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ZK
Verified CAS / Academic Author3 Decoded Studies

Prof. ZHENG Kai

Nanjing Medical University

Research Publications & English Decoded Briefs

Showing 3 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4242-1

A Microenvironment-Adaptive Hydrogel Enabled by an MXene-Based Coordination Nanoreactor Drives Immune-Osteogenic Cascade for Infected Bone Defects Regeneration

Infected bone defects remain a formidable clinical challenge due to the coupled pathologies of bacterial infection and impaired osteogenesis. Conventional treatments often fail to address the dynamic microenvironment, leading to persistent infection and inadequate bone repair. Here, we report a microenvironment-adaptive hydrogel incorporating a Ti3C2Tx MXene-based coordination nanoreactor that orchestrates an immune-osteogenic cascade. The nanoreactor, constructed by coordinating Fe3+ ions onto MXene nanosheets, exhibits pH- and reactive oxygen species (ROS)-responsive release of Fe3+ and MXene, enabling sequential antibacterial and pro-osteogenic activities. In vitro studies demonstrated that the hydrogel eradicated Staphylococcus aureus and Escherichia coli (>99.9% killing) within 6 h via synergistic photothermal and chemodynamic effects, while simultaneously scavenging excess ROS to mitigate oxidative stress. Notably, the released Fe3+ ions promoted M2 macrophage polarization, as evidenced by a 2.5-fold increase in CD206 expression, and subsequently enhanced osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs), with alkaline phosphatase activity elevated by 1.8-fold and alizarin red staining intensity increased by 2.2-fold. In a rat model of infected calvarial defects, the hydrogel significantly accelerated bone regeneration, achieving a bone volume fraction of 78.4% at 8 weeks post-implantation, compared to 35.2% in the untreated control. Micro-CT and histological analyses confirmed robust new bone formation and complete infection clearance. This study presents a paradigm for designing adaptive biomaterials that integrate infection control and bone regeneration, offering a promising strategy for treating infected bone defects.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3616-8

Performance enhancement, negative stiffness structural characterization, and energy absorption mechanisms of 3D-printed continuous carbon fiber reinforced composites

Negative stiffness (NS) structures exploit multi-stable mechanisms to achieve energy absorption, yet their practical application is limited by material and manufacturing constraints that compromise load-bearing capacity, reusability, and energy absorption efficiency. This study addresses these limitations by employing continuous carbon fiber reinforced thermoplastic polymers (CCFRTP) and three-dimensional (3D) printing to fabricate NS structures with cosine beam cells. A wet twisting method for continuous carbon fiber (CCF) was developed to enhance mechanical properties and elucidate failure behaviors and interfacial adhesion mechanisms. The resulting CCF/PLA/PVDF composites exhibited significant improvements in mechanical properties compared to untreated counterparts, with failure analysis revealing characteristic fiber breakage due to enhanced interfacial adhesion, as opposed to fiber pull-out and irregular fracture in untreated samples. A one-stroke path planning model was used to investigate bistability principles and energy absorption mechanisms. Displacement-controlled loading/unloading experiments assessed energy absorption in both energy-locked and repetitive modes. A dual-unit assembly structure was fabricated to validate the feasibility of a negative stiffness honeycomb structure. Composite layup simulations via Abaqus confirmed the deformation process and energy absorption mechanisms. The findings demonstrate that CCFRTP-based NS structures offer considerable potential for large deformation energy absorption applications in aerospace and naval fields.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3981-7

Phase-Purity Engineering in Quasi-2D Perovskites for Amplified Spontaneous Emission

Solution-processable quasi-2D perovskites are promising laser gain media due to their high exciton binding energy and improved stability relative to 3D counterparts. However, conventional synthesis yields mixed n-value phases, introducing interfacial defects and energetic disorder that impede charge injection into desired emission centers. Here, we report the first demonstration of stimulated emission from a phase-pure quasi-2D perovskite (n=8) achieved via a solvent-sieving method for selective phase removal. This dynamic purification yields near-unity phase purity (99.85%) with no detectable low-n phases, as confirmed by X-ray diffraction and ultraviolet-visible spectroscopy. The phase-pure film exhibits a narrower and more intense (001) diffraction peak (FWHM 0.16 nm, intensity 16,129) compared to pristine films (FWHM 0.22 nm, intensity 3,304), indicating enhanced crystallinity and increased grain size. Time-resolved photoluminescence reveals a prolonged carrier lifetime of 6.98 ns, suggesting reduced trap density. Atomic force microscopy shows a nearly pinhole-free surface with root mean square roughness of 1.18 nm. Consequently, the amplified spontaneous emission threshold is reduced to 13.82 μJ cm−2, a 12.5% improvement over conventional mixed-phase films (15.8 μJ cm−2). This work provides an efficient route to pure-phase quasi-2D perovskites for low-threshold lasers.