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Abstract In this study, crude cellulose derived from cornstalk, after bleaching, was used as raw material for the synthesis of sodium carboxymethyl cellulose (CMC) by reacting with the cellulose with NaOH and chloroacetic acid at 75 °C for 1.5 h. Effects of alkali dosage, concentration of chloroacetic acid on the physical and chemical properties of the CMC products were investigated. It was revealed that the reactants alkali reagent/chloroacetic acid/cellulose at the molar ratio of 4.6:2.8:1and 4:2.5:1, or at the molar ratio of NaOH/ClCH 2 COOH ≈1.6–1.64, resulted in CMC products of relatively high water solubility. The viscosity-average molecular weight M v of these two CMC products obtained at molar ratios of 4.0:2.5:1 and 4.6:2.8:1 is in the range of 1.94 × 10 4 –2.48 × 10 4 g mol −1 , and the average DS of the two products are 0.57 and 0.85, respectively. As the solute concentration is above 2 wt%, the viscosity of the CMC-water solution exhibits nonlinear (exponential) increasing with increasing the solute concentration (typical of non-Newton fluids).

Wide‐bandgap (WBG) perovskite solar cells (PSCs) are acknowledged as promising candidates for tandem solar cells and building photovoltaics. It is well known that cesium‐based all‐inorganic halide WBG perovskites possess the comparable optoelectronic properties as the organic–inorganic counterparts, but exhibit superior thermal stability. Among them, CsPbIBr2 is considered a feasible material for tandem solar cells after balancing the bandgap and stability of the inorganic perovskite. However, CsPbIBr2 PSCs are often subjected to drastic interfacial charge recombination especially in carbon‐based device structure derived from the chemical bonding defects (i.e., uncoordinated Pb2+) naked on CsPbIBr2 soft lattice, which dramatically limits overall efficiency of CsPbIBr2 WBG PSCs. Herein, a trimethyl ammonium salt hexyltrimethylammonium bromide is presented for CsPbIBr2/carbon interfacial modification. Benefiting from the −N+(CH3)3 passivation effect and −C6H13 hydrophobic alkyl chain, the optimal device with highly smooth morphology and sufficient charge extraction exhibits a champion power conversion efficiency of 11.24% and improved long‐term stability with 99.7% and 79.7% efficiency retention under dry air atmosphere and continuous 85 °C thermal stress, indicating the valuable potential application of the lattice solidified CsPbIBr2 WBG PSCs.

A template‐agent can affect defect formation as well as influence interface properties, due to the rapid growth of perovskite film from the solution. Herein, diethylammonium iodide (DAI) is used as an effective template‐agent to control the perovskite crystallization during preparation. It is found that a very small amount of DAI in chlorobenzene (CB) can slow down the perovskite growth of the CH3NH3PbI3 (MAPbI3) film with more large grain size and compacted crystal‐grains resulting in the lesser grain boundaries (GBs) in favor of carrier transport in perovskite solar cells (PSCs). Moreover, some redundant PbI2 can be digested to form DA2PbI4. One part of DA2PbI4 can form the sub‐grains with the composition of (DA2PbI4)0.2(PbI2)0.8 to passivate the GB defects, and other part can cover the surface to passivate the surface defects in large MAPbI3 grains. Using an optimized DAI concentration of 0.5 mg mL−1 in CB solution, the corrsponding MAPbI3 PSC achieves an increased power conversion efficiency of 20.31% with suppressed current–voltage hysteresis. This DAI passivation strategy provides a simple approach to effectively assist the grain‐growth for improved device performance.

AbstractA wide variety of diarylmethanes is synthesized by the title reaction.

New zinc phthalocyanine (ZnPc-TDA), peripherally functionalized with donor-acceptor conjugates was synthesized, and its optical, thermal, electrochemical, and photovoltaic properties were studied. The black ZnPc-TDA exhibited both excellent solubility in common organic solvents, and broad absorption covering the range 300-900 nm. The photovoltaic devices with the configuration of ITO/PEDOT-PSS/ZnPc-TDA:PCBM/LiF/Al produced short circuit current densities of 2.26 mA/cm(2), the open circuit voltage of 0.68 V and power conversion efficiency of 0.4% under AM1.5G illumination. (C) 2010 Elsevier B.V. All rights reserved.

The catalytic active sites of NiFe and NiFeCr (oxy)hydroxides are revealed byoperandospectroscopic techonologies for alkaline water oxidation.

SnOx attracts considerable attention as an anode of lithium‐ion batteries (LIBs) because of its high theoretical capacity. However, SnOx suffers from poor cyclability and rate capability caused by large volume change upon cycling and low conductivity, which severely limits its application for LIBs. Herein, a nanocomposite of Sn/SnO2/C is synthesized for the first time under an elevated pressure originated from the pyrolysis of dimethyltin oxide in a sealed vessel. The Sn/SnO2/C nanocomposite consists of a homogeneous dispersion of Sn and SnO2 nanocrystals (<10 nm) into the carbon matrix, which endows it with an enhanced lithium storage performance. The Sn/SnO2/C nanocomposite delivers an excellent cyclability (0.025% capacity loss per cycle during 1000 cycles at 1 A g−1) with an improved rate performance (243.8 mAh g−1 at 5 A g−1).

AbstractAu@Pd core–shell nanobricks (CNBs) with concave surfaces and Pd shells with a thickness of approximately 5 nm were synthesized by co‐reduction of HAuCl4 and H2PdCl4 in the presence of Au seeds and Ag ions. These as‐synthesized concave CNBs exhibit significantly enhanced catalytic activity for the electrooxidation of ethanol in alkaline media compared to the commercially‐used Pd black. The improved performance of the Au@Pd CNBs can be attributed to the exposed stepped surfaces, high‐index facets, and the synergistic effects of the core and shell metals.