Lithium-ion batteries(LIBs)featuring a Ni-rich cathode exhibit increased specific capacity,but the establishment of a stable interphase through the implementation of a functional electrolyte strategy remains challengi...Lithium-ion batteries(LIBs)featuring a Ni-rich cathode exhibit increased specific capacity,but the establishment of a stable interphase through the implementation of a functional electrolyte strategy remains challenging.Especially when the battery is operated under high temperature,the trace water present in the electrolyte will accelerate the hydrolysis of the electrolyte and the resulting HF will further erode the interphase.In order to enhance the long-term cycling performance of graphite/LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)LIBs,herein,Tolylene-2,4-diisocyanate(TDI)additive containing lone-pair electrons is employed to formulate a novel bifunctional electrolyte aimed at eliminating H_(2)O/HF generated at elevated temperature.After 1000 cycles at 25℃,the battery incorporating the TDI-containing electrolyte exhibits an impressive capacity retention of 94%at 1 C.In contrast,the battery utilizing the blank electrolyte has a lower capacity retention of only 78%.Furthermore,after undergoing 550 cycles at 1 C under45℃,the inclusion of TDI results in a notable enhancement of capacity,increasing it from 68%to 80%.This indicates TDI has a favorable influence on the cycling performance of LIBs,especially at elevated temperatures.The analysis of the film formation mechanism suggests that the lone pair of electrons of the isocyanate group in TDI play a crucial role in inhibiting the generation of H_(2)O and HF,which leads to the formation of a thin and dense interphase.The existence of this interphase is thought to substantially enhance the cycling performance of the LIBs.This work not only improves the performance of graphite/NCM811 batteries at room temperature and high temperature by eliminating H_(2)O/HF but also presents a novel strategy for advancing functional electrolyte development.展开更多
This work develops 2-Phenyl-1H-imidazole-1-sulfonate(PHIS)as a multi-functional electrolyte additive for H2O/HF scavenging and film formation to improve the high temperature performance of LiNi_(0.8)Co_(0.1)Mn_(0.1)O_...This work develops 2-Phenyl-1H-imidazole-1-sulfonate(PHIS)as a multi-functional electrolyte additive for H2O/HF scavenging and film formation to improve the high temperature performance of LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)/graphite batteries.After 450 cycles at room temperature(25℃),the discharge capacity retentions of batteries with blank and PHIS-containing electrolyte are 56.03%and 94.92%respectively.After 230 cycles at high temperatures(45℃),their values are 75.30%and 88.38%respectively.The enhanced electrochemical performance of the batteries with PHIS-containing electrolyte is supported by the spectroscopic characterization and theoretical calculations.It is demonstrated that this PHIS electrolyte additive can facilitate the construction of the electrode interface films,remove the H2O/HF in the electrolyte,and improve the electrochemical performance of the batteries.This work not only develops a sulfonate-based electrolyte but also can stimulate new ideas of functional additives to improve the battery performance.展开更多
LiNi0.8Co0.1Mn0.1O2 powder was prepared by mixing LiOH·H2O and co-precipitated Ni0.8Co0.1Mn0.1（OH）2 at a molar ratio of 1：1.05, followed by sintering at different temperatures. The effects of temperature on th...LiNi0.8Co0.1Mn0.1O2 powder was prepared by mixing LiOH·H2O and co-precipitated Ni0.8Co0.1Mn0.1（OH）2 at a molar ratio of 1：1.05, followed by sintering at different temperatures. The effects of temperature on the morphology, structure and electrochemical performance were extensively studied. SEM and XRD results demonstrate that the sintering temperature has large influence on the morphology and structure and suitable temperature is very important to obtain spherical materials and suppresses the ionic distribution. The charge-discharge tests show that the electrochemical performance of LiNi0.8Co0.1Mn0.1O2 powders becomes better with the increase of temperature from 700 ℃ to 750 ℃ and higher temperature will deteriorate the performance. Although both of materials obtained at 750 ℃ and 780 ℃ demonstrate almost identical cyclic stability at 2C rate, which delivers 71.9%retention after 200 cycles, the rate performance of powder calcined at 780 ℃ is much poorer than that at 750 ℃. The XRD results demonstrate that the poor performance is ascribed to more severe ionic distribution caused by higher temperature.展开更多
采用共沉淀-高温固相法制备LiNi_(0.6)Co_(0.1)Mn_(0.3)O_2锂离子正极材料,并使用X射线衍射仪(XRD)和扫描电镜(SEM)技术分别表征其结构和形貌.然后将所得LiNi_(0.6)Co_(0.1)Mn_(0.3)O_2正极材料组装成扣式电池,并表征其电化学性能,探讨...采用共沉淀-高温固相法制备LiNi_(0.6)Co_(0.1)Mn_(0.3)O_2锂离子正极材料,并使用X射线衍射仪(XRD)和扫描电镜(SEM)技术分别表征其结构和形貌.然后将所得LiNi_(0.6)Co_(0.1)Mn_(0.3)O_2正极材料组装成扣式电池,并表征其电化学性能,探讨烧结温度和锂配量对其电化学性能的影响.结果表明:所得LiNi_(0.6)Co_(0.1)Mn_(0.3)O_2正极材料的放电比容量随烧结温度的升高而增大,且在900℃时表现出最佳的电化学性能.室温下,1C倍率下,锂配量(n(Li)/n(Ni+Co+Mn)=1.09)时,正极材料的首次放电容量为143.7 m Ah/g,50次循环后,正极材料的放电比容量仍有141.3 m Ah/g,容量保持率为98.3%.展开更多
用溶胶-凝胶法合成锂离子电池用富锂正极材料Li[Li0.2Ni0.15Mn0.55Co0.1]O2,通过XRD、SEM、电感耦合等离子体发射光谱（ICP-OES）和电化学性能测试考察煅烧温度对合成材料结构和性能的影响。900℃下制备的材料具有典型的α-Na Fe O2层...用溶胶-凝胶法合成锂离子电池用富锂正极材料Li[Li0.2Ni0.15Mn0.55Co0.1]O2,通过XRD、SEM、电感耦合等离子体发射光谱（ICP-OES）和电化学性能测试考察煅烧温度对合成材料结构和性能的影响。900℃下制备的材料具有典型的α-Na Fe O2层状结构、较好的晶型结构及良好的电化学性能。在2.04.8 V充放电,20℃下的0.10 C首次放电比容量为235.4 m Ah/g,库仑效率为78.5%;依次以0.10 C、0.20 C、0.50 C、0.75 C和1.00 C循环10次,再以0.20 C放电,首次1.00 C放电比容量为149.7 m Ah/g,最后一次0.20 C放电比容量为首次0.10 C放电比容量的85.9%。展开更多
基金financially supported by the Scientific and Technological Plan Projects of Guangzhou City(202103040001),P.R.Chinathe Project of Science and Technology Department of Henan Province(222102240074)the Key Research Programs of Higher Education Institutions of Henan Province(24B150009)。
文摘Lithium-ion batteries(LIBs)featuring a Ni-rich cathode exhibit increased specific capacity,but the establishment of a stable interphase through the implementation of a functional electrolyte strategy remains challenging.Especially when the battery is operated under high temperature,the trace water present in the electrolyte will accelerate the hydrolysis of the electrolyte and the resulting HF will further erode the interphase.In order to enhance the long-term cycling performance of graphite/LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)LIBs,herein,Tolylene-2,4-diisocyanate(TDI)additive containing lone-pair electrons is employed to formulate a novel bifunctional electrolyte aimed at eliminating H_(2)O/HF generated at elevated temperature.After 1000 cycles at 25℃,the battery incorporating the TDI-containing electrolyte exhibits an impressive capacity retention of 94%at 1 C.In contrast,the battery utilizing the blank electrolyte has a lower capacity retention of only 78%.Furthermore,after undergoing 550 cycles at 1 C under45℃,the inclusion of TDI results in a notable enhancement of capacity,increasing it from 68%to 80%.This indicates TDI has a favorable influence on the cycling performance of LIBs,especially at elevated temperatures.The analysis of the film formation mechanism suggests that the lone pair of electrons of the isocyanate group in TDI play a crucial role in inhibiting the generation of H_(2)O and HF,which leads to the formation of a thin and dense interphase.The existence of this interphase is thought to substantially enhance the cycling performance of the LIBs.This work not only improves the performance of graphite/NCM811 batteries at room temperature and high temperature by eliminating H_(2)O/HF but also presents a novel strategy for advancing functional electrolyte development.
基金financially supported by the Scientific and Technological Plan Projects of Guangzhou City(202103040001)。
文摘This work develops 2-Phenyl-1H-imidazole-1-sulfonate(PHIS)as a multi-functional electrolyte additive for H2O/HF scavenging and film formation to improve the high temperature performance of LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)/graphite batteries.After 450 cycles at room temperature(25℃),the discharge capacity retentions of batteries with blank and PHIS-containing electrolyte are 56.03%and 94.92%respectively.After 230 cycles at high temperatures(45℃),their values are 75.30%and 88.38%respectively.The enhanced electrochemical performance of the batteries with PHIS-containing electrolyte is supported by the spectroscopic characterization and theoretical calculations.It is demonstrated that this PHIS electrolyte additive can facilitate the construction of the electrode interface films,remove the H2O/HF in the electrolyte,and improve the electrochemical performance of the batteries.This work not only develops a sulfonate-based electrolyte but also can stimulate new ideas of functional additives to improve the battery performance.
基金Project(2014CB643406)supported by the National Basic Research Program of China
文摘LiNi0.8Co0.1Mn0.1O2 powder was prepared by mixing LiOH·H2O and co-precipitated Ni0.8Co0.1Mn0.1（OH）2 at a molar ratio of 1：1.05, followed by sintering at different temperatures. The effects of temperature on the morphology, structure and electrochemical performance were extensively studied. SEM and XRD results demonstrate that the sintering temperature has large influence on the morphology and structure and suitable temperature is very important to obtain spherical materials and suppresses the ionic distribution. The charge-discharge tests show that the electrochemical performance of LiNi0.8Co0.1Mn0.1O2 powders becomes better with the increase of temperature from 700 ℃ to 750 ℃ and higher temperature will deteriorate the performance. Although both of materials obtained at 750 ℃ and 780 ℃ demonstrate almost identical cyclic stability at 2C rate, which delivers 71.9%retention after 200 cycles, the rate performance of powder calcined at 780 ℃ is much poorer than that at 750 ℃. The XRD results demonstrate that the poor performance is ascribed to more severe ionic distribution caused by higher temperature.
文摘采用共沉淀-高温固相法制备LiNi_(0.6)Co_(0.1)Mn_(0.3)O_2锂离子正极材料,并使用X射线衍射仪(XRD)和扫描电镜(SEM)技术分别表征其结构和形貌.然后将所得LiNi_(0.6)Co_(0.1)Mn_(0.3)O_2正极材料组装成扣式电池,并表征其电化学性能,探讨烧结温度和锂配量对其电化学性能的影响.结果表明:所得LiNi_(0.6)Co_(0.1)Mn_(0.3)O_2正极材料的放电比容量随烧结温度的升高而增大,且在900℃时表现出最佳的电化学性能.室温下,1C倍率下,锂配量(n(Li)/n(Ni+Co+Mn)=1.09)时,正极材料的首次放电容量为143.7 m Ah/g,50次循环后,正极材料的放电比容量仍有141.3 m Ah/g,容量保持率为98.3%.
