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Verified CAS / Academic Author2 Decoded Studies

Prof. GAO Zhan

Sun Yat-sen University

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3885-8

Optimizing Oxygen and Water Affinity in Aliphatic Acylhydrazone Covalent Organic Frameworks for Efficient H2O2 Photosynthesis from Water and Air

Photocatalytic production of hydrogen peroxide (H2O2) via oxygen reduction reaction (ORR) and water oxidation reaction (WOR) from water and air offers a sustainable alternative to conventional anthraquinone processes. However, the intrinsic kinetic mismatch—fast ORR (microseconds to milliseconds) versus sluggish WOR (seconds)—limits overall efficiency. Here, we report aliphatic acylhydrazone covalent organic frameworks (AA-COFs) synthesized by coupling aliphatic hydrazides with benzotrithiophene motifs via acylhydrazone linkages. The pore walls are decorated with abundant S, O, and N heteroatoms, enhancing affinity toward both O2 and H2O, thereby improving the kinetics of both half-reactions. Through single-carbon atomic engineering, the optimized AA-COF achieves a trade-off between ORR and WOR kinetics, enabling efficient overall H2O2 photosynthesis from water and air without sacrificial agents. The material exhibits a H2O2 production rate of 4777 μmol g−1 h−1 and an O2 utilization/conversion efficiency of 99.3%. This work demonstrates that rational design of heteroatom-rich COFs can synchronize ORR and WOR, overcoming a major bottleneck in artificial photosynthesis.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3404-8

Nanoparticulate lipid adjuvants induce robust immunity against RSV infection

Effective subunit vaccines against respiratory syncytial virus (RSV) require adjuvants that elicit both humoral and cellular immunity. Conventional adjuvants such as alum and squalene emulsions (MF59, AS03) potentiate antibody titers but fail to induce robust T cell responses, while the liposomal AS01 adjuvant, though clinically validated, relies on costly and resource-limited immunostimulants MPLA and QS21. This study introduces a nanoparticulate lipid adjuvant (NLA) platform based on ionizable lipid (IL) nanoparticles. A library of 124 structurally diverse ILs was synthesized via Ugi four-component reaction and formulated with helper lipids into 124 distinct nanoparticles. In vitro screening based on TNF-α production from splenocytes identified high-performance NLA candidates. Formulations with varied amine heads were assessed for immune cell activation, including bone marrow-derived dendritic cells and RAW264.7 macrophages. Leading NLAs upregulated TNF-α and costimulatory molecules CD80 and CD86. Co-administered with RSV pre-F antigen in mice via intramuscular injection, the optimized formulation induced robust cellular and humoral immunity, with significantly enhanced central and effector memory T cell responses. Challenge studies demonstrated superior protection against viral infection, comparable to an AS01e-like liposome adjuvant. Safety evaluations, including hematology, blood biochemistry, and histopathology, confirmed good biocompatibility. Using NLRP3 gene knockout cells, the inflammatory properties of NLAs were shown to depend primarily on the NLRP3 inflammasome pathway. These findings establish rationally designed IL-based NLAs as high-performing, accessible adjuvants for subunit vaccines.