Modified Wood Fibers Spontaneously Harvest Electricity from Moisture.

With the rapid development of modern society, our demand for energy is increasing. And the extensive use of fossil energy has triggered a series of problems such as an energy crisis and environmental pollution. A moisture-enabled electric generator (MEG) is a new type of energy conversion method, which can directly convert the ubiquitous moisture in the air into electrical energy equipment. It has attracted great interest for its renewable and environmentally friendly qualities. At present, most MEGs still have low power density, strong dependence on high humidity, and high cost. Herein, we report the development of a high-efficiency MEG based on a lignocellulosic fiber frame with high-power-density, all-weather, and low-cost characteristics using a simple strategy that optimizes the charge transport channel and ion concentration difference. The MEG devices we manufactured can generate the open-circuit voltage of 0.73 V and the short-circuit current of 360 µA, and the voltage can still reach 0.6 V at less than 30% humidity. It is possible to drive commercial electronic devices such as light-emitting diodes, electronic displays, and electronic calculators by simply connecting several electric generators in series. Biomass-based moisture-enabled electric generation has a low cost, is easy to integrate on a large scale, and is green and pollution-free, providing clean energy for low-humidity or high-electricity-cost areas.

Aldehyde modified cellulose-based dual stimuli responsive multiple cross-linked network ionic hydrogel toward ionic skin and aquatic environment communication sensors.

Recently, materials with complicated environmentally-sensitive abilities, high stretchability and excellent conductive sensitivity are interesting actuators in future applications. Herein, we fabricated a versatile and facile polyvinyl alcohol/polyacrylic acid/dialdehyde cellulose nanofibrils-Fe3+ hydrogel integrated with programmable dual-shape memory properties, high mechanical strength, good recoverability, and heat-induced self-healing capability. Benefiting from the synergistic effect of hydrogen bonds and dual metal coordination bonds of cellulose-based dialdehyde and carboxyl with Fe3+and then heating-freeze-thawing cycle treatment, the obtained hydrogel exhibited dual shape memory abilities, high tensile strain (up to 600 %), good self-recovery, and anti-fatigue properties. Moreover, the resultant hydrogel sensors showed revealed high strain sensitivity (gauge factor = 2.95) and satisfactory electrochemical performance; and such hydrogel-based sensor could be used as ionic skin to detect various human motions in real-time and barrier-free communication in the aquatic environment. The composite hydrogel with superior and versatile performances reported in this study could offer a great promise to be applied under extreme conditions as multifunctional sensors.