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Designing ultrastable P2/O3-type layered oxides for sodium ion batteries by regulating Na distribution and oxygen redox chemistry 被引量:3
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作者 Jieyou Huang Weiliang Li +3 位作者 Debin Ye Lin Xu Wenwei Wu Xuehang Wu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第7期466-476,共11页
P2/O3-type Ni/Mn-based layered oxides are promising cathode materials for sodium-ion batteries(SIBs)owing to their high energy density.However,exploring effective ways to enhance the synergy between the P2 and 03 phas... P2/O3-type Ni/Mn-based layered oxides are promising cathode materials for sodium-ion batteries(SIBs)owing to their high energy density.However,exploring effective ways to enhance the synergy between the P2 and 03 phases remains a necessity.Herein,we design a P2/O3-type Na_(0.76)Ni_(0.31)Zn_(0.07)Mn_(0.50)Ti_(0.12)0_(2)(NNZMT)with high chemical/electrochemical stability by enhancing the coupling between the two phases.For the first time,a unique Na*extraction is observed from a Na-rich O3 phase by a Na-poor P2 phase and systematically investigated.This process is facilitated by Zn^(2+)/Ti^(4+)dual doping and calcination condition regulation,allowing a higher Na*content in the P2 phase with larger Na^(+)transport channels and enhancing Na transport kinetics.Because of reduced Na^(+)in the O3 phase,which increases the difficulty of H^(+)/Na^(+) exchange,the hydrostability of the O3 phase in NNZMT is considerably improved.Furthermore,Zn^(2+)/Ti^(4+)presence in NNZMT synergistically regulates oxygen redox chemistry,which effectively suppresses O_(2)/CO_(2) gas release and electrolyte decomposition,and completely inhibits phase transitions above 4.0 V.As a result,NNZMT achieves a high discharge capacity of 144.8 mA h g^(-1) with a median voltage of 3.42 V at 20 mA g^(-1) and exhibits excellent cycling performance with a capacity retention of 77.3% for 1000 cycles at 2000 mA g^(-1).This study provides an effective strategy and new insights into the design of high-performance layered-oxide cathode materials with enhanced structure/interface stability forSIBs. 展开更多
关键词 Sodium-ion batteries P2/O3-type layered oxides na distribution Oxygen redox chemistry Hydrostability
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The Arabidopsis phosphatase PP2C49 negatively regulates salt tolerance through inhibition of At HKT1;1 被引量:12
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作者 Moli Chu Pengwang Chen +2 位作者 Sufang Meng Peng Xu Wenzhi Lan 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2021年第3期528-542,共15页
Type 2C protein phosphatases(PP2Cs)are the largest protein phosphatase family.PP2Cs dephosphorylate substrates for signaling in Arabidopsis,but the functions of most PP2 Cs remain unknown.Here,we characterized PP2 C49... Type 2C protein phosphatases(PP2Cs)are the largest protein phosphatase family.PP2Cs dephosphorylate substrates for signaling in Arabidopsis,but the functions of most PP2 Cs remain unknown.Here,we characterized PP2 C49(AT3G62260,a Group G PP2C),which regulates Na^(+)distribution under salt stress and is localized to the cytoplasm and nucleus.PP2C49 was highly expressed in root vascular tissues and its disruption enhanced plant tolerance to salt stress.Compared with wild type,the pp2c49 mutant contained more Na^(+)in roots but less Na^(+)in shoots and xylem sap,suggesting that PP2C49 regulates shoot Na^(+)extrusion.Reciprocal grafting revealed a root-based mechanism underlying the salt tolerance of pp2 c49.Systemic Na+distribution largely depends on AtHKT1;1 and loss of function of AtHKT1;1 in the pp2c49 background overrode the salt tolerance of pp2c49,resulting in salt sensitivity.Furthermore,compared with plants overexpressing PP2C49 in the wild-type background,plants overexpressing PP2C49 in the athtk1;1 mutant background were sensitive to salt,like the athtk1;1 mutants.Moreover,protein-protein interaction and two-voltage clamping assays demonstrated that PP2C49 physically interacts with AtHKT1;1 and inhibits the Na^(+)permeability of AtHKT1;1.This study reveals that PP2C49 negatively regulates AtHKT1;1 activity and thus determines systemic Na^(+)allocation during salt stress. 展开更多
关键词 ARABIDOPSIS At HKT1 1 na+distribution TRANSLOCATION PP2C PP2C49 salt stress
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