Coordination polymers (CPs) are a diverse class of multi-dimensional compounds that show promise as photocatalysts for degrading dyes in polluted water. Herein, a new 1D Cd(II)-based coordination polymer with the formula [Cd(bpyp)(nba)₂] (1) (bpyp = 2,5-bis(pyrid-4-yl)pyridine and Hnba = 4-nitrobenzoic acid) is synthesized and characterized. In 1, the two carboxyl groups of two different nba⁻ ligands show μ₂-η¹:η¹ and μ₁-η¹:η¹ coordination modes to connect the Cd^II centers and sit on either side of the chain along the b direction. The produced CP 1 was utilized as the photocatalyst in the process of the photodegradation of methyl blue (MB), methyl orange (MO), rhodamine B (RhB), and methyl violet (MV) dyes when exposed to UV light. The photocatalytic degradation activities of CP 1 were analyzed, and the results suggest that it exhibits an extraordinary efficiency in the degradation of MB, MV, MO, and RhB. RhB has a 95.52% efficiency of degradation, whereas MV has a 58.92% efficiency, MO has 35.44%, and MB has 29.24%. The photodecomposition of dyes is catalyzed mostly by •O₂⁻ and •OH⁻, as shown by research involving the trapping of radicals.

The fast rise of organic pollution has posed severe health risks to human beings and toxic issues to ecosystems. Proper disposal toward these organic contaminants is significant to maintain a green and sustainable development. Among various techniques for environmental remediation, advanced oxidation processes (AOPs) can non-selectively oxidize and mineralize organic contaminants into CO₂, H₂O, and inorganic salts using free radicals that are generated from the activation of oxidants, such as persulfate, H₂O₂, O₂, peracetic acid, periodate, percarbonate, etc., while the activation of oxidants using catalysts via Fenton-type reactions is crucial for the production of reactive oxygen species (ROS), i.e., •OH, •SO₄⁻, •O₂⁻, •O₃CCH₃, •O₂CCH₃, •IO₃, •CO₃⁻, and ¹O₂. Nanoscale zero-valent iron (nZVI), with a core of Fe⁰ that performs a sustained activation effect in AOPs by gradually releasing ferrous ions, has been demonstrated as a cost-effective, high reactivity, easy recovery, easy recycling, and environmentally friendly heterogeneous catalyst of AOPs. The combination of nZVI and AOPs, providing an appropriate way for the complete degradation of organic pollutants via indiscriminate oxidation of ROS, is emerging as an important technique for environmental remediation and has received considerable attention in the last decade. The following review comprises a short survey of the most recent reports in the applications of nZVI participating AOPs, their mechanisms, and future prospects. It contains six sections, an introduction into the theme, applications of persulfate, hydrogen peroxide, oxygen, and other oxidants-based AOPs catalyzed with nZVI, and conclusions about the reported research with perspectives for future developments. Elucidation of the applications and mechanisms of nZVI-based AOPs with various oxidants may not only pave the way to more affordable AOP protocols, but may also promote exploration and fabrication of more effective and sustainable nZVI materials applicable in practical applications.

Conjugated polymer photocatalysts for hydrogen production have the advantages of an adjustable structure, strong response in the visible light region, adjustable energy levels, and easy functionalization. Using an atom- and step-economic direct C–H arylation method, dibromocyanostilbene was polymerized with thiophene, dithiophene, terthiophene, and fused thienothiophene and dithienothiophene, respectively, to produce donor–acceptor (D-A)-type linear conjugated polymers containing different thiophene derivatives with different conjugation lengths. Among them, the D-A polymer photocatalyst constructed from dithienothiophene could significantly broaden the spectral response, with a hydrogen evolution rate up to 12.15 mmol h⁻¹ g⁻¹. The results showed that the increase in the number of fused rings on thiophene building blocks was beneficial to the photocatalytic hydrogen production of cyanostyrylphene-based linear polymers. For the unfused dithiophene and terthiophene, the increase in the number of thiophene rings enabled more rotation freedom between the thiophene rings and reduced the intrinsic charge mobility, resulting in lower hydrogen production performance accordingly. This study provides a suitable process for the design of electron donors for D-A polymer photocatalysts.

A series of aggregation-induced emission (AIE)-featured phenylmethylene pyridineacetonitrile derivatives named o-DBCNPy ((Z)-3-(4-(di-p-tolylamino)phenyl)-2-(pyridin-2-yl)acrylonitrile), m-DBCNPy ((Z)-3-(4-(di-p-tolylamino)phenyl)-2-(pyridin-3-yl)acrylonitrile), and p-DBCNPy ((Z)-3-(4-(di-p-tolylamino)phenyl)-2-(pyridin-4-yl)acrylonitrile) have been synthesized by tuning the substitution position of the pyridine ring. The linkage manner of the pyridine ring had influences on the molecular configuration and conjugation, thus leading to different photophysical properties. The absorption and fluorescence emission peak showed a bathochromic shift when the linking position of the pyridine ring changed from the meta to the ortho and para position. Meanwhile, o-DBCNPy exhibited the highest fluorescence quantum yield of 0.81 and the longest fluorescence lifetime of 7.96 ns as a neat film among all three isomers. Moreover, non-doped organic light-emitting diodes (OLEDs) were assembled in which the molecules acted as the light-emitting layer. Due to the relatively prominent emission properties, the electroluminescence (EL) performance of the o-DBCNPy-based OLED was superior to those of the devices based on the other two isomers with an external quantum efficiency (EQE) of 4.31%. The results indicate that delicate molecular modulation of AIE molecules could endow them with improved photophysical properties, making them potential candidates for organic photoelectronic devices.