Design strategy of a Cu-based catalyst for optimizing the performance in the electrochemical CO2 reduction reaction to multicarbon alcohols.

The electrochemical CO2 reduction reaction (ECRR) is a promising method to reduce excessive CO2 emissions and achieve a sustainable carbon cycle. Due to the high reaction kinetics and efficiency, copper-based catalysts have shown great application potential for preparing multicarbon (C2+) products. C2+ alcohols have high economic value and use-value, playing an essential role in modern industry. Therefore, we summarize the latest research progress of the ECRR to synthesize C2+ alcohols on Cu-based catalysts and discuss the state-of-the-art catalyst design strategies to improve CO2 reduction performance. Moreover, we analyzed in detail the specific reaction pathways for the conversion of CO2 to C2+ alcohols based on DFT calculations. Finally, we propose the problems and possible solutions for synthesizing C2+ alcohols with copper-based catalysts. We hope that this review can provide ideas for devising ECRR catalysts for C2+ alcohols.

The latest development of CoOOH two-dimensional materials used as OER catalysts.

Electrocatalytic water splitting, which is driven by renewable energy input to produce oxygen, has been widely regarded as a promising strategy in the future energy portfolio. The two-dimensional structure based on CoOOH nanosheets is easy to handle in the preparation process, low in cost, and has a small overpotential during water decomposition. Therefore, CoOOH two-dimensional materials have been widely used as electrocatalysts for the oxygen evolution reaction (OER). In this paper, we summarize the application of two-dimensional CoOOH nanosheets in the field of oxygen production from electrocatalytic water splitting. First, the different preparation methods of two-dimensional CoOOH nanosheets are briefly introduced. The structure-activity relationship of the two-dimensional CoOOH catalyst was analyzed from different viewpoints, such as doping, defects, etc. Finally, different catalytic mechanisms of CoOOH-based catalysts are discussed, and studies at the density functional theory (DFT) level are also provided to support the above mechanisms. To improve the readability of this review, a concise overview at the end of each section is given to illustrate some of the characteristics and trends of the studies in the corresponding part. The opportunities and challenges of two-dimensional CoOOH as an electrocatalyst in the future are summarized in the Conclusion section. This work will provide new insights and perspectives to the readers to understand the role of CoOOH nanosheets in the OER process.

Controlled Synthesis and Selective Adsorption Properties of Pr2CuO4 Nanosheets: a Discussion of Mechanism.

Tetragonal-phase Pr2CuO4 nanosheets with a thickness of about 60 nm were synthesized using the coordination compound methods (CCMs), then used as highly efficient selective adsorbent towards malachite green (MG) in aqueous solutions. The Pr2CuO4 samples were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectrum (DRS), and standard Brunauer-Emmett-Teller (BET) methods. The maximum adsorption capacity (Qm) of as-prepared samples was determined by adsorption isotherms with different adsorbent doses (m) of 0.03-0.07 g at 298, 318, and 338 K based on the Langmuir model. When m < 0.03 g or > 0.07 g, effects of systemic mass loss and particle aggregation were discussed on the data deviation from the Langmuir model at 298 K. Based on the hydrogen bond and coordination bond, a possible mechanism of selective adsorption of MG by Pr2CuO4 is proposed, which was further verified by the adsorption experiments of CuO and Pr2O3 towards MG and competing-ion experiments. Finally, the theoretic studies were performed at DFT level to reveal the possible adsorption process.

Synthesis and Absorption Properties of Hollow-spherical Dy2Cu2O5 via a Coordination Compound Method with [DyCu(3,4-pdc)2(OAc)(H2O)2]•10.5H2O Precursor.

Dy2Cu2O5 nanoparticles with perovskite structures were synthesized via a simple solution method (SSM) and a coordination compound method (CCM) using [DyCu(3,4-pdc)2(OAc)(H2O)2]•10.5H2O (pdc = 3,4-pyridinedicarboxylic acid) as precursor. The as-prepared samples were structurally characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), x-ray photoelectron spectroscopy (XPS) and standard Brunauer-Emmett-Teller (BET) methods. Compared to the aggregated hexahedral particles prepared by SSM, the Dy2Cu2O5 of CCM showed hollow spherical morphology composed of nanoparticles with average diameters of 100-150 nm and a larger special surface area up to 36.5 m2/g. The maximum adsorption capacity (Q m ) of CCM for malachite green (MG) determined by the adsorption isotherms with different adsorbent dosages of 0.03-0.07 g, reached 5.54 g/g at room temperature. The thermodynamic parameters of adsorption process were estimated by the fittings of the isotherms at 298, 318, and 338 K, and the kinetic parameters were obtained from the time-dependent adsorption isotherms. The results revealed that the adsorption process followed a pseudo-second-order reaction. Finally, the adsorption mechanism was studied using a competitive ion (CI) experiments, and the highly efficient selective adsorption was achieved due to strong O-Cu and O-Dy coordination bonds between Dy2Cu2O5 and MG.