A successive ‘‘conversion-deposition” mechanism achieved by micro-crystalline Cu2O modified current collector for composite lithium anode

Yifei Cai,Bin Qin,Chun Li,Xiaoqing Si,Jian Cao,Xiaohang Zheng,LIANG QIAO,Junlei Qi 한국공업화학회 2023 Journal of Industrial and Engineering Chemistry Vol.120 No.-

Lithium (Li) metal is a promising material for high-energy–density batteries, but it is still plagued byobvious capacity degradation and low average Coulombic efficiency resulting from dendrite Li propagation. One main reason is the electro-mechanic coupled failure of plated Li on the current collector, whichcontributes to non-dense Li deposition on the anode. Transition metal oxides (TMOs) with a conversiontypemechanism have been used directly as the anode materials for lithium ion batteries, which demonstratedbetter electro-mechanical stability than metal Li. Herein, a successive ’’conversion-deposition’’mechanism is ingeniously developed to restrain the generation of dendritic Li. Specifically, a microcrystallineCu2O modified current collector was prepared, in which Li+ are sequentially inserted intoCu2O and deposited in the form of Li metal at successive low potential. A Li-Cu half-cell based on thehybrid mechanism sustains a high Coulombic efficiency of over 99.3 % in up to 800 cycles. This work ingeniouslyinhibits the generation of dendrite Li by incorporating conversion-type materials withdeposition-dissolution type metal Li, which contributes to a novel concept for the design of functionalcurrent collectors for composite Li anodes.

Effect of Li Content on the Surface Film Formed on the Binary Mg–Li Alloys in NaCl Solution

Chuanqiang Li,Dahui Liang,Yejia Lin,Yong Dong,Binqing Shi,Changjian Yan,Zhengrong Zhang 대한금속·재료학회 2024 METALS AND MATERIALS International Vol.30 No.1

The surface film formed on the Mg–Li alloys with different Li content in 0.1 M NaCl solution were investigated via electrochemicaltesting, morphologies observation and chemical composition analysis in this work. The results revealed that thesurface film of Mg–14Li alloy (L14: body centred cubic (BCC)) possessed higher electrical resistivity and remained a highertolerating over-potential (0.1 V vs. open circuit potential) than those of Mg–4Li (L4: hexagonal closed-packed (HCP)) andMg–7.5Li (L7: HCP+BCC), resulting in a better corrosion performance. After 24 h immersion in NaCl solution, the wholesurface film of L14 remained undamaged and displayed weave-like and dense characteristic, while both L4 and L7 present aseverely damaged film. The cross-sectional details illustrated typical two layers of surface film formed on L14 with the outerlayer of ~ 1.5 μm and inner layer of ~ 2.5 μm in thickness, whilst only one layer of film with less than 2.5 μm in thicknesswas observed on L4 and L7. At last, combining analysis of X-ray diffraction, energy dispersive X-ray spectrometry, X-rayphotoelectron spectroscopy and transmission electron microscope confirmed the composition of outer layer of surface filmon the L14 contains much more Mg(OH)2 and Li-containing compounds, and the porous Mg(OH)2 film can be sealed by theLi-containing compounds, which is very different the single Mg(OH)2 film on the traditional magnesium and L4/L7 alloys. As a result, the best protective function of the surface film on the L14 alloy contribute to its high corrosion resistance.

The effect of S-functionalized and vacancies on V2C MXenes as anode materials for Na-ion and Li-ion batteries

Ya-Meng Li,Yong-Liang Guo,Zhao-Yong Jiao 한국물리학회 2020 Current Applied Physics Vol.20 No.2

The electrochemical properties of V2C and V2CT2 (T = O, S) MXenes with and without vacancy as anode materials for Na-ion and Li-ion batteries, have been studied using first-principles calculation. The present results indicate that the adsorption strength of Li-ion and Na-ion on V2CS2 are less than that of O-functionalized, together with a lower diffusion barrier. Simultaneously, V2CS2 monolayer exhibits lower open-circuit voltage (OCV) values of 0.72 and 0.49 V for Li- and Na-ion, respectively. Interestingly, the presence of atomic vanadium vacancy on V2CS2 monolayer exerts more prominent effects on enhancing adsorption strength than that of carbon vacancy for Li-ion and Na-ion, but with an exception for the diffusion of Li-ion and Na-ion on V2CS2 monolayer. The finding suggests that the V2CS2 monolayer is expected to be a potential candidate as anode material for Li-ion and Na-ion battery due to its lower open-circuit voltages and diffusion barriers.

Research on Li0.3Na0.18K0.52NO3 promoted Mg20Al-CO3 LDH/GO composites for CO2 capture

Ying Yang,Kai Chen,Liang Huang,Min Li,Taiping Zhang,Mi Zhong,Ping Ning,Junya Wang,Shikun Wen 한국공업화학회 2021 Journal of Industrial and Engineering Chemistry Vol.102 No.-

It has been reported that the addition of graphene oxide (GO) can increase the dispersion and heterogeneousnucleation of layered double hydroxide (LDH), thus providing more active sites, which is more conduciveto CO2 adsorption. Herein, we reported alkali metal nitrates ((Li0.3Na0.18K0.52)NO3) promoted LDHand GO composites (LDH/GO) as adsorbents for CO2 capture. The influence of mass ratio of LDH to GO, theimpregnation ratio of alkali metal nitrates, the calcination and adsorption temperature, as well as thecycling stability were investigated systematically. The results indicated that the CO2 capture capacityof LDH/GO composite with 30 mol% (Li0.3Na0.18K0.52)NO3 could reach 4.51 mmol g 1, which was 5.86times higher than LDH/GO1 without loading alkali metal nitrates. Moreover, it had outstanding CO2adsorption capacity in the range from 200 C to 320 C. In addition, the cyclic adsorption and desorptiontest manifested that the CO2 uptake of the material can reach 3.07 mmol g 1 after 22 cycles. We believethat this study will give a significant contribution to fabrication of LDH based composites as CO2 adsorbentsin future study.

Preparation of layered double hydroxides intercalated by tartaric acid anion and its application in boron adsorption

Lianmin Ji,Liang Cai,Yuze zhang,Xiaowu Peng,Dong Shi,Lijuan Li 한국공업화학회 2023 Journal of Industrial and Engineering Chemistry Vol.123 No.-

Based on the exchangeability of anions between the layers of magnesium-based LDHs, LDHs intercalatedby tartaric acid anion (TA-LDH) was prepared by co-precipitation method to adsorb boron, and confirmedby XRD and FT-IR that TA had successfully entered the interlayer of LDH. The adsorption kinetics showedthat the adsorption efficiency of B was mainly controlled by the chemisorption mechanism. The thermodynamicsrevealed that the relationship between the equilibrium concentration of B in solution and theadsorption capacity of TA-LDH for B was consistent with the Freundlich model. Cl or Li+ in solution hadlittle effect on the adsorption of B by TA-LDH, while SO4 2 had a great effect on that compared with NO3-LDH. Boron adsorption was accomplished through the interaction between the hydroxyl of TA anion inthe interlayer and that of B(OH)3 and B(OH)4. The elution efficiency of TA-LDH was greater than 70% withammonium chloride used as the eluent. While TA-LDH still maintained a good adsorption capacity after 5cycles, and the solubility loss efficiencies of Mg2+ in a single adsorption and elution were 1.5% and 5.4%,respectively. Our study can provide a new idea and method for the development and utilization of magnesiumresources.

Bromo-honaucin A inhibits osteoclastogenic differentiation in RAW 264.7 cells via Akt and ERK signaling pathways

( Mahesh Sapkota ),( Liang Li ),( Hyukjae Choi ),( William H Gerwick ),( Yunjo Soh ) 영남대학교 약품개발연구소 2016 영남대학교 약품개발연구소 연구업적집 Vol.26 No.-

Osteoclasts are unique bone remodeling cells derived from multinucleated myeloid progenitor cells. They play homeostatic vital roles in skeletal modeling and remodeling but also destroy bone masses in many pathological conditions such as osteoporosis and rheumatoid arthritis. Receptor activation of NF-KB li-gand (RANKL) is essential osteclastogenesis. In this study, we investigated the effects of bromo-honaucin A (Br-H A) isolated from Leptolyngbya crossbyana (cyanobacterium). To investigate the me-chanism of the inhibitory effect of Br-H A on osteoclstogenesis. we employed Br-H Ain RANKL-treated murine monocyte/macrophage RAW 264.7 cells for osteoclastic differentiation in-vitro. The inhibitory effects on in-vitro osteoclastogenesis was evaluated by counting the number of Tartarate resistant acid phospatase (TRAP) positive multinucleated cells and by measuring the expression level of osteoclast-specific genes like matrix metalloproteinase 9 (MMP9). cathepsin K (CATH K), GRB2-associated-binding protein 2 (GAB2), c-terminal myc kinase (C-MYC). C-terminal Src kinase (C-SRC) and Microphthalmia-associated transcription factor (MITF). Moreover, Br-H A blocked the resorbing capacity of RAW 264.7 cells on calcium phosphate-coated plates. Finally, Br-H A clearly decreased the expression of Akt and also decreased the activation of ERK. Thus, the study identifies Br-H A as potent inhibitor potentialin the treatment of diseases involving abnormal bone lysis such as osteoporosis. rheumatoid arthritis, and periodontal bone degradation.

Influence of multiple ultrasonic impact treatments on surface roughness and wear performance of SUS301 steel

Li, Liang,Kim, Miru,Lee, Seungjun,Bae, Munki,Lee, Deugwoo Elsevier 2016 Surface & coatings technology Vol.307 No.1

<P><B>Abstract</B></P> <P>This paper described an easy mechanical surface enhancement technique based on ultrasonic vibration, namely ultrasonic impact treatment (UIT). The effects of multiple ultrasonic impact treatments (UITs) on the surface properties of SUS301 steel were investigated using an optical microscope, a step profiler, a non-contact optical profiler, a micro hardness testing machine, X-ray diffraction (XRD), and a pin-on-disk tribotester. The results showed the effects of surface smoothing and hardening on the wear performance. An increase in the number of UITs resulted in a lower roughness and higher hardness. After three UITs, the surface roughness decreased from 0.694 to 0.112μm, and the hardness increased from 257.32 to 428.38HV. The evolution of surface morphology was also analyzed in detail over multiple UITs. Moreover, the volume fraction of plastic deformation-induced martensite increased with the number of UITs of the surface. The samples treated three passes showed better wear resistance than untreated samples under dry sliding conditions.</P> <P><B>Highlights</B></P> <P> <UL> <LI> An easy mechanical surface enhancement technique based on ultrasonic vibration was described. </LI> <LI> The roughness and hardness of SUS301 steel were respectively reduced and increased by this technique. </LI> <LI> The evolution of surface morphology was analyzed over multiple passes. </LI> <LI> This technique increased the wear resistance of SUS301 steel. </LI> </UL> </P>

NEDD8-activating enzyme inhibitor, MLN4924 (Pevonedistat) induces NOXA-dependent apoptosis through up-regulation of ATF-4

Liu, Xiaojun,Jiang, Yanan,Wu, Jianfu,Zhang, Wenjuan,Liang, Yupei,Jia, Lijun,Yu, Jinha,Jeong, L.S.,Li, Lihui Elsevier 2017 Biochemical and biophysical research communication Vol. No.

<P><B>Abstract</B></P> <P>It has been reported that MLN4924 can inhibit cell growth and metastasis in various kinds of cancer. We have reported that MLN4924 is able to inhibit angiogenesis through the induction of cell apoptosis both in vitro and in vivo models. Moreover, Neddylation inhibition using MLN4924 triggered the accumulation of pro-apoptotic protein NOXA in Human umbilical vein endothelial cells (HUVECs). However, the mechanism of MLN4924-induced NOXA up-regulation has not been addressed in HUVECs yet. In this study, we investigated how MLN4924 induced NOXA expression and cellular apoptosis in HUVECs treated with MLN4924 at indicated concentrations. MLN4924-induced apoptosis was evaluated by Annexin V-FITC/PI analysis and expression of genes associated with apoptosis was assessed by Quantitative RT-PCR and western blotting. As a result, MLN4924 triggered NOXA-dependent apoptosis in a dose-dependent manner in HUVECs. Mechanistically, inactivation of Neddylation pathway caused up-regulation of activating transcription factor 4 (ATF-4), a substrate of Cullin-Ring E3 ubiquitin ligases (CRL). NOXA was subsequently transactivated by ATF-4 and further induced apoptosis. More importantly, knockdown of ATF-4 by siRNA significantly decreased NOXA expression and apoptotic induction in HUVECs. In summary, our study reveals a new mechanism underlying MLN4924-induced NOXA accumulation in HUVECs, which may help extend further study of MLN4924 for angiogenesis inhibition treatment.</P> <P><B>Highlights</B></P> <P> <UL> <LI> MLN4924 triggered NOXA-dependent apoptosis in a dose-dependent manner in HUVECs. </LI> <LI> Inactivation of neddylation caused up-regulation of ATF4, a substrate of CRL. </LI> <LI> NOXA was transactivated by ATF4 and further induced apoptosis. </LI> <LI> Knockdown of ATF-4 significantly decreased NOXA expression and apoptotic induction. </LI> <LI> We revealed a new mechanism underlying MLN4924-induced NOXA accumulation in HUVECs. </LI> </UL> </P>

Pyrophosphate-triggered nanoaggregates with aggregation-induced emission

Li, Chun-Tao,Xu, You-Liang,Yang, Jian-Gong,Chen, Yong,Kim, Hyeong Seok,Cao, Qian-Yong,Kim, Jong Seung Elsevier Sequoia 2017 Sensors and actuators. B Chemical Vol.251 No.-

<P><B>Abstract</B></P> <P>A novel tetraphenylethene-based probe bearing bis-imidazolium anion donors is herein reported for pyrophosphate anion recognition. This probe can self-assemble finite, small sphere nanoaggregates with very weak emission in aqueous solution, and changes into large rod-like nanoaggregates with strong aggregation-induced emission upon binding with the pyrophosphate anion.</P> <P><B>Highlights</B></P> <P> <UL> <LI> A bis-imidazolium functionalized tetraphenylethene probe was prepared. </LI> <LI> This probe self-assemble finite small sphere nanoaggregates in aqueous solution. </LI> <LI> The probe can recognize pyrophosphate anion with strong aggregation-induced emission. </LI> <LI> The probe/pyrophosphate assembly can fluorescence assay alkaline phosphatase. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>A novel nanoaggregates for recognition of pyrophosphate anion with aggregation-induced emission in pure aqueous solution is introduced.</P> <P>[DISPLAY OMISSION]</P>

Rational design of common transition metal-nitrogen-carbon catalysts for oxygen reduction reaction in fuel cells

Zheng, Yongping,Yang, Dae-Soo,Kweun, Joshua M.,Li, Chenzhe,Tan, Kui,Kong, Fantai,Liang, Chaoping,Chabal, Yves J.,Kim, Yoon Young,Cho, Maenghyo,Yu, Jong-Sung,Cho, Kyeongjae Elsevier 2016 Nano energy Vol.30 No.-

<P><B>Abstract</B></P> <P>Bio-inspired non-precious-metal catalysts based on iron and cobalt porphyrins are promising alternatives to replace costly platinum-based catalysts for oxygen reduction reaction (ORR) in fuel cells. However, the exact nature of the active sites is still not clearly understood, and further optimization design is needed for practical applications. Here, we report a rational catalyst design process by combining density functional theory (DFT) calculations and experimental validations. Two sets of square-planar (MN<SUB>x</SUB>C<SUB>4−x</SUB>) and square-pyramid (MN<SUB>x</SUB>C<SUB>5−x</SUB>) active centers (M=Mn, Fe, Co, Ni) incorporated in graphene were examined using DFT. Fe-N<SUB>5</SUB> and Co-N<SUB>4</SUB> sites were identified theoretically to have the best performance in fuel cells, while Ni-N<SUB>x</SUB>C<SUB>4−x</SUB> sites catalyze the most H<SUB>2</SUB>O<SUB>2</SUB> byproduct. Graphene samples with well-dispersed incorporations of metals were synthesized, and the following electrochemical measurements show an excellent agreement with the theoretical predictions, indicating that a successful design framework and systematic understanding toward the catalytic nature of these materials are established.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Graphene based catalysts design for ORR is demonstrated by combining experiments and modellings. </LI> <LI> Iron porphyrin like active site is unraveled to be five nitrogen coordinated as FeN<SUB>5</SUB>. </LI> <LI> Cobalt porphyrin like active site is shown to be four nitrogen coordinated as CoN<SUB>4</SUB>. </LI> <LI> Nickel porphyrin like catalyst is potentially used for catalytic synthesis of H<SUB>2</SUB>O<SUB>2</SUB>. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>