Herein, a catalytic reductive fractionation of lignocellulose is presented using a heterogeneous cobalt catalyst and formic acid or formate as a hydrogen donor. The catalytic reductive fractionation of untreated birch wood yields monophenolic compounds in up to 34 wt % yield of total lignin, which corresponds to 76 % of the theoretical maximum yield. Model compound studies revealed that the main role of the cobalt catalyst is to stabilize the reactive intermediates formed during the organosolv pulping by transfer hydrogenation and hydrogenolysis reactions. Additionally, the cobalt catalyst is responsible for depolymerization reactions of lignin fragments through transfer hydrogenolysis reactions, which target the β‐O‐4′ bond. The catalyst could be recycled three times with only negligible decrease in efficiency, showing the robustness of the system.

A low-cost template-free solution chemical route to highly porous nanocrystalline sponges of ZnO-EuO 1.5 with 0−5 mol % Eu is presented. The process uses Zn− and Eu−acetate− nitrate and triethanolamine as precursors in methanol. After evaporation of the solvent and heating at 200 °C for 3 min, crystalline ZnO:Eu sponges with minor amounts of organic residues were obtained. Heating to 400 °C replaced the organics with carbonate, which in its turn was decomposed at temperatures below 600 °C, forming ZnO:Eu sponges. Samples heated to 200− 1000 °C for 3 min were studied with XRD, SEM, TEM, TG, XPS, and IR spectroscopy. The ZnO:Eu crystallite sizes could be tuned from below 10 nm for sponges prepared at 200−500 °C, to over 100 nm range at 900 °C, without sintering of the overall microstructure. XRD showed the presence of hexagonal ZnO:Eu (or at 700−1000 °C, ZnO:Eu and cubic Eu 2 O 3 ) as the only phases present. The ZnO:Eu had slightly larger unit cell dimensions than the literature value of ZnO for samples obtained at 200−600 °C, while the unit cells of samples obtained at higher temperatures were quite close to the value of undoped ZnO. XPS showed that Eu was mainly in its 3+ state and well-distributed within the sponges but segregated at the ZnO sponge surface upon heating at 700− 1000 °C, in accordance with XRD studies showing Eu 2 O 3 formation.

Structure–property relationships were established for undoped and europium-doped ZnO nanostructures, correlating their photocatalytic activity with optical and structural material properties.

Nanocrystalline ZnO sponges doped with 5 mol% EuO1.5 are obtained by heating metal–salt complex based precursor pastes at 200–900 °C for 3 min. X‐ray diffraction, transmission electron microscopy, and extended X‐ray absorption fine structure (EXAFS) show that phase separation into ZnO:Eu and c‐Eu2O3 takes place upon heating at 700 °C or higher. The unit cell of the clean oxide made at 600 °C shows only ≈0.4% volume increase versus undoped ZnO, and EXAFS shows a ZnO local structure that is little affected by the Eu‐doping and an average Eu3+ ion coordination number of ≈5.2. Comparisons of 23 density functional theory‐generated structures having differently sized Eu‐oxide clusters embedded in ZnO identify three structures with four or eight Eu atoms as the most energetically favorable. These clusters exhibit the smallest volume increase compared to undoped ZnO and Eu coordination numbers of 5.2–5.5, all in excellent agreement with experimental data. ZnO defect states are crucial for efficient Eu3+ excitation, while c‐Eu2O3 phase separation results in loss of the characteristic Eu3+ photoluminescence. The formation of molecule‐like Eu‐oxide clusters, entrapped in ZnO, proposed here, may help in understanding the nature of the unexpected high doping levels of lanthanide ions in ZnO that occur virtually without significant change in ZnO unit cell dimensions.

An efficient, template-free solution-chemical route to nanostructured ZnO sponges is presented: A mixture of Zn(NO)·6HO, Zn(OAc)·2HO, and triethanolamine in methanol was evaporated to a highly viscous liquid and rapidly heated to >200 °C for 1-3 min to achieve highly porous, nanocrystalline sponges of ZnO. The viscous precursor concentrate obtained on evaporation in air was characterized by TG, DSC, and IR spectroscopy, and the product ZnO sponges by XRD, SEM, TEM, and IR spectroscopy. The fast reaction forming ZnO started at 140 °C and finished within a few seconds. Scherrer analysis of the XRD peak broadening showed average crystallite sizes of 8 to 11 nm for ZnO prepared by annealing at 200-450 °C (3 min), while grain growth to 134 nm was observed from 500 to 900 °C (3 min). The ZnO powders obtained at 200-900 °C had cell dimensions of a = 3.25 Å and b = 5.21 Å, matching the ZnO literature data well. SEM and TEM analyses showed highly porous, bread-like 3D nanostructures built by ca. 30-70 nm thick walls of ZnO crystallites of the approximate average sizes given by the XRD Scherrer analysis. It seems that the crystal growth above 450 °C takes place within the ZnO 3D structure obtained at lower temperatures without much sintering of the larger porous structure.