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A Stable Open-Shell Conjugated Diradical Polymer with Ultra-High Photothermal Conversion Efficiency for NIR-Ⅱ Photo-Immunotherapy of Metastatic Tumor 被引量:1
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作者 Yijian Gao Ying Liu +7 位作者 Xiliang Li Hui Wang Yuliang Yang Yu Luo Yingpeng Wan Chun‑sing Lee Shengliang Li Xiao‑Hong Zhang 《Nano-Micro Letters》 SCIE EI CAS CSCD 2024年第2期1-14,共14页
Massive efforts have been concentrated on the advance of eminent near-infrared(NIR) photothermal materials(PTMs) in the NIR-Ⅱ window(1000–1700 nm), especially organic PTMs because of their intrinsic biological safet... Massive efforts have been concentrated on the advance of eminent near-infrared(NIR) photothermal materials(PTMs) in the NIR-Ⅱ window(1000–1700 nm), especially organic PTMs because of their intrinsic biological safety compared with inorganic PTMs. However, so far, only a few NIR-Ⅱresponsive organic PTMs was explored, and their photothermal conversion efficiencies(PCEs) still remain relatively low. Herein, donor–acceptor conjugated diradical polymers with open-shell characteristics are explored for synergistically photothermal immunotherapy of metastatic tumors in the NIR-Ⅱ window. By employing side-chain regulation, the conjugated diradical polymer TTB-2 with obvious NIR-Ⅱ absorption was developed, and its nanoparticles realize a record-breaking PCE of 87.7% upon NIR-Ⅱ light illustration. In vitro and in vivo experiments demonstrate that TTB-2 nanoparticles show good tumor photoablation with navigation of photoacoustic imaging in the NIR-Ⅱ window, without any side-effect. Moreover, by combining with PD-1 antibody,the pulmonary metastasis of breast cancer is high-effectively prevented by the efficient photo-immunity effect. Thus, this study explores superior PTMs for cancer metastasis theranostics in the NIR-Ⅱ window, offering a new horizon in developing radical-characteristic NIR-Ⅱ photothermal materials. 展开更多
关键词 NIR-Ⅱconjugated polymer PHOTOTHERMAL RADICAL Nanoparticles Cancer therapy
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Fundamental Understanding and Optimization Strategies for Dual‑Ion Batteries:A Review 被引量:6
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作者 Chong Chen Chun‑Sing Lee Yongbing Tang 《Nano-Micro Letters》 SCIE EI CAS CSCD 2023年第8期205-224,共20页
There has been increasing demand for high-energy density and longcycle life rechargeable batteries to satisfy the ever-growing requirements for nextgeneration energy storage systems.Among all available candidates,dual... There has been increasing demand for high-energy density and longcycle life rechargeable batteries to satisfy the ever-growing requirements for nextgeneration energy storage systems.Among all available candidates,dual-ion batteries(DIBs)have drawn tremendous attention in the past few years from both academic and industrial battery communities because of their fascinating advantages of high working voltage,excellent safety,and environmental friendliness.However,the dynamic imbalance between the electrodes and the mismatch of traditional electrolyte systems remain elusive.To fully employ the advantages of DIBs,the overall optimization of anode materials,cathode materials,and compatible electrolyte systems is urgently needed.Here,we review the development history and the reaction mechanisms involved in DIBs.Afterward,the optimization strategies toward DIB materials and electrolytes are highlighted.In addition,their energy-related applications are also provided.Lastly,the research challenges and possible development directions of DIBs are outlined. 展开更多
关键词 Dual-ion batteries Reaction mechanisms Optimization strategies Energy storage
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Fabricating Na/In/C Composite Anode with Natrophilic Na-In Alloy Enables Superior Na Ion Deposition in the EC/PC Electrolyte 被引量:1
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作者 Hui Wang Yan Wu +7 位作者 Ye Wang Tingting Xu Dezhi Kong Yang Jiang Di Wu Yongbing Tang Xinjian Li Chun-Sing Lee 《Nano-Micro Letters》 SCIE EI CAS CSCD 2022年第2期45-59,共15页
In conventional ethylene carbonate(EC)/propylene carbonate(PC)electrolyte,sodium metal reacts spontaneously and deleteriously with solvent molecules.This significantly limits the practical feasibility of high-voltage ... In conventional ethylene carbonate(EC)/propylene carbonate(PC)electrolyte,sodium metal reacts spontaneously and deleteriously with solvent molecules.This significantly limits the practical feasibility of high-voltage sodium metal batteries based on Na metal chemistry.Herein,we present a sodium metal alloy strategy via introducing NaIn and Na_(2)In phases in a Na/In/C composite,aiming at boosting Na ion deposition stability in the common EC/PC electrolyte.Symmetric cells with Na/In/C electrodes achieve an impressive long-term cycling capability at 1 mA cm^(-2)(>870 h)and 5 mA cm^(-2)(>560 h),respectively,with a capacity of 1 mAh cm^(-2).In situ optical microscopy clearly unravels a stable Na ion dynamic deposition process on the Na/In/C composite electrode surface,attributing to a dendrite-free and smooth morphology.Furthermore,theoretical simulations reveal intrinsic mechanism for the reversible Na ion deposition behavior with the composite Na/In/C electrode.Upon pairing with a highvoltage NaVPOF cathode,Na/In/C anode illustrates a better suitability in SMB s.This work promises an alternative alloying strategy for enhancing Na metal interfacial stability in the common EC/PC electrolyte for their future applications. 展开更多
关键词 EC/PC electrolyte Sodium metal batteries Na/In/C electrode Dendrite-free and smooth morphology Theoretical simulations
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Organic photovoltaic cells with copper(Ⅱ) tetra-methyl substituted phthalocyanine 被引量:2
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作者 许宗祥 Roy V. A. L 《Chinese Physics B》 SCIE EI CAS CSCD 2013年第12期533-536,共4页
Efficient heterojunction organic photovoltaic (OPV) cells are fabricated based on copper tetra-methyl phthalocyanine (CuMePc) as donor and fullerene (C60) as acceptor. The power conversion efficiency of CuMePc/C... Efficient heterojunction organic photovoltaic (OPV) cells are fabricated based on copper tetra-methyl phthalocyanine (CuMePc) as donor and fullerene (C60) as acceptor. The power conversion efficiency of CuMePc/C60 OPV cell (2.52%) is increased by 88% compared with that of the non-peripheral substituted copper phthalocyanine (CuPc)/C60 OPV cell (1.34%). The introduction of methyl substituent leads to stronger π–π interaction of CuMePc (~ 3.5 ?) than that of CuPc (~ 3.8 ?). The efficiency improvement is attributed to the enhanced carrier mobility of CuMePc thin film (1.1×10-3 cm2/V·s) and better film morphology by introducing methyl groups into the periphery of CuPc molecule. 展开更多
关键词 organic photovoltaic cell copper (Ⅱ) tetra-methyl substituted phthalocyanine π–π stacking GIXRD
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