Intelligent objects, autonomous factories and humans browsing the real world with artificial technology‐based capabilities is not the movie set of a new saga but what is going to happen with next‐generation electronics and bioelectronics fabricated with emerging materials, technologies, and devices. The emergence of (bio)electronics as a ubiquitous feature of an advanced modern society is posing the challenge of managing an ever‐increasing amount of e‐waste, also making the recovery more and more difficult. Thus, new design approaches are required considering that a possibly small but significant fraction of mass‐scale e‐products is inherently impossible to recover. In this perspective, organic materials and technologies can provide important solutions. This review presents and analyses green materials and technologies underpinning the development of sustainable organic transistors, which promise to become key components for Earth‐safe wide‐spread electronics and bioelectronics.

The eco-sustainable use of materials derived from agricultural and food processing waste will represent one of the most stimulating challenges shortly. Chitin and chitosan are two remarkable examples of how molecules with high added value can be extracted from food waste, such as crustaceans’ shells, fungi, mollusks, etc. This Perspective summarizes the current state of knowledge about chitin extraction, chitosan production, and hydrogel formation, highlighting the environmental critical steps in the common route (use of strong acids and basis, toxic solvents, and not eco-friendly crosslinkers). At the same time, promising green alternatives are described and analyzed. Examples are the employment of NADESs or DESs (such as choline chloride: urea or choline chloride: organic acids mixtures) for chitin extraction and dissolution, use of citric acid both in chitin extraction and hydrogel formation or utilization of natural extracts, like genipin, as green cross-linkers under mild conditions (heating at 37 °C for 12 h). In particular, this perspective aims to provide a stimulating basis for the development of processes based on the recycling and reusing of chemicals, during the different preparation steps, in line with “system chemistry” and “circular economy” principles.

In response to the European Union’s initiative toward achieving carbon neutrality, the utilization of water electrolysis for hydrogen production has emerged as a promising avenue for decarbonizing current energy systems. Among the various approaches, Solid Oxide Electrolysis Cell (SOEC) presents an attractive solution, especially due to its potential to utilize impure water sources. This study focuses on modeling a SOEC supplied with four distinct streams of treated municipal wastewaters, using the Aspen Plus software. Through the simulation analysis, it was determined that two of the wastewater streams could be effectively evaporated and treated within the cell, without generating waste liquids containing excessive pollutant concentrations. Specifically, by evaporating 27% of the first current and 10% of the second, it was estimated that 26.2 kg/m³ and 9.7 kg/m³ of green hydrogen could be produced, respectively. Considering the EU’s target for Italy is to have 5 GW of installed power capacity by 2030 and the mass flowrate of the analyzed wastewater streams, this hydrogen production could meet anywhere from 0.4% to 20% of Italy’s projected electricity demand.

Recovered ammonia, extracted from waste streams such as industrial leachates and organic waste, represents a unique opportunity to harness a sustainable, carbon-free energy resource. This paper focuses on the energy potential of ammonia recovered from waste, emphasizing its role as a critical element in the transition to a low-carbon economy. Integrating recovered ammonia into energy systems enables industries to reduce dependence on conventional ammonia production, lower greenhouse gas emissions, and advance circular economy practices. The study reviews advanced technologies for recovering ammonia from waste, as well as its application in combustion processes and fuel cells. Particular emphasis is placed on optimizing ammonia combustion to minimize nitrogen oxide (NOx) emissions and on utilizing recovered ammonia in direct ammonia fuel cells and hydrogen generation for fuel cells. Challenges associated with scaling waste recovery technologies and integrating recovered ammonia into existing energy infrastructures are critically examined. By providing an in-depth assessment of the environmental and economic benefits of using recovered ammonia as an energy source, this paper highlights its potential to decarbonize sectors such as transportation, industry, and power generation.

This study investigates the viability of developing chitosan-based hydrogels derived from waste shrimp shells for the removal of methylene blue and methyl orange, thereby transforming food waste into advanced materials for environmental remediation. Despite chitosan-based adsorbents being conventionally considered ideal for the removal of negative pollutants, through targeted functionalization with poly(3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT:PSS) at varying concentrations, we successfully enhance the hydrogels’ efficacy in also adsorbing positively charged adsorbates. Specifically, the incorporation of PEDOT:PSS at a concentration of 10% v/v emerges as a critical factor in facilitating the robust adsorption of dyes. In the case of the anionic dye methyl orange (MO, 10⁻⁵ M), the percentage of removed dye passed from 47% (for beads made of only chitosan) to 66% (for beads made of chitosan-PEDOT:PSS 10%), while, in the case of the cationic dye methylene blue (MB, 10⁻⁵ M), the percentage of removed dye passed from 52 to 100%. At the basis of this enhancement, there is an adsorption mechanism resulting from the interplay between electrostatic forces and π–π interactions. Furthermore, the synthesized functionalized hydrogels exhibit remarkable stability and reusability (at least five consecutive cycles) in the case of MB, paving the way for the development of cost-effective and sustainable adsorbents. This study highlights the potential of repurposing waste materials for environmental benefits, introducing an innovative approach to address the challenges regarding water pollution.

The selective hydrogenation of CO₂ for the production of net-zero fuels and essential chemical building blocks is a promising approach to combat climate change. Key to this endeavor is the development of catalysts with high activity and selectivity for desired hydrocarbon products in the C2–C5 range. The process involves a two-step reaction, starting with the reverse water–gas shift (RWGS) reaction and proceeding to the Fischer–Tropsch reactions under high pressure. Understanding the catalyst features that control the selectivity of these pathways is crucial for product formation, as well as identifying morphological changes in the catalysts during the reaction to optimize their performance. In this study, an innovative method for synthesizing iron–ruthenium bimetallic catalysts is introduced, capitalizing on the synergistic effects of these metals as active phases. This method leverages ionic liquids as solvents, allowing for the precise and uniform distribution of active metal phases. Advanced characterizations and extensive catalytic tests have demonstrated that the use of ionic liquids outperformed traditional colloid-based techniques, resulting in superior selectivity for target hydrocarbons. The success of this inventive approach not only advances the field of CO₂ hydrogenation catalysis, but also represents a significant stride towards sustainable e-fuel production.