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Verified CAS / Academic Author2 Decoded Studies

Prof. Na Yin

State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4482-6

Letting Polymer Semiconductors Crystallize Along Their Self-Templates: A Self-Templated Gradient Assembly Strategy for Multi-Scale Structural Ordering and Ultrahigh Charge Carrier Mobility

Polymer semiconductors offer solution processability, mechanical flexibility, and molecular tunability for flexible displays, wearable devices, and the Internet of Things, yet their charge transport properties remain substantially inferior to inorganic semiconductors. Efficient charge transport demands simultaneous structural order across molecular conformation, aggregate connectivity, and macroscopic orientation, but these length scales are strongly coupled: primary aggregates in solution, secondary nucleation during solvent evaporation, and final film solidification intertwine, rendering structural control dependent on empirical trial and error. Prior approaches—molecular design, solvent additives, thermal annealing, and shear coating—have improved crystallization and orientation, but two interrelated issues persist. First, enhancing aggregation does not guarantee higher mobility: insufficient aggregation yields small, loosely connected structures, while excessive aggregation causes premature nucleation, fiber twisting, and large grain boundaries. Second, direct observation of how solution aggregates evolve across molecular, mesoscopic, and macroscopic scales into solid films is often lacking. The fundamental challenge is not whether to promote crystallization, but how to cooperatively control aggregate type/size, internal order, connectivity, and assembly pathway, and to transform empirical solvent selection into predictive design rules. Zhao et al. report a self-templated gradient assembly (STGA) strategy that couples solubility parameters with vapor pressure to regulate both solution-state aggregation and assembly kinetics. Unlike conventional anti-solvent approaches that trigger rapid nucleation, STGA operates within mutually compatible solvent mixtures that retain polymer solubility and generate a continuous decline in solvent quality during evaporation. Preformed ordered aggregates become endogenous templates for subsequent assembly and crystallization rather than transient intermediates. Using a newly designed linear donor–acceptor polymer, PFIDTO-BT, and the relative energy difference (RED) index, cryogenic transmission electron microscopy confirmed that primary aggregates systematically enlarge as solvent quality decreases. Vapor pressure provides a second dimension, defining a solvent-selection matrix. For low-solubility, low-volatility components, the selectivity toward side chain/backbone parameter Ratio (S/B) further distinguishes aggregation pathways induced by different poor solvents. This framework connects solvent selection to hierarchical polymer organization through a semi-quantitative, experimentally testable methodology, enabling single-crystal-like polymer semiconductors with ultrahigh charge carrier mobility.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3484-6

Biodegradable Hollow MOFs-Based Nano-Modulator for Collaboratively Blocking Energy Metabolism for Immunotherapy of Orthotopic Gliomas

The immunosuppressive tumor microenvironment (TME) of gliomas renders conventional therapies suboptimal, and aberrant energy metabolism orchestrates tumorigenesis and immune evasion. This work constructs a biodegradable nano-modulator (ZIF-90@MnO2@GPNA, ZMG) based on ZIF-90 decorated with MnO2 and loaded with the glutamine transport antagonist L-γ-glutamyl-p-nitroanilide (GPNA) for glioma therapy via multi-pathway inhibition of energy metabolism and TME reshaping. Hyaluronic acid (HA) and lactoferrin (Lf) are functionalized on the surface (ZMGH-Lf) to cross the blood-brain barrier (BBB) and target gliomas. ZMGH-Lf biodegrades in response to TME stimulation, releasing Mn2+ that catalyzes H2O2 to ·OH, inducing mitochondrial dysfunction. It inhibits glycolysis by alleviating hypoxia and reducing NAD+ expression, while GPNA blocks compensatory glutamine uptake. This strategy achieves multi-pathway disruption of glioma metabolism, relieves immune resistance, and improves the immune TME. Findings demonstrate that ZMGH-Lf effectively inhibits gliomas through multi-way manipulation of energy metabolism and immunotherapy, providing a new strategy for glioma treatment.