Biomass-derived carbon materials for lithiumion batteries emerge as one of the most promising anodes from sustainable perspective.However,improving the reversible capacity and cycling performance remains a long-standi...Biomass-derived carbon materials for lithiumion batteries emerge as one of the most promising anodes from sustainable perspective.However,improving the reversible capacity and cycling performance remains a long-standing challenge.By combining the benefits of K2CO_(3) activation and KMnO_(4) hydrothermal treatment,this work proposes a two-step activation method to load MnO_(2) charge transfer onto biomass-derived carbon(KAC@MnO_(2)).Comprehensive analysis reveals that KAC@MnO_(2) has a micro-mesoporous coexistence structure and uniform surface distribution of MnO_(2),thus providing an improved electrochemical performance.Specifically,KAC@MnO_(2) exhibits an initial chargedischarge capacity of 847.3/1813.2 mAh·g^(-1) at 0.2 A·g^(-1),which is significantly higher than that of direct pyrolysis carbon and K2CO_(3) activated carbon,respectively.Furthermore,the KAC@MnO_(2) maintains a reversible capacity of 652.6 mAh·g^(-1) after 100 cycles.Even at a high current density of 1.0 A·g^(-1),KAC@MnO_(2) still exhibits excellent long-term cycling stability and maintains a stable reversible capacity of 306.7 mAh·g^(-1) after 500 cycles.Compared with reported biochar anode materials,the KAC@MnO_(2) prepared in this work shows superior reversible capacity and cycling performance.Additionally,the Li+insertion and de-insertion mechanisms are verified by ex situ X-ray diffraction analysis during the chargedischarge process,helping us better understand the energy storage mechanism of KAC@MnO_(2).展开更多
Currently,the conversion of waste plastics into high-value products via catalytic pyrolysis enables the advancement of plastics’open-loop recycling.However,enhancing selectivity remains a critical challenge.This stud...Currently,the conversion of waste plastics into high-value products via catalytic pyrolysis enables the advancement of plastics’open-loop recycling.However,enhancing selectivity remains a critical challenge.This study introduces a novel approach to catalytic pyrolysis,utilizing a combination of MCM-41 and modified gallium-based HZSM-5 catalysts,to achieve exceptional selectivity for aromatic liquid-phase products from linear low-density polyethylene.Firstly,to enhance the probability of dehydroaromatization optimization,the type and proportion of metal active sites within the HZSM-5 catalyst are fine-tuned,which would establish equilibrium with acid sites,resulting in a remarkable 15.72%increase in the selectivity of aromatic hydrocarbons.Secondly,to enhance the accessibility of volatiles to active sites,mesoporous MCM-41 with cracking capabilities is introduced.The doping ratio of MCM-41 is meticulously controlled to facilitate the diffusion of cracked volatiles to the active centers of modified gallium-based HZSM-5,enabling efficient reforming reactions.Experimental findings demonstrate that MCM-41 significantly enhances the dehydroaromatization activity of the modified gallium-based HZSM-5 catalyst.Under the influence of MCM-41:Zr_(2)Ga_(3)/HZSM-5=1:2 catalyst,the selectivity for aromatic hydrocarbons reaches an impressive 93.11%,with a notable 60.01%selectivity for benzene,toluene,ethylbenzene,and xylene.Lastly,this study proposes a plausible pathway for the generation of high-value aromatic hydrocarbons using the combined catalyst.展开更多
基金supported by the National Natural Science Foundation of China(Grant No.22078278)Hunan Innovative Talent Project(Grant No.2022RC1111)+1 种基金the Key project of Hunan Provincial Education Department(Grant No.22A0131)the State Key Laboratory of Clean Energy Utilization(Open Fund Project No.ZJUCEU2021009).
文摘Biomass-derived carbon materials for lithiumion batteries emerge as one of the most promising anodes from sustainable perspective.However,improving the reversible capacity and cycling performance remains a long-standing challenge.By combining the benefits of K2CO_(3) activation and KMnO_(4) hydrothermal treatment,this work proposes a two-step activation method to load MnO_(2) charge transfer onto biomass-derived carbon(KAC@MnO_(2)).Comprehensive analysis reveals that KAC@MnO_(2) has a micro-mesoporous coexistence structure and uniform surface distribution of MnO_(2),thus providing an improved electrochemical performance.Specifically,KAC@MnO_(2) exhibits an initial chargedischarge capacity of 847.3/1813.2 mAh·g^(-1) at 0.2 A·g^(-1),which is significantly higher than that of direct pyrolysis carbon and K2CO_(3) activated carbon,respectively.Furthermore,the KAC@MnO_(2) maintains a reversible capacity of 652.6 mAh·g^(-1) after 100 cycles.Even at a high current density of 1.0 A·g^(-1),KAC@MnO_(2) still exhibits excellent long-term cycling stability and maintains a stable reversible capacity of 306.7 mAh·g^(-1) after 500 cycles.Compared with reported biochar anode materials,the KAC@MnO_(2) prepared in this work shows superior reversible capacity and cycling performance.Additionally,the Li+insertion and de-insertion mechanisms are verified by ex situ X-ray diffraction analysis during the chargedischarge process,helping us better understand the energy storage mechanism of KAC@MnO_(2).
基金National Natural Science Foundation of China(Grant No.22078278)Hunan Innovative Talent Project(Grant No.2022RC1111)Key Project of Hunan Provincial Education Department(Grant No.22A0131).
文摘Currently,the conversion of waste plastics into high-value products via catalytic pyrolysis enables the advancement of plastics’open-loop recycling.However,enhancing selectivity remains a critical challenge.This study introduces a novel approach to catalytic pyrolysis,utilizing a combination of MCM-41 and modified gallium-based HZSM-5 catalysts,to achieve exceptional selectivity for aromatic liquid-phase products from linear low-density polyethylene.Firstly,to enhance the probability of dehydroaromatization optimization,the type and proportion of metal active sites within the HZSM-5 catalyst are fine-tuned,which would establish equilibrium with acid sites,resulting in a remarkable 15.72%increase in the selectivity of aromatic hydrocarbons.Secondly,to enhance the accessibility of volatiles to active sites,mesoporous MCM-41 with cracking capabilities is introduced.The doping ratio of MCM-41 is meticulously controlled to facilitate the diffusion of cracked volatiles to the active centers of modified gallium-based HZSM-5,enabling efficient reforming reactions.Experimental findings demonstrate that MCM-41 significantly enhances the dehydroaromatization activity of the modified gallium-based HZSM-5 catalyst.Under the influence of MCM-41:Zr_(2)Ga_(3)/HZSM-5=1:2 catalyst,the selectivity for aromatic hydrocarbons reaches an impressive 93.11%,with a notable 60.01%selectivity for benzene,toluene,ethylbenzene,and xylene.Lastly,this study proposes a plausible pathway for the generation of high-value aromatic hydrocarbons using the combined catalyst.
