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Verified CAS / Academic Author2 Decoded Studies

Prof. MAO Chenghui

Sichuan University

Co-Affiliations:Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-4086-4

4D Printable Semi-Interpenetrating Networks with Robust Tissue Adhesion for Smart Self-Deployable Vascular Closure

Interventional therapy has emerged as a transformative alternative to open surgery owing to its minimal invasiveness and fast recovery. However, it still presents risks of iatrogenic injury from vascular access, necessitating prompt and reliable vascular closure. Although various closure systems have been developed, they often suffer from complicated deployment procedures, potential for loosening, and risk of device migration. Herein, we develop a smart self-deployable vascular closure device enabled by a semi-interpenetrating network (sIPN) that synergistically integrates a programmable shape memory effect and robust tissue adhesion. The sIPN was designed by interpenetrating flexible, dopamine-functionalized poly(tetrahydrofuran) (PTD) chains into a photo-crosslinkable poly(ε-caprolactone)-based copolymer (PCC) network. The vascular closure model was fabricated via a UV-assisted fused deposition modeling printing strategy, significantly reducing mechanical anisotropy while facilitating structural customization. The resulting device exhibits autonomous self-deployment at 37 °C, along with reliable tissue adhesion under physiological conditions (maximum shear strength of 150.5 kPa). In vitro, the material demonstrates exceptional hemocompatibility (below 3%) and excellently enhanced cell migration (up to 38.9%). In vivo, immunofluorescence analysis reveals a promotion for CD31 (162.18%) and αSMA (154.93%) compared to the control group. These results highlight the PTD/PCC sIPN as a bioadaptive, multifunctional material platform for intelligent vascular closure, offering great promise for clinical translation in interventional therapies.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3510-0

Platinum single-atom catalysts anchored on van der Waals heterostructure support for durable hydrogen evolution

The activity and stability of single-atom catalysts (SACs) are intimately associated with the structure of supports. Herein, by employing a van der Waals (vdW) heterostructure support, we construct a highly active and durable Pt SAC for hydrogen evolution reaction (HER). The unique support consists of monolayer MoS2 attaching on hierarchical N-doped carbon nanocages (hNCNC), on which Pt presents as individual single atoms on the hNCNC and as island-like single-atom layers on the MoS2. The optimized Pt1-MoS2/hNCNC demonstrates low overpotential (11 mV at 10 mA cm−2) and high mass activity (5.6 A mgPt−1 at −20 mV) in 0.5 M H2SO4 solution, outperforming commercial Pt/C. Impressively, the Pt1-MoS2/hNCNC exhibits improved long-term stability in proton exchange membrane water electrolyzer relative to commercial Pt/C. The excellent HER performance is attributed to the regulated electronic structure, robust interaction of Pt atoms with MoS2/hNCNC and facilitated charge transfer. This study establishes an innovative strategy to develop a highly active and durable Pt SAC using vdW heterostructure supports.