Composite Functional Materials

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Strategies on enhancing piezocatalysis performance of ZnO-based catalysts for aquatic pollutants degradation: A review

Donghai Huang, Tengfei Wu, Daoyue Xie, Huinan Che, Yanhui Ao

Composite Functional Materials, 2025, 1(1): 20250104. DOI: 10.63823/20250104

Fig. 14. (a) XRD patterns of undoped ZnO, 3%-Cl-ZnO, 5%-Cl-ZnO, 10%-Cl-ZnO and (b) an magnifying view of the ZnO (100) peak. The amplitude butterfly loop for (c) ZnO and (d) 10%-Cl-ZnO coated onto an indium tin oxide under ±10 V DC bias field along radial direction. (e) Schematic diagram for the catalytic mechanism of the ZnO and Cl-ZnO under different external conditions. Reproduced from ref. [79] (Copyright 2020, Elsevier).

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Fig. 1. Amount of publications and citations using “piezo*”, “ZnO or zinc oxide”, and “decompos* or remov* or degrad* or eliminat*” as keywords from 2004 to 2024 in Web of Science.
Fig. 2. Different strategies for enhancing the piezocatalytic performance of the ZnO-based catalysts. These inset figures are reproduced from ref. [75] (Copyright 2018, Materials Research Society); ref. [76] (Copyright 2019, Zhang et al.); ref. [77] (Copyright 2023, Elsevier Ltd.); ref. [78] (Copyright 2020, WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim); ref. [54] (Copyright 2023, Wiley-VCH GmbH); ref. [79] (Copyright 2020, Elsevier); respectively.
Fig. 3. Timeline for the typical strategies on enhancing piezocatalysis performance of ZnO-based catalysts for aquatic pollutants degradation. These inset figures are reproduced from ref. [80], [81] and [82] (Copyright 2013, 2015 and 2017, Elsevier Ltd.); ref. [83] (Copyright 2017, Elsevier B.V.); ref. [76] (Copyright 2019, Zhang et al.); ref. [84] and [85] (Copyright 2020, Elsevier B.V.); ref. [86] (Copyright 2022, The Royal Society of Chemistry); ref. [87] (Copyright 2023, Elsevier B.V.); ref. [88] and [89] (Copyright 2022 and 2023, Elsevier Ltd.); ref. [90] and [54] (Copyright 2023, Wiley-VCH GmbH); ref. [91] (Copyright 2023, Elsevier B.V.); ref. [92] (Copyright 2023, Elsevier Ltd.); respectively.
Fig. 4. (a-c) Microscopic (FESEM) images of ZnO nanoparticles (in particular nanorods), 1D microwires and multipods-like microparticles. MB degradation at 20 kHz (d) and 858 kHz (e) ultrasound in the presence of ZnO nanoparticles (ZnO-np), 1D microwires (ZnO-mw) and multipods-like microparticles (ZnO-mps) and without ZnO particles. Reproduced from ref. [145] (Copyright 2023, Troia et al.). (f) Piezoelectric potential curve versus particle size in granular nano-ZnO (ZnO NPs) under the fixed pressure of 10⁸ Pa by COMSOL simulation. (g) Piezoelectric potential curve versus length in rod-like nano-ZnO (ZnO NRs) under the fixed diameter of 40 nm and cavitation pressure of 10⁸ Pa by COMSOL simulation. Reproduced from ref. [146] (Copyright 2020, Elsevier Inc.). DCF conversion degree using ZnO1, i.e. ZnO nanorods (h) and ZnO2, i.e. star-shaped clusters (i) under ultrasound (US), ultraviolet light (UV) and both of them (UV-US). Reproduced from ref. [147] (Copyright 2021, Meroni et al.).
Fig. 5. (a-g) Schematic illustration of the two-step fabrication process of the vertically aligned ZnO NW array on a polymer matrix. (h) Picture of the as-prepared ZP film (1 × 1 in.²). Scale bar: 1 in. (i) Degradation curves of the MB dye in the presence of an ultrasonic field and UV light irradiation. (j) Schematic diagram of the piezo-photocatalytic mechanism. Reproduced from ref. [76] (Copyright 2019, Zhang et al.).
Fig. 6. (a) SEM image and (b) HRTEM image of the GZn/PQz composite. (c) The oxidation of IBF by piezoelectric catalysis with different doses of GZn/PQz catalyst. (d) General mechanism of IBF oxidation over GZn/PQz as piezoelectric catalyst, photocatalyst, and piezo-photocatalyst. Reproduced from ref. [153] (Copyright 2021, Elsevier B.V.)
Table 1. Catalytic performance of different ZnO-based composites toward pollutant degradation.
Fig. 7. (a) Piezo-photocatalytic mechanism of 2% BTO//ZO JNM under stir + light irradiation. Reproduced from ref. [87] (Copyright 2023, Elsevier B.V.). (b) mechanism schematic of RhB degradation through piezo-photocatalysis of BNT-1%ZnO. Reproduced from ref. [77] (Copyright 2023, Elsevier Ltd.). (c) Formation of p-n heterojunction between BiOI and ZnO, and probable separation process of charge carriers in the BiOI/ZnO nanorods under light and ultrasonic vibration. Reproduced from ref. [84] (Copyright 2020, Elsevier B.V.).
Fig. 8. (a) Schematic illustration of lattice structure of ZnO/MoS₂ heterojunction. (b) MO degradation efficiencies under different conditions. Energy band diagrams of ZnO/MoS₂ without stirring (c) and under stirring (e). The migration of photogenerated charge carries and production of reactive oxygen species under sole sunlight irradiation (d) and stirring-sunlight irradiation (f). Reproduced from ref. [85] (Copyright 2020, Elsevier B.V.).
Fig. 9. (a) Illustration of the synthesis process of the ZnO/Cs₂AgBiBr₆ nanorod array. (b) Degradation efficiencies of RhB using ZC0.5 under different situations (visible light, simulated sunlight, visible light with stirring, simulated sunlight with stirring) and (c) corresponding calculated k values. (d) Proposed mechanism of piezoelectric field and photosource-modulated photocatalysis of ZnO/Cs₂AgBiBr₆ S-scheme heterojunction, (i, ii) ZnO under visible light irradiation (λ > 420 nm) and (iii, iv) ZnO under simulated sunlight irradiation in ZnO/Cs₂AgBiBr₆ S-scheme heterojunction under opposite piezoelectric field directions. Reproduced from ref. [163] (Copyright 2023, Elsevier Ltd.).
Fig. 10. (a, b) TEM images of C-ZnO nanorods. (c) Element mapping images of C-ZnO nanorods. (d) The results of piezoelectric potential distribution in ZnO and C-ZnO simulated by the finite element method. (e) The degradation of BPA over C-ZnO. Reproduced from ref. [90] (Copyright 2023, Wiley-VCH GmbH). (f) Mechanism of TC degradation with ZnO/CQDs/PVDF pipe piezoelectric catalytic system. Reproduced from ref. [88] (Copyright 2022, Elsevier Ltd.).
Fig. 11. (a) Schematic of the fabrication process of the asymmetric Au-ZnO and the symmetric Au-ZnO nanorod array. (b) Piezo-photocatalytic degradation of RhB with different catalysts, and control sample without catalysts. (c) Summarized histogram of the RhB degradation under different conditions for 75 min. (d) Mechanism of the enhanced catalytic activity induced by piezotronic effect and unique asymmetric nanostructure under light illumination and ultrasound stimulation (, Schottky Barrier; and, the conduction band energy and valence band energy of ZnO, respectively;, energy of the Fermi level). Reproduced from ref. [78] (Copyright 2020, WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim).
Fig. 12. Mechanism of the enhanced catalytic performance via piezo-phototronic effect and the unique structure under ultrasonic wave and light irradiation (C_B and V_B, the conduction band and valence band of ZnO, respectively; E_F, energy of the Fermi level). (a) AZA under light irradiation. (b) AZA under concurrent ultrasonic wave and light irradiation. (c) AZP under light irradiation. (d) and (e) AZP under concurrent ultrasonic wave and light irradiation. AZA, Au/ZnO/Au; AZP, Au/ZnO/Pt. Reproduced from ref. [185] (Copyright 2022, Elsevier Ltd.).
Fig. 13. (a, b) SEM images of TB-ZnO. (c) Degradation efficiencies of IBP in different catalytic systems. (d) IBP degradation mechanism with the TB-ZnO/piezo/PMS system. Reproduced from ref. [91] (Copyright 2023, Elsevier B.V.).
Fig. 15. (a) degradation curves of LVX under different conditions. (b) Transient piezoelectric current properties of ZnO and Co-ZnO with different systems. (c) Schematic diagram of piezo-promoted PS activation. Reproduced from ref. [89] (Copyright 2023, Elsevier Ltd.).
Fig. 16. (a) Profiles of free energy for catalytic oxidation of formaldehyde onto ZnO (100) surfaces. (b) The computed transitional states and intermediate state structures for catalytic oxidation of formaldehyde onto -12% ZnO (100) surface. Reproduced from ref. [214] (Copyright 2024, Elsevier B.V.). Where -12% indicates the degree of compressive strain. (c) The charge density difference of the O₂ molecule on cobalt-loaded ZnO with varying oxygen vacancy concentrations (the isosurface is adjusted to 0.0005 eV; the blue electronic cloud indicates electron gain and the yellow electronic cloud indicates electron loss). Reproduced from ref. [215] (Copyright 2024, Ran et al.). (d) H₂O adsorption energy on ZnO sites of Au-ZnO model. (e) O₂ adsorption energy on Au sites of Au-ZnO model. Reproduced from ref. [216] (Copyright 2024, Elsevier Ltd.).
Fig. 17. In situ DRIFTS of Cu/ZnO in (a) H₂/MeOH/H₂O, Ar, and N₂O atmospheres, (b) H₂/EtOH/H₂O, Ar, and N₂O atmospheres, (c) H₂/PrOH/H₂O, Ar, and N₂O atmospheres. Reproduced from ref. [226] (Copyright 2023, Wiley-VCH GmbH). (d) Normalized XANES spectra and (e) Fourier transforms of EXAFS spectra of 1ZnO/Cu(OH)₂(“1” denotes the number of ZnO atomic layer deposition cycles) during CO₂ hydrogenation under a pressure of 0.8 MPa at different temperatures. (f)First derivative of the Zn K edge spectra of the 1ZnO/Cu(OH)₂ inverse catalyst during CO₂ hydrogenation at different temperatures. Reproduced from ref. [227] (Copyright 2022, Wiley-VCH GmbH). (g) In situ DRIFTS spectra for photocatalytic conversion of CH₄ over ZnO-AuPd_2.7%. (h) In situ EPR signals of ZnO-AuPd_2.7% collected under different environments. Reproduced from ref. [228] (Copyright 2020, American Chemical Society).
Fig. 18. Challenges and prospects of ZnO-based piezoelectric materials.

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