Search

Effective glucose surveillance provides a strong guarantee for the high-quality development of human health. Au nanomaterials possess compelling applications in nonenzymatic electrochemical glucose biosensors owing to superior catalytic performances and intriguing biocompatibility properties. However, it has been a grand challenge to accurately control the architecture and composition of Au nanomaterials to optimize their optical, electronic, and magnetic properties for further improving the performance of electrocatalytic sensing. Herein, ultra-low content Bi-anchored Au aerogels are synthesized via a one-step reduction strategy. Benefiting from the unique structure of aerogels as well as the synergistic effect between Au and Bi, the optimized Au

In this study, a novel donor-acceptor conjugated polymer PDPPDTP was designed and synthesized by D-A polymerization using 2,6-di(trimethyltin)

Organic ligands can induce p–d orbital hybridization at the interface of CoFe LDH, resulting in a downshift of the d-band center of CoFe LDH and the optimization of the binding strength of intermediates during the OER.

The large-scale application of nanozymes remains a significant challenge owing to their unsatisfactory catalytic performances. Featuring a unique electronic structure and coordination environment, single-atom nanozymes provide great opportunities to vividly mimic the specific metal catalytic center of natural enzymes and achieve superior enzyme-like activity. In this study, the spin state engineering of Fe single-atom nanozymes (FeNC) is employed to enhance their peroxidase-like activity. Pd nanoclusters (Pd

Benefiting from the merits of high stability and superior activity, nanozymes are recognized as promising alternatives to natural enzymes. Despite the great leaps in the field of therapy and colorimetric sensing, the development of highly sensitive nanozyme-involved photoelectrochemical (PEC) biosensors is still in its infancy. Specifically, the investigation of multifunctional nanozymes facilitating different catalytic reactions remains largely unexplored due to the difficulty in synergistically amplifying the PEC signals. In this work, mesoporous trimetallic AuPtPd nanospheres were synthesized with both efficient oxidase and peroxidase-like activities, which can synergistically catalyze the oxidation of 4-chloro-1-naphthol to produce benzo-4-chlorohexadienone precipitation on the surface of photoactive materials, and thus lead to the decreased photocurrent as well as increased charge-transfer resistance. Inspired by the proton-dependent catalytic activity of nanozymes, a self-regulated dual-modal PEC and electrochemical bioassay of urease activity was innovatively established by in situ regulating the activity of AuPtPd nanozymes through urease-mediated proton-consuming enzymatic reactions, which can remarkably improve the accuracy of the assay. Meanwhile, the determination of urease activity in spiked human saliva samples was successfully realized, indicating the reliability of the biosensor and its application prospects in clinical diagnosis.

Graphite carbon nitride (g-C3N4) is a significant non-metal photocatalyst, but still challenging for photocatalytic degradation of pollutants because of its poor visible light utilization, easy recombination of photo-generated carriers and low surface reactive reaction sites. In this paper, perylene diimide (PDI), an electron-deficient building block for constructing n-type organic semiconductors, was introduced into the framework of g-C3N4 (PDI-g-C3N4) to build polymer with donor–acceptor structure for energy band amelioration, achieving the most expanded visible light response up to date. Besides, a large dihedral angle (90°) induced by PDI moiety in PDI-g-C3N4 changes the molecular aggregation behavior according to calculations, which is advantageous to increase surface area for the reactive site exposure. The most promising functional photocatalyst PDI-g-C3N4/MIL is constructed by in-situ generation of NH2-MIL-53(Fe) on the surface of PDI-g-C3N4 to further facilitate the separation and transfer of interfacial photo-induced carriers. Through a finely adjusting ratio of PDI-g-C3N4 in heterojunction, the target material of PDI-g-C3N4/MIL exhibits superior activity for the photodegradation of organic pollutants in the presence of H2O2 and visible light illumination, providing potential direction in practical application for wastewater treatment.

With high activity and specificity to conduct catalysis under mild conditions, enzymes show great promise in many fields. However, they are not acclimatized to environments in practice after leaving the familiar biological conditions. Aiming at this issue, nanobiocatalysis, a fresh area integrating nanotechnology and enzymatic catalysis, is expected to design biocatalysis based on materials science. Specifically, nano-integrated biocatalysis and bio-inspired nanocatalysis are considered as two effective nanobiocatalytic systems to meet different design needs. Notably, both systems are not entirely separated, and the combination of both further sparks more possibilities. This review summarizes the type, construction, and function of nanobiocatalytic systems, analyzing the pros and cons of different strategies. Moreover, the corresponding applications in bioassay, biotherapy, and environmental remediation are highlighted. We hope that the advent of nanobiocatalysis will help in grasping the inherence of biocatalysis and propel biocatalytic applications.

At present, enzyme-mediated signal amplification strategies have been widely applied in photoelectrochemical (PEC) biosensing systems, while the introduction of natural enzymes onto the surface of photoelectrodes inevitably obstructs the electron transfer due to their insulating properties as proteins, leading to severe damage to photocurrent. In this work, the PdPt bimetallic nanozymes with the efficient peroxidase-like activity were used as alternatives to natural enzymes and amplified PEC biosensing signals via their efficient enzymatic reaction and remarkable enhancement in photocurrent. As a result, photoactive CdS nanorods modified with PdPt bimetallic nanozymes showed a boosted PEC performance compared with the pristine CdS nanorods due to the localized surface plasmon resonance effect and Schottky junction. On the basis of the as-prepared CdS/PdPt photoelectrode, a sensitive split-type glucose oxidase-mediated PEC immunoassay for carcinoembryonic antigen (CEA) detection was successfully constructed. Along with the sandwich immunocomplexing, the subsequently produced hydrogen peroxide (H2O2) can oxidize 4-chloro-1-naphthol into insoluble precipitates to inhibit photocurrent and simultaneously trigger the bio-etching of CdS to further restrain photocurrent signals due to the excellent peroxidase-mimicking activity of PdPt nanozymes. Owing to the synergistic signal amplification fulfilled by PdPt nanozymes, an ultrasensitive immunoassay of CEA was realized with a wider linear range from 1 to 5000 pg/mL and a low detection limit of 0.21 pg/mL, opening a new avenue for building ultrasensitive PEC biosensors with nanozymes.

The conventional cathodic electrochemiluminescence (ECL) always requires a more negative potential to trigger strong emission, which inevitably damages the bioactivity of targets and decreases the sensitivity and specificity. In this work, iron single-atom catalysts (Fe-N-C SACs) were employed as an efficient co-reaction accelerator for the first time to achieve the impressively cathodic emission of a luminol-H

Tris(bipyridine) ruthenium(II)-based luminophores have been well developed in the area of electrochemiluminescence, while their applications in chemiluminescence (CL) are rarely studied due to the poor luminous efficiency and complicated CL reaction. Herein, a novel tris(bipyridine) ruthenium(II)-based ternary CL system is proposed by introducing cobalt single atoms integrated with graphene-encapsulated cobalt nanoparticles (Co SAs/Co@C) and peroxymonosulfate (PMS) as advanced coreaction accelerator and promising coreactant, respectively. On the basis of the experimental results and density functional theory calculations, it is concluded that Co@C can synergistically modulate the adsorption behavior of PMS on Co SAs and then efficiently activate PMS to produce massive singlet oxygen for remarkable CL emission. Under the optimum conditions, the as-prepared CL biosensor exhibits a good linear range, excellent sensitivity, and selectivity, holding great potential for the practical detection of prostate-specific antigen in human serum.

A highly sensitive photoelectrochemical (PEC) sensing platform was constructed for Hg2+ determination based on the Schottky heterojunction between an emerging 2D material Ti3C2TX MXene and a promising semiconductor material BiVO4. Through simply spin-coating the single-layer Ti3C2TX onto the surface of BiVO4 film, the modified electrode exhibited significantly enhanced PEC activity. However, the boost in photocurrent could be noticeably suppressed due to the consumption of hole-scavenging agents (reduced glutathione) by the added Hg2+. Owing to the selective decrease in the photocurrent with the addition of Hg2+, the PEC sensor based on BiVO4/Ti3C2TX displayed a wide linear range from 1 pM to 2 nM with the limit of detection down to 1 pM. Moreover, the PEC sensor also exhibited satisfactory accuracy and repeatability in practical sample water, the Yangtze River water, demonstrating the great potential for monitoring heavy metal ions in natural water resources.

The traditional luminol-H2 O2 electrochemiluminescence (ECL) sensing platform suffers from self-decomposition of H2 O2 at room temperature, hampering its application for quantitative analysis. In this work, for the first time we employ iron single-atom catalysts (Fe-N-C SACs) as an advanced co-reactant accelerator to directly reduce the dissolved oxygen (O2 ) to reactive oxygen species (ROS). Owing to the unique electronic structure and catalytic activity of Fe-N-C SACs, large amounts of ROS are efficiently produced, which then react with the luminol anion radical and significantly amplify the luminol ECL emission. Under the optimum conditions, a Fe-N-C SACs-luminol ECL sensor for antioxidant capacity measurement was developed with a good linear range from 0.8 μm to 1.0 mm of Trolox.

High-performance broadband photodetectors based on low-bandgap conjugated polymers are scarce due to a trade-off between the photoresponse range and device performance. In this work, the polymers with structural features responsible for both broad response and high detectivity are realized by using the combined electron deficient moieties at the molecular level. Based on the electron-deficient diketopyrrolopyrrole (DPP) and benzothiadiazole (BT), the combined units of DPP–DPP and DPP–BT–DPP are deemed more electron deficient and were successfully incorporated into the corresponding polymers. The arrangement of electron deficient moieties in the polymer main chain was found to be able to greatly affect the absorption profile, energy level, molecular stacking, and blend film morphology. Consequently, the photodetector based on the polymer with a DPP–BT–DPP acceptor exhibited a D* value of over 1012 Jones in the spectral region of 320–930 nm under −0.1 V bias.

In electrochemiluminescence sensing platforms, co-reaction accelerators are specific materials used to catalyze the dissociation of co-reactants into active radicals, which can significantly boost the ECL emission of luminophores. Deep insight into the correlation between the structure and ECL performance will guide the rational design of highly active co-reaction accelerators, which is imperative for constructing sensitive and reliable ECL biosensors. In this review, a brief introduction about the basic ECL mechanisms based on the co-reactant pathway is presented. After that, recent developments with various co-reaction accelerators are further discussed regarding different luminophore systems, including luminol, g-C3N4, quantum dots, nanoclusters and others. Furthermore, synergistic amplification strategies based on efficient co-reaction accelerators and enzyme immune and hybrid chain reactions are elucidated. Finally, the outlook for the preparation of high-performance ECL sensors with efficient co-reaction accelerators is discussed as well.

The investigations on the generation, separation, and interfacial-redox-reaction processes of the photoinduced carriers are of paramount importance for realizing efficient photoelectrochemical (PEC) detection. However, the sluggish interfacial reactions of the photogenerated carriers, combined with the need for appropriate photoactive layers for sensing, remain challenges for the construction of advanced PEC platforms. Here, as a proof of concept, well-defined Fe single-atom catalysts (Fe SACs) were integrated on the surface of semiconductors, which amplified the PEC signals

Tremendous efforts have been made in developing single-atomic site catalysts (SASCs) for oxygen reduction reaction (ORR), which is regarded as a pivotal cornerstone in electrochemical energy conversion. However, SASCs for ORR have not been explored for electrochemical sensing. Herein, a template-sacrificed strategy is reported for the synthesis of atomically dispersed Ir SASCs, serving as a sensing platform to detect organophosphorus pesticides (OPs) with high sensitivity and selectivity. Owing to abundant Ir single-atom active sites, Ir SASCs show excellent ORR activity and stability in a neutral medium. It is found that the ORR activity of Ir SASCs can be inhibited by thiocholine, which is the hydrolysate of acetylthiocholine. After being integrated with acetylcholinesterase (AChE), the AChE-Ir SASC-based electrochemical sensor is established and shows a superior sensitivity, which shows a wide detection range of 0.5-500 ng mL

Photoelectrochemical (PEC) enzymatic biosensors integrate the excellent selectivity of enzymes and high sensitivity of PEC bioanalysis, while the shortcomings of high cost, poor stability, as well as tedious immobilization of natural enzymes on photoelectrodes, severely suppress their applications. AgCu@CuO aerogel-based photoelectrode material with both remarkable enzyme-like activities and outstanding photoelectric properties was innovatively designed and synthesized to evaluate the activity of xanthine oxidase with a wide linear detection range and a low limit of detection.

Developing effective electrocatalysts to achieve highly sensitive and selective detection of heavy metal ions is one of the challenges in the field of environmental monitoring. Herein, bismuth (Bi) metallene (Bi-ene) in atomic thickness is successfully synthesized and applied as a conceptual application in electrochemical sensors for the detection of lead ion (Pb

Lead selenide (PbSe) colloidal quantum dots (CQDs) are promising candidates for optoelectronic applications. To date, PbSe CQDs capped by halide ligands exhibit improved stability and solar cells using these CQDs as active layers have reported a remarkable power conversion efficiency (PCE) up to 10%. However, PbSe CQDs are more prone to oxidation, requiring delicate control over their processability and compromising their applications. Herein, an efficient strategy that addresses this issue by an in situ cation-exchange process is reported. This is achieved by a two-phase ligand exchange process where PbI

Luminol-dissolved O2 electrochemiluminescence (ECL)-sensing platforms have been widely developed for sensitive and reliable detection, while their actual ECL mechanisms are still in controversy due to the involved multiple reactive oxygen species (ROS). Different from the structural complexity of nanomaterials, well-defined single-atom catalysts (SACs) as coreaction accelerators will provide great prospects for investigating the ECL mechanism at the atomic level. Herein, two carbon-supported nickel SACs with the active centers of Ni-N4 (Ni-N4/C) and Ni-N2O2 (Ni-N2O2/C) were synthesized as efficient coreaction accelerators to enhance the ECL signals of a luminol-dissolved O2 system. By modulating the surrounding environment of the center metal atoms, their corresponding oxygen reduction behaviors can be well controlled to selectively produce intermediate ROS, giving a great chance to study the following ECL process. According to the experimental and calculated results, the superoxide radical (O2•-) acts as the main radical for the ECL reaction and the Ni-N4/C catalyst with the four-electron pathway to activate dissolved O2 is preferential to enhance ECL emission.

Benefiting from the maximum atom-utilization efficiency and distinct structural features, single-atom catalysts open a new avenue for the design of more functional catalysts, whereas their bioapplications are still in their infancy. Due to the advantages, platinum single atoms supported by cadmium sulfide nanorods (Pt SAs-CdS) are synthesized to build an ultrasensitive photoelectrochemical (PEC) biosensing platform. With the decoration of Pt SAs, the PEC signal of CdS is significantly boosted. Furthermore, theory calculations indicate the positively charged Pt SAs could change the charge distribution and increase the excited carrier density of CdS. Meanwhile, it also suggests that Cu2+ can severely hinder the photoexcitation and electron-hole separation of CdS. As a proof of concept, prostate-specific antigen is chosen as the target analyte to demonstrate the superiority of the Pt SAs-CdS-based PEC sensing system. As a result, the PEC biosensor based on Pt SAs-CdS exhibits outstanding detection sensitivity and promising applicability.

Cell-free enzymatic catalysis (CFEC) is emerging biotechnology that simulates biological transformations without living cells. However, the high cost of separation and preparation of the enzyme has hindered the practical application of the CFEC. Enzyme immobilization technologies using solid supports to stabilize enzymes have been regarded as an efficient strategy to address this issue. Nevertheless, the activity and stability of the immobilized enzymes are still crucial challenges for working in vitro. Herein, an enzyme immobilization platform is developed by using PtCu hydrogels coated with amorphous metallic-organic frameworks (MOFs) as multifunctional carriers to encapsulate horseradish peroxidase (HRP). Specifically, PtCu hydrogels acting as a "reservoir of metal ions" can interact with the immobilized enzyme and facilitate electron transfer, leading to the boosted enzyme catalytic performances. Furthermore, amorphous MOFs on the surface of PtCu hydrogels serve as an "armor" to protect the internal enzymes from various perturbation environments. The resultant enzyme immobilization platform (PtCu@HRP@ZIF-8) not only shows an approximately 2.4-fold enhanced activity compared with free enzyme but also exhibits improved stability against harsh conditions. The PtCu@HRP@ZIF-8-based biosensor is constructed for sensitive sensing of organophosphorus pesticides (OPs). The proposed biosensor exhibits a favorable linear relationship with the concentration of paraoxon-ethyl from 6 to 800 ng/mL, with a low detection limit of 1.8 ng/mL. This work reveals the promising potential of our proposed enzyme immobilization platform in practical applications.

Multiple enzymes-induced biological cascade catalysis guides efficient and selective substrate transformations in vivo. The biomimetic cascade systems, as ingenious strategies for signal transduction and amplification, have a wide range of applications in biosensing. However, the fragile nature of enzymes greatly limits their wide applications. In this regard, metal-organic frameworks (MOFs) with porous structures, unique nano/microenvironments, and good biocompatibility have been skillfully used as carriers to immobilize enzymes for shielding them against hash surroundings and improving the catalytic efficiency. For another, nanomaterials with enzyme-like properties and brilliant stabilities (nanozymes), have been widely applied to ameliorate the low stability of the enzymes. Inheriting the abovementioned merits of MOFs, the performances of MOFs-immboilized nanozymes could be significantly enhanced. Furthermore, in addition to carriers, some MOFs can also serve as nanozymes, expanding their applications in cascade systems. Herein, recent advances in the fabrication of efficient MOFs-involving enzymes/nanozymes cascade systems and biosensing applications are highlighted. Integrating diversified signal output modes, including colorimetry, electrochemistry, fluorescence, chemiluminescence, and surface-enhanced Raman scattering, sensitive detection of various targets (including biological molecules, environmental pollutants, enzyme activities, and so on) are realized. Finally, challenges and opportunities about further constructions and applications of MOFs-involving cascade reaction systems are briefly put forward.

Generally, the photoactive materials are always tightly fixed on the photoelectrode of photoelectrochemical (PEC) sensors to produce excellent photocurrent response, while obvious and constant background currents will appear as well and then hamper the ultrasensitive sensing of target molecules. In this work, ultrasensitive detection of organophosphorus pesticides (OPs) is successfully fulfilled by using dissociable photoelectrode based on CdS nanocrystal-functionalized MnO2 nanosheets. With the assistance of acetylcholinesterase (AChE), acetylthiocholine (ATCh) is hydrolyzed into thiocholine (TCh) which can effectively etch the ultrathin MnO2 nanosheets, resulting in the dissociation of MnO2–CdS from the photoelectrode. Benefiting from the dissociation of photoactive materials, the background photocurrent induced by semiconductor itself dramatically decreases. OPs, as a specific inhibitor for AChE activity, can prevent the generation of TCh and the dissociation of MnO2 nanosheets, building a relationship between OPs concentration and photocurrent. Under the optimized test conditions, the PEC sensor for the detection of paraoxon displays a wide linear range from 0.05 to 10 ng/mL with a detection limit of 0.017 ng/mL. Furthermore, the PEC sensor shows good sensitivity, stability, and promising application in practical samples.

A highly sensitive photoelectrochemical (PEC) sensing platform was constructed for Hg

Transition-metal phosphides, as the promising alternatives to noble metal catalysts, have been widely used as efficient electrocatalysts for hydrogen evolution reaction (HER). In this work, three kinds of cobalt-8-hydroxyquinoline (Coqx) with different size and nanostructures are synthesized by varying the hydrothermal conditions, which was named as Coqx-L, Coqx-M and Coqx-S according to the decreased size. Accordingly, the CoxP/NC with three different size nanostructures (CoxP/NC-L, CoxP/NC-M and CoxP/NC-S) are obtained by the sequential carbonization and phosphidation of Coqx. The X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) results imply the identical chemical composition in these catalysts with different morphologies. Thus, systematic study is carried out to reveal the relationship between catalytic performance and morphologies of materials with the same chemical composition. The experimental result indicates that the morphology of CoxP/NC plays a crucial role on the surface area and electron transfer. Finally, the catalyst of CoxP/NC-S with the smallest size nanostructrue exhibits the best HER performance with a low overpotential at current density of 10 mA/cm2 (η = 56.9 and 115.6 mV) and a small Tafel slope (52.3 and 69.3 mV/dec) in both 0.1 M HClO4 and 1.0 M KOH as well as long-term stability.

A series of n-type semiconducting conjugated polymers based on naphthalene diimide (NDI) having three different side chains, 5-decylpentadecyl, 2-octyldodecyl and 4-(2-octyldodecyloxy)phenyl, were synthesized. Experimental results showed that the subtle structural changes at the side chains can influence the molecular packing, electron mobility, blend film morphology and thus performance of bulk-heterojunction polymer photodetectors using these NDI-based polymers as acceptors. The optimized all-polymer photodetector exhibited a specific detectivity (D*) of over 1013 Jones in the spectral region of 300–800 nm under −0.1 V bias, which is among the best D* values of the reported UV–vis–NIR all-polymer photodetectors and comparable to the best fullerene-based photodetectors.

A novel strategy to fabricate Co3O4 nanosheet arrays for the oxygen evolution reaction (OER) was developed by electrodeposition of Co(OH)2 on nickel foam (NF) and subsequent in situ electrochemical oxidation into Co3O4 during the OER. The produced Co3O4@NF-15, which was further engraved with air plasma, exhibits the best performance and long-term stability.

Metal-organic framework (MOF)-based materials are regarded as potential electrocatalysts for oxygen evolution reaction (OER) resulting from the abundant pore structures, large surface area and atomically dispersed metal centers, while their coordinately saturated metal nodes are inert to electrocatalysis. In this work, creating active sites while accelerating charge transport is proposed to improve the OER properties of MOF-derived layered double hydroxides (MLDH). By using multifunctional Ti3C2 MXene as support and post-treating MOF with an etching-coprecipitating process, the resultant CoFe MLDH/Ti3C2 exhibits prominent OER performance with ultralow overpotentials of only 170 and 238 mV to achieve the current density of 10 and 100 mA/cm2, respectively. In addition, the experimental and theoretical calculation results prove the strong electronic interaction between CoFe MLDH and Ti3C2 MXene could modulate the binding strength of intermediates for OER. This work gives a direction to prepare MOF-based efficient catalysts and enhance the intrinsic activity of (oxy)hydroxide-based catalysts.

Though nanozymes are successfully applied in various areas, the increasing demands facilitate the exploitation of nanozymes possessing higher activity and more functions. Natural enzyme-linked receptors (ELRs) are critical components for signal transductions in vivo by expressing activity variations after binding with ligands. Inspired by this, the defect-engineered carbon nitrides (DCN) are reported to serve as nanozyme-linked receptors (NLRs). For one thing, cyano defects increase the enzyme-like activity by a factor of 109.5. For another, DCN-based NLRs are constructed by employing cyano groups as receptors, and variable outputs are ensued upon the addition of ion ligands. Significantly, both the cascade effect and electronic effect are demonstrated to contribute to this phenomenon. Finally, NLRs are used for pattern recognition of metal ions, indicating the signal transduction ability of NLRs as well. This work not only provides great promise of defect engineering in nanozymes, but also contributes to the design of artificial ELRs.

A series of electron-acceptor polymers, copolymers and blends were used in all-polymer BHJ photodetectors and the effect of acceptor compositions on the key device parameters of dark current density and photocurrent was investigated. Compared with acceptor polymers and polymer blends, the devices based on acceptor copolymer showed lowered dark current and higher photocurrent, due to optimal molecular stacking and morphology of the BHJ active layer. The acceptor blends tend to cause a large phase separation and rough surface of the active layer, thus leading to a low detectivity of the device. Among all the acceptor compositions studied in this work, the all-polymer BHJ photodetector based on a donor polymer (PolyD) and an acceptor copolymer (PolyAA′50) exhibited the highest specific detectivity of over 1012 Jones in the spectral region of 320–980 nm under −0.1 V bias.

A novel donor unit dithienobenzotrithiophen (DTBTT) was designed and utilized in the synthesis of a series of donor–acceptor (D–A) polymers with the thienoisoindigo-based acceptor. The relationships between the structure of polymers and the absorption spectra, electrochemistry properties, hole mobility, and photovoltaic properties of these polymers have been studied. The results showed that low-bandgap D–A polymers containing DTBTT are suitable for use in broadband polymer photodetectors. Polymer photodetectors exhibited a specific detectivity (D*) in the order of 1012 Jones, low dark current and photoresponsivity at the wavelengths from 300 to 1600 nm.

A series of random copolymers containing the two electron-withdrawing units naphthalene diimide (NDI) and diketopyrrolopyrrole (DPP) and a thiophene (T) spacer were designed and synthesized as non-fullerene acceptors for all-polymer photodetectors. Increasing the number of DPP–T segments in the polymer backbone leads to a significant red shift in maximal absorption, bandgap narrowing, better film morphology and lower dark current density. A specific detectivity over 1012 Jones in a broad spectral region of 340–960 nm under −0.1 V bias was achieved with a photodetector using a blend of a donor polymer based on dithienopyrrole and diketopyrrolopyrrole (PDTP–DPP) and a copolymer (PNDI–DPP10) as an acceptor. In comparison, the device performance was found to be better than for the one based on PDTP–DPP and the PNDI homopolymer.

A series of four low-bandgap polymers containing diketopyrrolopyrrole (DPP) and dithienopyrrole (DTP) functionalized with four different side chains of 4-phenyl, 4-octylphenyl, 4-(octyloxy)phenyl and 4-(octylthio)phenyl were synthesized. Subtle changes in the side chains of polymers are found to effectively affect the molecular stacking and crystallinity, film morphology, and photodetector performance. The best polymer photodetector displays an average external quantum efficiency (EQE) of 40% and a specific detectivity (D*) of over 1013 Jones in the spectral region of 350–960 nm under −0.1 V bias, which is among the best EQE and D* values of all the known UV–vis–NIR polymer photodetectors reported to date.