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Solar‐blind ultraviolet (UV) photodetectors based on p‐organic/n‐Ga2O3 hybrid heterojunctions have attracted extensive attention recently. Herein, the multifunctional solar‐blind photodetector based on p‐type poly[N‐9′‐heptadecanyl‐2,7‐carbazole‐alt‐5,5‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothiadiazole)] (PCDTBT)/n‐type amorphous Ga2O3 (a‐Ga2O3) is fabricated and investigated, which can work in the phototransistor mode coupling with self‐powered mode. With the introduction of PCDTBT, the dark current of such the a‐Ga2O3‐based photodetector is decreased to 0.48 pA. Meanwhile, the photoresponse parameters of the a‐Ga2O3‐based photodetector in the phototransistor mode to solar‐blind UV light are further increased, that is, responsivity (R), photo‐detectivity (D*), and external quantum efficiency (EQE) enhanced to 187 A W–1, 1.3 × 1016 Jones and 9.1 × 104 % under the weak light intensity of 11 μW cm–2, respectively. Thanks to the formation of the built‐in field in the p‐PCDTBT/n‐Ga2O3 type‐II heterojunction, the PCDTBT/Ga2O3 multifunctional photodetector shows self‐powered behavior. The responsivity of p‐PCDTBT/n‐Ga2O3 multifunctional photodetector is 57.5 mA W–1 at zero bias. Such multifunctional p‐n hybrid heterojunction‐based photodetectors set the stage for realizing high‐performance amorphous Ga2O3 heterojunction‐based photodetectors. [ABSTRACT FROM AUTHOR]

Perovskite solar cells (PSCs) have exhibited tremendous potential in photovoltaic fields owing to their appreciable performance and simple fabrication. Nevertheless, device performances are still required to be further improved before commercial applications. As one‐dimensional materials, carbon nanotubes (CNTs) have been utilized to regulate stability and efficiency of PSCs because of their excellent chemical stability, flexibility, as well as tunable optical and electrical characteristics. In this review, we comprehensively summarize various functions of CNTs in PSCs, such as transparent electrodes, hole/electron‐transport layers, counter electrodes, perovskite additives, and interlayers. Additionally, applications of CNTs toward the advancement of flexible and semitransparent PSCs are provided. Finally, we preview the challenges and research interests of using CNTs in high‐efficiency and stable perovskite devices. [ABSTRACT FROM AUTHOR]

Perovskite solar cells (PSCs) are considered as a promising photovoltaic technology due to their high efficiency and low cost. However, their long‐term stability, mechanical durability, and environmental risks are still unable to meet practical needs. To overcome these issues, we designed a multifunctional elastomer with abundant hydrogen bonds and carbonyl groups. The chemical bonding between polymer and perovskite could increase the growth activation energy of perovskite film and promote the preferential growth of high‐quality perovskite film. Owing to the low defect density and gradient energy‐level alignment, the corresponding device exhibited a champion efficiency of 23.10 %. Furthermore, due to the formation of the hydrogen‐bonded polymer network in the perovskite film, the target devices demonstrated excellent air stability and enhanced flexibility for the flexible PSCs. More importantly, the polymer network could coordinate with Pb2+ ions, immobilizing lead atoms to reduce their release into the environment. This strategy paves the way for the industrialization of high‐performance flexible PSCs. [ABSTRACT FROM AUTHOR]

Compared with the single‐junction perovskite solar cells, the perovskite/perovskite tandem solar cells have the advantages of lower cost and higher power conversion efficiency (PCE). Herein, both two‐terminal (2‐T) and four‐terminal (4‐T) perovskite/perovskite tandem solar cells with all‐inorganic perovskite as the top cell absorption layer and narrow bandgap perovskite MASn0.5Pb0.5I3 material as the bottom cell absorption layer are studied. To effectively improve the photon absorption ratio and performance of the 4‐T tandem device, both reflection and parasitic absorption should be reduced. Afterward, by optimizing the doping concentration of the carrier transport layer, a 4‐T all‐perovskite tandem solar cell with a high PCE of 30.45% is obtained. For the 2‐T all‐perovskite tandem device, the all‐inorganic perovskites with different halogen components (CsPbI3−xBrx, 0 ≤ x ≤ 3) are used as the absorption layer of the top cell, respectively. Through the optimization of the current matching of the subcell, the photoelectric field distribution, the parasitic absorption of the device, etc., an optimal PCE of 27.86% is obtained based on 2‐T CsPbI2Br/MASn0.5Pb0.5I3 tandem device. This study provides a guide for achieving high performance perovskite/perovskite tandem solar cells. [ABSTRACT FROM AUTHOR]

CsPbI2Br perovskite solar cells have achieved rapid development owing to their exceptional optoelectronic properties and relatively outstanding stability. However, open‐circuit voltage (Voc) loss caused by band mismatch and charge recombination between perovskite and charge transporting layer is one of the crucial obstacles to further improve the device performance. Here, we proposed a bilayer electron transport layer ZnO(bottom)/SnO2(top) to reduce the Voc loss (Eloss) and promote device Voc by ZnO insert layer thickness modulation, which could improve the efficiency of charge carrier extraction/transfer and suppress the charge carrier recombination. In addition, guanidinium iodide top surface treatment is used to further reduce the trap density, stabilize the perovskite film and align the energy levels, which promotes the fill factor, short‐circuit current density (Jsc), and stability of the device. As a result, the champion cell of double‐side optimized CsPbI2Br perovskite solar cells exhibits an extraordinary efficiency of 16.25% with the best Voc as high as 1.27 V and excellent thermal and storage stability. [ABSTRACT FROM AUTHOR]

Generally, growing phase pure CsPbBr3 single crystals is challenging, and CsPb2Br5 or Cs4PbBr6 by‐products are usually formed due to the different solubilities of CsBr and PbBr2 in the single solvent. Herein, the growth of high‐quality phase pure CsPbBr3 perovskite single crystals at room temperature by a humidity controlled solvent evaporation method is reported first. Meanwhile, the room temperature phase transition process from three dimensional (3D) cubic CsPbBr3 to two dimensional (2D) layered tetragonal CsPb2Br5 and the detailed mechanism induced by humidity are revealed. Moreover, compared with the organic–inorganic perovskite, the prepared CsPbBr3 single crystals are much more stable under high humidity, which satisfies the long‐term working conditions of X‐ray detectors. The X‐ray detectors based on CsPbBr3 single crystals show a high sensitivity and a low detection limit of 1.89 μGyair s–1, all of which meet the needs of medical diagnosis. [ABSTRACT FROM AUTHOR]

Introduction: To investigate CD44 effects on the adriamycin‐resistant in chronic myelogenous leukaemia cells K562, we explored the role of CD44 in the K562 cells migration and apoptosis. Methods: GeneChip® screening is used for elucidating various chemoresistance‐related gene expression in the adriamycin‐resistant leukaemia cells K562/ADR. We constructed K562/CD44 cells by transfection of an EGFP‐SV40‐CD44 plasmid, and adriamycin‐resistant ability was confirmed by detecting migration and apoptosis‐related proteins and mRNA expression using Western blotting and Real‐time PCR respectively. Results: K562/CD44 cells were generated by the transfection of an EGFP‐SV40‐CD44 plasmid with high CD44 expression. mRNA expression levels of CD44 and P‐glycoprotein (P‐gp), along with the proliferation rate, were increased, while the apoptosis rate of K562/CD44 cells was decreased. Migration‐associated proteins such as MMP‐2 and MMP‐9 were upregulated, whereas apoptosis‐related protein Bax was downregulated and Bcl‐2 protein was not significantly altered in the K562/CD44 cells. Conclusions: CD44 might be involved in adriamycin resistance via regulation of P‐gp, MMP‐2, MMP‐9, and Bcl‐2/Bax. [ABSTRACT FROM AUTHOR]

All‐inorganic perovskites have been intensively investigated as potential optoelectronic materials because of their excellent thermal stability, especially for CsPbI2Br. Herein, the authors studied the effects of mixed passivation utilizing organic phenylethylammonium bromide and inorganic ionic cesium bromide (PEABr + CsBr) on the all‐inorganic perovskite (CsPbI2Br) solar cells for the first time. The treatment with different passivation mechanisms enhances the perovskite film quality, resulting in uniform surface morphology and compact film with low trap density. Besides, the passivation improves the energy level alignment, which benefits the hole extraction at the perovskite/HTL interface and drives the interface electron separation, suppressing the charge recombination and realizing a high open‐circuit voltage (Voc). Finally, the device represents a high power conversion efficiency (PCE) of 16.70%, a Voc of 1.30 V, and an excellent fill factor (FF) of 0.82. The Voc loss and high FF should be among the best values for CsPbI2Br based devices. Furthermore, the treated devices exhibit remarkable long‐term stability with only 8% PCE loss after storing in a glove box for more than 1000 h without encapsulation. [ABSTRACT FROM AUTHOR]

All‐inorganic perovskite/gallium arsenide (GaAs) tandem solar cells are of great interest for potential space applications. Herein, planar all‐inorganic four‐terminal (4‐T) and two‐terminal (2‐T) perovskite/GaAs tandem solar cells are simulated and optimized, respectively. To achieve higher absorption in the 4‐T configuration, the reflection and parasitic absorption have to be reduced through optimizing the thickness of the perovskite and GaAs base, reducing the thickness of SnO2 and the organic hole transport layer (HTL), and introducing an antireflection coating, respectively. To balance the short‐circuit current and open‐circuit voltage of the GaAs bottom cell, the doping concentration on GaAs is optimized to 1018 cm−3 that has resulted in a high power conversion efficiency (PCE) of 30.97%. Based on the results of 4‐T configuration, all‐inorganic perovskites with different halide compositions are used for current matching to achieve a high‐efficiency 2‐T configuration. After studying the effects of defect density and optimizing the doping concentration of the GaAs base, an extremely high PCE of 30.67% is achieved based on 2‐T CsPbIBr2/GaAs tandem solar cells. Furthermore, the current mismatching under the AM0 spectrum is eliminated for potential high altitude/space application, and the device offers a very competitive PCE of 27.23% compared with that of traditional GaAs double‐junction tandem solar cells. [ABSTRACT FROM AUTHOR]

With the power conversion efficiency (PCE) surpassing 25%, the eye‐catching and promising perovskite materials have proved to be potential competitors in photovoltaic field. Till now, massive efforts have been invested into this blooming flower to further raise its efficiency approaching the Shockley‐Queisser limit (SQ limit) and improve its stability for prolonging effective operation life. In details, various methods including component engineering, structure optimization and interfacial treatment have been used for realizing efficient and stable devices. Especially, the charge transport layers usually play critical roles in effective extraction and transportation of charge carriers. Compared with organic charge transport materials, inorganic materials generally demonstrate excellent stability due to their superior film qualities and inert chemical properties. Moreover, low cost, high charge mobility and material stability have been proved for inorganic electron and hole transport materials. This review summarizes the general progress of different inorganic hole transport materials in perovskite solar cells of recent years for better acquaintance of their contribution in efficient and stable devices. The discussions about performance improvement in the future directions are also provided. [ABSTRACT FROM AUTHOR]

Human hydroxysteroid dehydrogenase‐like 2 (HSDL2) is a potent regulator in cancers and is also involved in lipid metabolism, but the role of HSDL2 in cervical cancer and whether it regulates the progress of cervical cancer through lipid metabolism remains unclear. In this study, we found that the overexpression of HSDL2 was in relation with cervical cancer progression including lymph nodes metastasis and recurrence. HSDL2 could serve as a novel marker of early diagnosis in cervical cancer. HSDL2 also gave impetus to tumorigenesis by initiating and promoting proliferation, invasion and migration of cervical cancer cells (Hela, C33A and SiHa) through EMT. Interestingly, we also searched that HSDL2 participated in oncogenesis by regulating lipid metabolism. In sum, our results gave the novel insight of HSDL2 functions which could be the potential for being the biomarker of prognosis and new target of therapy. [ABSTRACT FROM AUTHOR]

Background and Aim: Aerobic glycolysis (the Warburg effect) is a distinctive metabolic hallmark of colon adenocarcinoma. Ezrin was a member of the Ezrin–Radixin–Moesin protein family and has been found profoundly implicated in tumorigenesis. However, the specific functional roles of Ezrin in metabolic reprogramming of colon adenocarcinoma remain poorly characterized and need to be explored. Methods: The expression of Ezrin in colon adenocarcinoma tissues was screened by bioinformatics analysis and immunohistochemical assay. Si‐RNA‐mediated transfection and overexpression plasmid transfection were performed in colon adenocarcinoma cells. The proliferation viability was measured using MTT, colony formation, and EdU assays. The migration ability was determined using wound healing and transwell assay. The expression of EMT markers and transcriptional factors was detected using immunofluorescence staining and western blot assays. Glucose uptake, lactate production, and ATP assay were performed to validate the effect of Ezrin on glycolysis‐mediated colon adenocarcinoma progression. Results: Ezrin was upregulated in colon adenocarcinoma tissues and associated with poor survival. Ezrin stimulated colon adenocarcinoma cell proliferation, migration, and the process of EMT. Ezrin aroused significant increase in glucose uptake, lactate production, and ATP level in colon adenocarcinoma cells. Further investigations demonstrated that treatment with a glycolytic inhibitor 2‐deoxy‐d‐glucose reversed the effects reduced by Ezrin on colon adenocarcinoma cells. Conclusions: Our results evidenced a novel mechanism for colon adenocarcinoma cells proliferation and migration induced by Ezrin via glycolysis. [ABSTRACT FROM AUTHOR]

Lead halide perovskites have attracted increasing attention in photovoltaic devices, light‐emitting diodes, photodetectors, and other fields due to their excellent properties. Besides optoelectronic devices, growing numbers of studies have focused on the perovskite‐based electrical devices in the past few years, such as transistors and resistive random access memories (RRAMs). Here, this article summarizes the recent progress the researchers have made of RRAM devices. Primarily, the working mechanism and the key parameters of RRAM are introduced. Generally, the working principles, including the conductive filament model (containing the types of the model of the metal cations‐induced filament and the model of the ions migration in bulk), the interface effect, and the electronic effect are the origins of the RRAM behaviors, and hence, various factors that affect the device performance are explored. Then, RRAMs based on organolead halide perovskite and all‐inorganic perovskite are discussed in terms of different structures, different compositions, and different fabrication methods. Finally, a brief conclusion and a broad outlook are given on the progress and challenges in the field of perovskite‐based RRAMs. [ABSTRACT FROM AUTHOR]

Ezrin, one of the ezrin‐radixin‐moesin (ERM) proteins, is involved in the formation of cell membrane processes and has been implicated in the promotion of cancer proliferation and metastasis. However, the possible role of ezrin in hepatocellular carcinoma (HCC) metastasis and glycolysis reprogramming has remained unclear. In this study, we found that ezrin was upregulated in HCC tissues, and its overexpression was linked with HCC patients' aggressive tumor characteristics and poor prognosis. Functional experiments further revealed that ezrin overexpression promoted HCC cell proliferation, epithelial‐to‐mesenchymal transition (EMT) progression and angiogenesis. In addition, by measuring glucose consumption, lactate production, ATP levels and the expression of glucose metabolism‐related markers in HCC cells, we investigated whether ezrin regulated glucose metabolism. Moreover, 2‐deoxy‐D‐glucose (2‐DG) affected ezrin‐mediated proliferation, migration and EMT of HCC cells, which suggested that ezrin may, at least in part, promote HCC progression by regulating glycolysis reprogramming. Based on our results, we proposed that ezrin was involved in HCC progression and may be a valid prognostic marker. [ABSTRACT FROM AUTHOR]

Understanding the crystal anisotropy effect of materials on optical and electrical properties is crucial for further comprehension of the device operating mechanism and device performance improvement. In this study, a detailed theoretical analysis is performed to explore the crystal anisotropy effect on the performance of perovskite solar cells by employing state‐of‐the‐art multiscale simulations connecting from the material (first‐principle theory) to the device (drift‐diffusion model). According to the results obtained from first‐principle calculation, the mobility and absorption coefficient of CsPbIBr2 and CsPbI2Br along the [001] orientation are larger than those along the [100] orientation, suggesting that the transport properties and optical properties along the [001] orientation are superior to those along the [100] orientation. According to the results obtained from the drift‐diffusion model, owing to the superior optical and transport characters along the [001] direction, the optimal power conversion efficiencies (PCEs) of CsPbI2Br (18.88%) and CsPbIBr2 (16.42%) solar cells can be obtained. In addition, the two‐terminal CsPbIxBr3‐x/silicon tandem solar cell is also investigated. By utilizing CsPbIBr2/silicon and CsPbI2Br/silicon tandem structures along the [001] orientation, ultrahigh efficiencies are achieved up to 26.32% and 31.39%, respectively. Therefore, the [001] crystal orientation of CsPbIBr2 and CsPbI2Br is more suitable for further applications of optoelectronic devices. [ABSTRACT FROM AUTHOR]

All‐inorganic perovskite CsPbI2Br have been regarded as a promising candidate to tackle the thermal instability issue of organic–inorganic perovskite solar cells. However, the serious interfacial charge recombination and large voltage potential loss in cells circumscribe their performance and commercialization. Herein, a facile approach is demonstrated in which the SnO2 electron transport layer is modified with short‐period deep‐ultraviolet (DUV) photoactivation process to decrease the work function and achieve better energy alignment with the conduction band of perovskites. Such modification triggers efficient charge transfer and reduces the charge recombination. Moreover, first‐principles calculation further demonstrates that DUV‐treated SnO2 can strengthen the interface interaction, reduce the interface stress caused by lattice mismatch, induce more ordered perovskite structure, enlarge transfer charge from 0.71 to 2.33 e, gain larger built‐in field (from 0.74 to 2.09 eV), lower work function, and smaller conduction band offset. Thus, all‐inorganic CsPbI2Br solar cells based on DUV‐treated SnO2 exhibit a significant enhancement in power conversion efficiency, and the champion cell achieves an elevated efficiency of 15.1% with a superior Voc of 1.22 V and better stability. [ABSTRACT FROM AUTHOR]

Recent research shows that the interface state in perovskite solar cells is the main factor which affects the stability and performance of the device, and interface engineering including strain engineering is an effective method to solve this issue. In this work, a CsBr buffer layer is inserted between NiOx hole transport layer and perovskite layer to relieve the lattice mismatch induced interface stress and induce more ordered crystal growth. The experimental and theoretical results show that the addition of the CsBr buffer layer optimizes the interface between the perovskite absorber layer and the NiOx hole transport layer, reduces interface defects and traps, and enhances the hole extraction/transfer. The experimental results show that the power conversion efficiency of optimal device reaches up to 19.7% which is significantly higher than the efficiency of the device without the CsBr buffer layer. Meanwhile, the device stability is also improved. This work provides a deep understanding of the NiOx/perovskite interface and provides a new strategy for interface optimization. [ABSTRACT FROM AUTHOR]

Valproic acid (2‐propylpentanoic acid, VPA) has been widely used as an anticonvulsant drug and is a choice drug for seizure treatment. VPA is also used as a short‐chain fatty acid HDAC inhibitor that affects proliferation and differentiation and induces cell apoptosis in both solid and haematologic malignancies. Here, we observed that VPA treatment inhibited HDAC1/2 activity and induced autophagy in gastric cancer cells, leading to apoptosis. VPA‐induced apoptosis occurred through inhibition of the HDAC1/PTEN/Akt signalling pathway and involved alterations in Bcl‐2 and Beclin‐1. The antitumour effects of VPA were verified in vivo using SGC‐7901 xenograft models. Moreover, we evaluated the expression of HDAC1/2 in gastric cancer patient samples and revealed a positive correlation between HDAC1/2 overexpression and poor prognosis. These findings indicate that VPA may serve as a potential therapeutic agent for gastric cancer and that HDAC1/2 might be a promising therapeutic biomarker for the disease. [ABSTRACT FROM AUTHOR]

This study focused on the expression of mortalin in colorectal cancer (CRC). Mortalin activated the Wnt/β‐catenin pathway to accelerate cell proliferation and the epithelial–mesenchymal transition (EMT) program. Data from online databases displayed that the expression of mortalin was high in CRC, which was further validated using clinical specimens. Meanwhile, high mortalin expression was positively associated with a poor overall survival rate. Suppression of mortalin inhibited CRC cell proliferation as evaluated by the 3‐(4,5‐dimethyl‐2‐thiazolyl)‐2,5‐diphenyl‐2‐H‐tetrazolium bromide (MTT), colony formation, and immunofluorescence staining assays. In addition, depletion of mortalin inhibited CRC cell EMT progression and deactivated the Wnt/β‐catenin pathway. Altogether, mortalin is highly expressed in CRC and may indicate a poor prognosis. Mortalin accelerated CRC progression by stimulating cell proliferation and the EMT program. This study may provide a potential clinical therapeutic target for CRC. [ABSTRACT FROM AUTHOR]

Perovskite CsPbIBr2 is attracting ever‐increasing attention for carbon‐based, all‐inorganic solar cells, owing to its well‐balanced band gap and stability features. However, significant interfacial recombination of charge carriers in solar cells fabricated with this active layer, which is intrinsically associated with the unwanted conduction band misalignment between CsPbIBr2 and the commonly used TiO2 electron transport layer, has limited power conversion efficiency (PCE) values. Herein, we demonstrate successful conduction band alignment engineering at the TiO2/CsPbIBr2 heterojunction by modifying TiO2 with CsBr clusters. Such modification triggers a beneficial increase in the conduction band minimum (CBM) of TiO2 from −4.00 to −3.81 eV and decreases the work function from 4.11 to 3.86 eV, thus promoting favorable band alignment at the heterojunction, suppressing recombination, and improving extraction and transport of charge carriers. As a result, the carbon‐based, all‐inorganic CsPbIBr2 solar cells exhibit over 20 % enhancement in average PCE. The champion device achieves a PCE of 10.71 %, a record among pure CsPbIBr2‐based cells, open‐circuit voltage of 1.261 V, and excellent stability. [ABSTRACT FROM AUTHOR]

Abstract: NiOx hole transporting layer has been extensively studied in optoelectronic devices. In this paper, the low temperature, solution–combustion‐based method is employed to prepare the NiOx hole transporting layer. The resulting NiOx thin films show better quality and preferable energy alignment with perovskite thin film compared to high temperature sol–gel‐processed NiOx. With this, high‐performance perovskite solar cells are fabricated successfully with power conversion efficiency exceeding 20% using a modified two‐step prepared MA1−yFAyPbI3−xClx perovskite. This efficiency value is among the highest values for NiOx‐based devices. Various characterizations and analyses provide evidence of better film quality, enhanced charge transport and extraction, and suppressed charge recombination. Meanwhile, the device exhibits much better device stability compared to sol–gel‐processed NiOx and poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate)‐based devices. [ABSTRACT FROM AUTHOR]

In this work, well-ordered periodic nanogroove structures are constructed on the surfaces of indium tin oxide (ITO) substrates through a simple and cost-effective patterning method, laser interference lithography (LIL). By using the nanopatterned ITO electrodes coated conformally with metal oxide thin films as the electron-selective interlayer (ESL) fabricated by low-temperature atomic layer deposition (ALD), periodically nanostructured cathode-active-layer interfaces are formed in the inverted organic solar cells (OSCs). Compared with a planar-ITO cathode, a nanopatterned ITO cathode with 30 nm high nanogrooves leads to considerably improved short-circuit current and power conversion efficiency for poly(3-hexylthiophene)/[6,6]-phenyl-C61-butyric acid methyl ester (P3HT/PCBM) based cells. The improvement in the photocurrent is caused by enhanced light absorption and improved charge-carrier generation in the devices with nanostructured cathode-active-layer interfaces. [ABSTRACT FROM AUTHOR]

To investigate the clinicopathological significance of DEK overexpression in breast cancers, a total of 196 cases, including 20 of normal tissues, 12 of intraductal hyperplasia, 31 of ductal carcinoma in situ (DCIS) and 133 of invasive ductal carcinoma of the breast, were selected from the Department of Pathology, Yanbian Tumor Hospital for immunohistochemical staining of DEK, estrogen (ER), progesterone (PR) and Ki-67 proteins. In results, DEK protein had higher positivity in DCIS, compared with the adjacent normal breast tissues. Also, DEK protein was strongly positive in invasive ductal carcinoma of the breast on immunohistochemistry, which was significantly higher than normal breast tissues. However, only two (2/12) cases of intraductal hyperplasia of the breast showed positive staining for DEK protein. Additionally, DEK overexpression was significantly correlated with the increased proliferating index of Ki-67. For the histological grade, DEK positive rate was only 39.6% in G1 breast cancers, but significantly higher in G2 (92.3%) and G3 (97.0%) cases ( P<0.05). Also, a strongly positive rate of DEK was lower in Stage-0 (21.4%) and Stage-I (40.9%) compared with Stage-IIa (87.5%), Stage-IIb (89.7%) and Stage-IIIa (92.3%) ( P<0.05). And DEK protein showed higher expression level in <3 years disease free survival breast cancers than it did in ≥3 years disease free survival cases ( P<0.05). However, no statistically difference was found among DEK expression, lymph node metastasis, and ER and PR expressions. In conclusion, DEK overexpression appears to be associated with breast cancer progression and DEK may potentially be used as a breast cancer biomarker for the early diagnosis, prognostic evaluation and therapeutic target for breast cancer. [ABSTRACT FROM AUTHOR]

The aim of the present study was to investigate the distribution of HPV genotypes in uterine cervical lesions in Yanbian, northern China. HPV-DNA chip (oligonucleotide microarray) and cervical biopsy were used for 322 women in 1998–2005. All the normal cervical epithelia were negative for HPV. The positive rate of high-risk HPV was 33.9% in cervical intra-epithelial neoplasia (CIN)-1, 51.6% in CIN-2, 57.7% in CIN-3, 66.7% in cervical glandular intra-epithelial neoplasia (CGIN), 91.7% in squamous cell carcinoma (SCC), and 78.6% in adenocarcinoma. HPV-16 was the major type in all CIN and SCC cervical lesions, but in cervical adenocarcinoma HPV-18 was the most common type, and HPV-16 was the second most common type. Several cases of CIN-3, SCC and adenocarcinoma had multiple types of HPV, but there was none in CIN-1/2. In summary, HPV-16 is the type most frequently involved in the development of SCC of the cervix, and this may be helpful for the prediction of the development and progress of CIN-2/3, whereas both HPV-18 and -16 play a prominent role in the development of adenocarcinoma and CGIN of the cervix in Yanbian, northern China. [ABSTRACT FROM AUTHOR]

The charge transport layer is crucial to the performance and stability of the perovskite solar cells (PSCs). Compared with other conventional metal oxide electron transport materials, SnO2 has a deeper conduction band and higher electron mobility, and can efficiently serve as an electron transport layer to facilitate charge extraction and transfer. Herein, an optimized low‐temperature solution‐processed SnO2 electron transport layer is achieved by doping polyethylenimine polyelectrolyte into SnO2 for the first time in the PSCs. It is found that the performance of all aspects of the doped SnO2 film is improved over that of the pristine SnO2 film. The better energy level alignment, larger built‐in field, enhanced electron transfer/extraction, and reduced charge recombination all contribute to the improved device performance. Finally, a PSC with a power conversion efficiency of 20.61% is successfully prepared under low temperature below 150 °C. Moreover, the stability of the doped SnO2‐based device is also greatly improved. [ABSTRACT FROM AUTHOR]

Lead‐free halide double perovskites Cs2AgB″X6 (B″═In, Bi; X═Cl, Br, I) are emerging as excellent photoelectric materials. Investigating their mechanical and thermodynamic properties under hydrostatic pressure is vital for designing high‐performance photoelectric devices. Although Cs2AgB″X6 exhibits similar cubic structures, the bond length and strength characteristics of Cs2AgInX6 are different to those of Cs2AgBiX6, and Cs2AgB″X6 exhibits obvious mechanical anisotropic. Upon experiencing pressure, the stablility of Cs2AgB″X6 is improved and without phase transition, and its bond characteristics are unified, which is different to lead halide perovskites. Compared to Cs2AgBiX6, Cs2AgInX6 may be more suitable to flexible devices due to its higher shear and bulk modulus. In addition, the thermal conductivities of Cs2AgBiX6 (X═Cl, Br) and Cs2AgBiX6 (X═Cl, Br, I) are 0.41, 0.32, 0.37, 0.29, 0.23 W m−1 K−1, and can be enlarged by pressure and surpass that of lead halide perovskite. Moreover, all the Cs2AgB″X6 (B″═In, Bi; X═Cl, Br, I) possess the same saturated heat capacity of about 249.3 J mol−1 K−1. These variations of mechanical and thermal properties are elucidated by the bonds. These results maybe also applicable to other double perovskites, and beneficial for designing devices with better optoelectronic performance. [ABSTRACT FROM AUTHOR]

The article looks at research regarding bandgap engineering strategies including impurity and pressure as well as their underlying mechanisms and mentions intermediate band and external electric field for bandgap structure.

Material passivation is essential to enhance the quality of perovskite materials and boost the performance of perovskite solar cells (PSCs). However, most of the previous reports only paid attention to improving the quality of perovskite films by adopting single passivation. Here, a facile strategy that can carry out double passivation to improve the performance of PSCs is demonstrated. By using the dilute halide salt PEABr solution to treat the perovskite film, PbI2 can precipitate from the perovskite. Both PEABr and PbI2 can passivate the perovskite film, and by combining PEABr and PbI2, the double passivation improves the performance of PSCs significantly. Very high short‐circuit current density of 24.30 mA cm−2, open‐circuit voltage of 1.10 V, and fill factor of 79.75% are achieved which lead to a surprising efficiency of 21.32% for the passivated device. The improved efficiency is mainly according to the available surface passivation of the perovskite material, leading to repressed nonradiative recombination and unhindered charge collection. In addition, the passivated device exhibits better power conversion efficiency stability relative to the control device. [ABSTRACT FROM AUTHOR]

In article number 1900293, Jingjing Chang and co-workers demonstrate a novel solution process to develop 2D/3D perovskites with modulated diffusion passivation by introducing a PEAI and DMF additive, which could effectively enhance device performance and long-term stability. The solar cells with passivation treatment exhibit a high fill factor of 83.6% and an average power conversion efficiency of 21.4%. [Extracted from the article]

Perovskite/copper indium gallium selenide (CIGS) tandem solar cells represent an attractive configuration to obtain ultrahigh efficiency. A detailed theoretical analysis is crucial for further improving the performance of tandem solar cells. Herein, four‐terminal and two‐terminal perovskite/CIGS tandem solar cells are intensively researched. For four‐terminal perovskite/CIGS tandem solar cell, the optimal thicknesses of CH3NH3PbI3 and CIGS are 0.5 and 3 μm, respectively, according to the simulation result. Reducing the thickness of TiO2 and Spiro‐OMeTAD can minimize the short‐wavelength parasitic absorption and long‐wavelength parasitic absorption, respectively. Meanwhile, using antireflection coating, such as 100 nm MgF2, is beneficial to increase the photon absorption. For two‐terminal perovskite/CIGS tandem solar cells, the thicknesses of perovskite and CIGS are tuned to meet the current matching. To further improve the efficiency of two‐terminal tandem cells, FTO thickness is reduced to minimize reflection, and the optimal doping concentration of CIGS (1 × 1018 cm−3) is used. In addition, results show that the quality of perovskite films should be improved by enlarging the grain size to decrease the trap states at grain boundary. Finally, the optimal efficiency of two‐terminal CH3NH3PbI2Br/CIGS tandem solar cells reaches 31.13%. [ABSTRACT FROM AUTHOR]

Understanding the interfacial properties of perovskite/SnO2 interface is important for perovskite solar cell design and optimization. Here, interfacial structure and transport properties of CH3NH3PbI3/SnO2 interfaces are investigated comprehensively by density functional theory and experiment. Forming CH3NH3PbI3/SnO2 interfaces weakens the gap states induced by CH3NH3PbI3 surfaces. The interfacial transport properties are strongly dependent on the interface atomic configurations. The CH3NH3PbI3/SnO2 interface with PbI and O terminations is more beneficial for hole blocking and electron transporting due to the largest valence band offset compared to the CH3NH3PbI3/SnO2 interface with other terminations. Moreover, it exhibits a larger electrostatic potential difference compared with CH3NH3PbI3/TiO2 interface, leading to the higher electron transfer efficiency. Hence, higher power conversion efficiency is achieved based on CH3NH3PbI3/SnO2 compared to CH3NH3PbI3/TiO2 structure in experiments. In addition, CH3NH3PbI3/SnO2 interfaces with PbI terminations are more stable than those with CH3NH3I terminations, suggesting PbI2 layer may be preferentially formed on SnO2 substrate during CH3NH3PbI3 fabrication process. Such results could provide a useful understanding on CH3NH3PbI3/SnO2 interface and contribute to new strategies for the interface optimization. [ABSTRACT FROM AUTHOR]

The discovery of two‐dimensional (2D) Ga2O3 has provided an effective way to further tune the performance of β‐Ga2O3. Understanding the effects of strain and electric field (E‐field) on 2D Ga2O3 is helpful to explore the mechanism and potential application in the flexible device. Here, transport and optical properties of monolayer Ga2O3 under uniaxial strain and E‐field are investigated. An indirect‐to‐direct band‐gap‐transition occurs under uniaxial tension due to the different variation of π bonding at the valence bands. The band‐gap exhibits a parabolic variation character from compression to tension, and relates to the direction of uniaxial strain. Interestingly, the transport characters are sensitive to the direction of uniaxial strain, and both compression and tension along b direction enhance the mobility of monolayer Ga2O3, which is inconsistent with that of electron effective mass. The mobility of tensile monolayer Ga2O3 can be enlarged to 48368.14 cm2V−1s−1, different to that of 2D layered materials. Interestingly, the ultra‐visible absorption coefficients are just enhanced significantly by compression along c direction. Upon monolayer Ga2O3 undergoes large E‐field (>0.5 eV Å−1), the band‐gap and anisotropic transport property decreases and even vanishes. The results are useful to reveal the mechanisms and potential of 2D Ga2O3 in the flexible devices. [ABSTRACT FROM AUTHOR]

ZnO is considered as a potential electron transport layer (ETL) in solar cells due to its high charge carrier mobility and low‐temperature processability. However, it is challenging to obtain highly efficient and stable perovskite solar cells (PSCs) using low‐temperature ZnO ETL due to the poor chemical compatibility between ZnO and perovskite films. Hence, proper surface passivation strategies of ZnO ETL are developed to enhance the ZnO/perovskite interface stability for highly efficient PSCs. In this study, low‐temperature TiOx post‐treatment is performed to passivate the ZnO surface, suppress the interface charge recombination, and stabilize the ZnO/perovskite interface. The fullerene treatment is further applied to enhance the electron transfer from perovskite to ZnO and reduce the hysteresis behavior. Finally, high‐performance PSCs with an efficiency of over 20% and improved stability are achieved. [ABSTRACT FROM AUTHOR]

Among all inorganic halide perovskite photovoltaic materials, CsPbIBr2 exhibits the most balanced features in terms of bandgap and stability. However, the poor quality of solution‐processed CsPbIBr2 films impedes further optimization of cells performance. Herein, a facile intermolecular exchange strategy for CsPbIBr2 film is demonstrated, wherein an optimized methanol solution of CsI is spin‐coated on CsPbIBr2 precursor film in conventional one‐step solution route. It surprisingly produces full‐coverage and pure‐phase CsPbIBr2 films featured with average grain size of ≈0.65 µm, few grain boundaries, high crystallinity, preferable (100) orientation, stoichiometric composition along with favorable electronic structures for effective dissociation and transfer of carriers. Hence, the cost‐effective, carbon‐based all‐inorganic planar perovskite solar cells based on them, yield an optimized efficiency of 9.16% with a stabilized value of 8.46% in ambient air conditions that highlight a particularly superb open‐circuit voltage of 1.245 V, all of which represent the highest values reported in pure CsPbIBr2 based cells so far. Moreover, the optimized cell without encapsulation shows excellent long‐term stability because it can retain 90% over 60 days and 97% over 7 days of its initial efficiency, when is stored controllably in ≈45% relative humidity at 25 or 85 °C at zero humidity, respectively. A carbon‐based all‐inorganic planar CsPbIBr2 solar cell with a record efficiency of 9.16%, an extremely high open‐circuit voltage of 1.245 V, and excellent long‐term stability is achieved by a facile intermolecular exchange strategy. Its impressive performance mainly derives from the desirable features of CsPbIBr2 film including full coverage, high crystallinity, preferable (100) orientation, and stoichiometric composition along with favorable electronic structure. [ABSTRACT FROM AUTHOR]