An environmentally friendly, low-cost, and lightweight biocompatible textile triboelectric material was made by in situ coating carbon fabric (CF) with nanostructured zinc oxide (ZnO) layers using the automatic Successive Ionic Layer Adsorption and Reaction (SILAR) method. Depending on the deposition mode, we created triboelectric CF/ZnO textiles with multidirectionally intergrown short ZnO nanorods or with arrays of ZnO nanosheets. The Raman spectra confirmed the hexagonal wurtzite structure of both types of ZnO layers and the unique a-axis texture of the nanosheets. In the developed triboelectric CF/ZnO/PET/ITO sensors, the upper tribonegative part was made of a polyethylene terephthalate film coated with a thin layer of indium-tin oxide, and the lower tribopositive part was made of CF/ZnO textile. In tests with repeated hand tapping at low frequency 1.3–13 Hz and a force of ∼ 5 N (pressure of ∼ 33 kPa), the open-circuit voltage pulses were ∼ 15 V for short ZnO nanorods and ∼ 30 V for ZnO nanosheets, their duration did not exceed a few milliseconds. Due to the nanosheet morphology of the ZnO layer, the maximum touch-induced surface charge density for the corresponding triboelectric textile (0.7 µC/m²) was almost twice than for the CF/ZnO textile with intergrown ZnO short nanorods (0.4 µC/m²). The touch sensor with ZnO nanosheets showed an output voltage of 3.6 V, a current density of 1.47 µA/cm², and a power density of 1.8 µW/cm². It can be used as a dual-mode sensor due to ability to recognize the hardness of objects by analyzing the output current peaks.

In the infrastructure of the future, based on intelligent computerized systems and control and monitoring devices, the smart home is part of the Internet of Things (IoT). However, in addition to the need to address energy consumption, the widespread adoption of smart homes may also exacerbate the growing problem of increasing amounts of non-recyclable e-waste from IoT devices. Compared to synthetic plastics, biopolymers offer many unique advantages such as robust structure, light weight, mechanical flexibility, biocompatibility, biodegradability and renewability. Biopolymers, which are abundant in natural products such as cellulose, silk fibroin, polylactic acid, chitosan, collagen, keratin, alginate, starch and gelatin, have great promise for the production of environmentally friendly Internet of Things devices. They are ideal candidates for the use of low-temperature sol–gel coating and ink-printing processes to facilitate the development of low-cost, large-area flexible electronic devices. This work presents developments known from the literature, as well as the results of original research on the use of biopolymer materials to create flexible, wearable and textile electronic devices, such as sensors, energy storage devices and nanogenerators, soft hydrogel actuators and wireless communication devices that are promising for the Internet of Things but have not yet been implemented in smart homes. Graphical Abstract

Chemiresistive ammonia gas sensors with a low limit of detection of 0.15 ppm and moisture-independent characteristics based on p-type copper iodide (CuI) semiconductor films have been developed. CuI films were deposited on glass and polyethylene terephthalate (PET) substrates using a Successive Ionic Layer Adsorption and Reaction method to fabricate CuI/glass and CuI/PET gas sensors, respectively. They have a nanoscale morphology, an excess iodine and sulfur impurity content, a zinc blende γ-CuI crystal structure with a grain size of ~34 nm and an optical band gap of about 2.95 eV. The high selective sensitivity of both sensors to NH₃ is explained by the formation of the [Cu(NH₃)₂]⁺ complex. At 5 °C, the responses to 3 ppm ammonia in air in terms of the relative resistance change were 24.5 for the CuI/glass gas sensor and 28 for the CuI/PET gas sensor, with short response times of 50 s to 210 s and recovery times of 10–70 s. The sensors have a fast response–recovery and their performance was well maintained after long-term stability testing for 45 days. After 1000 repeated bends of the flexible CuI/PET gas sensor in different directions, with bending angles up to 180° and curvature radii up to 0.25 cm, the response changes were only 3%.

In this work, to obtain textile triboelectric layers for wearable flexible triboelectric nanogenerators (TENGs), we used two modes of growing nanostructured zinc oxide (ZnO) arrays on a carbon fabric (CF) using the automatic Successive Ionic Layer Adsorption and Reaction (SILAR) method. To produce a CF/ZnO_nr triboelectric textile with an array of intergrown short ZnO nanorods, we used a pre-coating of carbon fibers with ZnO seed layers. When the ZnO layer was fabricated by automatic SILAR on bare carbon fabric, we obtained the CF/ZnO_ns textile with an array of interconnected ZnO nanosheets 50–100 nm thick. As a proof of concept, we developed and tested two prototypes of flexible vertical contact–separation mode CF/ZnO_nr/PET/ITO and CF/ZnO_ns/PET/ITO TENGs, in which a gap was involuntarily formed between the smooth PET layer and the woven carbon textile coated with nanostructured ZnO films. In pressing tests with a force of ~5 N (pressure ~33 kPa), the CF/ZnO_ns/PET/ITO TENG created a higher open-circuit voltage up to 30 V and a higher maximum surface charge density of 1.3 μC/m². In the successive press–release tests, this TENG showed an output voltage of 3.6 V, a current density of 1.47 μA/cm², and a power density of 1.8 µW/cm², confirming its effectiveness.