The rapid expansion of the photovoltaic industry has generated heavily oxidized waste silicon(wSi),which hinders efficient recycling owing to its small particle size and uncontrolled surface oxidation.This study intro...The rapid expansion of the photovoltaic industry has generated heavily oxidized waste silicon(wSi),which hinders efficient recycling owing to its small particle size and uncontrolled surface oxidation.This study introduces a molten salt electrochemical strategy for converting photovoltaic wSi into NiSi_(2)-silicon nanorods(NiSi_(2)-SiNRs)as high-performance anode materials for lithium-ion batteries.A stable oxidized passivation layer is formed on the wSi surface via controlled oxidation,and further in situ generated highly active NiSi_(2) droplets.The molten salt electric field modulates the surface energy of silicon,while particle integration drives localized directional growth,enabling the self-assembly of NiSi_(2)-SiNRs composites.These NiSi_(2)-SiNRs anodes exhibit rapid ion transport and effective strain buffering.The high aspect ratio of SiNRs and the presence of retained NiSi_(2) facilitate both longitudinal and transverse Li^(+) diffusion.Owing to their robust structural design,the NiSi_(2)-SiNRs anode achieves an excellent initial Coulombic efficiency of 91.61%and retains 72.99%of its capacity after 800 cycles at 2 A·g^(−1).This study establishes a model system for investigating silicide/silicon interfaces in molten salt electrochemical synthesis and provides an effective strategy for upcycling photovoltaic wSi into high-performance lithium-ion battery anodes.展开更多
While silicon/carbon(Si/C)is considered one of the most promising anode materials for the next generation of high-energy lithium-ion batteries(LIBs),the industrialization of Si/C anodes is hampered by high-cost and lo...While silicon/carbon(Si/C)is considered one of the most promising anode materials for the next generation of high-energy lithium-ion batteries(LIBs),the industrialization of Si/C anodes is hampered by high-cost and low product yield.Herein,a high-yield strategy is developed in which photovoltaic waste silicon is converted to cost-effective graphitic Si/C composites(G-Si@C)for LIBs.The introduction of a binder improves the dispersion and compatibility of silicon and graphite,enhances particle sphericity,and significantly reduces the loss rate of the spray prilling process(from about 25%to 5%).As an LIB anode,the fabricated G-Si@C composites exhibit a capacity of 605 mAh g^(-1) after 1200 cycles.The cost of manufacturing Si/C anode materials has been reduced to approximately$7.47 kg^(-1),which is close to that of commercial graphite anode materials($5.0 kg^(-1)),and significantly lower than commercial Si/C materials(ca.$20.74 kg^(-1)).Moreover,the G-Si@C material provides approximately 81.0 Ah/$of capacity,which exceeds the current best commercial graphite anodes(70.0 Ah/$)and Si/C anodes(48.2 Ah/$).The successful implementation of this pathway will significantly promote the industrialization of high-energydensity Si/C anode materials.展开更多
In widely studied organic-inorganic hybrid perovskites,the organic component tends to volatilize and decompose under high temperatures,oxygen,and humidity,which adversely affects the performance and longevity of the a...In widely studied organic-inorganic hybrid perovskites,the organic component tends to volatilize and decompose under high temperatures,oxygen,and humidity,which adversely affects the performance and longevity of the associated solar cells.In contrast,all-inorganic perovskites demonstrate superior stability under these conditions and offer photoelectric properties comparable to those of their hybrid counterparts.The potential of tandem solar cells(TSCs)made from all-inorganic perovskites is especially promising.This review is the first to address recent advancements in TSCs that use all-inorganic perovskites and crystalline silicon(c-Si),both domestically and internationally.This work provides a systematic and thorough analysis of the current challenges faced by these systems and proposes rational solutions.Additionally,we elucidate the regulatory mechanisms of all-inorganic perovskites and their TSCs when combined with c-Si,summarizing the corresponding patterns.Finally,we outline future research directions for all-inorganic perovskites and their TSCs with c-Si.This work offers valuable insights and references for the continued advancement of perovskitebased TSCs.展开更多
Silicon anodes are promising for high-energy-density lithium-ion batteries.Nevertheless,unsatisfied initial Coulombic efficiency(ICE)and structure collapse are two barriers still hindering their application.Here,we re...Silicon anodes are promising for high-energy-density lithium-ion batteries.Nevertheless,unsatisfied initial Coulombic efficiency(ICE)and structure collapse are two barriers still hindering their application.Here,we report a 5 at.%-vanadium hybriding strategy to stabilize Si film anode,which delivers a high initial Coulombic efficiency of 92.1%with a discharge capacity of 2434.9 mAh·g^(−1) and a desirable capacity retention of 80%after 100 cycles at 1 A·g^(−1).Physical and electrochemical analyses demonstrate the Li_(x)PO_(y)F_(z)-rich inorganic solid-electrolyte interphase(SEI)and the low film internal strain are two advantageous factors for the desirable Li-ion storage reversibility and stability.A full battery with a LiFePO_(4) cathode delivers the energy densities of 291.9 and 194.6 Wh·kg^(−1) under power densities of 145.9 and 389.2 W·kg^(−1),respectively.This result on Si anodes may pave the way to next-generation highenergy-density lithium-ion batteries.展开更多
基金supported by the Yunnan Province Basic Research General Program,China(No.202201BE070001-002)the Major Science and Technology Projects in Yunnan Province,China(No.202402AF 080005).
文摘The rapid expansion of the photovoltaic industry has generated heavily oxidized waste silicon(wSi),which hinders efficient recycling owing to its small particle size and uncontrolled surface oxidation.This study introduces a molten salt electrochemical strategy for converting photovoltaic wSi into NiSi_(2)-silicon nanorods(NiSi_(2)-SiNRs)as high-performance anode materials for lithium-ion batteries.A stable oxidized passivation layer is formed on the wSi surface via controlled oxidation,and further in situ generated highly active NiSi_(2) droplets.The molten salt electric field modulates the surface energy of silicon,while particle integration drives localized directional growth,enabling the self-assembly of NiSi_(2)-SiNRs composites.These NiSi_(2)-SiNRs anodes exhibit rapid ion transport and effective strain buffering.The high aspect ratio of SiNRs and the presence of retained NiSi_(2) facilitate both longitudinal and transverse Li^(+) diffusion.Owing to their robust structural design,the NiSi_(2)-SiNRs anode achieves an excellent initial Coulombic efficiency of 91.61%and retains 72.99%of its capacity after 800 cycles at 2 A·g^(−1).This study establishes a model system for investigating silicide/silicon interfaces in molten salt electrochemical synthesis and provides an effective strategy for upcycling photovoltaic wSi into high-performance lithium-ion battery anodes.
基金supported by the Major Science and Technology Projects in Yunnan Province(Grant No.202402AF080005)National Natural Science Foundation of China(Grant Nos.52274408,22468029,52274412)+2 种基金Yunnan Fundamental Research Projects(Grant No.202201AW070014)the Program for Innovative Research Team in University of Ministry of Education of China(Grant No.IRT 17R48)the German Research Foundation(DFG,Project number 501766751).
文摘While silicon/carbon(Si/C)is considered one of the most promising anode materials for the next generation of high-energy lithium-ion batteries(LIBs),the industrialization of Si/C anodes is hampered by high-cost and low product yield.Herein,a high-yield strategy is developed in which photovoltaic waste silicon is converted to cost-effective graphitic Si/C composites(G-Si@C)for LIBs.The introduction of a binder improves the dispersion and compatibility of silicon and graphite,enhances particle sphericity,and significantly reduces the loss rate of the spray prilling process(from about 25%to 5%).As an LIB anode,the fabricated G-Si@C composites exhibit a capacity of 605 mAh g^(-1) after 1200 cycles.The cost of manufacturing Si/C anode materials has been reduced to approximately$7.47 kg^(-1),which is close to that of commercial graphite anode materials($5.0 kg^(-1)),and significantly lower than commercial Si/C materials(ca.$20.74 kg^(-1)).Moreover,the G-Si@C material provides approximately 81.0 Ah/$of capacity,which exceeds the current best commercial graphite anodes(70.0 Ah/$)and Si/C anodes(48.2 Ah/$).The successful implementation of this pathway will significantly promote the industrialization of high-energydensity Si/C anode materials.
基金the National Natural Science Foundation of China(Grant Nos.52164050 and 51762043)Major Science and Technology Project of Yunnan Province(Grant No.202202AB080010).
文摘In widely studied organic-inorganic hybrid perovskites,the organic component tends to volatilize and decompose under high temperatures,oxygen,and humidity,which adversely affects the performance and longevity of the associated solar cells.In contrast,all-inorganic perovskites demonstrate superior stability under these conditions and offer photoelectric properties comparable to those of their hybrid counterparts.The potential of tandem solar cells(TSCs)made from all-inorganic perovskites is especially promising.This review is the first to address recent advancements in TSCs that use all-inorganic perovskites and crystalline silicon(c-Si),both domestically and internationally.This work provides a systematic and thorough analysis of the current challenges faced by these systems and proposes rational solutions.Additionally,we elucidate the regulatory mechanisms of all-inorganic perovskites and their TSCs when combined with c-Si,summarizing the corresponding patterns.Finally,we outline future research directions for all-inorganic perovskites and their TSCs with c-Si.This work offers valuable insights and references for the continued advancement of perovskitebased TSCs.
基金supported by the National Natural Science Foundation of China(Nos.22469010 and U24A2063)Yunnan Province Natural Science Fund(Nos.202501AT070331 and 202301AT070151)Yunnan Xingdian Young Talent Project(No.KKXX202452039).
文摘Silicon anodes are promising for high-energy-density lithium-ion batteries.Nevertheless,unsatisfied initial Coulombic efficiency(ICE)and structure collapse are two barriers still hindering their application.Here,we report a 5 at.%-vanadium hybriding strategy to stabilize Si film anode,which delivers a high initial Coulombic efficiency of 92.1%with a discharge capacity of 2434.9 mAh·g^(−1) and a desirable capacity retention of 80%after 100 cycles at 1 A·g^(−1).Physical and electrochemical analyses demonstrate the Li_(x)PO_(y)F_(z)-rich inorganic solid-electrolyte interphase(SEI)and the low film internal strain are two advantageous factors for the desirable Li-ion storage reversibility and stability.A full battery with a LiFePO_(4) cathode delivers the energy densities of 291.9 and 194.6 Wh·kg^(−1) under power densities of 145.9 and 389.2 W·kg^(−1),respectively.This result on Si anodes may pave the way to next-generation highenergy-density lithium-ion batteries.
