Recent advances in moisture-induced electricity generation based on wood lignocellulose: Preparation, properties, and applications.

Moisture-induced electricity generation (MEG), which can directly harvest electricity from moisture, is considered as an effective strategy for alleviating the growing energy crisis. Recently, tremendous efforts have been devoted to developing MEG active materials from wood lignocellulose (WLC) due to its excellent properties including environmental friendliness, sustainability, and biodegradability. This review comprehensively summarizes the recent advances in MEG based on WLC (wood, cellulose, lignin, and woody biochar), covering its principles, preparation, performances, and applications. In detail, the basic working mechanisms of MEG are discussed, and the natural features of WLC and their significant advantages in the fabrication of MEG active materials are emphasized. Furthermore, the recent advances in WLC-based MEG for harvesting electrical energy from moisture are specifically discussed, together with their potential applications (sensors and power sources). Finally, the main challenges of current WLC-based MEG are presented, as well as the potential solutions or directions to develop highly efficient MEG from WLC.

Rapid fabricated in-situ polymerized lignin hydrogel sensor with highly adjustable mechanical properties.

Conductive hydrogels have been widely used as sensors owing to their tissue-like properties. However, the synthesis of conductive hydrogels with highly adjustable mechanical properties and multiple functions remains difficult to achieve yet highly needed. In this study, lignin hydrogel characterized by frost resistance, UV resistance, high conductivity, and highly adjustable mechanical properties without forming by-products was prepared through a rapid in-situ polymerization of acrylic acid/zinc chloride (AA/ZnCl2) aqueous solution containing lignin extract induced by the reversible quinone-catechol redox of the ZnCl2-lignin system at room temperature. Results revealed that the PAA/ZnCl2/lignin hydrogel exhibited mechanical properties with tensile stress (ranging from 0.08 to 3.28 MPa), adhesion to multiple surfaces (up to 62.05 J m-2), excellent frost resistance (-70-20 °C), UV resistance, and conductivity (0.967 S m-1), which further endow the hydrogel as potential strain and temperature sensor with wide monitor range (0-300 %), fatigue resistance, and quick response (70 ms for 150 % strain). This study proposed and developed a green, simple, economical, and efficient processing method for a hydrogel sensor in flexible wearable devices and man-machine interaction fields.

Mussel-inspired cellulose nanofiber/poly(vinyl alcohol) hydrogels with robustness, self-adhesion and antimicrobial activity for strain sensors.

Flexible strain sensors have attracted substantial attention given their application in human-computer interaction and personal health monitoring. Due to the inherent disadvantages of conventional hydrogels, the manufacture of hydrogel strain sensors with high tensile strength, excellent adhesion, self-healing and antimicrobial properties in vitro, and conductive stability is still a challenge. Herein, a conductive hydrogel consisting of polydopamine-coated cellulose nanofibers (CNF@PDA), carbon nanotubes (CNT), and polyvinyl alcohol (PVA) was developed. The CNTs in PVA/CNF@PDA/CNT hydrogels were uniformly dispersed in the presence of CNF@PDA by hydrogen bonding, resulting in a nearly threefold increase in conductivity (0.4 S/m) over hydrogels without PDA. The hydrogel exhibited satisfactory tensile properties (tensile stress up to 0.79 MPa), good fatigue resistance, self-recovery and excellent antimicrobial activity in vitro. It showed excellent adhesion, especially the adhesion strength of pigskin was increased to 27 kPa. In addition, the hydrogel was used as a strain sensor, exhibiting excellent strain sensitivity (strain coefficient = 2.29), fast response (150 ms), and great durability (over 1000 cycles). The fabricated strain sensors can detect both large and subtle human movements (e.g., wrist bending and vocalization) with stable and repeatable electrical signals, indicating potential applications in personal health monitoring.

Self-healing hydrogel with multiple adhesion as sensors for winter sports.

Hydrogels are widely used as sensors in the field of wearable devices. However, the hydrogels were rarely designed to endure the harsh outdoor environment in winter, including extremely low temperature, ultraviolet (UV) radiation and variable humidity. In addition, physical damage is also a challenge for hydrogels. In this study, a self-healing hydrogel with adhesion was prepared as a sensor for winter sports using a one-pot method. Polyvinyl alcohol was used as the hydrogel matrix, providing the hydrogel preferable self-healing properties and adhesion to various surfaces such as porcine skin, metal, glass, and plastic. Lithium chloride was used for the chain entanglement of polyvinyl alcohol, forming a hydrogel with excellent ionic conductivity (24.29 S m-1 at room temperature, 13.45 S m-1 under -18 ℃) to detect human motion and temperature changes. Together with ethylene glycol, lithium chloride also provided successful water retention ability and frost resistance. The hydrogel remained stable after 30 d of storage at room temperature and -18 ℃. Sodium lignosulfonate was introduced to improve the mechanical properties and ultraviolet (UV) resistance of hydrogel, created nearly 100% UV shielding with a thickness of 0.5 mm. These advantages provide great potential to the hydrogel for application in flexible wearable devices for winter sports.

Frost-resistant and ultrasensitive strain sensor based on a tannic acid-nanocellulose/sulfonated carbon nanotube-reinforced polyvinyl alcohol hydrogel.

The operating temperature of hydrogels, especially at low temperatures, is crucial due to their wide applicability in soft robots, sensors, and electronic skin. Hydrogels are often used at room temperature, but their performance may deteriorate at low temperatures. Therefore, it is crucial to develop hydrogels that can be used at low temperatures to expand their range of use. Herein, we have proposed a simple one-pot method to prepare a frost-resistant (-70 °C) and conductive hydrogel consisting of a glycerol (Gly)-water binary solvent. We have added tannic acid (TA)-coated carboxymethylated cellulose nanofibrils (CMCNFs) to poly (vinyl alcohol) (PVA) as a functional filler to improve the hydrogel's mechanical properties. The introduction of sulfonated carbon nanotubes (SCNT) has provided the hydrogel with high conductivity (0.1 S/m), strain sensitivity (gauge factor of 3.76), and cyclic stability (1600 cycles). Due to the strong hydrogen bonding and physical entanglement effects between the components, the hydrogel exhibied excellent tensile properties (297 %), high toughness (0.44 MJ/m3), and a high Young's modulus (1.25 MPa). These characteristics ensure that the hydrogel is well suited for low-temperature environments, health monitoring, and wearable devices.