Low VOC Research Articles

Investigation of the effect of autoclave aging on polyurethane foams with low VOC content

Six flexible polyurethane foam recipes using low VOC additives were formulated and the prepared samples were analysed for their mechanical and acoustic properties pre and post autoclave aging. The results were compared with a reference foam comprising traditional additives. Promising results were obtained, particularly in acoustic performance, with two formulations (W2, W3) exhibiting superior sound absorption compared to the reference sample. However, after the autoclave aging the value of the sound absorption coefficient drops suddenly in a given frequency range, which may also indicate the degradation of the cell structure. The compressive strength of the samples were lower in case of four out of six samples, which can be due to their lower density. Adjustments in foaming reaction could potentially mitigate this issue. After the autoclave aging the compressive strength significantly reduced in all cases including the reference sample, which indicates that when the foams are utilized in wet environments for extended periods of time they cannot be further used for bearing applications.

Low-frequency EIS interpretation with the potential to predict the durability of protective coatings

Obtaining impedance response with predictive value for coating durability is central to meeting today's protective coatings end-user requirements. Here we present a novel approach to interpreting the low-frequency impedance of industrial coatings that takes into account the relevance of the coating properties that determine their barrier and adhesion durability. Modern, high adhesion, low VOC polymer coatings utilize cross-linking chemistry with polar or hydrogen bonding materials, leading to the apparent paradox that coatings exhibit corrosion creep values that are very low and inversely related to the barrier effect derived from the EIS response. In practice, once the corrosion creep rate is negligible, the ability of a coating to act as a long-term effective barrier, especially at edges and welds, becomes a major concern, and the improvement in durability relies on the improvement of the barrier. In the present study, we investigated the barrier effect of conventional partial and full offshore coating systems with epoxy and epoxy mastic layers applied without and with zinc-rich or zinc phosphate primers and polyurethane topcoats. The panels were aged for two years in an atmospheric offshore-like conditions and subsequently exhibited defects due to inadequate coating thickness, number of layers, surface preparation and inadequate application practice. EIS measurements were performed on the panels in the laboratory in dry and wet state. EIS provided a quantitative rating of the barrier effect that can serve as a basis for informed upgrading of coating solutions, application practices or workmanship quality, particularly in structures with limited access where high durability is an imperative.

An Optimization Path for Sb2(S,Se)3 Solar Cells to Achieve an Efficiency Exceeding 20.

Antimony selenosulfide, denoted as Sb2(S,Se)3, has garnered attention as an eco-friendly semiconductor candidate for thin-film photovoltaics due to its light-absorbing properties. The power conversion efficiency (PCE) of Sb2(S,Se)3 solar cells has recently increased to 10.75%, but significant challenges persist, particularly in the areas of open-circuit voltage (Voc) losses and fill factor (FF) losses. This study delves into the theoretical relationship between Voc and FF, revealing that, under conditions of low Voc and FF, internal resistance has a more pronounced effect on FF compared to non-radiative recombination. To address Voc and FF losses effectively, a phased optimization strategy was devised and implemented, paving the way for Sb2(S,Se)3 solar cells with PCEs exceeding 20%. By optimizing internal resistance, the FF loss was reduced from 10.79% to 2.80%, increasing the PCE to 12.57%. Subsequently, modifying the band level at the interface resulted in an 18.75% increase in Voc, pushing the PCE above 15%. Furthermore, minimizing interface recombination reduced Voc loss to 0.45 V and FF loss to 0.96%, enabling the PCE to surpass 20%. Finally, by augmenting the absorber layer thickness to 600 nm, we fully utilized the light absorption potential of Sb2(S,Se)3, achieving an unprecedented PCE of 26.77%. This study pinpoints the key factors affecting Voc and FF losses in Sb2(S,Se)3 solar cells and outlines an optimization pathway that markedly improves device efficiency, providing a valuable reference for further development of high-performance photovoltaic applications.

Dielectric barrier discharge plasma for chlorobenzene removal: Performance optimization, process modeling, and toxicity evaluation

Bio-purification has been recognized as an effective method of removal of volatile organic pollutants (VOCs), yet exist a technical bottleneck of low removal efficiency in the treatment of high toxicity and low water-soluble VOCs, especially chlorobenzene (CB). Herein, dielectric barrier discharge (DBD) technology was used as a pre-treatment technology, and the effect of process parameters (specific input of energy (SIE), inlet concentration of CB, humidity, and discharge length) of DBD on the removal performance of CB was analyzed, in order to investigate the feasibility of DBD as a pre-treatment approach for bio-purification. Taking energy yield, by-product analysis and exhaust evaluation as considerations, an SIE of 1,131.57 J·L-1, an inlet CB concentration of 300 ppm, a humidity of 50 %, and a discharge length of 10 cm were selected as the most suitable experimental conditions for the air DBD reactor. The temperature of gas flow was analyzed. Results suggested that DBD have no adverse thermal effect on the subsequent biotechnology (decreased by about 8 K during the discharge process). The temperature change caused by the degradation of CB (e.g., phenyl ring-opening and other processes) accounts for about 90 % of the total temperature change, where remaining part of temperature decreased caused by the large number of active substances produced by electron excitation, collision and cracking during discharge. The regulation of short-life active substances (e.g., ·NO, ·NO2,·OH, and O2–·) further reduced the toxicity of the outlet gas generated by DBD through affect the contents the long-life active substances (e.g., H2O2, and O3). This study provides a better understanding of the feasibility of DBD as a treatment for bio-purification and a new coupling technology for the effective removal of CB.

Preparation of high-performance water-based ink from acrylic-modified rosin resin

This study focuses on the preparation of a water-based ink binder using acrylic-modified rosin polyethylene glycol ester (ROPEGE). This binder is characterized by a low acid value (12.23 mg NaOH/g), low viscosity (5.40 mPa s), high fixed content (92.40 %), and excellent printability. Compared to reported water-based inks, the inks derived in this study exhibit higher fixed content (resulting in lower VOC emissions), low acid value (indicating high oxidation resistance), and low viscosity (enhancing print quality). The individual effects of emulsifier type, emulsifier content, initiator type, initiator content, acrylic acid content, and dispersant content are analyzed as single factors. The optimal formulation is achieved by selecting specific components: emulsifier PEG-400 (40 wt%/ROPEGE), initiator potassium persulfate (10 wt%/ROPEGE), functional monomer acrylic acid (10 wt% of ROPEGE), and wetting and dispersing agent OT-75 (10 wt%/ROPEGE). The enhancement of the water-based ink formulation is accomplished through the use of acrylic-modified rosin resin (AMRR) as the binder, dimethyl silicone oil as the defoamer, and malachite green as the pigment.

Dual polarity open circuit voltage in triboelectric nanogenerators originated from two states series impedance

Experimental and simulation studies demonstrated that the initial voltage setting significantly influences the open-circuit voltage (VOC) in triboelectric nanogenerators (TENGs). Utilizing diode configurations, we consistently observed two distinct VOCs independent of the initial settings. A lower VOC corresponded to the surface voltage (VSurface), while a higher VOC was amplified by the product of the VSurface and the TENG's characteristic impedance ratio. Notably, a lower measurement system capacitance provided a more precise representation of the inherent characteristics of the TENG. Conversely, an increase in system impedance led to a convergence of the two VOCs and a reduction in their magnitudes relative to VSurface. These findings suggest that optimizing the initial/repeated charge balancing and minimizing capacitive loads are crucial for maximizing TENG output power in practical applications.

Recyclable azine polyurethane thermosets and carbon fiber reinforced composites with excellent thermostability and mechanical properties

Carbon fiber reinforced composites (CFRCs) have received increasingly concerns and widely used in high-end applications, owing to their outstanding mechanical properties. Most of the polymers used in CFRCs were thermosets. However, a large number of applications brought enormous wastes due to the stable structure of thermosets which is difficult to degrade or recycle. CFRCs based on dynamic covalent polymers (DCPs) were developed to resolve the recycling problem. Polyurethanes were used for fabricating CFRCs applied in energy absorbing materials, vehicle interiors, sporting goods, and constructing materials, owing to excellent toughness, bonding abilities and low VOCs. Although some recyclable PU CFRCs were developed to resolve the recycling of CFs, there remain the problems of excess catalysts, low chemical resistance or thermostability due to the dynamic feature of DCPs. Herein, a series of azine polyurethane thermosets (APUTs) were prepared from hexamethylene diisocyanate (HDI) trimer and dihydroxy azines with different lengths of carbon chains. The resulting APUTs displayed excellent thermal stabilities with all Td, 5 % exceeding 320 °C, owing to high exchange temperature of azine moieties and high crosslinking density. APUTs-6 showed the highest tensile strength of 36.72 ± 1.18 MPa. APUTs-6 could be easily degraded in 0.1 M acetone/water solution at 50 °C. APUTs-6 showed excellent reprocessing properties and tensile strength could maintain 83.1 % of its initial one. The APUTs-6/CFs composites exhibited excellent mechanical properties, chemical resistance and recyclability. CFs could be readily recycled by acid degradation and maintain excellent mechanical properties. The tensile strength of recycled composites could recover 94.36 % of the original one after two times of recycling. The recovery ratio of tensile strength of recycled CF filaments was 95.7 %. The application of phenyl azine provided a feasible solution for the industrialization of recyclable CFRCs.

Enhanced Selective Contact Behavior in a‐Si:H/oxide Transparent Photovoltaic Devices via Dipole Layer Integration

Transparent photovoltaic (TPV) devices have the potential to revolutionize photovoltaic (PV) technology by enabling on‐site generation while minimizing visual impact. However, a major challenge in the development of TPV, as well as for many PV technologies, is the open‐circuit voltage (Voc) deficit, which limits their efficiency. In this work, the development of wide‐bandgap inorganic‐based TPV devices is reported with a focus on low‐cost, earth‐abundant, stable, and nontoxic materials. The device structure consists of an ultrathin hydrogenated amorphous silicon (a‐Si:H) absorber and metal‐oxide layers as selective contacts. Herein, novel approach is presented to significantly improve device performance, especially in Voc, by introducing molecular dipoles in the device electron‐transport layer. By incorporating polyethyleneimine or poly(amidoamine) G1 and G2 dipoles, Voc (from 410 mV up to 638 mV) is significantly increased without sacrificing the average photopic transmittance of the device, leading to a record efficiency for this particular approach in TPV. Measurements confirm excellent long‐term stability. This approach can potentially allow tuning the work function of the selective contacts enabling the use of low‐cost, earth‐abundant materials that are not optimized for a particular absorber. Furthermore, this solution circumvents the issue of low Voc by a simple interface treatment.

Development of nitrogen-rich hierarchical porous carbon for high selective adsorption of methanol in multi-VOCs waste gas recovery processes

Methanol is a typical polar volatile organic compound that has been commonly used as a solvent in industrial processes and is considered as an important resource. It often appears with aromatic compounds in practical application scenarios. Conducting methanol and aromatic compounds recycle technology can provide us with a sustainable carbon source for fuels and materials well beyond the fleeting fossil fuel era. Post-synthesis modification (PSM) has been utilized to incorporate 3-amino-1,2,4-triazole (Atz) into ZIF-8, thereby enabling the derivation of mesopore structure and enhancement of nitrogen content in ZIF-8 derived carbon. With this method the obtained carbon exhibited a highly polarizable micro-mesoporous structure, resulting in high adsorption capacity for methanol adsorption at low concentrations. The experimental results showed that the VOCs adsorption on porous carbon is primarily dictated by its microporous structure at high pressure, and predominantly governed by the presence of nitrogen functional groups and the micro-mesoporous properties at low pressure. DFT theoretical analysis also showed that nitrogen functional group can improve the absorption capacity of methanol by adsorbents through changing the electron distribution and surface polarity of carbon-based materials. Finally, based on the emission properties that is low concentration and high volume of VOCs waste gas in industrial application, ZIF8-24-700 and BACs-36 materials (Wang et al., 2023) were used to further prove the feasibility of this technology under low VOCs concentration, which achieve recovery rates of 99 % for toluene and 95 % for methanol, respectively.

Segmented Control of Selenization Environment for High-Quality Cu2ZnSn(S,Se)4 Films Toward Efficient Kesterite Solar Cells.

High-crystalline-quality absorbers with fewer defects are crucial for further improvement of open-circuit voltage (VOC) and efficiency of Cu2ZnSn(S,Se)4 (CZTSSe) solar cells. However, the preparation of high-quality CZTSSe absorbers remains challenging due to the uncontrollability of the selenization reaction and the complexity of the required selenization environment for film growth. Herein, a novel segmented control strategy for the selenization environment, specifically targeting the evaporation area of Se, to regulate the selenization reactions and improve the absorber quality is proposed. The large evaporation area of Se in the initial stage of the selenization provides a great evaporation and diffusion flux for Se, which facilitates rapid phase transition reactions and enables the attainment of a single-layer thin film. The reduced evaporation area of Se in the later stage creates a soft-selenization environment for grain growth, effectively suppressing the loss of Sn and promoting element homogenization. Consequently, the mitigation of Sn-related deep-level defects on the surface and in the bulk induced by element imbalance is simultaneously achieved. This leads to a significant improvement in nonradiative recombination suppression and carrier collection enhancement, thereby enhancing the VOC. As a result, the CZTSSe device delivers an impressive efficiency of 13.77% with a low VOC deficit.

Strain Regulation of Mixed-Halide Perovskites Enables High-Performance Wide-Bandgap Photovoltaics.

Wide-bandgap mixed-halogen perovskite materials are widely used as top cells in tandem solar cells. However, serious open-circuit voltage (Voc ) loss restricts the power conversion efficiency (PCE) of wide-bandgap perovskite solar cells (PSCs). Herein, it is shown that the resulting methylammonium vacancies induce lattice distortion in methylammonium chloride-assisted perovskite film, resulting in an inhomogeneous halogen distribution and low Voc . Thus, a lattice strain regulation strategy is reported to fabricate high-performance wide-bandgap PSCs. Rubidium (Rb) cations are introduced to fill the A-site vacancy caused by the methylammonium volatilization, which alleviates shrinkage strain of the perovskite crystal. The reduced lattice distortion and increased halide ion migration barrier result in a homogeneous mixed-halide perovskite film. Due to improved carrier transport and suppressed nonradiative recombination, the Rb-treated wide-bandgap PSC (1.68eV) achieves an excellent PCE of 21.72%, accompanied by a high Voc of 1.22V. The resulting device maintains more than 90% of its initial PCE after 1500h under 1-sun illumination conditions.

Dual mechanisms based on synergistic effects of evaporation potential and streaming potential for natural water evaporation

Electricity generation by natural water evaporation generators (NWEGs) using porous materials shows great potential for energy harvesting, but mechanistic investigations of NWEGs have mostly been limited to streaming potential studies. In this study, we propose the coexistence of an evaporation potential and streaming potential in a NWEG using ZSM-5 as the generation material. The iron probe method, salt concentration regulation, solution regulation, and side evaporation area regulation were used to analyze the NWEG mechanism. Our findings revealed that a streaming potential formed as water flowed inside the ZSM-5 nanochannels, driven by electrodynamic effects that increased from the bottom to the top of the generator. In addition, an evaporation potential existed at the surface interface between ZSM-5 and water, which decreased from the bottom to the top as the evaporation height of the generator increased. The resulting open-circuit voltage (Voc) depended on the balance between the evaporation and streaming potentials, both of which were influenced by the evaporation enthalpy (Ee) or vapor pressure. Generally, a higher Ee or lower vapor pressure led to a lower evaporation potential and subsequently a lower Voc. A dual mechanism involving synergistic evaporation potential and streaming potential is proposed to explain the mechanism of NWEGs.

Cu-Doped Sb2Se3 Thin-Film Solar Cells Based on Hybrid Pulsed Electron Deposition/Radio Frequency Magnetron Sputtering Growth Techniques

In recent years, research attention has increasingly focused on thin-film photovoltaics utilizing Sb2Se3 as an ideal absorber layer. This compound is favored due to its abundance, non-toxic nature, long-term stability, and the potential to employ various cost-effective and scalable vapor deposition (PVD) routes. On the other hand, improving passivation, surface treatment and p-type carrier concentration is essential for developing high-performance and commercially viable Sb2Se3 solar cells. In this study, Cu-doped Sb2Se3 solar devices were fabricated using two distinct PVD techniques, pulsed electron deposition (PED) and radio frequency magnetron sputtering (RFMS). Furthermore, 5%Cu:Sb2Se3 films grown via PED exhibited high open-circuit voltages (VOC) of around 400 mV but very low short-circuit current densities (JSC). Conversely, RFMS-grown Sb2Se3 films resulted in low VOC values of around 300 mV and higher JSC. To enhance the photocurrent, we employed strategies involving a thin NaF layer to introduce controlled local doping at the back interface and a bilayer p-doped region grown sequentially using PED and RFMS. The optimized Sb2Se3 bilayer solar cell achieved a maximum efficiency of 5.25%.

High performance wide bandgap perovskite solar cell with low VOC deficit less than 0.4 V

Wide bandgap perovskite solar cells (PSCs) have attracted significant attention because they can be applied to the top cells of tandem solar cells. However, high open-circuit voltage (VOC) deficit (>0.4 V) result from poor crystallization and high non-radiative recombination losses become a serious limitation in the pursuit of high performance. Here, the relevance between different PbI2 proportions and performance parameters are revealed through analysis of surface morphology, residual stress, and photostability. The increase of PbI2 proportion promotes crystal growth and reduces the work function of the perovskite film surface and promotes the energy level alignment with the carrier transport layer, which decreased the VOC deficit. However, residual PbI2 exacerbated the stress level of perovskite film, and the resulting lattice disorder deteriorated the photostability of the device. Ultimately, after the synergistic passivation of residual PbI2 and PEAI, the VOC achieves 1.266 V and VOC deficit is less than 0.4 V, the record value in wide bandgap PSCs.

Methanol as an anti-solvent to improve the low open-circuit voltage of CsPbBr3 perovskite solar cells prepared with water.

CsPbBr3 has received more and more attention in the field of optoelectronic devices due to its excellent stability. To address the cost and environmental concerns associated with the use of toxic methanol, water has been explored as a substitute solvent for CsBr in the preparation of CsPbBr3 perovskite solar cells (PSCs). In this study, we utilized methanol as an anti-solvent of the CsBr/H2O solution to regulate the detrimental effects of water on the CsPbBr3 film and control the crystallization process. From results of the experiment, it was found that methanol anti-solvent treatment greatly improved the crystallization of the CsPbBr3 film, increased the grain size, and reduced the defect density. After the introduction of methanol anti-solvent treatment, the power conversion efficiency (PCE) increased from 6.09% to 7.91%, while the open-circuit voltage (Voc) increased from 1.18 V to 1.39 V. Furthermore, we incorporated 2-hydroxyethylurea into the CsPbBr3 PSCs to improve the wettability of PbBr2 towards the CsBr/H2O solution and ensure the formation of pure-phase CsPbBr3 films. The introduction of 2-hydroxyethylurea resulted in an additional increase in Voc from 1.19 V to 1.42 V. The PCE further improved from 6.56% to 8.62% after methanol anti-solvent treatment. These results demonstrate that methanol treatment effectively addresses the low Voc issue observed in CsPbBr3 PSCs prepared with water as a solvent. Importantly, this approach significantly reduces the reliance on methanol compared to conventional fabrication methods for CsPbBr3 PSCs. Overall, this work presents a promising pathway for achieving high Voc and efficiency in CsPbBr3 PSCs by utilizing water as a solvent.

Enhancement of Interfacial Properties by Indoloquinoxaline‐Based Small Molecules for Highly Efficient Wide‐Bandgap Perovskite Solar Cells

AbstractInterfacial engineering in organic–inorganic hybrid perovskite solar cells (PSCs) has attracted significant attention, aiming to achieve high‐performing and highly stable devices. Here, newly designed organic small molecules based on quinoxaline and triphenylamine for inverted type wide‐bandgap PSCs are introduced, with the objective of enhancing the interfacial properties between perovskite and NiOx hole transport layer (HTL). The incorporation of an organic interlayer effectively reduces the energy level offset between the HTL and wide‐bandgap perovskite, while passivating defects within the perovskite layer. It leads to improved charge extraction and minimized non‐radiative recombination at the interface. Furthermore, the enhanced interfacial characteristics and hydrophobicity contribute to the improvement of perovskite film quality, resulting in larger grain size and higher crystallinity. As a result, the power conversion efficiency (PCE) of the PSC is enhanced from 18.9% to 20.1% with the incorporation of the IQTPAFlu interlayer, accompanied by an increase in Voc to ≈1.3 V, achieving a significantly low Voc deficit of 0.46 V. And the IQTPAFlu‐based devices demonstrate stable and consistent performance over 500 h, with ≈91% of their initial PCE retained. The highly stable wide‐bandgap PSCs, characterized by high Voc and PCEs, hold great promise as potential candidates for tandem solar cells.

Wavelength‐Recognizable SbSI:Sb2S3 Photovoltaic Devices: Elucidation of the Mechanism and Modulation of their Characteristics

AbstractThe output of photovoltaic (PV) devices is mostly independent of the wavelength of the incident light, whereas an anomalous wavelength‐dependent photovoltaic effect (WDPE) has recently been observed in antimony chalcohalide‐chalcogenide (SbSI:Sb2S3) PVs. Remarkably, the open‐circuit voltage (VOC) exhibits a reversible change between low VOC for short wavelengths and high VOC for long wavelengths. Herein, this work presents i) insights into the underlying mechanisms of this phenomenon by electron spin resonance (ESR) measurements and ii) the switchable character of WDPE depending on the hole transport material (HTM). Operando ESR measurements with light irradiation revealed that the hole density in the HTM is significantly suppressed when the ultraviolet component is included in the irradiation light. This indicated interfacial charge recombination rather than hole transfer to the HTM under short‐wavelength light irradiation, providing a basis for understanding the mechanism of WDPE. Furthermore, the use of poly(triarylamine) as the HTM unexpectedly exhibit the opposite wavelength‐VOC dependence, where a low VOC is observed with long‐wavelength light. In addition, the introduction of a polar gas accelerated the response speed of these effects. These findings shed light on the expansion of unique wavelength‐responsive single junction devices.

Improving the Device Performance of CZTSSe Thin-Film Solar Cells via Indium Doping.

Cation incorporation emerges as a promising approach for improving the performance of the kesterite Cu2ZnSn(S,Se)4 (CZTSSe) device. Herein, we report indium (In) doping using the chemical bath deposition (CBD) technique to enhance the optoelectronic properties of CZTSSe thin-film solar cells (TFSCs). To incorporate a small amount of the In element into the CZTSSe absorber thin films, an ultrathin (<10 nm) layer of In2S3 is deposited on soft-annealed precursor (Zn-Sn-Cu) thin films prior to the sulfo-selenization process. The successful doping of In improved crystal growth and promoted the formation of larger grains. Furthermore, the CZTSSe TFSCs fabricated with In doping exhibited improved device performance. In particular, the In-CZTSSe-2-based device showed an improved power conversion efficiency (PCE) of 9.53%, open-circuit voltage (Voc) of 486 mV, and fill factor (FF) of 61% compared to the undoped device. Moreover, the small amount of In incorporated into the CZTSSe absorber demonstrated reduced nonradiative recombination, improved carrier separation, and enhanced carrier transport properties. This study suggests a simple and effective way to incorporate In to achieve high efficiency and low Voc loss.

Efficient Exciton Dissociation on Ceria Chelated Cerium-Based MOF Isogenous S-Scheme Photocatalyst for Acetaldehyde Purification.

Long-term exposure to low concentration indoor VOCs of acetaldehyde (CH3CHO) is harmful to human health. Thus, a novel isogenous heterojunction CeO2/Ce-MOF photocatalyst is synthesized via a one-step hydrothermal method for the effective elimination of CH3CHO in this work. This CeO2/Ce-MOF photocatalyst performs well in CH3CHO removal and achieves an apparent quantum efficiency of 7.15% at 420nm, which presents ≈6.7 and 3.4times superior to those generated by CeO2 and Ce-MOF, respectively. The enhanced efficiency is due to two main aspects including i) an effective photocarrier separation ability and the prolonged reaction lifetime of excitons play crucial roles and ii) the formation of an internal electric field (IEF) is sufficient to overcome the considerable exciton binding energy, and increases the exciton dissociation efficiency by up to 50.4%. Moreover, the reasonable pathways and mechanisms of CH3CHO degradation are determined by in situ DRIFTS analysis and simulated DFT calculations. Those results demonstrated that S-scheme heterojunction successfully increases the efficiency of harmful volatile organic compounds elimination, and it offers essential guidance for designing rare earth-based MOF photocatalysts.

Indoor air VOCs biofiltration by bioactive coating packed bed bioreactors

Bioactive coatings are envisaged as a promising biotechnology to tackle the emerging problem of indoor air pollution. This solution could cope with the low concentrations, the wide range of compounds and the hydrophobicity of some indoor air VOCs, which are the most important bottlenecks regarding the implementation of conventional biotechnologies for indoor air treatment. A bioactive coating-based bioreactor was tested in this study for the abatement of different VOCs (n-hexane, toluene and α-pinene) at different empty bed residence times (EBRT) and inlet VOC concentrations. The performance of this reactor was compared with a conventional biofilm-based bioreactor operated with the same microbial inoculum. After an acclimation period, the bioactive coating-based bioreactor achieved abatements of over 50% for hexane, 80% for toluene and 70% for pinene at EBRTs of 112–56 s and inlet concentrations of 9–15 mg m−3. These results were about 25, 10 and 20% lower than the highest removals recorded in the biofilm-based bioreactor. Both bioreactors experienced a decrease in VOC abatement by ∼25% for hexane, 45% for toluene and 40% for pinene, after reducing the EBRT to 28 s. When inlet VOC concentrations were progressively reduced, VOC abatement efficiencies did not improve. This fact suggested that low EBRTs and low inlet VOCs concentration hindered indoor air pollutant abatement as a result of a limited mass transfer and bioavailability. Metagenomic analyses showed that process operation with toluene, hexane and pinene as the only carbon and energy sources favored an enriched bacterial community represented by the genera Devosia, Mesorhizobium, Sphingobacterium and Mycobacterium, regardless of the bioreactor configuration. Bioactive coatings were used in this work as packing material of a conventional bioreactor, achieving satisfactory VOC abatement similar to a conventional bioreactor.