Evaporable Fullerene Indanones with Controlled Amorphous Morphology as Electron Transport Layers for Inverted Perovskite Solar Cells.

Fullerenes are among the most commonly used electron-transporting materials (ETMs) in inverted perovskite solar cells (IPSCs). Although versatile functionalized fullerene derivatives have shown excellent performance in IPSCs, pristine [60]fullerene (C60) is still the most widely used in devices mainly because of its uniform morphology by thermal deposition. However, thermally evaporable fullerene derivatives have not yet been achieved. Herein, we developed a series of evaporable fullerene derivatives, referred to as fullerene indanones (FIDOs), affording IPSCs with high power conversion efficiency (PCE) and long-term storage stability. The FIDOs were designed with a unique architecture in which the fullerene moiety and a benzene ring moiety are linked via a five-membered carbon ring in benzene ring plane. This molecular arrangement affords exceptional thermal stability, allowing the FIDOs to withstand harsh thermal deposition conditions. Moreover, by manipulating the steric bulk of the functional groups, we could control the state of the organic film from crystalline to amorphous. Subsequently, we used FIDOs as an electron transport layer (ETL) in IPSCs. Thanks to the suitable energy level and dual-passivation effect of FIDOs compared with a reference ETL using C60, the device using FIDOs achieved an open-circuit voltage of 1.16 V and a fill factor of 0.77. As a result, the PCE reached 22.11%, which is superior to 20.45% of the best-performing reference device. Most importantly, the FIDO-based IPSC devices exhibited exceptional stability in comparison to the reference device due to the stability of the amorphous ETL films.

Sequential click modification of a lithium-ion endohedral fullerene connecting small molecules through a dieneazide linker.

A versatile method for the chemical modification of a lithium-ion endohedral fullerene (Li+@C60) to connect various small molecules is described. The designed dieneazide linker enables the facile connection of Li+@C60 with small molecules bearing a terminal alkyne via Huisgen annulation and a subsequent Diels-Alder reaction. This strategy significantly expands the diversity of small molecules to be attached by Li+@C60.

Face-mask-aware Facial Expression Recognition based on Face Parsing and Vision Transformer.

As wearing face masks is becoming an embedded practice due to the COVID-19 pandemic, facial expression recognition (FER) that takes face masks into account is now a problem that needs to be solved. In this paper, we propose a face parsing and vision Transformer-based method to improve the accuracy of face-mask-aware FER. First, in order to improve the precision of distinguishing the unobstructed facial region as well as those parts of the face covered by a mask, we re-train a face-mask-aware face parsing model, based on the existing face parsing dataset automatically relabeled with a face mask and pixel label. Second, we propose a vision Transformer with a cross attention mechanism-based FER classifier, capable of taking both occluded and non-occluded facial regions into account and reweigh these two parts automatically to get the best facial expression recognition performance. The proposed method outperforms existing state-of-the-art face-mask-aware FER methods, as well as other occlusion-aware FER methods, on two datasets that contain three kinds of emotions (M-LFW-FER and M-KDDI-FER datasets) and two datasets that contain seven kinds of emotions (M-FER-2013 and M-CK+ datasets).

Inkjet printing of mechanochromic fluorenylidene-acridane.

In mechanochromic material research, a serious problem is that mechanical treatment cannot be applied to the materials because of their responsiveness to stimuli. Inkjet printing is a useful solution deposition method for electronics, but materials must be processed to be suitable for an inkjet printer. Fluorenylidene-acridane (FA) exhibits ground-state mechanochromism with visual color changes and responds not only to mechanical pressure but also to alcohol. Alcohol inhibits the color change induced by mechanical stimulation because the mechanochromism of FA is based on a conformational change in its molecular structure. This phenomenon suggests that the mechanochromism of FA can be controlled using alcohol. For use in inkjet printing, minute particles of FA obtained by bead milling in ethanol were investigated for uniformity and size by scanning electron microscopy and gas adsorption measurement. Also, ink containing FA particles was prepared and examined for physical properties such as viscosity and surface tension. It was confirmed that the inkjet-printed pattern demonstrated visual color changes between yellow and green in response to mechanical pressure and alcohol. This report describing the control of mechanochromism and its specific application is expected to contribute to broadening the mechanochromic materials research field.

Detecting Human Actions in Drone Images Using YoloV5 and Stochastic Gradient Boosting.

Human action recognition and detection from unmanned aerial vehicles (UAVs), or drones, has emerged as a popular technical challenge in recent years, since it is related to many use case scenarios from environmental monitoring to search and rescue. It faces a number of difficulties mainly due to image acquisition and contents, and processing constraints. Since drones' flying conditions constrain image acquisition, human subjects may appear in images at variable scales, orientations, and occlusion, which makes action recognition more difficult. We explore low-resource methods for ML (machine learning)-based action recognition using a previously collected real-world dataset (the "Okutama-Action" dataset). This dataset contains representative situations for action recognition, yet is controlled for image acquisition parameters such as camera angle or flight altitude. We investigate a combination of object recognition and classifier techniques to support single-image action identification. Our architecture integrates YoloV5 with a gradient boosting classifier; the rationale is to use a scalable and efficient object recognition system coupled with a classifier that is able to incorporate samples of variable difficulty. In an ablation study, we test different architectures of YoloV5 and evaluate the performance of our method on Okutama-Action dataset. Our approach outperformed previous architectures applied to the Okutama dataset, which differed by their object identification and classification pipeline: we hypothesize that this is a consequence of both YoloV5 performance and the overall adequacy of our pipeline to the specificities of the Okutama dataset in terms of bias-variance tradeoff.

Synthesis of neutral Li-endohedral PCBM: an n-dopant for fullerene derivatives.

Li@PCBM, the first neutral Li@C60 derivative, was synthesized. The Li@PCBM exists in a monomer-dimer equilibrium in solution but as a monomer in the PCBM matrix. The fully dispersed Li@PCBM n-doped the surrounding empty PCBM, raising the Fermi level by 0.13 eV compared with the undoped PCBM film. The hybrid films were utilized as an ETL for PSCs, promoting the efficiency of the device.

Synthesis of n-type [60]Fullerene Derivatives with Sterically Bulky tert-Butyl Groups for Vacuum Deposition Processes.

[60]Fullerene derivatives with high thermal stability can be used for vacuum deposition under heating to fabricate thin films for organic electronic devices. Here, we investigated the thermal stability of [60]fullerene derivatives with various bulky substituents for thermal evaporation under vacuum by means of thermogravimetric analysis under reduced and normal pressure. We found sterically bulky groups such as tert-butyl groups of [60]fullerene derivatives lowered the vacuum deposition temperature. Also, we performed isothermal thermogravimetric analysis to examine the long-term thermal stability of the designed compounds under heating conditions. Furthermore, we investigated the UV-Vis absorption patterns of the deposited films. Absorption in the blue wavelength range, which was attributed to intermolecular HOMO-LUMO transitions among the molecular orbitals of adjacent [60]fullerenes, was dramatically modified. These results were associated with the prevention of aggregation among neighboring [60]fullerene by the sterically bulky groups. This concept could contribute to expanding the use of evaporable [60]fullerene derivatives in organic thin-film electronics research fields.

Deep learning, reinforcement learning, and world models.

Deep learning (DL) and reinforcement learning (RL) methods seem to be a part of indispensable factors to achieve human-level or super-human AI systems. On the other hand, both DL and RL have strong connections with our brain functions and with neuroscientific findings. In this review, we summarize talks and discussions in the "Deep Learning and Reinforcement Learning" session of the symposium, International Symposium on Artificial Intelligence and Brain Science. In this session, we discussed whether we can achieve comprehensive understanding of human intelligence based on the recent advances of deep learning and reinforcement learning algorithms. Speakers contributed to provide talks about their recent studies that can be key technologies to achieve human-level intelligence.

Triarylamine/Bithiophene Copolymer with Enhanced Quinoidal Character as Hole-Transporting Material for Perovskite Solar Cells.

Polytriarylamine is a popular hole-transporting materials (HTMs) despite its suboptimal conductivity and significant recombination at the interface in a solar cell setup. Having noted insufficient conjugation among the triarylamine units along the polymer backbone, we inserted a bithiophene unit between two triarylamine units through iron-catalyzed C-H/C-H coupling of a triarylamine/thiophene monomer so that two units conjugate effectively via four quinoidal rings when the molecule functions as HTM. The obtained triarylamine/bithiophene copolymer (TABT) used as HTM showed a high-performance in methylammonium lead iodide perovskite (MAPbI3 ) solar cells. Mesityl substituted TABT forms a uniform film, shows high hole-carrier mobility, and has an ionization potential (IP=5.40 eV) matching that of MAPbI3 . We fabricated a solar cell device with a power conversion efficiency of 21.3 % and an open-circuit voltage of 1.15 V, which exceeds the performance of devices using reference standard such as poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine (PTAA) and Spiro-OMeTAD.

Facile Multiple Alkylations of C60 Fullerene.

The reduction of fullerene (C60) with sodium dispersion in the presence of an excess amount of dipropyl sulfate was found to yield highly propylated fullerene, C60(nC3H7)n (max. n = 24), and C60(nC3H7)20 was predominantly generated as determined by mass spectroscopy.

Synthesis of Conjugated Donor-Acceptor Antiaromatic Porphyrins and Their Application to Perovskite Solar Cells.

A conjugated donor-acceptor antiaromatic porphyrin, composed of an antiaromatic thieno-fused porphyrin structure and a diketopyrrolopyrrole mioety, was synthesized and applied in a perovskite solar cell for the first time. Enhanced light absorption in the device by the antiaromatic porphyrin resulted in a significantly increased power conversion efficiency of 19.3%.

Controlled Removal of Surfactants from Double-Walled Carbon Nanotubes for Stronger p-Doping Effect and Its Demonstration in Perovskite Solar Cells.

Double-walled carbon nanotubes (DWNTs) have shown potential as promising alternatives to conventional transparent electrodes owing to their solution processability as well as high conductivity and transparency. However, their DC to optical conductivity ratio is limited by the surrounding surfactants that prevent the p-doping of the DWNTs. To maximize the doping effectiveness, the surfactants are removed from the DWNTs, with negligible damage to the nanotubes, by calcination in an Ar atmosphere. The effective removal of the surfactants is characterized by various analyses, and the results show that the optimal calcination temperature is 400 °C. The conductivity of the DWNTs films improves when doped by triflic acid. While the conductivity increase of the surfactants-wrapped DWNT films is 31.9%, the conductivity increase of the surfactants-removed DWNT is found to be 59.7%. Using the surfactants-removed, p-doped, solution-processed transparent electrodes, inverted-type perovskite solar cells are fabricated, resulting in a power conversion efficiency of 17.7% without hysteresis. This work advances the application of DWNTs in transparent conductors, as the efficiency obtained is the highest value achieved to date for carbon nanotube electrode-based perovskite solar cells and solution-processable transparent electrode-based solar cells.

An Adamantane Capsule and its Efficient Uptake of Spherical Guests up to 3 nm in Water.

Efficient uptake of small to large guests, with a large difference in relative size, is quite rare for synthetic host compounds. Herein we designed and prepared a micellar capsule, composed of bent amphiphiles bearing two adamantyl groups, as a new host with a well-defined nanostructure. Unlike previous covalent, coordination, and hydrogen-bonding hosts, the adamantane-based capsule displays unusual uptake abilities toward spherical molecules with small (∼0.6 nm in diameter; e.g., adamantane) to medium size (∼1 nm; e.g., fullerene) as well as large size (∼3 nm; i.e., metal-organic polyhedra (MOP)), where the size differences are up to 5-fold, in water. Moreover, the resultant MOP-uptaking capsule incorporates medium-sized molecules (e.g., perylene and eosin Y) into the polyhedral cavity to generate ternary core-shell structures.

Multi-Walled Carbon Nanotube-Assisted Encapsulation Approach for Stable Perovskite Solar Cells.

Perovskite solar cells (PSCs) are regarded as the next-generation thin-film energy harvester, owing to their high performance. However, there is a lack of studies on their encapsulation technology, which is critical for resolving their shortcomings, such as their degradation by oxygen and moisture. It is determined that the moisture intrusion and the heat trapped within the encapsulating cover glass of PSCs influenced the operating stability of the devices. Therefore, we improved the moisture and oxygen barrier ability and heat releasing capability in the passivation of PSCs by adding multi-walled carbon nanotubes to the epoxy resin used for encapsulation. The 0.5 wt% of carbon nanotube-added resin-based encapsulated PSCs exhibited a more stable operation with a ca. 30% efficiency decrease compared to the ca. 63% decrease in the reference devices over one week under continuous operation. Specifically, the short-circuit current density and the fill factor, which are affected by moisture and oxygen-driven degradation, as well as the open-circuit voltage, which is affected by thermal damage, were higher for the multi-walled carbon nanotube-added encapsulated devices than the control devices, after the stability test.

One-step direct oxidation of fullerene-fused alkoxy ethers to ketones for evaporable fullerene derivatives.

Ketones are widely applied moieties in designing functional materials and are commonly obtained by oxidation of alcohols. However, when alcohols are protected/functionalized, the direct oxidation strategies are substantially curbed. Here we show a highly efficient copper bromide promoted one-step direct oxidation of benzylic ethers to ketones with the aid of a fullerene pendant. Mechanistic studies unveil that fullerene can serve as an electron pool proceeding the one-step oxidation of alkoxy group to ketone. In the absence of the fullerene pendant, the unreachable activation energy threshold hampers the direct oxidation of the alkoxy group. In the presence of the fullerene pendant, generated fullerene radical cation can activate the neighbour C-H bond of the alkoxy moiety, allowing a favourable energy barrier for initiating the direct oxidation. The produced fullerene-fused ketone possesses high thermal stability, affording the pin-hole free and amorphous electron-transport layer with a high electron-transport mobility.

Denatured M13 Bacteriophage-Templated Perovskite Solar Cells Exhibiting High Efficiency.

The M13 bacteriophage, a nature-inspired environmentally friendly biomaterial, is used as a perovskite crystal growth template and a grain boundary passivator in perovskite solar cells. The amino groups and carboxyl groups of amino acids on the M13 bacteriophage surface function as Lewis bases, interacting with the perovskite materials. The M13 bacteriophage-added perovskite films show a larger grain size and reduced trap-sites compared with the reference perovskite films. In addition, the existence of the M13 bacteriophage induces light scattering effect, which enhances the light absorption particularly in the long-wavelength region around 825 nm. Both the passivation effect of the M13 bacteriophage coordinating to the perovskite defect sites and the light scattering effect intensify when the M13 virus-added perovskite precursor solution is heated at 90 °C prior to the film formation. Heating the solution denatures the M13 bacteriophage by breaking their inter- and intra-molecular bondings. The denatured M13 bacteriophage-added perovskite solar cells exhibit an efficiency of 20.1% while the reference devices give an efficiency of 17.8%. The great improvement in efficiency comes from all of the three photovoltaic parameters, namely short-circuit current, open-circuit voltage, and fill factor, which correspond to the perovskite grain size, trap-site passivation, and charge transport, respectively.

Solvation-Free Li+ Lewis Acid Enhancing Reaction: Kinetic Study of [5,6]-Li+@PCBM to [6,6]-Li+@PCBM.

Kinetic parameters for the [5,6]- to [6,6]-[Li+@PCBM]TFSI- transformation were determined experimentally, revealing a ca. 700-fold faster reaction rate at 423 K than empty PCBM and a 57.4 kJ mol-1 lower activation energy. The encapsulated Li+ can be considered as solvation-free Li+, forming a 1:1 complex with the substrate.

Nickel-Catalyzed Deaminative Acylation of Activated Aliphatic Amines with Aromatic Amides via C-N Bond Activation.

Deaminative functionalization of aliphatic primary amines has great synthetic utility. Herein, we describe a Ni-catalyzed reductive deaminative cross-electrophile coupling reaction between Katritzky salts and aromatic amides. This work provides examples of the synthesis of various ketones from alkylpyridinium salts, including both primary and secondary alkylamines. Given its mild reaction conditions and high functional group tolerance, this cross-coupling strategy is expected to be useful for late-stage functionalization of complex compounds.

Equilibrium and thermodynamic studies of chromic overcrowded fluorenylidene-acridanes with modified fluorene moieties.

Chromic materials, an important class of stimuli-responsive materials, have aroused extensive attention in recent years. Normally, their color is based on changes in morphology. Few examples of chromic material based on conformational isomerization, such as in overcrowded alkenes, have been reported previously. Furthemore, experimental thermodynamic studies of overcrowded bistricyclic aromatic enes have not been carried out to our knowledge. Here, we show that N-phenyl-substituted fluorenylidene-acridanes, with a properly modified fluorene moiety, performs chromisms originating from conformational changes. Thermodynamic studies determine equilibrium constants, changes in enthalpy, entropy, and free energy in solution, enabling in-depth understanding of the equilibrium behavior of overcrowded alkenes and providing useful information for designing functional chromic compounds. Single-crystal X-ray diffraction analysis of fluorenylidene-acridanes in this work clearly shows well-tuned charge transfer from the acridane to the fluorene moiety. Various chromic behaviors such as mechanochromism, thermochromism, solvatochromism, vapochromism, and proton-induced chromism also support understanding of conformational isomerism.

Recent progress in porphyrin- and phthalocyanine-containing perovskite solar cells.

In this review, we summarize the application of porphyrins and phthalocyanines in perovskite solar cells to date. Since the first porphyrin- and phthalocyanine-based perovskite solar cells were reported in 2009, their power conversion efficiency has dramatically increased from 3.9% to over 20%. Porphyrins and phthalocyanines have mostly been used as the charge selective layers in these cells. In some cases, they have been used inside the perovskite photoactive layer to form two-dimensional perovskite structures. In other cases, they were used at the interface to engineer the surface energy level. This review gives a chronological introduction to the application of porphyrins and phthalocyanines for perovskite solar cells depending on their role. This review article also provides the history of porphyrin and phthalocyanine derivative development from the perspective of perovskite solar cell applications.