通过在镍钴双金属氢氧化物(Ni-Co LDH)的合成体系中引入胺修饰板钛矿TiO2得到了Ni-Co LDH/TiO2复合光催化材料,并对其光催化降解环丙沙星(CIP)抗生素的活性进行了研究。扫描电子显微镜(SEM)显示Ni-Co LDH将棒状的板钛矿TiO2完全包裹,增...通过在镍钴双金属氢氧化物(Ni-Co LDH)的合成体系中引入胺修饰板钛矿TiO2得到了Ni-Co LDH/TiO2复合光催化材料,并对其光催化降解环丙沙星(CIP)抗生素的活性进行了研究。扫描电子显微镜(SEM)显示Ni-Co LDH将棒状的板钛矿TiO2完全包裹,增大了材料与环丙沙星分子的接触面积。当TiO2与LDH的摩尔比为1:4时,复合材料表现出最佳的催化活性且Ni-Co LDH/TiO2(1:4)在四次循环实验后仍未出现明显的活性下降,说明其具有优异的稳定性。光电化学结果证明这种结构为光催化环丙沙星降解提供了更多的活性位点,其优异的光生电子与空穴的分离和传输效率是其具有最佳催化活性的主要原因。Ni-Co LDH/brookite TiO2 composite is prepared by adding amine-modified TiO2 into the fabrication system of Ni-Co layered bimetallic hydroxide (Ni-Co LDH), and its photocatalytic degradation of ciprofloxacin (CIP) antibiotic is studied. Scanning electron microscopy (SEM) images show that Ni-Co LDH wrapped on the brookite TiO2 increases the contact area between the catalyst and ciprofloxacin molecules. It is found that when the mole ratio of TiO2 to Ni-Co LDH is 1:4, the composite exhibits the best catalytic activity, and the activity of Ni-Co LDH/TiO2(1:4) has no decrease significantly after four cycles tests, indicating that it has excellent stability. The photochemical results show that this structure provides more active sites for photocatalytic ciprofloxacin degradation, and its excellent separation and transfer efficiency of photogenerated electrons and holes are the main reason for its optimal catalytic activity.展开更多
Lithium-sulfur(Li-S)batteries with high energy density are considered promising energy storage devices for the next generation.Nevertheless,the shuttle effect and the passive layer between the separator and the electr...Lithium-sulfur(Li-S)batteries with high energy density are considered promising energy storage devices for the next generation.Nevertheless,the shuttle effect and the passive layer between the separator and the electrodes still seriously affect the cycle stability and life.Herein,a bimetallic Ni-Co metal-organic framework(MOF)with adsorption and catalytic synergism for polysulfides was successfully synthesized as an electrospinning separator sandwich for Li-S batteries.Introducing porous Ni-Co MOF coatings into the separator provides more adsorption catalytic sites for polysulfides,prevents their diffusion to the anode,and enhances sulfur utilization.Consequently,the improved Li-S batteries with a Ni-Co MOF@PAN(NCMP)electrospun separator delivered excellent rate performance and outstanding cycle stability,yielding an ultra-high initial capacity of 1560 mA h g^(-1)at 0.1 C.Notably,remarkable Li-S battery performance with a discharge capacity of 794 mA h g^(-1)(84.1%capacity retention)was obtained after500 cycles,while delivering a low capacity decay rate of 0.032%during long-term cycling(up to 500cycles)at 1 C.Surprisingly,even at the current density of 2 C,the capacity attenuation rate of 2000 cycles is only 0.034%per cycle.In addition,compared with the Celgard separator,the NCMP separator also had high thermal stability(keeping the separator outline at 200℃)that ensured battery safety and excellent electrolyte wettability(73%porosity and 535%electrolyte absorption)and significantly enhanced the ionic conductivity and Li^(+) transfer number,and protected the surface integrity of the anode.展开更多
文摘通过在镍钴双金属氢氧化物(Ni-Co LDH)的合成体系中引入胺修饰板钛矿TiO2得到了Ni-Co LDH/TiO2复合光催化材料,并对其光催化降解环丙沙星(CIP)抗生素的活性进行了研究。扫描电子显微镜(SEM)显示Ni-Co LDH将棒状的板钛矿TiO2完全包裹,增大了材料与环丙沙星分子的接触面积。当TiO2与LDH的摩尔比为1:4时,复合材料表现出最佳的催化活性且Ni-Co LDH/TiO2(1:4)在四次循环实验后仍未出现明显的活性下降,说明其具有优异的稳定性。光电化学结果证明这种结构为光催化环丙沙星降解提供了更多的活性位点,其优异的光生电子与空穴的分离和传输效率是其具有最佳催化活性的主要原因。Ni-Co LDH/brookite TiO2 composite is prepared by adding amine-modified TiO2 into the fabrication system of Ni-Co layered bimetallic hydroxide (Ni-Co LDH), and its photocatalytic degradation of ciprofloxacin (CIP) antibiotic is studied. Scanning electron microscopy (SEM) images show that Ni-Co LDH wrapped on the brookite TiO2 increases the contact area between the catalyst and ciprofloxacin molecules. It is found that when the mole ratio of TiO2 to Ni-Co LDH is 1:4, the composite exhibits the best catalytic activity, and the activity of Ni-Co LDH/TiO2(1:4) has no decrease significantly after four cycles tests, indicating that it has excellent stability. The photochemical results show that this structure provides more active sites for photocatalytic ciprofloxacin degradation, and its excellent separation and transfer efficiency of photogenerated electrons and holes are the main reason for its optimal catalytic activity.
基金supported by the 2022 Yeungnam University Research Grant。
文摘Lithium-sulfur(Li-S)batteries with high energy density are considered promising energy storage devices for the next generation.Nevertheless,the shuttle effect and the passive layer between the separator and the electrodes still seriously affect the cycle stability and life.Herein,a bimetallic Ni-Co metal-organic framework(MOF)with adsorption and catalytic synergism for polysulfides was successfully synthesized as an electrospinning separator sandwich for Li-S batteries.Introducing porous Ni-Co MOF coatings into the separator provides more adsorption catalytic sites for polysulfides,prevents their diffusion to the anode,and enhances sulfur utilization.Consequently,the improved Li-S batteries with a Ni-Co MOF@PAN(NCMP)electrospun separator delivered excellent rate performance and outstanding cycle stability,yielding an ultra-high initial capacity of 1560 mA h g^(-1)at 0.1 C.Notably,remarkable Li-S battery performance with a discharge capacity of 794 mA h g^(-1)(84.1%capacity retention)was obtained after500 cycles,while delivering a low capacity decay rate of 0.032%during long-term cycling(up to 500cycles)at 1 C.Surprisingly,even at the current density of 2 C,the capacity attenuation rate of 2000 cycles is only 0.034%per cycle.In addition,compared with the Celgard separator,the NCMP separator also had high thermal stability(keeping the separator outline at 200℃)that ensured battery safety and excellent electrolyte wettability(73%porosity and 535%electrolyte absorption)and significantly enhanced the ionic conductivity and Li^(+) transfer number,and protected the surface integrity of the anode.
