ion Storage in Small Molecular Crystal

Rechargeable calcium-ion batteries have become intriguing alternatives for grid-scale energy storage devices. However, the strong electrostatic interaction caused by the intrinsic divalent nature of Ca2+ leads to sluggish ion diffusion kinetics, thus resulting in low capacity. Herein, a small molecular crystal organic material is employed as the electrode material for the aqueous calcium-ion batteries. This kind of organic material could not only bypass the sluggish ion diffusion through carbonyl enolization but also avoid electrode inevitable dissolution due to the intermolecular hydrogen bonding, and flexible structure. In addition, the robust crystal structure allows fast Ca-ion diffusion and storage. Electrochemical characterization including electrochemical quartz crystal microbalance combined with first-principles density calculations and in(ex)-situ spectroscopy methods reveals the whole Ca-ion storage mechanism at the atomistic and macroscopic levels. The reversible enolization redox process, diffusion path, and structure change of molecular crystals have been clearly clarified. Consequently, the materials yield a premier rate capability (70.2 mAh g−1 at 5 A g−1), and excellent cycling stability (retention of 80.3% over 1000 cycles at 2 A g−1). This study extends the boundary of molecular crystal systems for battery chemistry to construct high-performance multivalent ion batteries.

Fluorinated Pentafulvalene‐Fused Hole‐Transporting Material Enhances the Performance of Perovskite Solar Cells with Efficiency Exceeding 23%

AbstractOrganic small molecular materials with coplanar π‐conjugated system as HTMs in perovskite solar cells (PSCs) have attracted considerable attention due to their high charge transport capability and thermal stability. Herein, three novel pentafulvalene‐fused derivatives with or without fluorine atoms incorporated (YSH‐oF and YSH‐mF and YSH‐H, respectively) are designed, synthesized, and applied as hole‐transporting materials (HTMs) in PSCs fabrication. The fluorinated HTMs, YSH‐oF and YSH‐mF, exhibited higher hole mobility and better charge extraction at the perovskite/HTM interface than non‐fluorinated one do, presumably due to the closer intermolecular π–π packing interactions. As a result, small‐area (0.09 cm2) PSCs made with YSH‐oF and YSH‐mF achieved an impressive power conversion efficiency (PCE) of 23.59% and 22.76% respectively, with negligible hysteresis, in contrast with the 20.57% for the YSH‐H‐based devices. Furthermore, for large‐area (1.00 cm2) devices, the PSCs employing YSH‐oF exhibited a PCE of 21.92%. Moreover, excellent long‐term device stability is demonstrated for PSCs with F‐substituted HTMs (YSH‐oF and YSH‐mF), presumably due to the higher hydrophobicity. This study shows the great potential of fluorinated pentafulvalene‐fused materials as low‐cost HTM for efficient and stable PSCs.

2D-Self-Assembled Organic Materials in Undoped Hole Transport Bilayers for Efficient Inverted Perovskite Solar Cells.

Interfaces between photoactive perovskite layer and selective contacts play a key role in the performance of perovskite solar cells (PSCs). The properties of the interface can be modified by the introduction of molecular interlayers between the halide perovskite and the transporting layers. Herein, two novel structurally related molecules, 1,3,5-tris(α-carbolin-6-yl)benzene (TACB) and the hexamethylated derivative of truxenotris(7-azaindole) (TTAI), are reported. Both molecules have the ability to self-assemble through reciprocal hydrogen bond interactions, but they have different degrees of conformational freedom. The benefits of combining these tripodal 2D-self-assembled small molecular materials with well-known hole transporting layers (HTLs), such as PEDOT:PSS and PTAA, in PSCs with inverted configuration are described. The use of these molecules, particularly the more rigid TTAI, enhanced the charge extraction efficiency and reduced the charge recombination. Consequently, an improved photovoltaic performance was achieved in comparison to the devices fabricated with the standard HTLs.

Accurate structure models and absolute configuration determination using dynamical effects in continuous-rotation 3D electron diffraction data

Continuous-rotation 3D electron diffraction methods are increasingly popular for the structure analysis of very small organic molecular crystals and crystalline inorganic materials. Dynamical diffraction effects cause non-linear deviations from kinematical intensities that present issues in structure analysis. Here, a method for structure analysis of continuous-rotation 3D electron diffraction data is presented that takes multiple scattering effects into account. Dynamical and kinematical refinements of 12 compounds—ranging from small organic compounds to metal–organic frameworks to inorganic materials—are compared, for which the new approach yields significantly improved models in terms of accuracy and reliability with up to fourfold reduction of the noise level in difference Fourier maps. The intrinsic sensitivity of dynamical diffraction to the absolute structure is also used to assign the handedness of 58 crystals of 9 different chiral compounds, showing that 3D electron diffraction is a reliable tool for the routine determination of absolute structures.

Small molecular donor materials based on electron withdrawing benzobisthiazole core unit enable an efficiency of 11.8% for organic solar cells

All-small-molecule (ASM) organic solar cells (OSCs) are in advantage of their defined molecular structures and good reproducibility. However, the state-of-art donor molecules are usually based on benzodithiophene (BDT) as the core unit, which limits the modulation of energy levels, optical absorption, and opto-electronic properties. In this research, we designed and synthesized two small molecular donors (BBTSM-1 and BBTSM-2) with electron withdrawing benzobisthiazole (BBT) as the core unit, developing a type of A-π-A'-π-A conjugated system. The molecules exhibit reduced energy levels, high charge carrier mobilities, and ordered edge-on molecular packing in thin films. High power conversion efficiency of 11.8% was achieved in solar cells based on BBTSM-1:Y6, which indicating that small molecular donors based on the weak electron withdrawing BBT unit would be promising candidates for high-performance organic solar cells.

Stimulus-Responsive Organic Phosphorescence Materials Based on Small Molecular Host-Guest Doped Systems.

Small molecular host-guest doped materials exhibit superiority toward high-efficiency room-temperature phosphorescence (RTP) materials due to their structural design diversity and ease of preparation. Dynamic RTP materials display excellent characteristics, such as good reversibility, quick response, and tunable luminescence ability, making them applicable to various cutting-edge technologies. Herein, we summarize the advances in host-guest doped dynamic RTP materials that respond to external and internal stimuli and present some insights into the molecular design strategies and underlying mechanisms. Subsequently, specific viewpoints are described regarding this promising field for the development of dynamic RTP materials. This Perspective is highly beneficial for future intelligent applications of dynamic RTP systems.

Terminal Cyano-Functionalized Fused Bithiophene Imide Dimer-Based n-Type Small Molecular Semiconductors: Synthesis, Structure-Property Correlations, and Thermoelectric Performances.

n-Doped small molecular organic thermoelectric materials (OTMs) hold advantages of high Seebeck coefficient and better performance reproducibility over their polymeric analogues; however, high-performance n-type small molecular OTMs are severely lacking. We report here a class of small molecular OTMs based on terminal cyanation of a bithiophene imide-based ladder-type heteroarene BTI2. It was found that the cyanation could effectively lower the lowest unoccupied molecular orbital (LUMO) level from -2.90 eV (BTI2) to -4.14 eV (BTI2-4CN) and thus lead to significantly improved n-doping efficiency. Additionally, terminal cyano-functionalization can maintain the close packing and efficient intermolecular charge transfer between these cyanated molecules, thus yielding high electron mobilities of up to 0.40 cm2 V-1 s-1. Benefiting from its low LUMO-enabled efficient n-doping and high electron mobility, an encouraging n-type electrical conductivity of 0.43 S cm-1 and power factor (PF) of 6.34 μW m-1 K-2 were achieved for tetracyanated BTI2-4CN, significantly outperforming those of its noncynated BTI2 (<10-7 S cm-1, PF undetectable) and dicyanated BTI2-2CN (0.24 S cm-1, 1.78 μW m-1 K-2). These results suggest the great potential of the terminal cyanation strategy of ladder-type heteroarenes for developing high-performance small molecular OTMs.

Near thermal-electric field controlled electrohydrodynamic 3D printing of high aspect ratio microstructures

Electrohydrodynamic (EHD) printing is an effective method for high-resolution two-dimensional patterning because of its high material compatibility. The latest research on three-dimensional (3D) structure fabrication has been reported for metal nanoparticles, small molecular materials, and phase change materials by process regulation. One of the main challenges in conventional EHD 3D printing of polymers is the low accuracy of filament deposition and stacking at the microscale. It is difficult to achieve a high aspect ratio (AR) for printed structures. This study develops an external field-assisted EHD printing process for polymer materials, where the filament formation can be improved by the near thermal field and the stacking accuracy of filaments is further promoted by applying an alternating voltage between layers. The feasibility of this method is demonstrated by printing polystyrene, a typical polymer material, on the silicon substrate with. The regulatory effect of the process parameters on the filament width is explored. The influence of the external thermal field on filament formation and deposition is discussed, and a promotion mechanism is revealed of alternating voltage for accurate deposition. Based on these combinative effects, micro-scale 3D structures with a high AR are successfully printed on the insulating substrate with three kinds of polymers.