Interfacial Ce-S bonds enhanced Mo-doped ZnIn2S4/oxygen-deficient CeO2 S-scheme heterojunction for efficient photocatalytic overall water splitting
Junchao Zhou , Sibi Liu , Siman Mao , Yijin Wang , Fei Yan , Ruiqing Zou , Weiheng Ding , Shujie Zhang , Youzi Zhang , Xuanhua Li
InfoScience ›› 2025, Vol. 2 ›› Issue (1) : e12028
Interfacial Ce-S bonds enhanced Mo-doped ZnIn2S4/oxygen-deficient CeO2 S-scheme heterojunction for efficient photocatalytic overall water splitting
Photocatalytic overall water splitting (OWS) can convert solar energy into hydrogen (H2) and oxygen (O2), which is significant in reducing the reliance on fossil fuels. Constructing S-scheme heterojunctions is an effective method for facilitating charge transfer, but the huge interfacial charge transfer barrier poses a challenge to advance the efficiency of photocatalytic OWS. Here, a low-interfacial barrier Ce-S bond-enhanced Mo-doped ZnIn2S4/oxygen-deficient CeO2 (Mo-ZIS/OV-CeO2) S-scheme heterojunction photocatalyst was designed via a doping-defect coupling strategy. The abundant unsaturated S atoms generated by doping Mo atoms in ZnIn2S4 combine with the unpaired electrons on the Ce atom in OV-CeO2, forming the interfacial Ce-S bonds, which induce a 43% decrease in carrier transport activation energy and a 2.1-fold increase in build-in electric field intensity compared to ZIS/OV-CeO2. Reduced carrier transport activation energy and increased built-in electric field intensity provide a strong driving force for charge separation following the S-scheme pathway. Benefiting from the interfacial Ce-S bonds and the S-scheme transfer path, Mo-ZIS/OV-CeO2 exhibits H2 and O2 evolution rates of 512.7 and 256.3 μmol g-1 h-1, respectively, along with a solar-to-hydrogen efficiency of 0.14%. This study proposes an innovative insight into developing and constructing S-scheme heterojunction photocatalysts with efficient charge migration interfaces.
doping-defect coupling / interfacial bonding / overall water splitting / S-scheme heterojunction / ZnIn2S4
| [1] |
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| [2] |
|
| [3] |
|
| [4] |
|
| [5] |
|
| [6] |
|
| [7] |
|
| [8] |
|
| [9] |
|
| [10] |
|
| [11] |
|
| [12] |
|
| [13] |
|
| [14] |
|
| [15] |
|
| [16] |
|
| [17] |
|
| [18] |
|
| [19] |
|
| [20] |
|
| [21] |
|
| [22] |
|
| [23] |
|
| [24] |
|
| [25] |
|
| [26] |
|
| [27] |
|
| [28] |
|
| [29] |
|
| [30] |
|
| [31] |
|
| [32] |
|
| [33] |
|
| [34] |
|
| [35] |
|
| [36] |
|
| [37] |
|
| [38] |
|
| [39] |
|
| [40] |
|
| [41] |
|
| [42] |
|
| [43] |
|
| [44] |
|
| [45] |
|
| [46] |
|
| [47] |
|
| [48] |
|
| [49] |
|
| [50] |
|
| [51] |
|
| [52] |
|
| [53] |
|
| [54] |
|
| [55] |
|
| [56] |
|
| [57] |
|
| [58] |
|
| [59] |
|
| [60] |
|
2025 The Author(s). InfoScience published by UESTC and John Wiley & Sons Australia, Ltd.
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