Search

• Comprehensive utilization of solar energy to get hydrogen energy and fresh water was studied. • 2D lamellar membrane based on the semiconductor BiOCl nanosheet was designed. • PHE and PWE were closely related to the light-to-thermal conversion and water state. • The PWE rate of BOC-CNF@CNT lamellar membrane was up to 2.05 kg·m−2·h−1. Solar energy can help solve the energy and water shortage crisis. Developing a single material that can exhibit both photocatalytic hydrogen evolution (PHE) and photothermal water evaporation (PWE) represents a new concept to simultaneously realize green energy and fresh water supply. In this study, a series of 2D lamellar membranes (2DLMs) based on a conventional semiconductor BiOCl nanosheet was designed as an ensemble, and its combined application for PHE and PWE was explored, in which cellulose nanofibers (CNFs), carbon nanotubes (CNTs), and a self-assembly of CNF@CNT were also used. The PHE and PWE efficiencies are closely related to the conversion of solar energy and the state of the water molecules. Owing to the high light-to-thermal conversion, enhanced water transfer, and the low evaporation enthalpy of confined water, a composite made of BiOCl and CNF@CNT 2DLM (BOC-CNF@CNT) could rapidly reach a surface temperature of 46.6 °C, with its PWE rate reaching up to 2.05 kg·m−2·h−1. Moreover, owing to the high photogenerated carrier transport, strong photothermal effect, and the action of confined water, the PHE rate of BOC-CNF@CNT is 1.99-fold that of the composite made of BiOCl and CNF 2DLM (BOC-CNF) and 1.42-fold that of the composite made of BiOCl and CNT 2DLM (BOC-CNT). This work provides a new and effective strategy for a comprehensive utilization of solar energy to simultaneously produce clean hydrogen and fresh water. [ABSTRACT FROM AUTHOR]

Due to the natural cellulose encapsulated in both lignin and hemicellulose matrices, as well as in plant cell walls with a compact and complex hierarchy, extracting cellulose nanofibers (CNFs) from lignocellulosic biomass is challenging. In this study, a sustainable high yield strategy with respect to other CNF preparations was developed. The cellulose was liberated from plant cell walls and fibrillated to a 7–22 nm thickness in one bath treatment with H3PO4 and H2O2 under mild conditions. The cellulose underwent swelling, the lignin underwent oxidative degradation, and the hemicellulose and a small amount of cellulose underwent acid hydrolysis. The CNFs' width was about 12 nm, with high yields (93% and 50% based on cellulose and biomass, respectively), and a 64% crystallinity and good thermal stability were obtained from bagasse. The current work suggests a strategy with simplicity, mild conditions, and cost-effectiveness, which means that this method can contribute to sustainable development for the preparation of CNFs. [ABSTRACT FROM AUTHOR]

Separating the fibers, deconstructing both the interlamellar structures and the intermicrofibrils structures in the cell wall, and cleaving the amorphous regions of cellulose (all reached in one bath chemical-assisted treatment), then extracting cellulose nanofibers (CNFs) from biomass, is both challenging and imperative. A simple, cost-effective and green strategy for extracting CNFs from bamboo using nitric acid and hydrogen peroxide (NCHP), to enable fibrillation via a cooperative mechanism, is demonstrated herein. NCHP-CNFs 13.1 ± 2.0 nm wide, with a high aspect ratio, 74% crystallinity, excellent UV resistance and high thermal stability, were successfully extracted by treatment in HNO3 aqueous solution, at a concentration of 3.2 mol/L, and treatment with 60.00 mmol/g H2O2 at 50 °C for 48 h. The yields of NCHP-CNFs reached 73% and 99% based on biomass and cellulose, respectively, due to the high delignification selectivity of OH+ and the mild aqueous conditions during the NCHP treatment. These NCHP-CNFs with excellent UV resistance can potentially be applied in the field of UV-resistant coatings, to replace organic and inorganic materials. [ABSTRACT FROM AUTHOR]