首先以Hummers法制备还原态氧化石墨烯(RGO),其次通过溶胶-凝胶法和水热法分别制备TiO_(2)和TiO_(2)/RGO复合材料,然后向硝酸银溶液滴加氨水沉淀出纳米Ag并掺杂到TiO_(2)上,再以聚乙烯吡咯烷酮(PVP)为分散剂,以RGO为基体材料,用一步水...首先以Hummers法制备还原态氧化石墨烯(RGO),其次通过溶胶-凝胶法和水热法分别制备TiO_(2)和TiO_(2)/RGO复合材料,然后向硝酸银溶液滴加氨水沉淀出纳米Ag并掺杂到TiO_(2)上,再以聚乙烯吡咯烷酮(PVP)为分散剂,以RGO为基体材料,用一步水热法合成Ag@TiO_(2)/RGO复合光催化剂。复合材料通过FT-IR、XRD、SEM、DRS和BET等进行结构、组成、形貌和孔径大小的表征。将Ag@TiO_(2)/RGO用来光催化降解罗丹明B(RhB)溶液,结果表明,0.020 g该催化剂对50 mL 5 mg/L的RhB溶液在pH值为5、室温条件下的降解效果最好;经6次循环利用后,降解率依然能达到80%。展开更多
1T-MoS_(2)nanosheets,with metallic conductivity and high capacity,hold great potential for lithium-ion capacitors(LICs),but suffer from sluggish reaction kinetics due to dense stacking.Herein,1T-MoS_(2)nanosheets with...1T-MoS_(2)nanosheets,with metallic conductivity and high capacity,hold great potential for lithium-ion capacitors(LICs),but suffer from sluggish reaction kinetics due to dense stacking.Herein,1T-MoS_(2)nanosheets with enlarged interlayer spacing,vertically bonded to reduced graphene oxide(rGO)(1T-MoS_(2)/rGO),were designed using a hydrothermal-assisted dispersion and intercalation strategy.The active nitrogen species derived from N,N-dimethylformamide(DMF)not only bridge the rGO and MoS_(2)through strong Mo-N-C bonds to promote the formation of dispersed MoS_(2)nanosheets,but also intercalate into the MoS_(2)structure,further enlarging the interlayer spacing.This unique structure synergistically enhances meso-and microscale mass transfer outside and inside of the few-layered nanosheets,significantly improving electrochemical reaction kinetics and reducing the kinetic mismatch between the anode and cathode.Consequently,the resulting 1T-MoS_(2)/rGO achieves a capacity of 500 mAh g^(-1)after 500 cycles at 5 A g^(-1)and a high rate performance of 587 mAh g^(-1)at a high rate of 10 A g^(-1).Moreover,the assembled 3D vertical 1T-MoS_(2)/rGO//AC LIC delivers a high energy density of 100.3 Wh kg^(-1)at a power density of1.0 kW kg^(-1),and long cycle stability with capacity retention as high as 91.02%after 5000 cycles at 2 A g^(-1).This work provides a generalizable strategy for engineering two-dimensional material-based electrodes,offering new insights into high-performance energy storage systems.展开更多
文摘首先以Hummers法制备还原态氧化石墨烯(RGO),其次通过溶胶-凝胶法和水热法分别制备TiO_(2)和TiO_(2)/RGO复合材料,然后向硝酸银溶液滴加氨水沉淀出纳米Ag并掺杂到TiO_(2)上,再以聚乙烯吡咯烷酮(PVP)为分散剂,以RGO为基体材料,用一步水热法合成Ag@TiO_(2)/RGO复合光催化剂。复合材料通过FT-IR、XRD、SEM、DRS和BET等进行结构、组成、形貌和孔径大小的表征。将Ag@TiO_(2)/RGO用来光催化降解罗丹明B(RhB)溶液,结果表明,0.020 g该催化剂对50 mL 5 mg/L的RhB溶液在pH值为5、室温条件下的降解效果最好;经6次循环利用后,降解率依然能达到80%。
基金the financial support from the National Natural Science Foundation of China(No.52225208 and 51802131)the Training Program for academic and technical leaders in major disciplines of Jiangxi Province-Young Talents(No.20212BCJ23021)the Natural Science Foundation of Jiangxi Province,China(No.20232BAB204020).
文摘1T-MoS_(2)nanosheets,with metallic conductivity and high capacity,hold great potential for lithium-ion capacitors(LICs),but suffer from sluggish reaction kinetics due to dense stacking.Herein,1T-MoS_(2)nanosheets with enlarged interlayer spacing,vertically bonded to reduced graphene oxide(rGO)(1T-MoS_(2)/rGO),were designed using a hydrothermal-assisted dispersion and intercalation strategy.The active nitrogen species derived from N,N-dimethylformamide(DMF)not only bridge the rGO and MoS_(2)through strong Mo-N-C bonds to promote the formation of dispersed MoS_(2)nanosheets,but also intercalate into the MoS_(2)structure,further enlarging the interlayer spacing.This unique structure synergistically enhances meso-and microscale mass transfer outside and inside of the few-layered nanosheets,significantly improving electrochemical reaction kinetics and reducing the kinetic mismatch between the anode and cathode.Consequently,the resulting 1T-MoS_(2)/rGO achieves a capacity of 500 mAh g^(-1)after 500 cycles at 5 A g^(-1)and a high rate performance of 587 mAh g^(-1)at a high rate of 10 A g^(-1).Moreover,the assembled 3D vertical 1T-MoS_(2)/rGO//AC LIC delivers a high energy density of 100.3 Wh kg^(-1)at a power density of1.0 kW kg^(-1),and long cycle stability with capacity retention as high as 91.02%after 5000 cycles at 2 A g^(-1).This work provides a generalizable strategy for engineering two-dimensional material-based electrodes,offering new insights into high-performance energy storage systems.
