The hydrogen evolution reaction (HER) is one of the most effective and sustainable ways to produce hydrogen gas as an alternative clean fuel. The rate of this electrocatalytic reaction is highly dependent on the properties (dispersity and stability) of electrocatalysts. Herein, we developed well-dispersed and highly stable platinum nanoparticles (PtNPs) supported on a covalent organic framework (COF-bpyTPP), which exhibit excellent catalytic activities toward HER as well as the hydride reduction reaction. The nanoparticles have an average size of 2.95 nm and show superior catalytic performance compared to the commercially available Pt/C under the same alkaline conditions, producing 13 times more hydrogen with a far more positive onset potential (-0.13 V vs.-0.63 V) and ca. 100% faradaic efficiency. The reaction rate of the hydride reduction of 4-nitrophenol was also 10 times faster in the case of PtNPs@COF compared to the commercial Pt/C under the same loading and conditions. More importantly, the PtNPs@COF are highly stable under the aqueous reactions conditions and can be reused without showing noticeable aggregation and activity degradation.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c9nr09112bDOI Listing

Publication Analysis

Top Keywords

covalent organic
8
platinum nanoparticles
8
highly stable
8
hydride reduction
8
organic framework-supported
4
framework-supported platinum
4
nanoparticles efficient
4
efficient electrocatalysts
4
electrocatalysts water
4
water reduction
4

Similar Publications

Aromatic ring compounds with different conjugation degrees in a boronic acid matrix to realize multicolor phosphorescence for time division colorful multiplexing.

Nanoscale

January 2025

Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education International Center for Dielectric Research & Shaanxi Engineering Research Center of Advanced Energy Materials and Devices, Xi'an Jiaotong University, 710049 Xi'an, China.

Long lifetime multicolor phosphorescence materials possess excellent optical properties and have important application prospects in the fields of advanced anti-counterfeiting and information encryption. However, realizing long lifetime and color-tunable room temperature phosphorescent (RTP) carbon dot (CD) materials has proved challenging. In this study, the organic precursor molecules 2-phenethylamine (2-Ph), 9-aminophenanthrene (9-Ph) and 1-aminopyrene (1-Py) with different degrees of conjugation were selected to synthesize RTP CD composites: 2-Ph@BA, 9-Ph@BA and 1-Py@BA were synthesized by mixing with a boric acid (BA) matrix under high temperature pyrolysis.

View Article and Find Full Text PDF

Pairing photocatalytic 1,2,3,4-tetrahydroisoquinoline semi-dehydrogenation reaction (THIQ-SDR) with two-electron oxygen reduction reaction (2e- ORR) is a green solar to chemical strategy by simultaneously utilizing the photo-excited electrons and holes. However, it is still short of high-efficiency photocatalyst to drive two reactions above. In the present work, crystalline pyrene-thiourea/urea covalent organic frameworks (COF-Py-S and -O) were synthesized and demonstrated as high-performance metal-free photocatalysts.

View Article and Find Full Text PDF

Construction and Band Gap-Regulation of Ordered Macro-Microporous Single Crystals of an Amine-Linked Covalent Organic Framework.

ACS Appl Mater Interfaces

January 2025

State Key Laboratory of Bioinspired Interfacial Materials Science, Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Suzhou 215123, China.

Heterogeneity engineering provides an effective route to manipulate the chemical and physical properties of covalent organic frameworks (COFs) but is still under development for their single-crystal form. Here, we report the strategy based on a combination of the template-assisted modulated synthesis with a one-pot crystallization-reduction method to directly construct ordered macro-microporous single crystals of an amine-linked three-dimensional (3D) COF (OM-COF-300-SR). In this strategy, the colloidal crystal-templating synthesis not only assists the formation of ordered macropores but also greatly facilitates the in situ conversion of linkages (from imine to amine) in the COF-300 single crystals.

View Article and Find Full Text PDF

Piezoelectric catalysis possesses the potential to convert ocean wave energy into and holds broad prospects for extracting uranium from seawater. Herein, the Z-type ZnO@COF heterostructure composite with excellent piezoelectric properties was synthesized through in situ growth of covalent organic frameworks (COFs) on the surface of ZnO and used for efficient uranium extraction. The designed COFs shell enables ZnO with stability, abundant active sites and high-speed electron transport channels.

View Article and Find Full Text PDF

The exploration of pure organic ultra-long room temperature phosphorescence (RTP) materials has emerged as a research hotspot in recent years. Herein, a simple strategy for fabricating long-afterglow polymer aerogels with three-dimensional ordered structures and environmental monitoring capabilities is proposed. Based on the non-covalent interactions between pectin (PC) and melamine formaldehyde (MF), a composite aerogel (PCMF@phenanthrene) (PCMF@PA) doped with phosphorescent organic small molecules was constructed.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!