Electron Transport Research Articles

Controllable Heavy n–type Behaviours in Inverted Perovskite Solar Cells with Non‐Conjugated Passivants

AbstractInterfacial issues between the perovskite film and electron transport layer greatly limit the efficiency and stability of inverted (p‐i‐n) perovskite solar cells (PSCs). Despite organic ammonium passivants have been widely established as interfacial layers, they failed to improve electron extraction. Here, we reported that the heavy n‐type characteristics in a low band gap perovskite film could be modulated by incorporating non‐conjugated ammonium passivants with strong electron‐withdrawing abilities. This resulted in a significant enhancement of electron extraction in the heavily n‐type doped perovskite. The passivant‐treated PSCs exhibited a power conversion efficiency of 25.74 % with an excellent fill factor of 85.4 % and a high open‐circuit voltage of 1.166 V, which are significantly higher than that of the control device. The unencapsulated devices maintained 88 % of their initial PCEs after 1,200 hours at 85 °C.

Stabilizing Wide‐Bandgap Perovskite with Nanoscale Inorganic Halide Barriers for Next‐Generation Tandem Technology

AbstractWide‐bandgap (WBG) perovskite solar cells (PSCs) play a crucial role in advancing perovskite‐based tandem solar cells. In WBG perovskite films, grain boundary (GB) defects are the main contributors to open‐circuit voltage (VOC) deficits and performance degradation. This report presents an effective strategy for passivating GBs by incorporating an inorganic protective layer and reducing the density of GBs in perovskite films. This is achieved by integrating potassium thiocyanate (KSCN) into I‐Br mixed halide WBG perovskites. It is reported for the first time that the incorporation of KSCN creates band‐shaped barriers along the GBs. In addition, KSCN enlarges the grains of perovskite film. Elemental and structural analyses reveal that these barriers are composed of potassium lead halide. Incorporating KSCN significantly enhances the fill factor and VOC of WBG single‐junction PSCs by reducing trap density. This results in high power conversion efficiencies of 19.22% (bandgap of 1.82 eV), 20.45% (1.78 eV), and 21.54% (1.70 eV) with a C60/bathocuproine electron transport layer, and 18.51% (1.82 eV) with a C60/SnO2. Furthermore, both operational and shelf stabilities are significantly improved due to reduced light‐induced halide segregation. By using inorganic‐halide‐passivated WBG sub‐cells, a monolithic all‐perovskite tandem solar cell with an efficiency of 27.04% is demonstrated.

First-principles study on thermal and electrical transport properties of NbGe2 and NbSi2: the role of electron-phonon coupling

Abstract We study coupled electron and phonon transport in NbX2 with X=Ge, Si, in which experimental evidence of strong electron-phonon coupling and hydrodynamic transport has been reported. Based on first-principles calculations at the density functional theory level, we report their thermal and electrical transport properties. We find that phonon-electron scattering strongly affects their phonon thermal conductivity (κ ph) and leads to weak temperature dependence of κ ph, instead of normal inverse temperature dependence when anharmonic three phonon scattering dominates. Moreover, κ ph contributes to quarter of the total thermal conductivity, which differs from typical metals where total thermal conductivity is predominantly from electron part. Different from previous numerical study, our results of electrical resistivity agree well with experimental measurement. The anisotropic property of the transport coeffcients is attributed to the electron and phonon dispersion relation. Moreover, we find negligible effect of electron-phonon drag on the transport property, contrary to expectation from a strongly coupled electron-phonon fluid.

Aging, ROS, and cellular senescence: a trilogy in the progression of liver fibrosis.

Ageing is an inevitable and multifaceted biological process that impacts a wide range of cellular and molecular mechanisms, leading to the development of various diseases, such as liver fibrosis. Liver fibrosis progresses to cirrhosis, which is an advanced form due to high amounts of extracellular matrix and restoration of normal liver structure with failure to repair damaged tissue and cells, marking the end of liver function and total liver failure, ultimately death. The most important factors are reactive oxygen species (ROS) and cellular senescence. Oxidative stress is defined as an impairment by ROS, which are by-products of the mitochondrial electron transport chain and other key molecular pathways that induce cell damage and can activate cellular senescence pathways. Cellular senescence is characterized by pro-inflammatory cytokines, growth factors, and proteases secreted by senescent cells, collectively known as the senescence-associated secretory phenotype (SASP). The presence of senescent cells, which disrupt tissue architecture and function and increase senescent cell production in liver tissues, contributes to fibrogenesis. Hepatic stellate cells (HSCs) are activated in response to chronic liver injury, oxidative stress, and senescence signals that drive excessive production and deposition of extracellular matrix. This review article aims to provide a comprehensive overview of the pathogenic role of ROS and cellular senescence in the aging liver and their contribution to fibrosis.

Efficient and Stable Quantum‐Dot Light‐Emitting Diodes with Trilayer PIN Architecture

AbstractAlthough the performance of quantum dot light‐emitting diodes (QLEDs) has been greatly improved in recent years, the multilayer device structure has become increasingly complex, limiting the practical application of QLEDs. Here, a novel trilayer PIN QLED with only three functional layers, which are Spiro‐OMeTAD:TFB bulk‐heterojunction (BHJ) hole transport layer (HTL), quantum‐dot emitting layer and ZnMgO electron transport layer is demonstrated. Due to the enhanced hole injection capability and suppressed electron leakage of Spiro‐OMeTAD:TFB BHJ HTL, the trilayer PIN QLED can show an excellent external quantum efficiency (EQE) of 25.1% and an impressive brightness of 299300 cd m−2 at only 8 V, which are significantly higher than those of conventional QLED. Moreover, the device stability is also remarkably improved due to the mitigation of hole accumulation and removal of unstable PEDOT:PSS. By using liquid alloy EGaIn as cathode, a fully solution‐processed vacuum‐free trilayer PIN QLED with a higher EQE of 27.3% can be further realized. The developed trilayer PIN QLEDs, with better performance and fewer functional layers, can promote the commercialization of QLED technology.

BHLHE40-mediated transcriptional activation of GRIN2D in gastric cancer is involved in metabolic reprogramming.

Gastric cancer (GC) is the third leading cause of death in developed countries. The reprogramming of energy metabolism represents a hallmark of cancer, particularly amplified dependence on aerobic glycolysis. Here, we aimed to illustrate the functional role of glutamate ionotropic receptor N-methyl-D-aspartate type subunit 2D (GRIN2D) in the regulation of glycolysis in GC and the mechanisms involved. Differentially expressed genes were analyzed using the GEO and GEPIA databases, followed by prognostic value prediction using the Kaplan-Meier Plotter database. The effect of GRIN2D knockdown on the malignant behavior and glycolysis of GC cells was explored. GRIN2D expression was upregulated in GC cells and promoted the malignant behavior of GC cells by activating glycolysis. Class E basic helix-loop-helix protein 40 (BHLHE40) was overexpressed in GC cells and mediated transcriptional activation of GRIN2D. The anti-tumor effects of BHLHE40 knockdown on GC cells in vitro and in vivo were reversed by GRIN2D overexpression. Knockdown of GRIN2D or BHLHE40 downregulated the expression of mRNA of electron transport chain subunits and phosphorylation of p38 MARK and inhibited calcium efflux in GC cells. Overexpression of GRIN2D promoted calcium efflux, phosphorylation of p38 MARK protein, and proliferation of GES1 cells. Altogether, the findings derived from this study suggest that BHLHE40 knockdown suppresses the growth, mobility, and glycolysis of GC cells by inhibiting GRIN2D transcription and disrupting the BHLHE40/GRIN2D axis may be an attractive therapeutic strategy for GC.

High‐Performance MCNTs@MoS2(1‐x)Se2x Nanocomposites in Catalytic Hydrogen Evolution

AbstractAdvances in electrocatalysis require the development of high specific surface area materials with high electron conductivity. In this study, a series of MCNTs@MoS2(1‐x)Se2x nanocomposites has been prepared for application in catalytic hydrogen evolution. A uniform growth of MoS2(1‐x)Se2x nanoflower spheres on MCNTs has been achieved, circumventing stacking and aggregation. The introduction of the conducting material accelerated the electron transport rate in the electrode reaction. Structural characterization has confirmed that S doping increased the specific surface area of the catalyst, exposing more edge defects. As a result, the MCNTs@MoS2(1‐x)Se2x nanocomposites exhibited enhanced catalytic activity. Electrochemical tests have established that MCNTs@MoS1.5Se0.5 possessed the lowest overpotential (146 mV) at a current density of 10 mA/cm2 with the smallest Tafel slope (45.1 mV/dec).

Extreme electron-hole drag and negative mobility in the Dirac plasma of graphene.

Coulomb drag between adjacent electron and hole gases has attracted considerable attention, being studied in various two-dimensional systems, including semiconductor and graphene heterostructures. Here we report measurements of electron-hole drag in the Planckian plasma that develops in monolayer graphene in the vicinity of its Dirac point above liquid-nitrogen temperatures. The frequent electron-hole scattering forces minority carriers to move against the applied electric field due to the drag induced by majority carriers. This unidirectional transport of electrons and holes results in nominally negative mobility for the minority carriers. The electron-hole drag is found to be strongest near room temperature, despite being notably affected by phonon scattering. Our findings provide better understanding of the transport properties of charge-neutral graphene, reveal limits on its hydrodynamic description, and also offer insight into quantum-critical systems in general.

Improving Vietnam’s law on contracts for international carriage of goods by sea: a comparative analysis with international conventions

ABSTRACT This paper critically examines the Vietnamese legal framework governing contracts for the international carriage of goods by sea, particularly in comparison to international conventions such as the Hague-Visby Rules, Hamburg Rules, and Rotterdam Rules. Despite its strategic maritime importance and extensive coastline, Vietnam has not fully aligned its maritime transport laws with these international standards. Through a detailed comparative analysis, the paper identifies key shortcomings in Vietnamese law, particularly in areas such as carrier liability, limitation periods for legal actions, and the adoption of electronic transport documents. The paper proposes specific legal reforms to enhance Vietnam's maritime legal system, making it more consistent with international norms and better suited to the nation's economic conditions. By adopting these recommendations, Vietnam can improve its maritime legal framework, fostering greater integration into the global marine economy and better protecting the rights and interests of all parties involved in maritime transport.

Menaquinone production in genetically engineered E. coli.

Menaquinone (MK) is an important electron transporter in Escherichia coli. This isoprenoid quinone can transfer electrons to many terminal acceptors, such as fumarate and nitrate, which helps this organism survive under diverse and challenging conditions. As the isoprenoid quinones with various length of isoprenyl tail are widely distributed in nature, the heterologous expression of polyprenyl diphosphate synthases (PDSs) has been investigated using its counterpart, ubiquinone (UQ). In this study, we investigated the MK production by the expression of various heterologous PDS genes from prokaryotic and eukaryotic species, including Saccharomyces cerevisiae COQ1 (hexa-PDS), Haemophilus influenzae hi0881 (hepta-PDS), Synechocystis sp. strain PCC6803 slr0611 (nona-PDS) and Glunocobacter suboxydans ddsA (deca-PDS) in E. coli. We detected specific isoforms of MK, including MK7, MK9, and MK10, via the expression of HI0881, Slr0611 and DdsA respectively, but rarely detect MK6 via the expression of Coq1. As UQ6 was detected in E. coli harboring COQ1, the acceptance of the side chain lengths by MenA (prenyl transferase for MK) was narrower than UbiA (prenyl transferase for UQ). We also identified a mutation in menA in the E. coli AN386 strain and a transposon insertion of IS186 in menC in E. coli KO229 (∆ispB) and its parental strain FS1576. Taken together, these results elucidate the different nature of MenA from UbiA.

Atomic Layer Deposition of ZnO on CsPbBr3 Perovskite Nanocrystals: Surface-Dependent Mechanistic Insights.

In this study, we investigate the atomic layer deposition (ALD) process on all-inorganic CsPbBr3 perovskite nanocrystals (PNCs) to introduce an inorganic electron transport layer (ETL) in light-emitting diode (LED) devices. Two types of CsPbBr3 PNCs were synthesized with oleate (OA) and oleylammonium (OLA) ligands on the surface. We found that CsPbBr3 PNCs with Cs oleate surfaces experienced severe photoluminescence (PL) quenching after the ALD process, while those with oleylammonium bromide surfaces did not show any significant PL drop. Transmission electron microscopy and X-ray photoelectron spectroscopy revealed that significant Pb metal formation and Ruddlesden-Popper planar faults, linked to uncoordinated Pb2+ ion defects, were generated in CsPbBr3 PNCs terminated with Cs oleate after ALD ZnO. Finally, we fabricated LEDs using PNCs with an ALD ZnO process to introduce inorganic ZnMgO nanoparticles as the ETL. The devices processed with ALD exhibited superior luminance and external quantum efficiency compared to those without the ALD process. This research provides crucial insights into the surface-dependent chemistry of PNCs and the surface-dependent performance of perovskite-based optoelectronic devices.

First-principles study of the electron and phonon transport properties in monolayer boron monosulfide

Abstract Motivated by the excellent electronic properties of theoretical proposed monolayer boron monosulfides (BS) binary materials, which belong to a light-element member of the group IIIA chalcogenides family, we have investigated the electron and phonon transport properties of three monolayer phases of BS (α, β and γ) using first-principles and Boltzmann transport theory methods. The calculated electronic structures show that α- and β-BS are semiconductors with indirect bandgaps of 4.01 eV and 3.87 eV, respectively, whereas the γ-BS is a semiconductor with a direct bandgap of 2.97 eV. Additionally, due to their light carrier effective masses, superior high carrier mobilities are observed, thus bringing high Seebeck coefficients. We also find that due to the absence of imaginary phonon frequencies, the three monolayer phases of BS show dynamical stability. The phonon group velocity and relaxation time are also calculated to analyze the phonon thermal conductivity. We find that strong phonon scattering makes γ-BS monolayer possess extremely low phonon thermal conductivity (1.2 and 2.7 Wm−1K−1 along the x and y directions at 300 K, respectively), whereas α- and β-BS monolayers show a relatively high phonon thermal conductivity. Therefore, the highest predicted ZT value of 1.7 ( n -type) at 700 K is obtained for monolayer γ-BS along the x direction. However, α- and β-BS monolayers have extremely low ZT values. Our results reveal that the γ-BS monolayer has wider promising applications in high performance thermoelectric material than α- and β-BS monolayers.

Comparing the Efficacies of Electrospun ZnO and TiO2 Nanofibrous Interlayers for Electron Transport in Perovskite Solar Cells

ZnO and TiO2 are both well-known electron transport materials. Their comparison of performance is considered advantageous and novel. Therefore, a viable electrospinning route was considered for the development of highly polycrystalline TiO2 and ZnO nanofibers as an electron transport material (ETM) for perovskite solar cells. The materials were well-characterized in terms of different analytical techniques. The X-ray diffraction detected polycrystalline structural properties corresponding to TiO2 and ZnO. Morphological analysis by scanning electron microscopy revealed that the nanofibers are long, uniform, and polycrystalline, having a diameter in the nanometer range. Optoelectronic properties showed that TiO2 and ZnO exhibit absorption values in the ultraviolet and visible ranges, and band gap values for TiO2 and ZnO were 3.3 and 3.2 eV, respectively. TiO2 bandgap and semiconductor nature were more compatible with Electron Transport Layer (ETL) compared to ZnO. Electrical studies revealed that TiO2 nanofibers have enhanced values of conductivity and sheet carrier mobility compared to ZnO nanofibers. Therefore, higher photovoltaic conversion efficiency was achieved for TiO2 nanofibers (10.4%) compared to ZnO (8.5%).

Creating Spin Channels in SrCoO3 through Trigonal-to-Cubic Structural Transformation for Enhanced Oxygen Evolution/Reduction Reactions.

Oxygen evolution and reduction reactions (OER and ORR) play crucial roles in energy conversion processes such as water splitting and air batteries, where spin dynamics inherently influence their efficiency. However, the specific contribution of spin has yet to be fully understood. In this study, we intentionally introduce a spin channel through the transformation of trigonal antiferromagnetic SrCoO2.5 into cubic ferromagnetic SrCoO3, aiming to deepen our understanding of spin dynamics in catalytic reactions. Based on the results from spherical-aberration-corrected microscopy, synchrotron absorption spectra, magnetic characterizations, and density functional theory calculations, it is revealed that surface electron transfer is predominantly governed by local geometric structures, while the presence of the spin channel significantly enhances the bulk transport of spin-polarized electrons, particularly under high current densities where surface electron transfer is no longer the limiting factor. The overpotential for OER is reduced by at least 70 mV at 150 mA cm-2 due to the enhanced conductivity from spin-polarized electrons facilitated by spin channels, with an expectation of even more significant reductions at higher current densities. This work provides a clearer picture of the role of spin in oxygen-involved electrocatalysis, providing critical insights for the design of more efficient catalytic systems in practical applications.

Electrospun Micro/Nanofiber-Based Electrocatalysts for Hydrogen Evolution Reaction: A Review

Hydrogen is regarded as an ideal energy carrier to cope with the energy crisis and environmental problems due to its high energy density, cleanliness, and renewability. Although there are several primary methods of industrial hydrogen production, hydrogen evolution reaction (HER) is an efficient, eco-friendly, and sustainably green method for the preparation of hydrogen which has attracted considerable attention. However, this technique is characterized by slow reaction kinetics and high energy potential owing to lack of electrocatalysts with cost-effective and high performance which impedes its scale-up. To address this issue, various studies have focused on electrospun micro/nanofiber-based electrocatalysts for HER due to their excellent electron and mass transport, high specific surface area, as well as high porosity and flexibility. To further advance their development, recent progress of highly efficient HER electrospun electrocatalysts is reviewed. Initially, the characteristics of potential high-performance electrocatalysts for HER are elucidated. Subsequently, the advantages of utilizing electrospinning technology for the preparation of electrocatalysts are summarized. Then, the classification of electrospun micro/nanofiber-based electrocatalysts for HER are analyzed, including metal-based electrospun electrocatalyst (noble metals and alloys, transition metals, and alloys), metal–non-metal electrocatalysts (metal sulfide-based electrocatalysts, metal oxide-based electrocatalysts, metal phosphide-based electrocatalysts, metal nitride-based electrocatalysts, and metal carbide-based electrocatalysts), metal-free electrospun micro/nanofiber-based electrocatalysts, and hybrid electrospun micro/nanofiber-based electrocatalysts. Following this, enhancement strategies for electrospun micro/nanofiber-based electrocatalysts are discussed. Finally, current challenges and the future research directions of electrospun micro/nanofiber-based electrocatalysts for HER are concluded.

Fibin is a crucial mitochondrial regulatory gene in skeletal muscle development.

Fin bud initiation factor homolog (Fibin) is a secreted protein that is relatively conserved among species. It is closely related to fin bud development and can regulate a variety of cellular processes. In our previous high-throughput chromosome conformation capture (Hi-C) study of pig embryonic muscle development, it was found that Fibin has high expression and activity during the development of pig primary muscle fibers. Therefore, we speculated Fibin participated in myogenesis severely. Specific deletion of Fibin in mouse skeletal muscle resulted in abnormal primary muscle fiber development during the embryonic period and a substantial decrease in skeletal muscle mass in adulthood. In vitro, knocking out Fibin in C2C12 cells promoted cell proliferation; however, after myogenic induction, cells lacking Fibin had almost no ability to differentiate into myotubes. During myogenic differentiation, loss of Fibin disrupts the normal function of mitochondria and impairs oxidative phosphorylation, resulting in decrease of NADH and FADH in the electron transport chain. Transmission electron microscopy also showed that mitochondrial morphology of Fibin-deficient C2C12 was impaired. In conclusion, our research has unveiled a novel mechanism of myogenesis regulation in mitochondrial function and potential target Fibin, and improved understanding of a broad range of mitochondrial muscle diseases.

Co-Carbonization of Straw and ZIF-67 to the Co/Biomass Carbon for Electrocatalytic Nitrate Reduction

Electrocatalytic nitrate reduction enables the recovery of nitrate from water under mild conditions and generates ammonia for nitrogen fertilizer feedstock in an economical and green means. In this paper, Co/biomass carbon (Co/BC) composite catalysts were prepared by co-carbonization of straw and metal–organic framework material ZIF-67 for electrocatalytic nitrate reduction using hydrothermal and annealing methods. The metal–organic framework structure disperses the catalyst components well and provides a wider specific surface area, which is conducive to the adsorption of nitrate and the provision of more reactive active sites. The introduction of biomass carbon additionally enhances the electrical conductivity of the catalyst and facilitates electron transport. After electrochemical testing, Co/BC-100 exhibited the best performance in electrocatalytic nitrate reduction to ammonia, with an ammonia yield of 3588.92 mmol gcat.−1 h−1 and faradaic efficiency of 97.01% at −0.5 V vs. RHE potential. This study provides a promising approach for the construction of other efficient cobalt-based electrocatalysts.

Tribute to Kenneth Sauer (1931-2022): a mentor, a role-model, and an inspiration to all in the field of photosynthesis.

Kenneth (Ken) Sauer was a mainstay of research in photosynthesis at the University of California, Berkeley and the Lawrence Berkeley National Laboratory (LBNL) for more than 50years. Ken will be remembered by his colleagues, and other workers in the field of photosynthesis as well, for his pioneering work that introduced the physical techniques whose application have enriched our understanding of the basic reactions of oxygenic photosynthesis. His laboratory was a training ground for many students and postdocs who went on to success in the field of photosynthesis and many others. Trained as a physical chemist, he always brought that quantitative approach to research questions and used several spectroscopic methods in his research. His broad scientific interests concerned the role of manganese in oxygen evolution, electronic properties of chlorophylls, energy transport in antenna complexes, and electron transport reactions. He was also an enthusiastic teacher, an enormously successful mentor who leaves behind a legion of scientists as his abiding legacy, a lover of music and the outdoors with many interests beyond science, and a dedicated family man with a great sense of humility. In this tribute, we summarize some aspects of Ken Sauer's life and career, illustrated with selected research achievements, and describe his approach to research and life as we perceived it, which is complemented by reminiscences of several current researchers in photosynthesis and other fields. The supporting material includes Ken Sauers's CV and publication list, as well as a list of the graduate students and postdocs he trained and of researchers that spent a sabbatical in his lab.

Toward Commercial-Scale Perovskite Solar Cells: The Role of ALD-SnO2 Buffer Layers in Performance and Stability.

Hybrid organic-inorganic perovskite solar cells (PSCs) have shown significant potential in photovoltaic applications due to their superior optoelectronic properties. However, the conventional electron transport layer (ETL) of C60 in PSCs poses challenges such as incomplete coverage and metal diffusion, leading to reduced performance and stability. This work explores the efficacy of atomic layer deposition (ALD) of SnO2 as an interlayer between C60 and electrode to enhance the performance and stability of devices. Devices with varying SnO2 thicknesses were fabricated, revealing that a 15 nm ALD-SnO2 layer optimally improved the power conversion efficiency (PCE) to 23.85%, compared to the 22.86% achieved with a BCP layer. Moreover, the SnO2-based devices exhibited superior open-circuit voltage (VOC), short-circuit current density (JSC), and fill factor (FF). Modules (30 × 30 cm) with ALD-SnO2 demonstrated notable enhancements in efficiency and uniformity, suggesting the potential for scalable commercial applications. Photoluminescence (PL) and electrochemical impedance spectroscopy (EIS) analyses confirmed the improved charge extraction and reduced recombination with the SnO2 buffer layer. This research indicates that ALD-SnO2 is a promising interlayer candidate for PSCs, providing a pathway toward higher efficiency and stability in perovskite solar technology.

Impact of Cr doping on Hall resistivity and magnetic anisotropy in SrRuO3 thin films.

Hall effects, including anomalous and topological types, in correlated ferromagnetic oxides provide an intriguing framework to investigate emergent phenomena arising from the interaction between spin-orbit coupling and magnetic fields. SrRuO3 is a widely studied itinerant ferromagnetic system with intriguing electronic and magnetic characteristics. The electronic transport of SrRuO3 is highly susceptible to the defects (O/Ru vacancy, chemical doping, ion implantation), and interfacial strain. In this regard, we investigate the impact of Cr doping on the magnetic anisotropy and the Hall effect in SrRuO3 thin films. The work encompasses a comprehensive analysis of the structural, spectroscopic, magnetic, and magnetotransport properties of Cr-doped SrRuO3 films grown on SrTiO3(001) substrates. Cross-sectional transmission electron microscopy reveals a sharp and coherent interface between the layers. Notably, perpendicular magnetic anisotropy is preserved in doped films with thicknesses up to 113 nm. The resistivity exhibits a T^2 dependence below the Curie temperature, reflecting the influence of disorder and correlation-induced localization effects. Interestingly, in contrast to the undoped parent compound SrRuO3, an anomaly in the Hall signal has been observed up to a large thickness (56 nm) attributed to the random Cr doping and Ru vacancy. Based on our measurements, a field-temperature (H -T) phase diagram of anomalous Hall resistivity is constructed.