Periodic Reporting for period 2 - CATCH (Cross-dimensional Activation of Two-Dimensional Semiconductors for Photocatalytic Heterojunctions)
Période du rapport: 2022-11-01 au 2024-04-30
The ERC-funded project CATCH focuses on a cross-dimensional activation strategy to implement practical photocatalysis. It benefits dimensional features of the 2D matrices, from which the activations involve the participants of nanomaterials of 0D, 1D, and 2D to form photocatalytic heterostructures. Synergic impacts crossing 2D-nD are expected to lead to > 95%/hour rates for removals of selected pollutants and >20% apparent quantum efficiencies for H2 evolution under visible light. It is supported by three subobjectives (SOs) of compatible host and guest materials designs, realizations and functionalization of heterojunctions, and mechanistic studies to understand photocatalysis crossing the dimensionalities.
CATCH establishes a possible blueprint for 2D photocatalysts crossing materials dimensionalities. It considers physical and electronic merits from the planar hosts and their variants when combining with low-dimensional guests. Materials activation strategy for the 2D materials also benefits activations of materials of other dimensions for applications beyond photocatalysis, e.g. in electronics, optics etc. The high-performance photocatalysts developed in CATCH are envisaged as base materials in photocatalytic reactors where the end-product of hydrogen will be collected and used in various fields. CATCH practices methodological transfers obtained from photocatalysis to other relevant fields, e.g. surface wetting, electrocatalysis, and optoelectronics.
CATCH offers the solutions to practical photocatalysis to benefit human’s sustainability. The high-performance and durable photocatalysts applied to harvest solar energy for pollutant removal and hydrogen production are foreseen to possibly alleviate two urgent crises of environmental pollution and clean energy shortage.
In general, the project has been well implemented according to the plan. In the period, 25 peer-reviewed journal articles, including 2 reviews, were published. In hetero-site selections (related to WP1, SO1) and materials realizations (related to WP2, SO2), after thoroughly surveying the 2D databases, computationally we have predicted various new 2D semiconductor matrices, such as 2D transition metal dichlorides, defective trihalide monolayers, and Ni tellurate. The tellurate was synthesized successfully in the lab. A machine learning algorithm was established to predict the heterojunctions with materials from 2D materials databases. Experimentally (related to WP2, SO2), shape-controlled synthesis has been performed and many synthetic materials have been realized. In activations, 0D decorates were loaded on to Ce metal–organic framework, nickel composites composed of flakes and 2D hydroxides. We realized high performances of photocatalysts, despite some of their morphologies are mixed. An apparent quantum efficiency of 20.45% at visible light region (420 nm) was reached for hydrogen evolution, and a removal rate of 95.6% for Cr (VI) under sunlight in 30 minutes. The 0D+2D Co3O4/Co(OH)2 was capable in photocatalytic hydrogen production and degradation of persistent microplastics under visible light. In mechanistic study (WPs 3,4 and SO3), the in-situ x-ray studies were performed along with density functional theory investigations of reaction intermediates during the photocatalysis.
Research endeavours in cross-dimensional activations are expected to reach 2D+0D, 2D+1D and 2D+2D photocatalysts. Variants of the 2D matrices may get along with the individual slabs for materials activations. Mechanistic studies of photocatalysis down to nanosecond scales are also in a reasonable reach. Along with continuous enhancements of the quantum efficiency of photocatalytic hydrogen evolutions on activated 2D-materials-based heterostructures, photocatalysts resulted from CATCH are expected to be mounted on scalable photocatalytic reactors for practical hydrogen evolution under solar/visible light.