Value-added Upcycling of PET to 1,4-Cyclohexanedimethanol by a Hydrogenation/Hydrogenolysis Relay Catalysis.

We present an innovative process for directly transforming poly(ethylene terephthalate) (PET), a polymer extensively used in food and beverage packaging, into trans-isomer-enriched 1,4-cyclo- hexanedimethanol (CHDM), a key ingredient in advanced specialty polymers. Our approach leverages a dual-catalyst system featuring palladium on reduced graphene oxide (Pd/r-GO) and oxalate-gel-derived copper-zinc oxide (og-CuZn), utilizing hydrogenation/hydrog- enolysis relay catalysis. This method efficiently transforms PET into polyethylene-1,4-cyclohexanedicarboxylate (PECHD), which is then converted into CHDM with an impressive overall yield of 95% in a two-stage process. Our process effectively handles various post-consumer PET plastics, converting them into CHDM with yields between 78% and 89% across different substrates. Additionally, we demonstrate the applicability and scalability of this approach through a temperature-programmed three-stage relay process on a 10-gram scale, which results in purified CHDM with an isolated yield of 87% and a notably higher trans/cis ratio of up to 4.09/1, far exceeding that of commercially available CHDM. This research not only provides a viable route for repurposing PET waste but also enhances the control of selectivity patterns in multistage relay catalysis.

Functionalization of Covalent Organic Frameworks with Peptides by Polymer-Assisted Surface Modification and the Application for Protein Detection.

Although covalent organic frameworks (COFs) have received extensive attention for biomedical research due to their unique properties, their application is still hindered by the challenges of incorporating COFs with functional biomolecules. Since peptides have shown advantages in biomedical applications, herein, we propose the functionalization of COFs with peptides by a polymer-assisted surface modification strategy. Furthermore, a method based on the peptide-functionalized COFs for protein detection has also been developed to demonstrate their application potential. With the help of the polymers, peptides and horseradish peroxidase are attached onto COFs with a high surface density, and the developed method has achieved simple and sensitive detection of the secreted protein acidic and rich in cysteine. We speculate that the facile method proposed in this work to prepare peptide-functionalized COFs can not only benefit protein detection but also promote more biomedical applications of COFs.

Study on processing synthetic aperture radar data based on an optical 4f system for fast imaging.

Due to the huge amount of collected echo data caused by the working principle of synthetic aperture radar (SAR), the use of digital processing relies heavily on the performance of digital chips. Because of the limitation of Moore's law, the technology of digital signal processing exposes the limitation of computing speed and power consumption in the face of SAR processing. Against this background, the optical processing method based on the optical 4f system is introduced into SAR imaging. A spatial light modulator (SLM) is placed on the input surface and spectrum surface of the 4f system to load the echo data of the SAR and the matched filter function of the SAR. Using optical Fourier transform to realize the core calculation of SAR data processing can solve the difficulty of processing time-consuming due to the large amount of calculation. In the process of Fourier transform, instead of using a solid glass lens, we use a phase-type Fresnel lens diagram in the SLM to realize the function of Fourier, which avoids the need for special design of Fourier lens. It also greatly reduces the volume and weight of the whole machine, which provides a reference method for real-time imaging of spaceborne SAR.

Programmable optical real-time processing system for ultra-wide bandwidth electronic reconnaissance.

Electronic reconnaissance is to detect signals, extract their parameters, modulation types or direction of arrival and so on from a wide bandwidth range. It is difficult for digital signal processing device to process in real time under an ultra-wide bandwidth environment. This paper proposed a programmable optical system which can process signals from an instantaneous bandwidth up to 40GHz in real time. In the optical system, the signals are reconstructed at wavefront of a laser beam. The laser beam carrying signals passes through an optical system composed by lens, beam splitter, light modulator, etc. Signal processing operation is accomplished when laser beam arrives at a focal plane, and processing results are acquired by a high-speed camera. Typical pulse description words can be yielded from the results. The proposed optical system has a nano-second processing delay due to its meter-length light path.

Optical SAR data processing configuration with simultaneous azimuth and range matching filtering.

The real-time processing of synthetic aperture radar (SAR) data has a high requirement for the processor, which is a difficult problem in SAR real-time processing. With the rapid development of optoelectronic devices, traditional electrical SAR data processing can be converted into optoelectronic processing to improve the processing speed. In this paper, a new type of optical device is proposed to improve the processing speed of SAR data. With the help of a spatial light modulator (SLM), the initial SAR signal and matched filter function are loaded on the input plane and spectrum plane of the 4f system, respectively. Using an optical lens with the function of the Fourier transform, the Fourier transform and inverse Fourier transform of the SAR signal are carried out to realize the fast imaging of SAR. In theory, the processing speed of SAR data is the speed of light. Compared with traditional methods such as the range-Doppler (RD) algorithm, it is no longer necessary to carry out a one-dimensional Fourier transform but to carry out matching filtering for the azimuth and range of the spectrum plane of 4f system at the same time. In this way, it is not necessary to introduce a cylindrical lens, only a spherical lens is needed to realize the Fourier transform imaging of SAR. Finally, a two-dimensional SAR processing optical system is built to obtain the SAR image in real time.

Electrocatalytic Oxidation of Benzaldehyde on Gold Nanoparticles Supported on Titanium Dioxide.

The electrooxidation of organic compounds offers a promising strategy for producing value-added chemicals through environmentally sustainable processes. A key challenge in this field is the development of electrocatalysts that are both effective and durable. In this study, we grow gold nanoparticles (Au NPs) on the surface of various phases of titanium dioxide (TiO2) as highly effective electrooxidation catalysts. Subsequently, the samples are tested for the oxidation of benzaldehyde (BZH) to benzoic acid (BZA) coupled with a hydrogen evolution reaction (HER). We observe the support containing a combination of rutile and anatase phases to provide the highest activity. The excellent electrooxidation performance of this Au-TiO2 sample is correlated with its mixed-phase composition, large surface area, high oxygen vacancy content, and the presence of Lewis acid active sites on its surface. This catalyst demonstrates an overpotential of 0.467 V at 10 mA cm-2 in a 1 M KOH solution containing 20 mM BZH, and 0.387 V in 100 mM BZH, well below the oxygen evolution reaction (OER) overpotential. The electrooxidation of BZH not only serves as OER alternative in applications such as electrochemical hydrogen evolution, enhancing energy efficiency, but simultaneously allows for the generation of high-value byproducts such as BZA.

Hybrid homogeneous/heterogeneous relay catalysis for efficient synthesis of 5-aminomethyl-2-furancarboxylic acid from HMF.

Here we present a hybrid catalytic pathway for efficient synthesis of 5-aminomethyl-2-furancarboxylic acid (AMFC), a bio-based nylon-6 analogue monomer, from 5-hydroxymethylfurfural (HMF). This method combines homogeneous-catalyzed selective oxidation of HMF to 5-formyl-2-furancarboxylic acid (FFCA) with heterogeneous-catalyzed reductive amination using ammonia as the nitrogen source. Through this relay strategy, we achieve significant enhancements in overall efficiency, resulting in isolation yields of up to 92% for highly selective and scalable AMFC production from HMF.

Upgrading Waste Polylactide via Catalyst-Controlled Tandem Hydrolysis-Oxidation.

As plastic waste pollution continues to pose significant challenges to our environment, it is crucial to develop eco-friendly processes that can transform plastic waste into valuable chemical products in line with the principles of green chemistry. One major challenge is breaking down plastic waste into economically valuable carbon resources. This however presents an opportunity for sustainable circular economies. In this regard, a flexible approach is presented that involves the use of supported-metal catalysts to selectively degrade polylactide waste using molecular oxygen. This protocol has several advantages, including its operation under organic solvent-free and mild conditions, simplicity of implementation, and high atom efficiency, resulting in minimal waste. This approach enables the chemical upcycling of polylactide waste into valuable chemicals such as pyruvic acid, acetic acid, or a mixture containing equimolar amounts of acetic acid and formaldehyde, providing a viable alternative for accessing key value-added feedstocks from waste and spent plastics.

Hierarchical iron-doped CoP heterostructures self-assembled on copper foam as a bifunctional electrocatalyst for efficient overall water splitting.

A bifunctional electrocatalyst with peculiarly hierarchical snowflake-like iron-doped CoP heterostructures self-assembled on copper foam (CoFeP/CF) was synthesized via a facile hydrothermal-phosphidation pathway. The excellent electrochemical performance of CoFeP/CF can be attributed to the synergistic effect of cobalt and iron atoms, tuneful interaction between metal atoms and phosphorus, and the large electrochemical active surface area origined from its peculiarly hierarchical snowflake-like heterostructures with high surface roughness. With the small Tafel slope values (of 73.0 mV dec-1 for OER and 90.4 mV dec-1 for HER), CoFeP/CF demands the diminutive overpotentials (of 277.9 mV for OER and 152.6 mV for HER) to desire the current density of 50 mA cm-2 in alkaline electrolyte. Furthermore, CoFeP/CF exhibits outstanding electrochemical performance for the overall water splitting with the cell potential of 1.495 V to attain 10 mA cm-2 in a two-electrode cell.

Synthesis of Metal Phosphide Nanoparticles Supported on Porous N-Doped Carbon Derived from Spirulina for Universal-pH Hydrogen Evolution.

Transition metal phosphides (TMPs) are regarded as highly active electrocatalysts for the hydrogen evolution reaction (HER). However, traditional synthetic routes usually use expensive and dangerous precursors as P donors. The development of a low-cost and ecofriendly method for the synthesis of TMPs is significant for sustainable energy development. Herein, cobalt phosphides anchored on or embedded in a spirulina-derived porous N-doped carbon matrix (Co2 P/NC) was fabricated by two-step hydrothermal treatment and carbonization method, which utilized the intrinsic C, N, and P of biomass cleverly as the sources of C, N, and P, respectively. As a result of the high surface area and porosity that enhance the mass-transfer dynamics, Co2 P/NC shows good electrocatalytic activity at all pH values in the HER. This work not only provides a facile and effective method for the fabrication of TMP nanoparticles loaded onto carbon materials but also opens a new strategy for the utilization of the intrinsic ingredients of biomass for the preparation of other functional electrocatalysts.

Nitrogen and phosphorus dual-doping carbon shells encapsulating ultrafine Mo2C particles as electrocatalyst for hydrogen evolution.

Electrochemical hydrogen evolution reaction (HER) from water splitting is a promising way to promote the utilization of renewable energy. Designing and fabricating electrocatalysts with low cost, high catalytic activity and robust stability is desirable. In response, we prepared carbon shells encapsulating ultrafine ß-Mo2C nanoparticles with N and P dual-doping as advanced electrocatalyst used for HER in both acidic and alkaline mediums. This paper gives a discussion on element doping and porosity which have influence on the HER performance. As introducing heteroatoms into carbon matrix to create active sites and enhance electron transfer capacity, the as-prepared electrocatalyst exhibits high catalytic activity with low overpotential of 117 mV and 121 mV to achieve current density of 10 mA cm-2 in acidic and alkaline solutions. Due to the strategy of carbon shells encapsulating, the catalyst presents robust stability for a long time at various applied potential. Furthermore, the design idea of using multiple strategies preparing catalysts may serve some inspiration to fabricate advanced electrocatalysts.