S-Scheme Interface Between K-CN and FePS Fosters Photocatalytic H Evolution.

ACS Appl Mater Interfaces

Chair for Photonics and Optoelectronics, Nano-Institute Munich, Physics Department, Ludwig Maximilians-Universität München, Königinstr. 10, 80539 Munich, Germany.

Published: November 2024


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

In photocatalysis, photogenerated charge separation is pivotal and can be achieved through various mechanisms. Building heterojunctions is a promising method to enhance charge separation, where effective contact and charge exchange between heterojunction components remains challenging. Mostly used synthesis processes for making heterostructures require high temperatures, difficult processes, or expensive materials. Herein, a heterojunction of potassium intercalated graphitic carbon nitride (K-CN) and nanoflakes of iron phosphor trisulfide (FPS) is designed via a simple mechanical grinding process to boost the hydrogen evolution by a factor of more than 25 compared to pure K-CN. This significant improvement is rarely reached by other combinations of two semiconductors without cocatalysts, such as platinum. It can be attributed to the band alignment and band bending of an S-scheme that is validated via optical and X-ray photoelectron spectroscopy. As a consequence, strong quenching of the photoluminescence and significant H evolution occur for this unique heterojunction. Furthermore, the excellent durability of the designed photocatalytic heterostructure is confirmed by monitoring the catalysts' H-evolution rate and crystal structure after 72 h under light illumination. This study opens up promising and simple pathways for constructing efficient S-scheme heterojunctions for photocatalytic water-splitting.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.4c15236DOI Listing

Publication Analysis

Top Keywords

charge separation
8
s-scheme interface
4
interface k-cn
4
k-cn feps
4
feps fosters
4
fosters photocatalytic
4
photocatalytic evolution
4
evolution photocatalysis
4
photocatalysis photogenerated
4
photogenerated charge
4

Similar Publications

Charged hadron elliptic anisotropies (v_{2}) are presented over a wide transverse momentum (p_{T}) range for proton-lead (pPb) and lead-lead (PbPb) collisions at nucleon-nucleon center-of-mass energies of 8.16 and 5.02 TeV, respectively.

View Article and Find Full Text PDF

Femtosecond laser excitation of nanometer thin heterostructures comprising a heavy metal and a magnetically ordered material is known to result in the emission of terahertz radiation. However, the nature of the emitted radiation from heavy metal/antiferromagnet heterostructures has sparked debates and controversies in the literature. Here, we unambiguously separate spin and charge contributions from Pt/NiO heterostructures by introducing an unprecedented methodology combining high external magnetic fields with a symmetry analysis of the emitted terahertz polarization.

View Article and Find Full Text PDF

CpG-A induces liquid-liquid phase separation of HMGB1 to activate the RAGE-mediated inflammatory pathway.

Proc Natl Acad Sci U S A

September 2025

State Key Laboratory of Green Biomanufacturing, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China.

High-mobility group box protein 1 (HMGB1) is a chromatin-associated nonhistone protein widely distributed in the nucleus of eukaryotic cells. It is transported extracellularly as a proinflammatory mediator or late warning protein to induce immune and inflammatory reactions upon stimuli such as microbial infection. Here, we have found that HMGB1 directly interacts with bacterial DNA analogue CpG-A in the extracellular environment to undergo liquid-liquid phase separation (LLPS) via its positively charged DNA-binding domain.

View Article and Find Full Text PDF

This review delivers a focused and critical evaluation of recent progress in the green synthesis of carbon quantum dots (CQDs), with particular attention to state-of-the-art approaches utilizing renewable biomass as precursors. The main objective is to systematically examine innovative, environmentally friendly methods and clarify their direct influence on the core properties and photocatalytic performance of CQDs. The novelty of this review stems from its comprehensive comparison of green synthetic pathways, revealing how specific processes determine key structural, optical, and electronic attributes of the resulting CQDs.

View Article and Find Full Text PDF

Photocatalysis holds significant promise for the reduction of CO to valued chemicals under mild conditions. However, its potential is severely limited by weak CO adsorption and slow proton-coupled electron transfer (PCET) rates. In this work, ZnInS-based catalysts with varying hydroxyl contents were synthesized via the solvothermal method.

View Article and Find Full Text PDF