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Graft-versus-host-disease-free, relapse-free survival (GRFS) is a useful composite endpoint that measures survival without relapse or significant morbidity after allogeneic hematopoietic stem cell transplantation (allo-HSCT). We aimed to develop a novel analytical method that appropriately handles right-censored data and competing risks to understand the risk for GRFS and each component of GRFS. This study was a retrospective data-mining study on a cohort of 2207 adult patients who underwent their first allo-HSCT at the Kyoto Stem Cell Transplantation Group (KSCTG), a multi-institutional joint research group of 17 transplantation centers in Japan. The primary endpoint was GRFS. A stacked ensemble of Cox proportional hazard regression and seven machine learning algorithms was applied to develop a prediction model. The median age of patients was 48 years. For GRFS, the stacked ensemble model achieved better predictive accuracy evaluated by C-index than other top-of-the-art competing risk models (ensemble model: 0.670, Cox-PH: 0.668, Random Survival Forest: 0.660, Dynamic DeepHit: 0.646). The probability of GRFS after 2 years was 30.54% for the high-risk and 40.69% for the low-risk group, respectively (hazard ratio [HR] compared to the low-risk group: 2.127; 95% CI: 1.19-3.80). We developed a novel predictive model for survival analysis that showed superior risk stratification to existing methods using a stacked ensemble of multiple machine learning algorithms., アンサンブル学習を用いた造血幹細胞移植予後予測モデルの開発 --機械学習を用いた新規生存時間解析手法の実装--. 京都大学プレスリリース. 2021-12-28.

Since the discovery of the ferroelectric perovskite-type oxide BaTiO3 in 1943, numerous materials have been surveyed as candidates for new ferroelectrics. Perovskite-type materials have played a leading role in basic research and applications of ferroelectric materials since the last century. Experimentalists and theoreticians have developed a new materials design stream for post-perovskite materials. In this stream, we have mainly focused on the role of covalency in the evolution of ferroelectricity for displacive-type ferroelectrics in oxides. This perspective surveys the following topics: (1) crossover from quantum paraelectric to ferroelectric through a ferroelectric quantum critical point, (2) the role of cation–oxygen covalency in ferroelectricity and the crossover to quantum paraelectric in perovskite-type compounds, (3) off-centerinduced ferroelectricity in perovskites, (4) second-order Jahn–Teller effect enhancement of ferroelectricity in lithium-niobate-type oxides, (5) the presence of four ferroelectric phases and structural transitions of phases of AFeO3 with decreasing radius of A (A = La–Al), (6) tetrahedral ferroelectrics of perovskiterelated Bi2SiO5 and wurtzites, (7) a rare type of polarization switching system in which the coordination number of ions in κ-Al2O3 systems changes between 4 and 6, and (8) lone-pair-electron-induced ferroelectrics in langasite-type compounds.

Four distinct classes of multiferroics are usually being discussed in the literature, in which ferroelectricity is respectively driven by electronic lone pairs, geometry, charge ordering, and magnetism. Each class has its own shortcomings for technological applications. Here, through a combined experimental and theoretical investigation, we propose a mechanism to achieve multiferroicity in a single phase by engineering the anionic network and creating local geometric distortions in fluorinated, vacancy-ordered brownmillerite Ca2Mn2O5−xFy. The system exhibits both ferroelectricity and an antiferromagnetic order above room temperature, pointing toward a novel route to multiferroicity by anion mixing.

Side reactions of the charge/discharge in Li-ion batteries (LIBs) generate a solid-electrolyte interface (SEI) onto an electrode surface, resulting in the degradation of the lifetime of a cell. The suppression of SEI formations has attracted much attention for achieving longer cyclable LIBs. Our research group has previously reported that few SEI were observed at triple-phase interfaces (TPIs) consisting of BaTiO3, LiCoO2, and electrolyte interfaces in LIBs with excellent cyclability and ultrahigh-speed chargeability. An investigation on the suppression mechanisms of SEI formations at TPIs should yield important information on understanding the undesirable side reactions. Therefore, we have explored the suppression mechanisms of SEI formations by preparing epitaxial thin films and evaluating the surface of the samples after the electrochemical treatment. The results of X-ray photoelectron spectroscopy and scanning electron microscopy with energy-dispersive X-ray analysis measurements suggested that the decomposition of LiPF6 was suppressed at TPIs, implying that the generation of PF5 via the decomposition of LiPF6 contributed to SEI formation.

The alkylating agent busulfan is commonly used as conditioning in allogeneic hematopoietic stem cell transplantation for acute myeloid leukemia (AML). However, a consensus has not yet been reached regarding the optimal busulfan dose in cord blood transplantation (CBT). Therefore, we conducted this large nationwide cohort study to retrospectively analyze the outcomes of CBT in patients with AML receiving busulfan at intermediate (6.4 mg/kg i.v.; BU2) or higher (12.8 mg/kg i.v.; BU4) doses within a fludarabine/i.v. busulfan (FLU/BU) regimen. Among 475 patients who underwent their first CBT following FLU/BU conditioning between 2007 and 2018, 162 received BU2 and 313 received BU4. Multivariate analysis identified BU4 as a significant factor for longer disease-free survival (hazard ratio [HR], .85; 95% confidence interval [CI], .75 to .97; P = .014) and a lower relapse rate (HR, .84; 95% CI, .72 to .98; P = .030). No significant differences were observed in non-relapse mortality between BU4 and BU2 (HR, 1.05; 95% CI, .88-1.26; P = .57). Subgroup analyses showed that BU4 provided significant benefits for patients who underwent transplantation while not in complete remission (CR) and those age

The antiferroelectric (AFE) phase, in which nonpolar and polar states are switchable by an electric field, is a recent discovery in promising multiferroics of hexagonal rareearth manganites (ferrites), h-RMn(Fe)O3. However, this phase has so far only been observed at 60−160 K, which restricts key investigations into the microstructures and magnetoelectric behaviors. Herein, we report the successful expansion of the AFE temperature range (10−300 K) by preparing h-DyFeO3 films through epitaxial stabilization. Room-temperature scanning transmission electron microscopy reveals that the AFE phase originates from a nanomosaic structure comprising AFE P3̅c1 and ferroelectric P63cm domains with small domain sizes of 1− 10 nm. The nanomosaic structure is stabilized by a low c/a ratio derived from the large ionic radius of Dy3+. Furthermore, weak ferromagnetism and magnetocapacitance behaviors are observed. Below 10 K, the film exhibits an M-shaped magnetocapacitance versus magnetic field curve, indicating unusual magnetoelectric coupling in the AFE phase.

Although allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the key strategy to cure patients with mature T and natural killer (NK) cell lymphomas/leukemia, especially those with relapsed/refractory diseases, there is no consensus strategy for donor selection. We retrospectively analyzed the outcomes of allo-HSCT in 111 patients in 15 Japanese institutions as a multi-institutional joint research project. Thirty-nine patients received bone marrow or peripheral blood stem cell transplantation from related donors (rBMT/rPBSCT), 37 received BMT/PBSCT from unrelated donors (uBMT/uPBSCT), and 35 received cord blood transplantation (CBT). Overall survival (OS) and progression-free survival (PFS) at 4 years were 42% and 34%, respectively. The cumulative incidences of relapse and nonrelapse mortality were 43% and 25%. In multivariate analysis, CBT showed comparable OS with rBMT/rPBSCT (rBMT/rPBSCT versus CBT: hazard ratio [HR], 1.63; P = .264) and better OS compared with uBMT/uPBSCT (HR, 2.99; P = .010), with a trend toward a lower relapse rate (rBMT/rPBSCT versus CBT: HR, 2.60; P = .010; uBMT/uPBSCT versus CBT: HR, 2.05; P = .082). This superiority of CBT was more definite in on-disease patients (OS: rBMT/rPBSCT versus CBT: HR, 5.52; P = .021; uBMT/uPBSCT versus CBT: HR, 6.80; P = .007). Better disease control was also strongly associated with better OS and PFS with lower relapse rate. In conclusion, allo-HSCT is beneficial for the survival of patients with mature T and NK cell lymphomas/leukemia if performed in a timely fashion. Since CBT showed favorable survival with a lower relapse risk, it could be a preferred alternative, especially in on-disease patients.

Background Inactive aldehyde dehydrogenase-2 (ALDH2) is a well-known deterrent to the development of alcohol use disorder (AUD), and however, some individuals with inactive ALDH2 do go on to develop AUD. These alcoholics are likely to have strong risk factors for the development of this disorder. Using a model of alcoholics with inactive ALDH2 (the AIA model), we investigated the unique characteristics of alcoholics with inactive ALDH2 in an attempt to identify the risk factors for AUD. In this study, we focused on comorbid psychiatric and personality disorders as potential risk factors for AUD. Methods The subjects were 103 male alcoholics with inactive ALDH2 (AIAs), 87 age- and ADH1B genotype-matched alcoholics with active ALDH2 (AAAs) and 200 age-matched healthy men. The alcoholics were divided into 4 subgroups according to their ALDH2 and ADH1B genotypes (inactive ALDH2 vs. active ALDH2, usual ADH1B vs. superactive ADH1B). To assess the participants' comorbid psychiatric disorders, we conducted semi-structured interviews using the Japanese translation of SSAGA version 2. We compared the prevalence of comorbid psychiatric and personality disorders among groups with different combinations of the ALDH2 and ADH1B genotypes. Results The prevalence of attention-deficit/hyperactivity disorder (ADHD) was significantly higher in the AIAs with usual ADH1B than in the other 3 subgroups of alcoholics. In contrast, the prevalence rates of agoraphobia and panic disorder were significantly lower in the AIAs with superactive ADH1B than in the other 3 subgroups of alcoholics. Conclusions This study suggested that (i) ADHD is a risk factor for AUD, consistent with previous reports; (ii) agoraphobia and panic disorder may have deterrent effects against the development of AUD in individuals with inactive ALDH2, probably attributable to the similarity between the symptoms of agoraphobia and panic disorder and the adverse reactions to consumption of alcohol in subjects with inactive ALDH2.

Zn-deficient spinel-type ZnGa2O4:Mn2+ phosphor thin films were prepared using pulsed laser deposition. With an increase (decrease) in the Zn deficiency (concentration) of the films, changes in lattice constant, optical band gap, and photoluminescence spectra were observed. All films without γ-Ga2O3:Mn showed green luminescence attributable to the transition from the 4T1 state to the 6A1 state. In addition, the spectral shape changed depending on the temperature. The luminescence spectra have two peaks resulting from the Mn2+ ions located in the tetrahedral and octahedral sites. These peaks had different thermal quenching temperatures, which were around 320 and 260 K, respectively. Therefore, the spectral shape changed with increasing temperature. The spectral shape also depended on the Zn concentration. With an increase (decrease) in the Zn concentration (deficiency) of the films, the intensity of emission from Td increased in comparison with that from Oh. Therefore, the position of Mn2+ was controlled by Zn deficiency similarly to the effect of crystal-site engineering.

Next-generation nonvolatile memory devices require many functionalities such as high-speed processing, low power consumption, lightweight, and a simple structure. The use of heterostructures with r...

Polar magnets are important materials in fundamental science and technology. However, the requirements for a polar nature are generally incompatible with those for magnetism, and thus there are few polar magnets. At the order and disorder boundaries of cations in ABO3 compounds, two polar ferromagnets of ScFeO3 with polar-corundum-type and LiNbO3-type structures were previously prepared by high-pressure synthesis. Here, we prepared a third ScFeO3 polar ferromagnet with an YMnO3-type structure using a heteroepitaxial film technique and characterized its physical properties. The YMnO3-type ScFeO3 film on a perovskite electrode showed a ferroelectric P–E hysteresis loop with Pr ∼ 4.9 μC cm−2. Only YMO-type ScFeO3 has switchable polarization by the external electric field among the three ScFeO3 polar magnets. Magnetic measurements confirmed weak ferromagnetism (TN = 195 K), which is the highest observed in the hexagonal family.

AlxFe2−xO3 (x-AFO) thin films, belonging to the κ-Al2O3 family, are interesting because they show room temperature ferrimagnetism and have a polar crystal structure. These types of materials are being studied to observe simultaneous ferrimagnetism and ferroelectricity, and the possibility of coupling between the two. However, it is difficult to realise ferroelectric properties at room temperature, due to the low resistivity of the films. In this work, we have optimized the synthesis conditions to obtain x-AFO (0.5 ≤ x ≤ 1) thin films with high resistance. While magnetic measurements confirmed room temperature ferrimagnetism of the films, the maximum magnetization was observed for the composition x = 0.8. In addition, the Curie temperature was found to be influenced by oxygen pressure during deposition. Ferroelectric measurements on the films showed small remnant polarization (∼0.5–2 μC cm−2). In contrast, the predicted polarization from first principles calculations was calculated to be between 21 and 26 μC cm−2. The analysis also suggested that ferroelectric domain-switching occurs through shearing of in-plane oxygen layers. The presence of multiple in-plane domains, which oppose polarization switching of adjacent domains, is suggested to be the cause of the small observed polarization. The magnetocapacitance measurements showed weak magnetic coupling with the capacitance.

Viral infection is one of the lethal adverse events after cord blood transplantation (CBT). Human leukocyte antigen (HLA) and killer immunoglobulin-like receptor (KIR) ligand divergences can increase the risk of viral infection due to conflicting interactions between virus-infected cells and immune cells. However, the relationship between these disparities and the frequency of viral infection after CBT remains to be evaluated. Herein, we have conducted a retrospective multicenter study to assess the effect of HLA and KIR ligand mismatches on viral infections after CBT. The study included 429 patients, among which 126 viral infections occurred before day 100. Viral infection was significantly associated with poorer overall survival (OS; hazard ratio [HR] 1.74, p 0.01). Patients harboring ≥3 mismatches in the HLA allele and inhibitory KIR ligand mismatches (HLAKIR mismatches) had a significantly greater prevalence of viral infection (HR 1.66, p = 0.04). Thus, patients with HLAKIR mismatches had poorer outcomes in terms of non-relapse mortality (HR 1.61, p = 0.05). Our study demonstrates the unfavorable impacts of HLAKIR mismatches on viral infections and non-relapse mortality after CBT. Evaluating the viral infection risk and performance of an appropriate and early intervention in high-risk patients and optimizing the graft selection algorithm could improve the outcome of CBTs.

The phase stability, ferroelectricity, and magnetism of highly crystalline epitaxial e-Fe2O3 films deposited on SrTiO3(111) substrates are reported. Temperature-dependent x-ray diffraction measurements revealed that α-Fe2O3 appeared as a secondary phase after samples were annealed up to 1000 °C. A clear saturated and opened polarization–electric field hysteresis loop with the remnant polarization ∼2.6 μC cm−2 and coercive electric field ∼100 kV cm−1 was obtained at room temperature using a conventional ferroelectric measurement technique. The magnetic phase transition was observed at 155 K. Magnetization–magnetic field measurements revealed that magnetic softening via the phase transition accompanied a reduction in the coercive field from 10 to 6.8 kOe, which is smaller than the coercive field reduction previously observed for e-Fe2O3 nanoparticles.

Present energy issues have increasingly stimulated the demand for the development of clean and sustainable energy platforms which can achieve net zero carbon emissions. Renewable energy resources are quite promising candidates for the construction of sustainable decarbonized society. One of examples of harnessing renewable energy-derived electricity is the electrolysis of earth-abundant water into hydrogen, which is a prominent carbon-free chemical fuel with a high weight energy density. Compared with polymer electrolyte water electrolysis in acidic environment, electrochemical alkaline water splitting can employ inexpensive nonprecious metals as electrocatalysts, which can make this technology a large-scale and cost-effective process. However, the anodic oxygen evolution reaction (OER) in the water splitting has a large overpotential, and it is a great bottleneck for widespread use. Thus, highly active and inexpensive electrocatalysts for OER are desired to overcome this concern. Iron (Fe) is a very earth-abundant element that is a quite cheap and non-toxic metal, and thus it is a potential candidate as electrocatalyst for OER. Previous studies have reported several multimetal oxides with Fe and other metallic elements, such as perovskite and brownmillerite types, which have attracted great attentions due to their facile synthesis and easily tunable OER activities by element substitution and doping. However, most of these studies focused on the choice of elements. Contrarily, the effects of crystal structures on OER activity have not yet been sufficiently interpreted, and it can be a crucial aspect to understand the OER electrocatalysis on Fe-based oxides and for the rational design of outstanding OER catalysts. In this study, we aim to comprehensively understand the effects of crystal structures on electrocatalytic OER activities on Fe-based oxides. To obtain versatile insights into OER electrocatalysis, we collected OER performances of Fe-based simple and bimetal oxides from our experiments and literature, and their structural characteristics were obtained from databases for inorganic compounds. Thus, we found that OER efficiencies on the Fe-based oxides were correlated with Fe–O bond lengths in their crystals; i.e., a shorter Fe–O bond length led to a higher OER activity.[1] We then exploited databases to mine potential candidates based on the structure–activity relationship and selected unreported Fe-based bimetal and trimetal oxides with various structures, which can dramatically accelerate our catalyst research. We synthesized these Fe-based multimetal oxides and evaluated their OER activity in alkaline media; remarkably, the OER efficiency on the unreported Fe-based multimetal oxides also exhibited excellent correlation with Fe–O bond lengths, as plotted in Figure 1. It is notable that the trend in the Fe–O bond length and OER activity is applicable to a wide variety of Fe-based simple, bimetal, and trimetal oxides regardless of chemical compositions, crystal categories, and Fe valence states. Furthermore, machine learning analysis proved that Fe–O bond length is the most dominant structural descriptor for OER efficiency compared with other structural parameters.[2] However, it is required to overcome the abovementioned catalytic trend because theoretical Fe–O bond length in Fe-based oxides is limited, and superior OER catalysts cannot be achieved according to this design guideline. Hence, we attempted to switch the OER electrocatalytic mechanism on a Fe-based oxide by the arrangement of crystal structure because different mechanisms should be involved in different descriptors; i.e., the mechanism switch could surpass the abovementioned catalytic trend. Thus, we found post-spinel CaFe2O4 that comprises a large amount of edge-shared FeO6 connectivity in its crystal. DFT calculations unveiled that the structural characteristics induced an unprecedented OER mechanism, multi-iron-site mechanism, where OER process goes through a reaction intermediate with an O–O bridge on multiple Fe sites as depicted in upper side in Figure 1. Consequently, CaFe2O4 exhibited prominent OER activity despite long Fe–O bond length in its crystal.[3] These findings provide a novel insight into the OER electrocatalysis on Fe-based oxides and contribute to the innovation of electrochemical hydrogen production. The part of this paper is based on results obtained from a project, JPNP14021, commissioned by the New Energy and Industrial Technology Development Organization (NEDO). Authors acknowledge the PRESTO program (No. JPMJPR15S3) of the JST. The part of DFT calculations was carried out on the supercomputers at NIMS, Hokkaido Univ., Kyushu Univ., and the HPCI systems (project codes: hp180115, hp200131). The part of this work was supported by JSPS KAKENHI Grant Number 20H00314 and 20K15087. References [1] Y. Sugawara, K. Kamata, E. Hayashi, M. Itoh, Y. Hamasaki, T. Yamaguchi ChemElectroChem, 2021, 8, 4466. [2] Y. Sugawara. S. Ueno, K. Kamata, T. Yamaguchi, ChemElectroChem, 2022, 9, in press. [3] Y. Sugawara, K. Kamata, A. Ishikawa, Y. Tateyama, T Yamaguchi, ACS Appl. Energy Mater., 2021, 4, 3057. Figure 1

High-speed rechargeability is essential for next-generation secondary batteries. We previously reported that a surface-supporting material deposited on a cathode material accelerates Li-ion motions between an electrode−electrolyte interface by an electric field concentration at a supporting material–cathode–electrolyte (triple-phase) interface (TPI). In addition, a high relative permittivity material was found to be a promising supporting material with which to reinforce the electric field concentration at TPIs. However, the TPI's effects on anode materials remains to be revealed. To demonstrate those effects, we prepared CeO2 or BaTiO3 micropads deposited on Li4Ti5O12 epitaxial thin films. Compared with the cathodes, CeO2 micropads deposited on Li4Ti5O12 film showed the best performance at a high C-rate. Because the rate-determining step of Li4Ti5O12 epitaxial thin films is inner diffusion, reinforcing the surface electric field by the deposition of a low relative permittivity materials could promote high C-rate performance even in anode materials.

Nanodot BaTiO3 supported LiCoO2 cathode thin films can dramatically improve high-rate chargeability and cyclability. The prepared BaTiO3 nanodot is

Single-phase multiferroic materials have attracted considerable attention among scientists, due to the strong drive in industry towards device miniaturization, addition of new functionalities, etc. Currently, most of the discovered materials have at-least one ferroic order active only at low temperatures, thereby hindering their induction into practical devices. κ-Al2O3-type AlxFe2-xO3 (x-AFO) oxides belong to a new class of metastable multiferroic compounds (space group: Pna21), with relatively high Curie temperatures. The current work investigates the effect of thin film deposition conditions on the ferroelectric and ferrimagnetic properties of Al0.5Fe1.5O3 (0.5-AFO). Substrate temperature and oxygen partial pressure during deposition were found to be the critical parameters in obtaining high quality films. Optimizing the deposition conditions of 0.5-AFO enabled observation of both ferroelectricity and ferrimagnetism at room temperature.

κ-Al2O3-type GaFeO3 is a promising multiferroic material due to the coexistence of a large spontaneous magnetization and polarization near room temperature. In the current study, we present the magnetic properties of single crystalline GaFeO3 and compare it with that of e-Fe2O3. Magnetic measurements revealed that spontaneous magnetization appears below 540 K in two steps, similar to that reported for e−Fe2O3. Partial magnetic ordering takes place at 540 K (TN1), with Fe3+ ions in two distorted octahedral sites ordering antiparallel to one another. Upon further cooling at 200 K (TN2), the remaining Fe3+ ions in regular octahedra and tetrahedra order antiparallel to one another. Substitution of Ga for Fe in e-Fe2O3 leads to a decrease in TN1 and TN2 from 850 to 540 K and from 480 to 200 K, respectively, caused by a dilution of magnetic Fe by nonmagnetic Ga and preferential site occupation of Ga.

Lithium ion batteries with high-rate performance have been demanded since electric and hybrid vehicles are released. It is known that high interfacial resistance between electrode and electrolyte prevents intercalation of lithium ions. We investigated high-rate capability of typical LiCoO2 cathode with various surface morphologies using epitaxial thin films prepared by pulsed laser deposition. As a result, high-rate performance in (104)LiCoO2 thin films was enhanced by an increase of (110)LiCoO2 facet density because diffusion coefficient of (110)LiCoO2 was larger than that of (104)LiCoO2. Therefore, a control of crystal plane at the surface is a key point for high-rate performance.

GaFeO

GaFeO3-type iron oxides are promising multiferroics due to the coexistence of large spontaneous magnetization and polarization near room temperature. However, the high leakage current and difficulties associated with synthesizing single crystals make it difficult to achieve two important features in the system: a large ferroelectric polarization switching and magnetoelectric coupling at a high-temperature region. Herein, we report successful achievement of these features by preparing high-quality Sc-doped GaFeO3 single crystals (ScxGa1-x/2Fe1-x/2O3 with x = 0-0.3) using the floating zone method. The x ≥ 0.05 crystals exhibit a leakage current 104 times lower than the x = 0 crystals, highlighting the importance of Sc doping. Because of the reduced leakage current, the Sc-doped crystals exhibit large ferroelectric polarization switching along the c-axis with a remanent polarization of 22-25 μC/cm2, which is close to the theoretically predicted polarization value of 25-28 μC/cm2. In addition, the Sc-doped crystals exhibit ferrimagnetism with magnetic anisotropy along the a-axis. Furthermore, a magnetic-field-induced modulation of polarization is observed in the x = 0.15 crystal even at a relatively high temperature, i.e., 100 K.

Spontaneous polarization (

Spontaneous polarization (Ps) of novel order-disorder type lead-free ferroelectric CaMnTi2O6 was successfully enhanced by partial V4+ substitution for Ti4+. A synchrotron X-ray diffraction study revealed that the polar displacement of octahedrally coordinated (Ti, V) in CaMn(Ti1-xVx)2O6 (0 ≤ x ≤ 0.4) increases with V4+ substitution having Jahn-Teller activity owing to the d1 electronic configuration. Our magnetic study suggested the presence of antisite disorder between Ca2+ and square planar coordinated Mn2+ associated with Mn-V intermetallic charge transfer for x ≥ 0.4, resulting in decreases in spontaneous polarization and the ferroelectric-paraelectric transition temperature. This is the first report on the enhanced polarization owing to the Jahn-Teller distortion of V4+ without stereochemical Pb2+ or Bi3+.

We report measurements of the thermal Hall effect in single crystals of both pristine and isotopically substituted strontium titanate. We discovered a 2 orders of magnitude difference in the thermal Hall conductivity between SrTi^{16}O_{3} and ^{18}O-enriched SrTi^{18}O_{3} samples. In most temperature ranges, the magnitude of thermal Hall conductivity (κ_{xy}) in SrTi^{18}O_{3} is proportional to the magnitude of the longitudinal thermal conductivity (κ_{xx}), which suggests a phonon-mediated thermal Hall effect. However, they deviate in the temperature of their maxima, and the thermal Hall angle ratio (|κ_{xy}/κ_{xx}|) shows anomalously decreasing behavior below the ferroelectric Curie temperature T_{c}∼25 K. This observation suggests a new underlying mechanism, as the conventional scenario cannot explain such differences within the slight change in phonon spectrum. Notably, the difference in magnitude of thermal Hall conductivity and rapidly decreasing thermal Hall angle ratio in SrTi^{18}O_{3} is correlated with the strength of quantum critical fluctuations in this displacive ferroelectric. This relation points to a link between the quantum critical physics of strontium titanate and its thermal Hall effect, a possible clue to explain this example of an exotic phenomenon in nonmagnetic insulating systems.

Zn-deficient spinel-type ZnGa

We have investigated the structural, magnetic, and dielectric properties of the Pb-based langasite compound ${\mathrm{Pb}}_{3}{\mathrm{TeMn}}_{3}{\mathrm{P}}_{2}{\mathrm{O}}_{14}$ both experimentally and theoretically in light of metal-oxygen covalency, and the consequent generation of multiferroicity. It is known that the large covalency between Pb $6p$ and O $2p$ plays an instrumental role behind the stereochemical lone pair activity of Pb. The same happens here, but a subtle structural phase transition above room temperature changes the degree of such lone pair activity and the system becomes ferroelectric below 310 K. Interestingly, this structural change also modulates the charge densities on different constituent atoms and consequently the overall magnetic response of the system while maintaining the global paramagnetism behavior of the compound. This single origin of modulation in polarity and paramagnetism inherently connects both functionalities and the system exhibits mutiferroicity at room temperature.

ϵ-Fe2O3, a metastable phase of iron oxide, is widely known as a room-temperature multiferroic material or as a superhard magnet. Element substitution into ϵ-Fe2O3 has been reported in the literature; however, the substituted ions have a strong site preference depending on their ionic radii and valence. In this study, in order to characterize the crystal structure and magnetic properties of ϵ-Fe2O3 in the Fe2+/Fe3+ coexisting states, Li+ was electrochemically inserted into ϵ-Fe2O3 to reduce Fe3+. The discharge and charge of Li+ into/from ϵ-Fe2O3 revealed that Li+ insertion was successful. X-ray magnetic circular dichroism results indicated that the reduced Fe did not exhibit site preference. Increasing the Li+ content in ϵ-Fe2O3 resulted in decreased saturation magnetization and irregular variation of the coercive field. We present a comprehensive discussion of how magnetic properties are modified with increasing Li+ content using transmission electron microscopy images and considering the Li+ diffusion coefficient. The results suggest that inserting Li+ into crystalline ϵ-Fe2O3 is a useful tool for characterizing crystal structure, lithiation limit, and magnetic properties in the coexistence of Fe2+/Fe3+

Transplant-associated thrombotic microangiopathy (TA-TMA) is a fatal complication of allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, so far, no large cohort study determined the risk factors and the most effective therapeutic strategies for TA-TMA. Thus, the present study aimed to clarify these clinical aspects based on a large multicenter cohort. This retrospective cohort study was performed by the Kyoto Stem Cell Transplantation Group (KSCTG). A total of 2425 patients were enrolled from 14 institutions. All patients were aged ≥16 years, presented with hematological diseases, and received allo-HSCT after the year 2000. TA-TMA was observed in 121 patients (5.0%) on day 35 (median) and was clearly correlated with inferior overall survival (OS) (hazard ratio [HR], 4.93). Pre- and post-HSCT statistically significant risk factors identified by multivariate analyses included poorer performance status (HR, 1.69), HLA mismatch (HR, 2.17), acute graft-versus-host disease (aGVHD; grades 3-4) (HR, 4.02), Aspergillus infection (HR, 2.29), and veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS; HR, 4.47). The response rate and OS significantly better with the continuation or careful reduction of calcineurin inhibitors (CNI) than the conventional treatment strategy of switching from CNI to corticosteroids (response rate, 64.7% vs 20.0%). In summary, we identified the risk factors and the most appropriate therapeutic strategies for TA-TMA. The described treatment strategy could improve the outcomes of patients with TA-TMA in the future.