JOURNAL OF POWER SOURCES
·
2020
·
IF 8.247
Wenxin Li,Bo Yu,Yang Hu,Xinqiang Wang,Bin Wang,Xiaojuan Zhang,Dongxu Yang,Zegao Wang,Yuanfu Chen
Exploring highly efficient, stable and nonprecious electrocatalysts for both hydrogen and oxygen evolutions is greatly desirable for sustainable energy conversion, but still a huge challenge. Herein, we construct a unique three-dimensional (3D) porous electrocatalyst with hollow (Co,Fe)P nanoframes encapsulated into N,P-codoped graphene aerogel (CFP NFs@NPGA) through one-step in situ encapsulation and selective etching, followed by phosphorization. Due to its uniqure 3D porous nanoarchitecture, CFP NFs@NPGA displays superior electrocatalytic performance. As a highly efficient catalyst for hydrogen evolution reaction , the CFP NFs@NPGA catalyst only needs low overpotential of 155 mV to afford 10 mA cm −2 under alkaline condition. Meanwhile, the hybrid reveals remarkable oxygen revolution reaction activity with a small overpotential of 278 mV to afford 10 mA cm −2 in alkaline electrolyte . When adopted as both cathode and anode in overall water-splitting cell, the hybrid requires only 1.59 V to achieve 10 mA cm −2 with nearly 100% faradaic efficiency, and the experimentally measured H 2 and O 2 gas genenaration rates are about 0.18 and 0.09 mmol h −1 , respectively, showing outstanding long-term stability even over 48 h. The present results manifest that the combination of hollow nanostructure and hetero-atom-doped carbon matrix is an effective strategy to enhance water-splitting performance of transition metal phosphides.
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DOI
高影响因子
JOURNAL OF POLYMER RESEARCH
·
2012
·Vol. 19
·期 11
·1-7
·
IF 1.733
Yu Wei-Na,Liu Shou-Xin,Wang Hong-Mei,Tian Rong
Temperature-responsive P(NIPAM- co -HMAM)- b -PEO- b -P(NIPAM- co -HMAM) triblock copolymers were synthesized by an atomic transfer radical polymerization (ATRP) method without freeze–pump–thaw cycles. The composition, structure, and molecular weight of the synthesized block copolymer were characterized by 1 H NMR and GPC. The phase transitions induced by temperature for different copolymers in dilute aqueous solutions have been studied using transmittance measurements, laser particle size measurements, viscosity analysis, and surface tension measurement, which showed that the HMAM content and the PEO (or PEG) chain length in the synthesized triblock copolymer affects the copolymer’s lower critical solution temperature (LCST). The micellization behavior of each temperature-responsive triblock copolymer was investigated by fluorescence probe measurements and transmission electron microscopy (TEM), which showed that the triblock copolymers form stable micelles above the LCST. The introduction of the HMAM component and the formation of micelles represent the first steps in the development of an injectable gel that forms in situ through chemical and physical crosslinking.
研究领域:
高分子化学
·
生物材料
·
药物递送系统
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DOI
高影响因子
ACS Applied Energy Materials
·
2022
·
IF 6.959
Xiaochun Zheng,Yidi Wang,Shoutian Ren,Qixiao Gai,Wenjun Liu,Quanli Dong
Interface defects are one of the main factors for inefficient photoelectric conversion of nanocomposites, which is also suitable for the photocatalytic nanosystem containing photosensitizers and co-catalysts, so the efficient passivation of interface defects can enhance their photocatalytic performance. In this work, P-doped C3N4 (P–C3N4) was prepared by the thermal polymerization of urea with phytic acid as the P doping source. Then, the doped P atoms could act as anchoring sites for photodeposited Ni nanoparticles (NPs) on P–C3N4, and Ni–P–N bonds were spontaneously formed between Ni NPs and P–C3N4 with doped P as the bridging ligand. The optimal H2 evolution rate of P–C3N4/Ni-20 is 1.56 mmol g–1 h–1, which is 52.0 and 6.0 times that of C3N4 and C3N4/Ni-30, respectively, and even 2.0 times that of P–C3N4/Pt-2%. Its apparent quantum efficiency of 4.35% at 420 nm was 6.9 times that of reference C3N4/Ni-30 without P doping. The optimized interface transfer of carriers by the formed Ni–P–N bonds between P–C3N4 and Ni NPs was the main factor for the enhanced photocatalytic performance of C3N4.
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产品关联
DOI
高影响因子
POLYMER
·
2020
·
IF 4.231
Abdul Haleem,Jun Chen,Xiao-Xiao Guo,Jia-Yun Wang,Hui-Juan Li,Peng-Yun Li,Sheng-Qi Chen,Wei-Dong He
Temperature-responsive macro-porous cryogels of poly( N -iospropylacryamide- co -acrylamido-2-methylpropane sulfonic acid) [P(NIPAM- co -AMPS)] were prepared through redox-initiated cryo-polymerization at −12, −18 and −24 °C. Silver or gold nanoparticles (AgNPs or AuNPs) were formed inside P(NIPAM- co -AMPS) cryogels through the thermal reduction of absorbed AgNO 3 or HAuCl 4 , resulting in hybrid cryogels immobilized with AgNPs or AuNPs. Fourier transform infrared spectroscopy , thermal gravimetric analysis and X-ray diffraction confirmed the chemical composition . Cryogel morphology and nanoparticle distribution were investigated through scanning and transmission electron microscopies . By checking swelling ratio in neutral water, the temperature response of cryogels was identified. The hybrid cryogels were used as the catalysts to reduce p -nitrophenol with NaBH 4 at different temperatures and pHs. The hybrid cryogel with AuNPs had the higher catalytic activity than the counterpart hybrid cryogel with AgNPs. The catalytic activity of hybrid cryogels increased with temperature and pH. The temperature response of cryogels facilitated their isolation from the reaction mixture. Since AuNPs were fixed tightly onto the cryogel pore-wall and hardly lost, hybrid cryogels with AuNPs demonstrated no decrease in catalytic activity for 5 cycles of p -nitrophenol reduction.
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DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2020
·
IF 6.182
Yi Zhang,Qi Wang,Dongming Liu,Qian Wang,Tong Li,Zhou Wang
A novel isotype (p-p) heterojunction, on the basis of Cu 2 O coupled with BiOI, has been designed and synthesized via a facile two-step electro-deposition approach at room temperature. The morphology, phase compositions and chemical bonding state were verified by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction measurements (XRD) and X-ray photoelectron spectra (XPS). The optimized Cu 2 O/BiOI hybrid electrode exhibited boosted photoelectrochemical (PEC) H 2 O 2 non-enzymatic sensing performance under visible light illumination, with a phenomenally broad linear range (1.99 µM ~ 17.54 mM), a high sensitivity of 213.87 µA mM −1 cm −2 , as well as a low detection limit of 0.44 µM (S/N = 3). Additionally, the sensor presented satisfying selectivity, repeatability, stability and its feasibility in real samples was corroborated. The photoelectrochemical sensing mechanism was clarified in the view of band structure and p-p heterojunction. Our work would enlighten the perspective research on the application of isotype heterojunction in PEC bio-sensing and provide a promising non-enzymatic biosensor platform for effective detection of H 2 O 2 in food, biomedical and environment analysis.
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高影响因子
JOURNAL OF FOOD SCIENCE
·
2018
·Vol. 83
·期 2
·565-573
·
IF 2.018
Lingying Luo,Yun Bai,Guanghong Zhou
3-Amino-1,4-dimethyl-5H-pyrido[4,3-b]indole (Trp-P-1) is a group 2B carcinogen characterized by the International Agency for Research on Cancer (IARC) and great efforts have been taken to reduce Trp-P-1 mutagenicity to humans. In this study, the effect of a reduction of Trp-P-1 on intestinal absorption as a promising strategy was investigated. The data showed that when 20 mM Trp-P-1 cotransported with 10 mM of sodium carboxymethyl cellulose (CMC), xanthan gum, or carrageenan, the absorption rate of Trp-P-1 was reduced by 31.5%, 49.5%, or 72.9% in MDCK-MDR1 cell monolayer, respectively; and 64.6%, 83.4%, or 64.1% in rat intestinal tissues, correspondingly. These 3 polysaccharides also reduced pharmacokinetic parameters, that is, C max , AUC 0-t , and AUC 0-∞ , after Trp-P-1 was given to rats intragastrically. However, gum arabic did not exhibit similar effects on Trp-P-1 absorption in vitro or in vivo . The Ames test showed that these 3 polysaccharides reduced Trp-P-1 mutagenicity to Salmonella typhimurium TA98, but gum arabic did not. Isothermal titration calorimetry assay indicated that Trp-P-1 interacted with these 3 polysaccharides. Thermodynamic study showed that the actual value of △ H <0, but its absolute value greater than the corresponding value of T∆S, suggest a specific interaction between Trp-P-1 and these 3 polysaccharides, probably through the hydrogen bond and/or ion interaction. Reduction of Trp-P-1 intestinal absorption using food additives could be one of the strategies to suppress Trp-P-1-induced carcinogenesis in human. Practical Application 1. This study provides insightful information for the food industry how gum arabic, xanthan gum, kappa carrageenan, and sodium carboxymethyl cellulose affect the absorption of Trp-P-1. 2. This study also provides novel information regarding a better formulation for meat products to reduce Trp-P-1 absorption.
研究领域:
营养学
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毒理学
·
食品科学
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DOI
PubMed
高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2026
·
IF 6.2
Hainan Song,Weiwei Cao,Xiushi Chen,Siqi Peng,Wenlong Sun,Xiaojun Yang,Mahmoud Salah,Mohamed A. Farag,Yajing Fang
Effects of four flavonoid inhibitors (FIs, quercetin, kaempferol, luteolin, and flavone) at different concentrations on dynamically increasing dihydroquercetin (DHQ) uptakes and regulating P-glycoprotein (P-gp)’s mRNA and protein levels were evaluated in KB/MDR1 cells. DHQ’s bidirectional transport was measured in Caco-2 monolayers. The low uptakes of DHQ were dynamically increased by four FIs (better than elacridar) in the order of quercetin > luteolin > kaempferol > flavone. Four FIs significantly increased DHQ40’s uptakes in a dose-independent manner. Four FIs alone or with DHQ significantly decreased P-gp’s mRNA and protein expressions. DHQ was poorly absorbed (efflux ratios >20) in Caco-2 monolayers, especially at high concentrations. Four FIs improved DHQ’s absorption by significantly increasing (reversing) its influx (efflux) at most time points (1, 2, 4, and 6 h), especially for DHQ100 rather than DHQ40. Docking results explained that quercetin competitively occupies DHQ’s binding site or binds to the inhibitor site of P-gp. These results were valuable for improving DHQ absorption.
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF POWER SOURCES
·
2025
·
IF 7.9
Jinnuo Yang,Jiahui Lv,Yanqing Feng,Jiang Yan,Shuo Zhao,Yang Liu,Lei Zu,Huiqin Lian
Lithium-ion batteries (LIBs) attract widespread attention as promising energy storage devices owing to their superior energy density, excellent cycle life, and absence of memory effect. However, they still encounter challenges in high-rate performance and structural stability, necessitating further optimization. This study focuses on a composite anode material constructed from black phosphorus (BP), tungsten disulfide (WS 2 ), and ultra-high-purity whisker carbon nanotubes (UWCNTs) (BP-WS 2 -UWCNTs). The research investigates the regulatory effects of phosphorus–carbon (P–C) and phosphorus–sulfur (P–S) bonds at the material interface on electrochemical performance. Characterization indicates the establishment of P–C and P–S bonds at the composite interface, which enhance structural integrity and improve electron/ion transport capabilities. Electrochemical performance evaluations validate the combined effect of these interfacial bonds: at 2.0 A g −1 , the BP-WS 2 -UWCNTs anode delivers 605.8 mAh g −1 for 2000 cycles, and retains 252.2 mAh g −1 after 3000 cycles even at 15.0 A g −1 , exhibiting remarkable rate performance and prolonged cycling durability. In practical applications of LIBs, the composite anode maintains robust structural integrity and outstanding electrochemical performance. This work highlights that the combined effect of interfacial P–C and P–S chemical linkages effectively facilitates lithium-ion diffusion and stabilizes the electrode structure, offering valuable insights and viable strategies for advancing high-capacity anode design in LIBs.
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高影响因子
KOREAN JOURNAL OF CHEMICAL ENGINEERING
·
2019
·Vol. 36
·期 6
·942-953
·
IF 2.476
Rong Yachan,Han Runping
Magnetic activated carbon (MAC) was prepared by co-precipitation. These particles had attractive adsorption capacity and could be easily separated from aqueous. MAC was used as adsorbent to remove p -chlorophenol ( p -CP) and p -nitrophenol ( p -NP) from solution in single and binary systems. In a single system, the equilibrium time was 60 min, the best initial pH was 3-8 and 3-6 for p -CP or p -NP adsorption, respectively. The existence of salt ions had little influence on the adsorption process, while surfactant had negative influence. The adsorption quantity from experiments was up to 97.3 mg·g −1 for p-CP and 116 mg·g −1 for p -NP at 293 K, respectively. Freundlich model and pseudo-second-order kinetic model fitted well the adsorption behavior. Thermodynamic parameters were calculated and the results showed that the process was spontaneous, exothermic and entropy production in nature. In addition, p -CP or p -NP-loaded MAC could be well reused by 0.01 mol·L −1 sodium hydroxide solution as regeneration agent. Kinetic process of desorption was fitted best by pseudo-second-order kinetic model. Results from the binary system showed that competitive adsorption existed during the process, and p -NP adsorption on MAC was easier than p -CP. Freundlich model well fitted the adsorption behavior in the binary system. Hydrogen-bonding, electron donor-acceptor and π-π interactions may be the main mechanisms of adsorption. MAC proved to be an excellent adsorbent for the removal of p -CP and p -NP from solution.
研究领域:
环境科学
·
化学工程
·
水处理
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DOI
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2025
·
IF 4.7
Ruihan Yang,Ying Ouyang,Longxiao Yang,Jianqiang Liu,Enhui Xing,Yibin Luo,Xingtian Shu
P-La modification has been industrially demonstrated as a successful approach to enhance the hydrothermal stability of ZSM-5 zeolites. ZSM-5 is widely used as the catalytic component in processes such as fluid catalytic cracking (FCC) and methanol-to-propylene (MTP), which involve harsh reaction/regeneration conditions. With the P-La modified ZSM-5 as the research subject, the interactions among phosphorus, lanthanum, and ZSM-5 during modification and their influence on catalytic performance were systematically investigated through characterization methods including XRD, 27 Al, 29 Si, 31 P MAS NMR, and 2D 31 P{ 27 Al} D-HMQC MAS NMR. The mechanism on enhancement of hydrothermal stability of ZSM-5 zeolite through interactions among P, La and ZSM-5 was proposed. Specifically, during the modification, phosphorus and lanthanum tends to form LaPO 4 and lanxthanum polyphosphate species. This P-La interaction not only suppresses channel blocking and damage in ZSM-5 caused by lanthanum, but also significantly reduces the degree of phosphorus polymerization, facilitating the re-dispersion of phosphorus during hydrothermal treatment and ultimately strengthening the interaction between phosphorus and ZSM-5. Directed by the mechanism, the P-La modified approach was optimized, and the subsequent impregnation of P and La onto ZSM-5 strategy was developed to further improve the hydrothermal stability of ZSM-5.
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DOI
高影响因子
Nature Communications
·
2026
·
IF 18.1
Zhai Mengde,Wu Tianhao,Du Kaihuai,Chen Cheng,Shibayama Naoyuki,Narmandakh Khongorzul,Khan Abdul Haseeb Hassan,Wang Ying-Chiao,Shang Juan,Staykov Aleksandar,Song Jun Tae,Ida Shintaro,Wang Pangpang,Yamada Sunao,Tamada Kaoru,Zhao Shuai,Wang Aili,Guo Zhanglin,Matsushima Toshinori,Miyasaka Tsutomu,Cheng Ming
Self-assembled molecules are widely used as bottom interfacial layers in inverted perovskite solar cells, yet their application to perovskite top surfaces remains poorly understood. Here, we develop two self-assembled molecules for perovskite surface modification and interfacial optimization with the hole transport layer. Through solvent engineering, ordered and uniform molecular packing is achieved on the perovskite surface. These molecules optimize surface energetics and promote efficient hole transfer when coupled with a homologous hole transport layer. Their large molecular dipoles tune interfacial energy alignment and reduce energetic offsets, thereby accelerating charge extraction from the perovskite layer. This dipole-driven interfacial modulation is effective in both normal and inverted device architectures. As a result, a power conversion efficiency of 26.18% (certified 26.23%) is achieved in normal-structure devices, together with improved operational stability under maximum power point tracking. This work establishes a viable strategy for perovskite surface engineering using self-assembled molecules.
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产品关联
DOI
PubMed
高影响因子
Small
·
2019
·Vol. 15
·期 10
·1804546
·
IF 10.856
Jing Yang,Donghua Guo,Shulin Zhao,Yue Lin,Rui Yang,Dongdong Xu,Naien Shi,Xiaoshu Zhang,Lingzhi Lu,Ya-Qian Lan,Jianchun Bao,Min Han
As one class of important functional materials, transition metal phosphides (TMPs) nanostructures show promising applications in catalysis and energy storage fields. Although great progress has been achieved, phase-controlled synthesis of cobalt phosphides nanocrystals or related nanohybrids remains a challenge, and their use in overall water splitting (OWS) is not systematically studied. Herein, three kinds of cobalt phosphides nanocrystals encapsulated by P-doped carbon (PC) and married with P-doped graphene (PG) nanohybrids, including CoP@PC/PG, CoP-Co 2 P@PC/PG, and Co 2 P@PC/PG, are obtained through controllable thermal conversion of presynthesized supramolecular gels that contain cobalt salt, phytic acid, and graphene oxides at proper temperature under Ar/H 2 atmosphere. Among them, the mixed-phase CoP-Co 2 P@PC/PG nanohybrids manifest high electrocatalytic activity toward both hydrogen and oxygen evolution in alkaline media. Remarkably, using them as bifunctional catalysts, the fabricated CoP-Co 2 P@PC/PG || CoP-Co 2 P@PC/PG electrolyzer only needs a cell voltage of 1.567 V for driving OWS to reach the current density at 10 mA cm −2 , superior to their pure-phase counterparts and recently reported bifunctional catalysts based devices. Also, such a CoP-Co 2 P@PC/PG || CoP-Co 2 P@PC/PG device exhibits outstanding stability for OWS. This work may shed some light on optimizing TMPs nanostructures based on phase engineering, and promote their applications in OWS or other renewable energy options.
研究领域:
材料科学
·
电催化
·
能源化学
·
纳米材料
·
可再生能源
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DOI
高影响因子
危险品化学品经营许可证（带存储）