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The efficient immobilization of GaPt liquid metal alloy droplets onto tailored supports improves catalytic performance by preventing coalescence and subsequent loss of active surface area. Herein, we use tailored supraparticle (SP) supports with controlled nanopores to systematically study the influence of pore sizes on the catalytic stability of GaPt supported catalytically active liquid metal solution (SCALMS) in propane dehydrogenation (PDH). Initially, GaPt droplets were prepared via an atom-efficient and scalable ultrasonication method with recycling loops to yield droplets <300 nm. Subsequently, these droplets were immobilized onto SiO-based SPs with controlled pore sizes ranging from 45 to 320 nm. Catalytic evaluations in PDH revealed that GaPt immobilized on SPs with larger pores demonstrated superior stability over 15 h time-on-stream evidenced by reduced deactivation rates from 0.046 to 0.026 h. Nanocomputed tomography and identical location SEM confirmed the successful immobilization of GaPt droplets within the interstitial sites formed by the primary particles constituting the SPs. These remained unchanged before and after the catalytic reaction, demonstrating efficient coalescence prevention. Our findings underscore the importance of support pore size engineering for improving the stability of GaPt SCALMS catalysts and highlight, particularly, the high potential of using SPs in this context.
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http://dx.doi.org/10.1021/acsanm.4c03577 | DOI Listing |
J Biomed Mater Res A
July 2025
G.E.R.N. Center for Tissue Replacement, Regeneration & Neogenesis, Department of Orthopedics and Trauma Surgery, Faculty of Medicine, Albert-Ludwigs-University of Freiburg, Freiburg, Germany.
This work highlights the potential of porous, bioactive coatings to advance implant technology and address critical clinical challenges. A key issue in implant coatings is to achieve the balance between infection prevention and successful osseointegration. Although titanium implants are widely used due to their mechanical strength and biocompatibility, their bioinert nature limits integration with bone tissue.
View Article and Find Full Text PDFACS Appl Mater Interfaces
July 2025
Department of Biomedical Engineering, College of Engineering and Applied Sciences, Nanjing University, 22 Han-Kou Road, Nanjing City, 210093, Jiangsu Province, China.
Poly(esters), especially poly(lactic--glycolic acid) (PLGA), are currently the materials of choice for clinical sustained-drug-release formulations based on polymer nanoparticles, due to the long history of safe clinical use of these polymers. The existing poly(ester) nanoparticles suffer from limitations in low colloidal stability or/and low drug loading. Here, we present a poly(ester)-based nanoparticle with ultrahigh colloidal stability (>210 days) and ultrahigh drug loading (∼40% for doxorubicin, or DOX).
View Article and Find Full Text PDFACS Appl Nano Mater
November 2024
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Lehrstuhl für Chemische Reaktionstechnik (CRT), 91058 Erlangen, Germany.
Adv Mater
August 2024
College of Chemistry, Key Laboratory of Radiation Physics & Technology, Ministry of Education, Sichuan University, Chengdu, 610064, P.R. China.
Superstructures with complex hierarchical spatial configurations exhibit broader structural depth than single hierarchical structures and the associated broader application prospects. However, current preparation methods are greatly constrained by cumbersome steps and harsh conditions. Here, for the first time, a concise and efficient thermally responsive dynamic synthesis strategy for the preparation of multidimensional complex superstructures within soluble covalent organic networks (SCONs) with tunable morphology from 0D hollow supraparticles to 2D films is presented.
View Article and Find Full Text PDFACS Nano
January 2024
International Joint Research Laboratory for Biointerface and Biodetection, Jiangnan University, Wuxi, Jiangsu 214122, People's Republic of China.
Titanium dioxide (TiO) has attracted significant attention in the fields of antibacterial activity and pollutant degradation due to its well-known photocatalytic properties. However, the application of TiO is significantly limited by its large band gap width, which only allows excitation by ultraviolet light below 400 nm. Here, we propose the use of surface chiral functionalization of TiO to tune its band gap width, thus enabling it to be excited by near-infrared-region light (NIR), resulting in the effective separation of electron-hole pairs.
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