Advancing Solid Oxide Fuel Cell Performance: Enhanced Electrochemical Properties of Pr1-xCaxBaFe2O5+δ Nanofiber Cathodes via Ca Doping.

The double perovskite oxide PrBaFe2O5+δ has great potential as a cathode material for solid oxide fuel cells (SOFCs). However, the electrochemical characteristics of Fe-based double perovskites are relatively inferior. To improve its electrochemical performance, Ca is investigated to partially replace Pr, forming Pr1-xCaxBaFe2O5+δ (PCBFx, x = 0.0-0.3) by an electrospinning technique. The PCBFx nanofibers exhibited a crystalline structure characterized by orthorhombic symmetry and space group P4/mmm. Furthermore, these PCBFx nanofibers displayed exceptional chemical compatibility with the Sm0.2Ce0.8O1.95 (SDC) electrolyte when sintered at a temperature of 900 °C for 5 h. The X-ray photoelectron spectroscopy (XPS) analysis reveals a progressive increase in the Fe4+ concentration as the Ca doping level rises. The polarization resistances (Rp) of the PCBF00, PCBF01, PCBF02, and PCBF03 nanofiber cathodes were 0.103, 0.079, 0.056, and 0.048 Ω cm2 at 750 °C. In the meantime, doping Ca increases the peak power density of the single cell by 46%, from 762.80 (PCBF00) to 1114.85 (PCBF03) mW cm-2 at 750 °C. The results demonstrate that PCBF03 double perovskite nanofibers exhibit great potential as cathode materials for SOFCs.

Building a Charge Transfer Bridge between g-C3N4 and Perovskite with Molecular Engineering to Achieve Efficient Perovskite Solar Cells.

Effective defect passivation and efficient charge transfer within polycrystalline perovskite grains and corresponding boundaries are necessary to achieve highly efficient perovskite solar cells (PSCs). Herein, focusing on the boundary location of g-C3N4 during the crystallization modulation on perovskite, molecular engineering of 4-carboxyl-3-fluorophenylboronic acid (BF) on g-C3N4 was designed to obtain a novel additive named BFCN. With the help of the strong bonding ability of BF with both g-C3N4 and perovskite and favorable intramolecular charge transfer within BFCN, not only has the crystal quality of perovskite films been improved due to the effective defects passivation, but the charge transfer has also been greatly accelerated due to the formation of additional charge transfer channels on the grain boundaries. As a result, the champion BFCN-based PSCs achieve the highest photoelectric conversion efficiency (PCE) of 23.71% with good stability.

Simultaneous photocatalytic degradation and SERS detection of tetracycline with self-sustainable and recyclable ternary PI/TiO2/Ag flexible microfibers.

Facile and efficient photocatalysts using sunlight, as well as fast and sensitive surface-enhanced Raman spectroscopy (SERS) substrates, are urgently needed for practical degradation of tetracycline (TC). To meet these requirements, a new paradigm for PI/TiO2/Ag organic‒inorganic ternary flexible microfibers based on semiconducting titanium dioxide (TiO2), the noble metal silver (Ag) and the conjugated polymer polyimide (PI) was developed by engineering a simple method. Under sunlight, the photocatalytic characteristics of the PI/TiO2/Ag flexible microfibers containing varying amounts of Ag quantum dots (QDs) were evaluated with photocatalytic degradation of TC in aqueous solution. The results demonstrated that the amount of Ag affected the photocatalytic activity. Among the tested samples, PI/TiO2/Ag-0.07 (93.1%) exhibited a higher photocatalytic degradation rate than PI/TiO2 (25.7%), PI/TiO2/Ag-0.05 (77.7%), and PI/TiO2/Ag-0.09 (63.3%). This observation and evaluation conducted in the present work strongly indicated a charge transfer mechanism. Moreover, the PI/TiO2/Ag-0.07 flexible microfibers exhibited highly sensitive SERS detection, as demonstrated by the observation of the Raman peaks for TC even at an extremely low concentration of 10-10 moles per liter. The excellent photocatalytic performance and SERS detection capability of the PI/TiO2/Ag flexible microfibers arose from the Schottky barrier formed between Ag and TiO2 and also from the outstanding plasmonic resonance and visible light absorptivity of Ag, along with immobilization by the PI. The successful synthesis of PI/TiO2/Ag flexible microfibers holds significant promise for sensitive detection and efficient photocatalytic degradation of antibiotics.

Break through the Steric Hindrance of Ionic Liquids with Carbon Quantum Dots to Achieve Efficient and Stable Perovskite Solar Cells.

Overcoming the negative impact of residual ionic liquids (ILs) on perovskite films based on an in-depth understanding of chemical interactions between ionic liquids and preparing perovskite precursor solutions is a great challenge when aiming to simultaneously achieve long-term stability and high efficiency within IL-based perovskite solar cells (PSCs). Herein, 1-butyl-3-methylimidazolium tetrafluoroborate (BMIMBF4), a type of IL, was introduced into the perovskite precursor solution, and carbon quantum dots (CQDs) were further introduced into the antisolvent to enhance the photovoltaic properties of PSCs. Both ILs and CQDs synergistically manipulate the crystallization process and passivate defects to obtain high-quality perovskite films. Besides serving as passivation sites to strengthen the collaboration between additives and perovskite materials, the cointroduction of CQDs further promotes the carrier transport process since it not only provides carrier channels at grain boundaries but also forms better energy alignment, which effectively overcomes the charge transfer loss caused by the steric hindrance of ILs. Based on such a synergistic effect of ILs and CQDs, the n-i-p MAPbI3-based PSCs achieve the highest efficiency of 20.84% with improved stability. This simple and low-cost synergistic integration method will subsequently provide direction for optimizing ILs to improve the photovoltaic performance of PSCs.

Managing intermediate phase transition of perovskite film with gearbox-like molecule for efficient and stable solar cells.

The smooth and dense light-absorbing layer is an essential factor in polycrystalline solar cells to achieve high photovoltaic performance, while it remains challenging in perovskite solar cells because of the difficulty balancing the speed of crystal nucleation and growth in a solution way. Here, we explored a perovskite nucleation/growth compatible model via manipulating the intermediate complex induced by n-hexylamine (NHA) molecule, guiding us to adjustments perovskite nucleation and growth process. We found that the NHA can act as a gearbox-like molecule to sequentially reduce the perovskite nucleation barrier, promote the nucleation velocity, and retard the perovskite growth simultaneously to obtain uniform perovskite films; correspondingly, this modulation also yields the buried interface with fewer voids and low defects density. In addition, the hydrophobic NHA with long alkyl chain improves the moisture tolerance of the perovskite. The treated solar cell power conversion efficiency was 21.91 %. Importantly, in âˆ¼ 70 % humidity at 25 °C for 30 days, the efficiency of the device declined less than 5 %, exhibiting a good stability performance.

Advanced Development of Molecularly Imprinted Membranes for Selective Separation.

Molecularly imprinted membranes (MIMs), the incorporation of a given target molecule into a membrane, are generally used for separating and purifying the effective constituents of various natural products. They have been in use since 1990. The application of MIMs has been studied in many fields, including separation, medicine analysis, solid-phase extraction, and so on, and selective separation is still an active area of research. In MIM separation, two important membrane performances, flux and permselectivities, show a trade-off relationship. The enhancement not only of permselectivity, but also of flux poses a challenging task for membranologists. The present review first describes the recent development of MIMs, as well as various preparation methods, showing the features and applications of MIMs prepared with these different methods. Next, the review focuses on the relationship between flux and permselectivities, providing a detailed analysis of the selective transport mechanisms. According to the majority of the studies in the field, the paramount factors for resolving the trade-off relationship between the permselectivity and the flux in MIMs are the presence of effective high-density recognition sites and a high degree of matching between these sites and the imprinted cavity. Beyond the recognition sites, the membrane structure and pore-size distribution in the final imprinted membrane collectively determine the selective transport mechanism of MIM. Furthermore, it also pointed out that the important parameters of regeneration and antifouling performance have an essential role in MIMs for practical applications. This review subsequently highlights the emerging forms of MIM, including molecularly imprinted nanofiber membranes, new phase-inversion MIMs, and metal-organic-framework-material-based MIMs, as well as the construction of high-density recognition sites for further enhancing the permselectivity/flux. Finally, a discussion of the future of MIMs regarding breakthroughs in solving the flux-permselectivity trade-off is offered. It is believed that there will be greater advancements regarding selective separation using MIMs in the future.

Modulating Crystallization and Defect Passivation by Butyrolactone Molecule for Perovskite Solar Cells.

The attainment of a well-crystallized photo-absorbing layer with minimal defects is crucial for achieving high photovoltaic performance in polycrystalline solar cells. However, in the case of perovskite solar cells (PSCs), precise control over crystallization and elemental distribution through solution processing remains a challenge. In this study, we propose the use of a multifunctional molecule, α-amino-γ-butyrolactone (ABL), as a modulator to simultaneously enhance crystallization and passivate defects, thereby improving film quality and deactivating nonradiative recombination centers in the perovskite absorber. The Lewis base groups present in ABL facilitate nucleation, leading to enhanced crystallinity, while also retarding crystallization. Additionally, ABL effectively passivates Pb2+ dangling bonds, which are major deep-level defects in perovskite films. This passivation process reduces recombination losses, promotes carrier transfer and extraction, and further improves efficiency. Consequently, the PSCs incorporating the ABL additive exhibit an increase in conversion efficiency from 18.30% to 20.36%, along with improved long-term environmental stability. We believe that this research will contribute to the design of additive molecular structures and the engineering of components in perovskite precursor colloids.

Toward low-cost and sustainable SERS substrate: novel ultrasensitive AMS5 nanoflowers.

Surface-enhanced Raman scattering (SERS) is an analytical technique for the rapid detection of low-concentration analytes. However, the lack of uniform, stable, and recyclable substrate limits its wide applications. Here, Ag-doped MoS2 (AMSx) was prepared by the hydrothermal method. Band structures, LSV, and EIS characteristics confirmed that Ag doping can reduce the indirect band gap and increase the charge transfer between substrates and molecules. As a SERS substrate, AMSx displays excellent reproducibility, stability, and recyclability, which is beneficial for the application of the SERS substrate. Meanwhile, AMSx has excellent sensitivity with an enhancement factor of 4.07 × 106, comparable to that of precious metals. In addition, AMSx exhibits ultrahigh sensitivity in sensing bilirubin and Bisphenol A (BPA); the corresponding detection limit of both is 10-9 M, also better than that of previously reported semiconductors. This work provided a novel idea to synthesize low-cost ultrasensitive SERS substrates and the strategy of improving metal-chalcogenide semiconductor sensing.

Hierarchical CoMoS3.13/MoS2 hollow nanosheet arrays as bifunctional electrocatalysts for overall water splitting.

Hollow hetero-nanosheet arrays have attracted great attention due to their efficient catalytic abilities for water splitting. We successfully fabricated ZIF-67-derived hollow CoMoS3.13/MoS2 nanosheet arrays on carbon cloth in situ through a two-step heating-up hydrothermal method, in which the MoS2 nanosheets were suitably distributed on the surface of the hollow CoMoS3.13 nanosheet arrays. There was a distinct synergistic effect between CoMoS3.13 and MoS2, and a large number of defective and disordered interfaces were formed, which improved the charge transfer rate and provided abundant electrochemical active sites. CMM 0.5, with the optimal Mo doping concentration of 0.5 mmol, exhibited the best catalytic properties. The overpotential values of CMM 0.5 at 10 mA cm-2 were only 107 and 169 mV for the HER and OER, respectively, and it had nearly 100% faradaic efficiency. A dual-electrode electrolytic cell assembled with CMM 0.5 required a voltage of only 1.507 V at 10 mA cm-2 for overall water splitting, and it displayed remarkable long-term durable bifunctional stability.

Diluted-CdS Quantum Dot-Assisted SnO2 Electron Transport Layer with Excellent Conductivity and Suitable Band Alignment for High-Performance Planar Perovskite Solar Cells.

An electron transport layer (ETL) with excellent conductivity and suitable band alignment plays a key role in accelerating charge extraction and transfer for achieving highly efficient planar perovskite solar cells (PSCs). Herein, a novel diluted-cadmium sulfide quantum dot (CdS QD)-assisted SnO2 ETL has been developed with a low-temperature fabrication process. The slight addition of CdS QDs first enhances the crystallinity and flatness of SnO2 ETLs so that it provides a promising workstation to obtain high-quality perovskite absorption layers. It also amazingly increases the conductivity of the SnO2 ETL by an order of magnitude and regulates the energy level matching between the SnO2 ETL and perovskite. These outstanding properties greatly accelerate the charge extraction and transfer. Thus, the MAPbI3-based PSCs with such a diluted-CdSQD-assisted SnO2 ETL achieve a maximum power conversion efficiency of 20.78% and obtain a better stability of devices in air. These findings testify the importance and potential of semiconductor QD modification on ETLs, which may pave the way for developing such composite ETLs for further enhancing photovoltaic performance of planar PSCs.

In-situ surface-enhanced Raman scattering based on MTi20 nanoflowers: Monitoring and degradation of contaminants.

Real-time and in-situ monitoring of chemical reactions has attracted great attention in many fields. In this work, we in-situ monitored the photodegradation reaction process of methylene blue (MB) by Surface enhanced Raman scattering (SERS) technique. An effective and versatile SERS platform assembled from MoS2 nanoflowers (NFs) and TiO2 nanoparticles (NPs) was prepared successfully. The optimized MoS2/TiO2 substrate (MTi20) exhibits not only an ultra-high SERS response but also the excellent catalytic degradation performance to the contaminant MB, which provided a new material for real-time and in-situ monitoring the photodegradation process. Experiments prove that the detection limit is as low as 10-13 M, and degradation rate is as high as 97.2% in 180 s, respectively. And the activity of the substrate kept in the air for 90 days is almost unchanged. Furthermore, as a practical SERS substrate, MTi20 can also detect trace amounts of other harmful substances including malachite green (MG), bisphenol A (BPA) and endosulfan. Thus, this study come up with a new orientation at the real-time and in-situ monitoring of photocatalytic reaction and may be applied in environmental monitoring and food security fields in the future.

Biomass derived the V-doped carbon/Bi2O3 composite for efficient photocatalysts.

This work focused on the utilization of biological extract for the preparation of lignin-based carbon composites materials and used in the field of photocatalysis. A straightforward one-step carbonization way has been developed to prepare vanadium-doped lignin-based carbon/Bi2O3 composites photocatalyst by using sodium lignosulfonate as the carbon source and catalyst. The application of lignin as the carbon source to form photocatalyst support tends to control the uniform distribution. At the same time, sodium lignosulfonate as the catalyst could break down the BiVO4 during carbonization process. A series of characterizations demonstrated the BiVO4 was transformed into Bi2O3 and vanadium-doped lignin-based carbon. The possible synthesis process was proposed. Moreover, the novel V-doped carbon/Bi2O3 composites photocatalyst displayed higher photocatalytic activity than bare BiVO4. A possible photocatalytic mechanism was also discussed. This work provided new insight into the lignin-based carbon materials.

High-sensitive imprinted membranes based on surface-enhanced Raman scattering for selective detection of antibiotics in water.

Poly(vinylidene fluoride) (PVDF) is known as one of the widely used membrane separation materials with excellent physical and chemical properties. In this work, we combine surface-enhanced Raman scattering (SERS) detection technology, membrane separation technology and molecular imprinting technology (MIT) to improve sensitivity and selectivity for selective detection of the enrofloxacin hydrochloride in water. In this investigation, PVDF membranes were used as the support materials and different experiment parameters were investigated to obtain the best property. Meanwhile, the Ag nanoparticles (Ag NPs) modified by 3-methacryloxypropyltrimethoxysilane (KH-570) were used as the SERS substrates and they were uniformly dispersed on the surface of the membrane. Finally, Ag-based SERS imprinted membranes (ASIMs) with specific recognition property were successfully prepared with enrofloxacin hydrochloride as the template molecule, acrylamide (AM) as the functional monomer, ethylene glycol dimethacrylate (EGDMA) as the cross-linker agent and 2,2'-azobis(2-methylpropionitrile) (AIBN) as the initiator by a facile and versatile precipitation polymerization strategy. Under the optimal condition, it was presented good linear relationship (R2 = 0.994) between the Raman signal (at 1390.8 cm-1) and the concentration (10-3 mol·L-1-10-7 mol·L-1) of the templates, and the limit of detection was determined as 10-7 mol·L-1. The morphology and characters were investigated and the results proved that the SERS imprinted membranes could be used into the selective detection of antibiotics and it provided a novel approach of antibiotics detection.

One-pot synthesis of ZnS nanowires/Cu7S4 nanoparticles/reduced graphene oxide nanocomposites for supercapacitor and photocatalysis applications.

The zinc sulfide (ZnS) nanowires (NWs)/analite (Cu7S4) nanoparticles (NPs)/reduced graphene oxide (rGO) nanocomposites were fabricated for the first time using a one-pot hydrothermal method, and the resulting nanocomposites can be used as a photocatalyst and the electrode for a supercapacitor. The ZnS NWs/Cu7S4 NPs/rGO nanocomposites showed excellent electrochemical performance with the maximum specific capacitance of 1114 F g-1 at a current density of 1 A g-1, good cycling stability with capacitance retention of 88% after 5000 cycles and low charge transfer resistance of 0.011 Ω. The ZnS NWs/Cu7S4 NPs/rGO nanocomposites were used as the positive electrode together with active carbon as the negative electrode for the fabrication of an asymmetric supercapacitor device, which exhibited a maximum energy density of 22 W h kg-1 as well as a power density up to 595 W kg-1 with capacitance retention of 77% after 5000 cycles. Furthermore, ZnS NWs/Cu7S4 NPs/rGO nanocomposites exhibited superior photocatalytic activity under ultraviolet and visible light irradiation because of the high surface area, small interface transfer resistance and efficient separation of photogenerated electrons and holes caused by the synergistic effect between ZnS NWs, Cu7S4 NPs and rGO.

Novel Insight into the Role of Chlorobenzene Antisolvent Engineering for Highly Efficient Perovskite Solar Cells: Gradient Diluted Chlorine Doping.

Chlorobenzene and diethyl ether were chosen as an antisolvent to control the crystallization of CH3NH3PbI3. Under the condition of similar crystallization for both perovskite films, the obvious larger short-circuit current density for CH3NH3PbI3 film treated by chlorobenzene prompted us to unveil the roles of chlorobenzene in the perovskite films via adjusting the dropping amount of chlorobenzene. A novel insight of chlorobenzene function was revealed, that is, gradient diluted chlorine doping in the CH3NH3PbI3 film, which forms a gradient band gap in the perovskite films, prompts photogenerated carriers accumulating at the interface, makes the electron transport faster, and effectively enhances the power conversion efficiency (PCE) of solar cells. The maximum PCE of 20.58% has been achieved under standard AM1.5 conditions. Moreover, this technique exhibits very high reproducibility, and 20 devices fabricated in one batch can yield an average PCE of 20.31%.

Fabrication of P(NIPAAm-co-AAm) coated optical-magnetic quantum dots/silica core-shell nanocomposites for temperature triggered drug release, bioimaging and in vivo tumor inhibition.

ZnS:Mn2+ quantum dots (QDs) Fe3O4 QDs/SiO2/P(NIPAAm-co-AAm) core-shell-shell nanocomposites have been successfully fabricated by free radical polymerization method. The average diameter and LCST of ZnS:Mn2+ QDs Fe3O4 QDs/SiO2/P(NIPAAm-co-AAm) (NIPAAm:AAm=90:10) nanocomposites was about 200 nm and 41.1°. It possessed a strong yellow-orange emission peak centered at 589 nm from the Mn2+ 4T1-6A1 transition and the desired superparamagnetic property at room temperature. The DOX encapsulation efficiency and loading capacity was 88% and 15.3 wt%, respectively. The nanocomposites showed the faster drug release behavior at 43 °C than that at 25 °C in vitro release experiment, and exhibited no significant cytotoxicity against the HeLa, HepG2 and HEK293 cell lines. Red fluorescence was observed in the cytoplasm of HeLa cells, confirming its application for biolabeling. Effective tumor inhibition was realized in vivo without the induction of toxicity in mice. ZnS:Mn2+ (QDs) Fe3O4 QDs/SiO2/P(NIPAAm-co-AAm) nanocomposites showed the red fluorescence in the cytoplasm of HeLa cells, faster drug release behavior at 43 °C than that at 25 °C in vitro, and effective tumor inhibition in vivo, confirming its application for drug delivery.

Enhanced Magnetic Properties of BiFeO3 Thin Films by Doping: Analysis of Structure and Morphology.

The improvement of ferromagnetic properties is critical for the practical application of multiferroic materials, to be exact, BiFeO3 (BFO). Herein, we have investigated the evolution in the structure and morphology of Ho or/and Mn-doped thin films and the related diversification in ferromagnetic behavior. BFO, Bi0.95Ho0.05FeO3 (BHFO), BiFe0.95Mn0.05O3 (BFMO) and Bi0.95Ho0.05Fe0.95Mn0.05O3 (BHFMO) thin films are synthesized via the conventional sol-gel method. Density, size and phase structure are crucial to optimize the ferromagnetic properties. Specifically, under the applied magnetic field of 10 kOe, BHFO and BFMO thin films can produce obvious magnetic properties during magnetization and, additionally, doping with Ho and Mn (BHFMO) can achieve better magnetic properties. This enhancement is attributed to the lattice distortions caused by the ionic sizes difference between the doping agent and the host, the generation of the new exchange interactions and the inhibition of the antiferromagnetic spiral modulated spin structure. This study provides key insights of understanding the tunable ferromagnetic properties of co-doped BFO.

Tailoring Blue-Green Double Emissions in Carbon Quantum Dots via Co-Doping Engineering by Competition Mechanism between Chlorine-Related States and Conjugated π-Domains.

Representing single-layer to tens of layers of graphene in a size less than 30 nm, carbon quantum dots (CQDs) is becoming an advanced multifunctional material for its unique optical, electronic, spin and photoelectric properties induced by the quantum confinement effect and edge effect. In present work, upon co-doping engineering, nitrogen and chlorine co-doped CQDs with uniquely strong blue-green double emissions are developed via a facile and one-pot hydrothermal method. The crystalline and optical properties of CQDs have been well manipulated by tuning the mole ratio of nitrogen/chlorine and the reaction time. The characteristic green emission centered at 512 nm has been verified, originating from the chlorine-related states, the other blue emissions centered at 460 nm are attributed to the conjugated π-domain. Increasing the proportion of 1,2,4-benzentriamine dihydrochloride can effectively adjust the bandgap of CQDs, mainly caused by the synergy and competition of chlorine-related states and the conjugated π-domain. Prolonging the reaction time promotes more nitrogen and chlorine dopants incorporate into CQDs, which inhibits the growth of CQDs to reduce the average size of CQDs down to 1.5 nm, so that the quantum confinement effect dominates into play. This work not only provides a candidate with excellent optical properties for heteroatoms-doped carbon materials but also benefits to stimulate the intensive studies for co-doped carbon with chlorine as one of new dopants paradigm.

A polydopamine-based molecularly imprinted polymer on nanoparticles of type SiO2@rGO@Ag for the detection of λ-cyhalothrin via SERS.

A new method is described for the determination of the pesticide λ-cyhalothrin (LC). It combines SERS detection with molecular imprinting and largely improves selectivity. A multilayer surface imprinted nanocomposite was synthesized in two steps on a nanostructure of type SiO2@rGO@Ag acting as a substrates. Firstly, the surface of the SiO2@rGO@Ag composite was modified with self-polymerized dopamine. Secondly, surface-initiated polymerization was carried out to prepare a molecularly imprinted polymer (MIP) using LC as the template. The use of this SiO2@rGO@Ag-MIP allows for excellent SERS based detection and has high selectivity for LC. The Raman intensity and LC concentration present perfect linear relationship between 10-5 to 10-9 mol L-1 and the detection limit is 3.8×10-10 mol L-1. All the procedures are conducted in aqueous or ethanol solution. Graphical abstract Schematic of a new method for determination of the pesticide λ-cyhalothrin. It combines SERS detection with molecular imprinting and largely improves selectivity. A multilayer surface imprinted nanocomposite was synthesized in two steps on a nanostructure of type SiO2@rGO@Ag acting as a substrates.

Correlation between structural change and electrical transport properties of Fe-doped chrysotile nanotubes under high pressure.

Fe3+ doped chrysotile nanotubes (NTs) have been synthesized under controlled hydrothermal conditions, and have been characteristic of layered-walls and room-temperature ferromagnetism. High-pressure in situ impedance spectra and synchrotron XRD measurements are performed on Fe-doped chrysotile NTs to reveal the electrical transport and structural properties under compression. Sample resistance (R sum) was found to increase with the pressure elevation, accompanying the step decrease in the grain boundary relaxation frequency (f gb), which reflects the bandgap broadening and dipoles polarization weakening due to the application of pressure. Furthermore, it is found that both R sum and f gb change their pressure dependences at ~5.0 GPa, which is attributed to the nonlinear compressibility of c-axis and even the underlying lattice distortion of monoclinic structure obtained in the XRD observations.