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Electrochemical water splitting offers an advancing approach to producing highly pure hydrogen and oxygen, motivated by the prevalence of a low‐carbon economy and the goal of a sustainable future. The customized modulation of electronic structures enables the electrocatalyst to directionally promote hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), which is a promising shortcut to overall water splitting (OWS). Herein, 3D homologous WSeS/CoSeS heterojunction nanoarrays (WSeS/CoSeS NAs) and W‐doped CoSeS nanoarrays (W‐CoSeS NAs) are investigated. Abundant heterointerfaces within WSeS/CoSeS NAs facilitate HER kinetics, boosting mass diffusivity, and increasing carrier separation and transfer process. High‐valence W6+ doping into CoSeS prevents phase separation and stabilizes Co sites by charge offset effect, leading to enhanced OER. Consequently, the WSeS/CoSeS NAs and W‐CoSeS NAs reach 10 mA cm−2 at an overpotential of 43.8 and 233.3 mV in 1.0 m KOH electrolyte for HER and OER, respectively. Moreover, when asymmetrically engaged as an electrolyzer, this configuration exhibits extraordinary electrocatalytic performances (cell voltage of 1.51 V at 10 mA cm−2) with satisfying stability and mechanical robustness (over 1000 h at 1000 mA cm−2). The modulation and manufacture of reaction‐property‐oriented materials are experimentally and theoretically validated potential, illuminating the light of inspiration for multiple applications. [ABSTRACT FROM AUTHOR]

Discovering a competent charge transport layer promoting charge separation in photoelectrodes is a perpetual pursuit in photoelectrochemical (PEC) water splitting to achieve high solar‐to‐hydrogen (STH) conversion efficiency. Here, a conjugated polythiophene framework (CPF‐TTB) on Ta3N5 is elaborately electropolymerized, substantiating the hole transport behavior in their heterojunction. Tailored band structures of the CPF‐TTB/Ta3N5 reinforce the separation of photogenerated carriers, elevating a fill factor of the photoanode modified with a cocatalyst. The enhanced hole extraction enables the NiFeOx/CPF‐TTB/Ta3N5/TiN photoanode to generate a remarkable water oxidation photocurrent density of 9.12 mA cm−2 at 1.23 V versus the reversible hydrogen electrode. A tandem device combining the photoanode with a perovskite/Si solar cell implements an unbiased solar water splitting with a STH conversion efficiency of 6.26% under parallel illumination mode. This study provides novel strategies in interface engineering for metal nitride‐based photoelectrodes, suggesting a promise of the organic–inorganic hybrid photoelectrode for high‐efficiency PEC water splitting. [ABSTRACT FROM AUTHOR]

Normalized signal intensity (SI) obtained from magnetic resonance imaging (MRI) has been used to track anterior cruciate ligament (ACL) postoperative remodeling. We aimed to assess the effect of MRI sequence (PD: proton density‐weighted; T2: T2‐weighted; CISS: constructive interference in steady state) on postoperative changes in healing ACLs/grafts. We hypothesized that CISS is better at detecting longitudinal SI and texture changes of the healing ACL/graft compared to the common clinical sequences (PD and T2). MR images of patients who underwent ACL surgery were evaluated and separated into groups based on surgical procedure (Bridge‐Enhanced ACL Repair (BEAR; n = 50) versus ACL reconstruction (ACLR; n = 24)). CISS images showed decreasing SI across all timepoints in both the BEAR and ACLR groups (p < 0.01), PD and T2 images showed decreasing SI in the 6‐to‐12‐ and 12‐to‐24‐month postoperative timeframes in the BEAR group (p < 0.02), and PD images additionally showed decreasing SI between 6‐ and 24‐months postoperation in the ACLR group (p = 0.02). CISS images showed texture changes in both the BEAR and ACLR groups, showing increases in energy and decreases in entropy in the 6‐to‐12‐ and 6‐to‐24‐month postoperative timeframes in the BEAR group (p < $\lt $ 0.04), and increases in energy, decreases in entropy, and increases in homogeneity between 6 and 24 months postoperation in the ACLR group (p < 0.04). PD images showed increases in energy and decreases in entropy between 6‐ and 24‐months postoperation in the ACLR group (p < 0.008). Finally, CISS was estimated to require a smaller sample size than PD and T2 to detect SI differences related to postoperative remodeling. [ABSTRACT FROM AUTHOR]

Magnetic microrobots and nanoparticles offer unique capabilities for medical applications by granting unprecedented access to intricate and delicate anatomical structures. Nevertheless, an intuitive manipulation approach remains a challenge due to their small size and limited feedback. This study presents a new method for magnetic microrobot and nanoparticle control that employs virtual reality (VR), creating an immersive and realistic view of the bodily anatomy and the microrobot within. This study compares three manipulation modes: a traditional mode using 2D displays, VR mode using a VR headset and touch controllers, and VR autonomous programmed maneuvering. It is shown that VR‐assisted modes reduce the manipulation time by improving spatial awareness. Nanoparticles in a VR environment are also manipulated. The proposed method will find applications in terms of intuitive, immersive microrobots or magnetic nanoparticle control in complex biological environments, thus in many medical procedures and for drug and cell delivery. The immersive nature of this approach enhances the ability of the user to perceive and understand complex anatomical structures, facilitating better navigation within delicate environments; both dexterity and spatial awareness are improved. Thus, it is shown how microrobots and magnetic nanoparticles can be controlled using immersive simulations to improve both visualization and manipulation. [ABSTRACT FROM AUTHOR]

Continuous Li monitoring is vital in ensuring the safety and treatment efficacy of probationers with psychotic disorders, such as bipolar disorder, depression, and mania. This study introduced a validated quantitative analysis method using ion chromatography (IC) to monitor Li+ concentration in urine. The methodology involved centrifuging the urine sample, diluting the supernatant with deionized water, and subsequent IC analysis using guard and analytical columns for precise Li+ concentration measurement. The method quantified Li+ within the range of 2–400 ng/mL, demonstrating its excellent linearity (r2 = 0.9983) with a weighting factor of 1/x. Precision levels below 12.8% were observed for both intraday and interday measurements with an accuracy of −5.9% to 15.2%. The detection limit was identified as 0.12 ng/mL. The method conformed to analytical standards in terms of selectivity, matrix effect, process efficiency, dilution integrity, and stability. Moreover, the method distinctly quantified Li+ while effectively eliminating interference from Na+, which had a similar retention time as Li+ with higher concentrations. Further, the developed method was successfully applied to analyze forensic urine samples of Li users, demonstrating its applicability for medication compliance monitoring using urine samples of mentally disordered probationers. [ABSTRACT FROM AUTHOR]

The fabrication of kesterite Cu2ZnSn(S,Se)4 (CZTSSe) thin‐film solar cells using the electrochemical deposition (ED), which is valued for its industrial feasibility, offers a cost‐effective and environmentally friendly approach to the carbon‐free and clean energy production. However, the reported power conversion efficiency of approximately 10 % for electrodeposited CZTSSe thin‐film solar cells is lower compared to the alternative methods like sputtering and spin‐coating, which is mainly attributed to the phase inhomogeneity and the rough morphology generated during the ED process. Ensuring the microscopic and macroscopic uniformity of the electrodeposited films is crucial for the improvement of the film quality and the device performances. In this review, strategies to address these challenges including the intrinsic film control such as the deposition mode, pH, concentration of metal ions, and complexing agents, as well as the extrinsic approaches such as doping, substitution of metal elements, and the introduction of interfacial layers. In addition, the prospects for the electrochemically deposited CZTSSe solar cells were presented, focusing on the promising applications in tandem, flexible, and solar water‐splitting devices. Finally, this review will provide technical insights into the ED process for preparing CZTSSe solar cells, outlining a perspective for the future development of highly efficient CZTSSe thin film solar cells. [ABSTRACT FROM AUTHOR]

Over the past couple of decades, immense research has been carried out to understand the photo‐physics of an organic solar cell (OSC) that is important to enhance its efficiency and stability. Since OSCs undergoes complex photophysical phenomenon, studying these factors has led to designing new materials and implementing new strategies to improve efficiency in OSCs. In this regard, the invention of the non‐fullerene acceptorshas greatly revolutionized the understanding of the fundamental processes occurring in OSCs. However, such vital fundamental research from device physics perspectives is carried out on glovebox (GB) processed OSCs and there is a scarcity of research on air‐processed (AP) OSCs. This review will focus on charge carrier dynamics such as exciton diffusion, exciton dissociation, charge‐transfer states, significance of highest occupied molecular orbital‐offsets, and hole‐transfer efficiencies of GB‐OSCs and compare them with the available data from the AP‐OSCs. Finally, key requirements for the fabrication of efficient AP‐OSCs will be presented from a charge‐carrier dynamics perspective. The key aspects from the charge‐carrier dynamics view to fabricate efficient OSCs either from GB or air are provided. [ABSTRACT FROM AUTHOR]

Ultraviolet photoacoustic microscopy (UV‐PAM), based on the high intrinsic optical absorption of DNA/RNA, holds great promise for intraoperative label‐free histopathological imaging modalities. Although clinical histopathology requires high‐resolution images to observe individual cell structures, conventional UV‐PAM suffers from relatively low resolution compared to the clinical histological modalities. Notably, opto‐ultrasound beam combiners or ring‐shaped ultrasound transducers, which have been used as geometrically coaxial methods of conventional reflection‐mode UV‐PAMs, restrict the numerical apertures (NA) due to their long working distances and/or hollow structures. Here, an ultraviolet‐transparent ultrasound transducer (UV‐TUT) is demonstrated that enables high‐resolution reflection‐mode UV‐PAM by improving the NA (0.38) and consequent spatial resolution (0.47 ± 0.03 µm). The study has successfully demonstrated its superior performance with mouse brain tissue and performed photoacoustic histopathology with cancerous animal tissues. This work proposes the ultimate form of a label‐free reflection‐mode UV‐PAM system with the potential to boost the practical use of intraoperative photoacoustic histopathology. [ABSTRACT FROM AUTHOR]

A non‐precious metal‐based catalyst for water electrolysis provides great promise for cost‐effective and highly efficient sustainable hydrogen production. It herein rationally synthesizes uniform superminiature CoNi nanoparticles (2.6 nm) embedded in 3D N‐doped randomly oriented and erected porous carbon nanosheets (CoNi@N‐PCNS). Taking advantage of the large specific surface area, expedited intermediate transport, and effectively exposed active sites of the hierarchical architecture, located CoNi nanoparticles yield a high atom utilization efficiency. Density functional theory calculations indicate that synergetic and cooperative interactions inside CoNi alloy modulate the d‐band center, leading to a moderate adsorption and desorption energy of reaction intermediates, further accelerating both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) kinetics. Accordingly, the as‐synthesized CoNi@N‐PCNS catalyst establishes superb catalytic activities for HER and OER, revealing overpotentials of 71.2 and 263.8 mV at 10 mA cm−2, respectively. Remarkably, when assembled as a two‐electrode electrolyzer, a satisfying cell voltage of 1.59 V at 10 mA cm−2, and superior stability are demonstrated, highlighting great promise toward water electrolysis. [ABSTRACT FROM AUTHOR]

In spite of the high potential economic feasibility of the tandem solar cells consisting of the halide perovskite and the kesterite Cu2ZnSn(S,Se)4 (CZTSSe), they have rarely been demonstrated due to the difficulty in implementing solution‐processed perovskite top cell on the rough surface of the bottom cells. Here, we firstly demonstrate an efficient monolithic two‐terminal perovskite/CZTSSe tandem solar cell by significantly reducing the surface roughness of the electrochemically deposited CZTSSe bottom cell. The surface roughness (Rrms) of the CZTSSe thin film could be reduced from 424 to 86 nm by using the potentiostatic mode rather than using the conventional galvanostatic mode, which can be further reduced to 22 nm after the subsequent ion‐milling process. The perovskite top cell with a bandgap of 1.65 eV could be prepared using a solution process on the flattened CZTSSe bottom cell, resulting in the efficient perovskite/CZTSSe tandem solar cells. After the current matching between two subcells involving the thickness control of the perovskite layer, the best performing tandem device exhibited a high conversion efficiency of 17.5% without the hysteresis effect. [ABSTRACT FROM AUTHOR]

As a more efficient alternative to the crystalline Si (c‐Si) cell whose performance is approaching its theoretical limit, perovskite (PVSK)/Si tandem solar cells (TSCs) are attracting attention from academia and industry. The tandem device, which can benefit from the maturity of the c‐Si cells and the high performance of the PVSK solar cell, has undergone tremendous development. The expectation for its commercialization is increasing as the device shows conversion efficiencies surpassing those of single‐junction solar cells. In this perspective article, the recent progress of the PVSK/Si TSC is summarized from a viewpoint balanced between academia and industry, by regrouping reported devices depending on the types of Si bottom cells: passivated emitter rear contact, heterojunction with intrinsic thin layer, and polysilicon‐passivated contact. In addition, opto‐electronic characterization methods of the PVSK/Si TSCs are reviewed, which can provide an in‐depth analysis of the subcells that can facilitate the development. [ABSTRACT FROM AUTHOR]

Bifunctional catalysts based on noble metals have achieved practical‐level performances in round‐trip energy conversion systems. However, the required amount of noble metals should be substantially reduced via a new catalyst design that can pursue the synergy of the constituent materials' intrinsic properties and architectural maneuver over reactant/product transport. In this study, cross‐stacked Ir and Pt nanowires resolved the bottlenecks of two reactions essential for the hydrogen‐based energy system: i) hydrogen spillover phenomenon between Pt and Ir nanowires to expedite the hydrogen oxidation reaction and ii) spacing Ir nanowires sufficiently to enhance the mass transport of the oxygen evolution reaction. Simultaneously accommodating the different strategies within the single catalyst layer, a new horizon to design a bifunctional electrode is proposed with the high performance of polymer electrolyte membrane unitized regenerative fuel cells: 47% of round‐trip efficiency at 0.5 A cm−2 with total noble metal loading < 0.3 mg cm−2. [ABSTRACT FROM AUTHOR]

Organometal halide perovskites are promising semiconducting materials for photodetectors because of their favorable optoelectrical properties. Although nanoscale perovskite materials such as quantum dots (QDs) show novel behavior, they have intrinsic stability issues. In this study, an effectively silane barrier‐capped quantum dot (QD@APDEMS) is thinly applied onto a bulk perovskite photosensitive layer for use in photodetectors. QD@APDEMS is synthesized with a silane ligand with hydrophobic CH3‐terminal groups, resulting in excellent dispersibility and durability to enable effective coating. The introduction of the QD@APDEMS layer results in the formation of a low‐defect perovskite film with enlarged grains. This is attributed to the grain boundary interconnection effect via interaction between the functional groups of QD@APDEMS and uncoordinated Pb2+ in grain boundaries. By passivating the grain boundaries, where various trap sites are distributed, hole charge‐carrier injection and shunt leakage can be suppressed. Also, from the energy point of view, the deep highest occupied molecular orbital (HOMO) level of QD@APDEMS can work as a hole charge injection barrier. Improved charge dynamics (generation, transfer, and recombination properties) and reduced trap density of QD@APDEMS are demonstrated. When this perovskite film is used in a photodetector, the device performance (especially the detectivity) stands out among existing perovskites evaluated for energy sensing device applications. [ABSTRACT FROM AUTHOR]

Two‐dimensional metal‐organic frameworks (MOFs) are regarded as promising electrocatalysts because of their high surface area and tunable compositions. Herein, a novel nickel‐based 2D MOF for efficient oxygen evolution reaction (OER) has been developed. Ni‐NDC MOF nanosheets (NDC = naphthalene‐2,6‐dicarboxylic acid) are successfully synthesized on a nickel foam (NF) through a surfactant‐assisted one‐step hydrothermal method. The resulting Ni‐NDC@NF possessing a high electrochemically active surface area of 3.06 mF cm−2 exhibits excellent OER performance with a low overpotential of 249 mV at 10 mA cm−2, a small Tafel slope of 74 mV dec−1, 100% faradaic efficiency, and long‐term stability of 24 h at least. For the application of a bifunctional catalyst, NiMo alloy is electrodeposited on the Ni‐NDC@NF to enhance hydrogen evolution reaction activity. The overall water splitting in a two‐electrode configuration of NiMo/Ni‐NDC@NF electrodes as both anode and cathode require only a 1.56 V for 20 mA cm−2. The photovoltaic‐electrocatalysis system powered by the tandem solar cell represents a high solar‐to‐hydrogen efficiency of ≈22%. This work will contribute to inspiring the design of novel MOF composite catalysts using vertically aligned 2D MOF nanosheet architecture, thereby enlarging the potential of MOFs on next‐generation electrocatalysts and energy devices. [ABSTRACT FROM AUTHOR]

Increase in incident light and surface modification of the charge transport layer are powerful routes to achieve high‐performance efficiency of perovskite solar cells (PSCs) by improving the short‐circuit current density (JSC) and charge transport characteristics, respectively. However, few techniques are studied to reduce reflection loss and simultaneously improve the electrical performance of the electron transport layer (ETL). Herein, an inclined fluorine (F) sputtering process to fabricate high‐performance PSCs is proposed. The proposed process simultaneously implements the antireflection effect of F coating and the effect of F doping on a TiO2 ETL, which increases the amount of light transmitted into the PSC due to the extremely low refractive index (≈1.39) and drastically improves the electrical properties of TiO2. Consequently, the JSC of the F coating and doping perovskite solar cell (F‐PSC) increased from 25.05 to 26.01 mA cm−2, and the power conversion efficiency increased from 24.17% to 25.30%. The unencapsulated F‐PSC exhibits enhanced air stability after 900 h of exposure to ambient environment atmosphere (30% relative humidity, 25 °C under dark condition). The inclined F sputtering process in this study can become a universal method for PSCs from the development stage to commercialization in the future. [ABSTRACT FROM AUTHOR]

The development of new heterostructures with high photoactivity is a breakthrough for the limitation of solar‐driven water splitting. Here, we first introduce indium oxide (In2O3) nanorods (NRs) as a novel electron transport layer for bismuth vanadate (BiVO4) with a short charge diffusion length. In2O3 NRs reinforce the electron transport and hole blocking of BiVO4, surpassing the state‐of‐the‐art photoelectrochemical performances of BiVO4‐based photoanodes. Also, a tannin–nickel–iron complex (TANF) is used as an oxygen evolution catalyst to speed up the reaction kinetics. The final TANF/BiVO4/In2O3 NR photoanode generates photocurrent densities of 7.1 mA cm−2 in sulfite oxidation and 4.2 mA cm−2 in water oxidation at 1.23 V versus the reversible hydrogen electrode. Furthermore, the "artificial leaf," which is a tandem cell with a perovskite/silicon solar cell, shows a solar‐to‐hydrogen conversion efficiency of 6.2% for unbiased solar water splitting. We reveal significant advances in the photoactivity of TANF/BiVO4/In2O3 NRs from the tailored nanostructure and band structure for charge dynamics. [ABSTRACT FROM AUTHOR]

Although semiconducting single‐walled carbon nanotubes (sc‐SWNTs) exhibit excellent sensing properties for various gases, commercialization is hampered by several obstacles. Among these, the difficulty in reproducibly fabricating sc‐SWNT films with uniform density and thickness is the main one. Here, a facile fabrication method for sc‐SWNT‐based hydrogen (H2) sensors with excellent reproducibility, high sensitivity, and selectivity against CO, CO2, and CH4 is reported. Uniform‐density and monolayer sc‐SWNT films are fabricated using chemical immobilized through the click reaction between azide‐functionalized polymer‐wrapped sc‐SWNTs and immobilized alkyne polymer on a substrate before decorating with Pd nanoparticles (0.5–3.0 nm). The optimized sc‐SWNT sensor has a high room‐temperature response of 285 with the response and recovery times of 10 and 3 s, respectively, under 1% H2 gas in air. In particular, this sensor demonstrates highly selective H2 detection at room temperature (25 °C), compared to other gases and humidity. Therefore, the chemical immobilization of the monolayer SWNT films with reproducible and uniform density has the potential for large‐scale fabrication of robust room‐temperature H2 sensors. [ABSTRACT FROM AUTHOR]

Power conversion efficiencies (PCEs) of glove‐box (GB) processed, two‐component, single‐junction organic solar cells (OSCs) have recently exceeded 18%. However, their mass‐scale manufacture using roll‐to‐roll (R2R) coating techniques is impracticable if they must be fabricated in an air‐free environment. From a commercialization perspective, efficient air‐processed OSCs are of much greater interest than GB‐processed devices since the vast majority of R2R‐manufacturing infrastructure is designed to operate in the air. Herein, it is reported that controlling the crystallinity of non‐fullerene acceptors plays a key role in determining the properties of blend films. Notably, Y6‐hu (a Y6‐derivative) is shown to exhibits a higher degree of crystallinity when processed in air. Air‐processed OSCs show an outstanding PCE of 17.38%, which, to the best of the authors' knowledge, is the highest PCE yet reported for two‐component‐based OSCs processed in air using halogen‐free solvents. Moreover, opaque large‐area OSC sub‐modules with PCEs of 12.44%, and red‐green‐blue colored semi‐transparent OSC sub‐modules with PCEs of >10% are demonstrated. By understanding how morphological features relate to the charge‐generation dynamics of air‐processed OSCs, a new window is opened for the fabrication of efficient and stable air‐processable organic electronics. [ABSTRACT FROM AUTHOR]

Pb‐free Sn‐based perovskite solar cells (PSCs) have significant potential for application in photovoltaic devices because of their suitable bandgap, low exciton binding energy, high carrier mobility, and long diffusion length. However, their performance is hampered by several issues. Sn‐based perovskites are highly susceptible to oxidation, which induces a high concentration of defects and degrades the chemical stability of the perovskite crystals. Herein, the anion formate (HCOO−) can effectively suppress the oxidation of Sn in the pure formamidinium tin triiodide (FASnI3) perovskite without using A‐site cationic additives. Moreover, the presence of formate results in a uniform pinhole‐free perovskite film with a low trap density, reduced charge carrier recombination, and improved charge extraction. Density functional theory calculations show that formate‐treated FASnI3 has improved stability against oxidative Sn degradation. The formate‐treated PSC achieves a power conversion efficiency of 12.11% at a high open‐circuit voltage of 0.71 V. The device exhibits improved stability in ambient air in which it maintained over 80% of its initial power conversion efficiency after 180 min because oxidation is inhibited owing to the strong interaction between Sn and formate. [ABSTRACT FROM AUTHOR]

The brain has a complex structure composed of hundreds of regions, forming networks to cooperate body functions. Therefore, understanding how various brain regions communicate with each other and with peripheral organs is important to understand human physiology. The suprachiasmatic nucleus (SCN) in the brain is the circadian pacemaker. The SCN receives photic information from the environment and conveys this to other parts of the brain and body to synchronize all circadian clocks. The circadian clock is an endogenous oscillator that generates daily rhythms in metabolism and physiology in almost all cells via a conserved transcriptional–translational negative feedback loop. So, the information flow from the environment to the SCN to other tissues synchronizes locally distributed circadian clocks to maintain homeostasis. Thus, understanding the circadian networks and how they adjust to environmental changes will better understand human physiology. This review will focus on circadian networks mediated by the SCN to understand how the environment, brain, and peripheral tissues form networks for cooperation. [ABSTRACT FROM AUTHOR]

Quasi‐2D perovskite materials have promise to unlock the full potential of blue perovskite light‐emitting diodes (PeLEDs). However, the efficiency of blue emissive PeLEDs still lags behind the green‐ and red‐emitting counterparts. Here, a multifunctional passivating molecule of (2‐(3,6‐dichloro‐9H‐carbazol‐9‐yl)ethyl)phosphonic acid (36ClCzEPA) that can form a self‐assembled monolayer (SAM) on the indium tin oxide (ITO) electrode is reported. The 36ClCzEPA SAM facilitates hole injection by increasing the work function of ITO through the strong interfacial dipole layer formation at the interface between the perovskite emitter and the ITO electrode. Moreover, it allows a pure‐blue emission and reduces the exciton quenching of luminescence in the perovskite emitter considerably because of its neutral nature, compared to the commonly used acidic PEDOT:PSS. Furthermore, chlorine atoms in the 36ClCzEPA promote well‐ordered crystalline 2D perovskite phases and decrease interfacial trap‐assisted deactivation channels by interfacial passivation. These beneficial characteristics of the 36ClCzEPA SAM yield the excellent luminescence property of PeLEDs with a maximum luminance of 1253 cd m−2 and a peak external quantum efficiency of 4.80% at 473 nm. This work demonstrates that a well‐designed molecule forming an interfacial SAM can be an important component for enhancing the luminescence property of pure‐blue PeLEDs. [ABSTRACT FROM AUTHOR]

6‐Bromoindirubin (6BrIR), found in Murex sea snails, is a precursor of indirubin‐derivatives anticancer drugs. However, its synthesis remains limited due to uncharacterized biosynthetic pathways and difficulties in site‐specific bromination and oxidation at the indole ring. Here, we present an efficient 6BrIR production strategy in Escherichia coli by using four enzymes, that is, tryptophan 6‐halogenase fused with flavin reductase Fre (Fre‐L3‐SttH), tryptophanase (TnaA), toluene 4‐monooxygenase (PmT4MO), and flavin‐containing monooxygenase (MaFMO). Although most indole oxygenases preferentially oxygenate the electronically active C3 position of indole, PmT4MO was newly characterized to perform C2 oxygenation of 6‐bromoindole with 45% yield to produce 6‐bromo‐2‐oxindole. In addition, 6BrIR was selectively generated without indigo and indirubin byproducts by controlling the reducing power of cysteine and oxygen supply during the MaFMO reaction. These approaches led to 34.1 mg/L 6BrIR productions, making it possible to produce the critical precursor of the anticancer drugs only from natural ingredients such as tryptophan, NaBr, and oxygen. [ABSTRACT FROM AUTHOR]

The photoactive layer of non‐fullerene organic solar cells (OSCs) generally consists of a low band‐gap acceptor and conjugated polymer with a deep highest occupied molecular orbital (HOMO) because the hole transfer from the acceptor to the donor as well as the electron transfer from the donor polymer to the acceptor is very important to achieve better performance. Therefore, energy level matching between the HOMO of the donor polymer and the work‐function (WF) of the hole transport layer is required. Since the intrinsic p‐type NiO has a lower WF value, the efficiency of NiO‐based PBDB‐T‐2F:Y6 OSCs is somewhat suppressed. In this work, the energy barrier between the NiO (5.1 eV) and HOMO of PBDB‐T‐2F (5.6 eV) by modifying the NiO surface using a 4‐(trifluoromethyl)benzoic acid (PTF‐BOA) dipole layer (NiO‐PTF‐BOA) is successfully eliminated. The carboxyl group of PTF‐BOA is bonded with Ni atoms on the NiO surface, while the CF3 group attracts electrons, thus resulting in a partial negative charge on the CF3 side. This PTF‐BOA dipole layer induces the vacuum level upshift thus enhancing the work function of NiO‐PTF‐BOA to 5.5 eV. The PBDB‐T‐2F:Y6 OSCs with NiO‐PTF‐BOA exhibit an efficiency of 16.36%, which is the highest reported efficiency for NiO‐based OSCs. [ABSTRACT FROM AUTHOR]

To successfully develop a regioregular polymer, poly[4,8‐bis(5‐(2‐hexyldecyl)thiophen‐2‐yl)benzo[1,2‐b:4,5‐b′]dithiophene][5,5′‐bis(7‐(4‐(2‐butyloctyl)thiophen‐2‐yl)‐6‐fluorobenzo[c][1,2,5]thiadiazol‐4‐yl)‐2,2′‐bithiophene] (PDBD‐FBT), a symmetric monomer synthesized in high yield by tin homo‐coupling reactions. PDBD‐FBT is suitable as a donor material in organic photovoltaics (OPVs) because it shows high crystallinity and strong face‐on packing properties. These properties were amplified by thermal annealing (TA). This causes a power conversion efficiency (PCE) enhancement in PDBD‐FBT‐based OPVs. Using PDBD‐FBT as a polymer donor and 2,2′‐((2Z,2′Z)‐((12,13‐bis(2‐heptylundecyl)‐3,9‐diundecyl‐12,13‐dihydro‐[1,2,5]thiadiazolo[3,4‐e]thieno[2″,3″:4′,5′]thieno[2′,3′:4,5]pyrrolo[3,2‐g]thieno[2′,3′:4,5]thieno[3,2‐b]indole‐2,10‐diyl)bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile (Y6‐HU) as an electron acceptor, a PCE of 7.91% was achieved without any additive and TA at optimized active layer film thickness of approximately 100 nm. After TA, a PCE of 12.53% was achieved with a 58% increase compared with the reference devices. Owing to the strong crystallinities, trap‐assisted recombination occurs by excessively formed grain boundaries; however, efficient exciton dissociation sufficiently covers these drawbacks. Even in the approximately 340 nm‐thick film condition, this tendency is more pronounced (73% PCE enhancement is observed from 6.17% to 10.69% of PCE in the without and with TA devices, respectively). Our study demonstrates that it is possible to manufacture thickness‐insensitive OPVs based on regioregular polymers with strong crystallinity and face‐on characteristics, thereby providing a solution to the thickness variation of large‐area organic solar cell modules. [ABSTRACT FROM AUTHOR]

Cerium oxide nanoparticles (CNPs) are investigated as radical scavengers to increase the durability of polymer electrolyte membrane fuel cells (PEMFCs). However, the practical application of CNPs in PEMFCs is hindered by the low stability of the CNPs during cell operation and the low compatibility of the CNPs with PEM. In this study, as effective antioxidants for PEMs, surface‐engineered CNPs, passivated with dopamine‐based copolymer ligands containing multidentate catechol pendant groups (CNP@DPLs), are reported. The DPLs provide enhanced colloidal and chemical stability in acidic and radical environments, thanks to the robust catechol binding groups and polymer backbone shielding. It is highlighted that they also improved the redox cycling ability of the CNPs, with catechol's additional radical scavenging. Using the CNP@DPLs as a model system, the effect of surface charge is also examined. Negatively charged sulfonic acid‐functionalized CNPs (CNP@DSAs) exhibit the highest compatibility with PEMs. Coherently, the CNP@DSA‐based reinforced composite membrane (CNP@DSA‐RCM) shows the lowest disintegration rate in Fenton's test. The PEMFC based on the CNP@DSA‐RCM outperforms previously reported antioxidant‐based PEMFCs. Importantly, while the pristine PEMFC and Ce salt‐based one undergoes degradation after 40 h, the CNP@DSA based PEMFC retains its performance even after 100 h. [ABSTRACT FROM AUTHOR]

This study is to investigate the optimal treatment option for synchronous bilateral breast cancer (SBBC) by comparing dosimetric and radiobiological parameters of intensity‐modulated radiotherapy (IMRT) and volumetric modulated arc therapy (VMAT) plans using single and dual isocenters. Twenty patients with SBBC without lymph node involvement were selected retrospectively. Four treatment plans were generated for each patient using the Eclipse treatment planning system (Varian Medical System, Palo Alto, CA, USA) following two delivery techniques with two isocenter conditions—IMRT using a single isocenter (IMRT_Iso1), VMAT using a single isocenter (VMAT_Iso1), IMRT using dual isocenters (IMRT_Iso2), and VMAT using dual isocenters (VMAT_Iso2). A dose of 42.56 Gy in 16 fractions was prescribed for the planning target volume (PTV). All plans were calculated using the Acuros XB algorithm and a photon optimizer for a 6‐MV beam of a Vital Beam linear accelerator. PTV‐related dosimetric parameters were analyzed. Further, the homogeneity index, conformity index, and conformation number were computed to evaluate plan quality. Dosimetric parameters were also measured for the organs at risk (OARs). In addition, the equivalent uniform dose corresponding to an equivalent dose related to a reference of 2 Gy per fraction, the tumor control probability, and the normal tissue complication probability were calculated based on the dose–volume histogram to investigate the radiobiological impact on PTV and OARs. IMRT_Iso1 exhibited similar target coverage and a certain degree of dosimetric improvement in OAR sparing compared to the other techniques. It also exhibited some radiobiological improvement, albeit insignificant. Although IMRT_Iso1 significantly increased monitor unit compared to VMAT_Iso1, which is the best option in terms of delivery efficiency, there was only a 22% increase in delivery time. Therefore, in conclusion, IMRT_Iso1, the complete treatment of which can be completed using a single setup, is the most effective method for treating SBBC. [ABSTRACT FROM AUTHOR]

The two members of the cytoplasmic FMR1‐interacting protein family, CYFIP1 and CYFIP2, are evolutionarily conserved multifunctional proteins whose defects are associated with distinct types of brain disorders. Even with high sequence homology between CYFIP1 and CYFIP2, several lines of evidence indicate their different functions in the brain; however, the underlying mechanisms remain largely unknown. Here, we performed reciprocal immunoprecipitation experiments using CYFIP1‐2 × Myc and CYFIP2‐3 × Flag knock‐in mice and found that CYFIP1 and CYFIP2 are not significantly co‐immunoprecipitated with each other in the knock‐in brains compared with negative control wild‐type (WT) brains. Moreover, CYFIP1 and CYFIP2 showed different size distributions by size‐exclusion chromatography of WT mouse brains. Specifically, mass spectrometry‐based analysis of CYFIP1‐2 × Myc knock‐in brains identified 131 proteins in the CYFIP1 interactome. Comparison of the CYFIP1 interactome with the previously identified brain region‐ and age‐matched CYFIP2 interactome, consisting of 140 proteins, revealed only eight common proteins. Investigations using single‐cell RNA‐sequencing databases suggested non‐neuronal cell‐ and neuron‐enriched expression of Cyfip1 and Cyfip2, respectively. At the protein level, CYFIP1 was detected in both neurons and astrocytes, while CYFIP2 was detected only in neurons, suggesting the predominant expression of CYFIP1 in astrocytes. Bioinformatic characterization of the CYFIP1 interactome, and co‐expression analysis of Cyfip1 with astrocytic genes, commonly linked CYFIP1 with focal adhesion proteins. Immunocytochemical analysis and proximity ligation assay suggested partial co‐localization of CYFIP1 and focal adhesion proteins in cultured astrocytes. Together, these results suggest a CYFIP1‐specific association with astrocytic focal adhesion, which may contribute to the different brain functions and dysfunctions of CYFIP1 and CYFIP2. Cover Image for this issue: https://doi.org/10.1111/jnc.15410 [ABSTRACT FROM AUTHOR]

The need for high‐resolution wind resource maps is increasing with the increase in the supply and development of wind power. Many physical downscaling models have been developed and applied to make these maps. However, as the existing models require extensive computations and time, statistical models with higher efficiency are being studied. Statistical models such as regression and machine learning models can quickly calculate wind resource maps, but they have a problem of low accuracy. This study proposes a machine learning model with new topography‐derived variables to interpret the physical characteristics of the wind. As the shape of topography, which was unable to be interpreted in previous studies, can be considered with new derived variables, a significant performance improvement was identified. The analysis was conducted using 1 km Weather Research and Forecasting (WRF) results and ERA5 reanalysis data from South Korea. Two Weibull distribution parameter maps were calculated and used as input and output data. Three collections of derived variables were devised and compared. Therefore, the multi‐resolution topography data showed the highest improvements with approximately 15% reduction in root mean square error (RMSE) for both the linear regression and machine learning models. In particular, the land area showed a decrease of 20%. The best proposed models showed an RMSE of 7% and 8% for two Weibull parameters. The results are expected to serve as a reference for continuing research and utilization of statistical models. [ABSTRACT FROM AUTHOR]

2'‐Fucosyllactose (2'‐FL) is the most abundant oligosaccharide in human milk and one of the most actively studied human milk oligosaccharides (HMOs). When 2'‐FL is produced through biological production using a microorganism, like Escherichia coli, d‐lactose is often externally fed as an acceptor substrate for fucosyltransferase (FT). When d‐glucose is used as a carbon source for the cell growth and d‐lactose is transported by lactose permease (LacY) in lac operon, d‐lactose transport is under the control of catabolite repression (CR), limiting the supply of d‐lactose for FT reaction in the cell, hence decreasing the production of 2'‐FL. In this study, a remarkable increase of 2'‐FL production was achieved by relieving the CR from the lac operon of the host E. coli BL21 and introducing adequate site‐specific mutations into α‐1,2‐FT (FutC) for enhancement of catalytic activity and solubility. For the host engineering, the native lac promoter (Plac) was substituted for tac promoter (Ptac), so that the lac operon could be turned on, but not subjected to CR by high d‐glucose concentration. Next, for protein engineering of FutC, family multiple sequence analysis for conserved amino acid sequences and protein–ligand substrate docking analysis led us to find several mutation sites, which could increase the solubility of FutC and its activity. As a result, a combination of four mutation sites (F40S/Q150H/C151R/Q239S) was identified as the best candidate, and the quadruple mutant of FutC enhanced 2'‐FL titer by 2.4‐fold. When the above‐mentioned E. coli mutant host transformed with the quadruple mutant of futC was subjected to fed‐batch culture, 40 g l−1 of 2'‐FL titer was achieved with the productivity of 0.55 g l−1 h−1 and the specific 2'‐FL yield of 1.0 g g−1 dry cell weight. [ABSTRACT FROM AUTHOR]

Designing an efficient and durable electrocatalyst for the sluggish oxygen evolution reaction (OER) at the anode remains the foremost challenge in developing proton exchange membrane (PEM) electrolyzers. Here, a highly active and durable cactus‐like nanoparticle with an exposed heterointerface between the IrO2 and the low oxidation state Ru by introducing a trace amount of Mn dopant is reported. The heterostructure fabrication relies on initial mixing of the Ru and Ir phases before electrochemical oxidation to produce a conjoined Ru/IrO2 heterointerface. Benefitting from electron transfer at the heterointerface, the low oxidation state Ru species shows excellent initial activity, which is maintained even after 180 h of continuous OER test. In a half‐cell test, the Mn‐doped RuIr nanocactus (Mn‐RuIr NCT) achieves a mass activity of 1.85 A mgIr+Ru−1 at 1.48 VRHE, which is 139‐fold higher than that of commercial IrO2. Moreover, the superior electrocatalytic performance of Mn‐RuIr NCT in the PEM electrolysis system ensures its viability in practical uses. The results of the excellent catalytic performance for acidic OER indicate that the heterostructuring robust rutile IrO2 and the highly active Ru species with a low oxidation state on the catalyst surface drive a synergistic effect. [ABSTRACT FROM AUTHOR]

Transition metal phosphides (TMPs) as ever‐evolving electrocatalytic materials have attracted increasing attention in water splitting reactions owing to their cost‐effective, highly active and stable catalytic properties. This work presents a facile synthetic route to NiCoP nanoparticles with Ru dopants which function as highly efficient electrocatalysts for oxygen evolution reaction (OER) in alkaline media. The Ru dopants induced a high content of Ni and Co vacancies in NiCoP nanoparticles, and the more defective Ru doped NiCoP phase than undoped NiCoP ones led to a greater number of catalytically active sites and improved electrical conductivity after undergoing electrochemical activation. The Ru doped NiCoP catalyst exhibited high OER catalytic performance in alkaline media with a low overpotential of 281 mV at 10 mA cm−2 and a Tafel slope of 42.7 mV dec−1. [ABSTRACT FROM AUTHOR]

The initiation of infection of host tissues by Staphylococcus aureus requires a family of staphylococcal adhesive proteins containing serine–aspartate repeat (SDR) domains, such as ClfA. The O‐linked glycosylation of the long‐chain SDR domain mediated by SdgB and SdgA is a key virulence factor that protects the adhesive SDR proteins against host proteolytic attack in order to promote successful tissue colonization, and has also been implicated in staphylococcal agglutination, which leads to sepsis and an immunodominant epitope for a strong antibody response. Despite the biological significance of these two glycosyltransferases involved in pathogenicity and avoidance of the host innate immune response, their structures and the molecular basis of their activity have not been investigated. This study reports the crystal structures of SdgB and SdgA from S. aureus as well as multiple structures of SdgB in complex with its substrates (for example UDP, N‐acetylglucosamine or SDR peptides), products (glycosylated SDR peptides) or phosphate ions. Together with biophysical and biochemical analyses, this structural work uncovered the novel mechanism by which SdgB and SdgA carry out the glycosyl‐transfer process to the long SDR region in SDR proteins. SdgB undergoes dynamic changes in its structure such as a transition from an open to a closed conformation upon ligand binding and takes diverse forms, both as a homodimer and as a heterodimer with SdgA. Overall, these findings not only elucidate the putative role of the three domains of SdgB in recognizing donor and acceptor substrates, but also provide new mechanistic insights into glycosylation of the SDR domain, which can serve as a starting point for the development of antibacterial drugs against staphylococcal infections. [ABSTRACT FROM AUTHOR]

Minimizing optical losses of the incident light at the window layers is one of the effective strategies for high photoresponse to achieve highly efficient perovskite/silicon tandem cells. The enhancement of the photoresponse of monolithic tandem cells via rationally controlling their window layers consisting of C60 and indium tin oxide (ITO) is reported. The optical simulation and experimental results are consistent that employing thinner C60 and ITO layers would reduce the optical losses caused by absorption/reflection of the incident, which should lead to the increased photocurrent density. However, it is found that the enhanced optical properties have to be balanced with the changes in the electrical and structural properties. The thickness of layers is optimized to function as charge collection and protection (during sputtering process) layers. As a result, the optimum design of the window layers maximizes the photoresponse without degrading the device performances, leading to a highly efficient two‐terminal perovskite/silicon tandem solar cell with a power conversion efficiency of 25.63%. [ABSTRACT FROM AUTHOR]

During cancer resection surgeries, intraoperative histopathologic examination of the surgical specimen is crucial for tumor margin identification. A conventional frozen‐section analysis requires complex tissue processing, which prolongs surgery and potentially introduces interpretation errors. Here, as a novel approach to label‐free intraoperative histopathology, a high‐speed reflection‐mode ultraviolet photoacoustic microscopy (UV‐PAM) system employing a waterproof 1‐axis microelectromechanical systems scanner is demonstrated. Label‐free nuclear imaging is photoacoustically verified using tissue sections excised from mice and humans. Moreover, by imaging clinical specimens from cancer patients and numerically quantifying the histopathologic results, it is successfully demonstrated that the proposed UV‐PAM system has great potential as an alternative intraoperative histopathology method with minimal tissue preparation processes. [ABSTRACT FROM AUTHOR]

Herein, planar heterojunctions comprising a nonfullerene small molecular acceptor (NFA) and a polymer donor are demonstrated by transferring polymer films on a water surface on top of NFA layers. So far, most solution‐processed layer‐by‐layer architectures have been reported as sequentially deposited bulk heterojunctions or pseudo‐bilayers because mixed regions at the donor/acceptor interface are inevitable in these methods. By virtue of the unique properties of conjugated polymers such as hydrophobicity and spontaneous film formation on a water surface, the fabrication of NFA/polymer bilayer nanostructures is clearly demonstrated by dramatically simplified methods. These bilayers are successfully rendered into bilayer organic solar cells achieving a power conversion efficiency of up to 7.47%. This reflects that these bilayers have appropriate morphological and optoelectrical properties to be operated as photoactive layers in photovoltaic devices. Further, ultrafast charge transfer from the polymer donor to the NFA and fast carrier mobility are investigated by transient‐absorption spectroscopy and photoinduced charge‐extraction measurements. Fast carrier dynamics are observed, which are essential for the efficient harvest of excitons in photovoltaic devices. It is believed that the formation of planar heterojunctions on water can offer technical diversity for the fabrication methods of the photovoltaic devices. [ABSTRACT FROM AUTHOR]