Citation: Xiaodie Li, Meiru Hou, Yu Fu, Lingli Wang, Yifan Wang, Dagang Lin, Qingchao Li, Dongdong Hu, Zhaohui Wang. A chronological review of photochemical reactions of ferrioxalate at the molecular level: New insights into an old story[J]. Chinese Chemical Letters, ;2023, 34(5): 107752. doi: 10.1016/j.cclet.2022.107752 shu

A chronological review of photochemical reactions of ferrioxalate at the molecular level: New insights into an old story

Xiaodie Li ^a ,
Meiru Hou ^a ,
Yu Fu ^a ,
Lingli Wang ^a ,
Yifan Wang ^a ,
Dagang Lin ^a ,
Qingchao Li ^a ,
Dongdong Hu ^a ,
Zhaohui Wang ^{a, b, c, *,}

a.
Shanghai Key Lab for Urban Ecological Processes and Eco-Restoration, School of Ecological and Environmental Sciences, East China Normal University, Shanghai 200241, China
b.
Technology Innovation Center for Land Spatial Eco-Restoration in Metropolitan Area, Ministry of Natural Resources, Shanghai 200062, China
c.
Shanghai Engineering Research Center of Biotransformation of Organic Solid Waste, Shanghai 200241, China

zhwang@des.ecnu.edu.cn

Received Date: 22 April 2022
Revised Date: 5 July 2022
Accepted Date: 16 August 2022
Available Online: 18 August 2022

Figures(4)

Owing to its outstanding photoactivity, ferrioxalate is originally used as an actinometer and subsequent work has discovered that photochemistry of ferrioxalate is also fundamentally or technically important in atmospheric chemistry and water treatment. While the overall products generated from photolysis of ferrioxalate are known to include Fe(Ⅱ), a series of oxidizing (e.g., ^•OH, O₂^•−/HO₂^•−) or reducing (C₂O₄^•−/CO₂^•−) radicals and H₂O₂, however, at the molecular level, the primary step of the photoreaction of ferrioxalate remains as an unsolved mystery due to the difficulty in examining such ultrafast processes. Benefiting from the development of time-resolved spectroscopy, this old question has been studied with increasing vigor recently, by means of such ever-more-sophisticated techniques (e.g., flash photolysis, time-resolved X-ray absorption spectroscopy (XAS), femtosecond infrared (IR) absorption spectroscopy, ultrafast photoelectron spectroscopy (PES)). There are two contrary views on the primary reaction mechanism: (1) Intramolecular electron transfer (ET) precedes the cleavage of the metal-ligand bond; (2) The dissociation of C–C or Fe–O bond occurs before intramolecular ET. Thus, this review presents a comprehensive summary about the overall reaction mechanism and molecular level mechanism of ferrioxalates. In chronological order, we have elaborated two predominant but controversial views from the perspectives of different experimental approaches. Some challenges and research opportunities in this active field are also briefly discussed.
- Ferrioxalate,
- Photolysis,
- Ligand-to-metal charge transfer (LMCT),
- Time-resolved spectroscopy
1. [1]
  K. Kawamura, S. Steinberg, I. Kaplan, Int. J. Environ. Anal. Chem. 19 (1985) 175–188. doi: 10.1080/03067318508077028
2. [2]
  J. Calvert, A. Lazrus, G. Kok, et al., Nature 317 (1985) 27–35. doi: 10.1038/317027a0
3. [3]
  T. Fox, N. Comerford, Soil Sci. Soc. Am. J. 54 (1990) 1139–1144. doi: 10.2136/sssaj1990.03615995005400040037x
4. [4]
  Y. Zuo, J. Hoigne, Environ. Sci. Technol. 26 (1992) 1014–1022. doi: 10.1021/es00029a022
5. [5]
  K. Kawamura, S. Bikkina, Atmos. Res. 170 (2016) 140–160. doi: 10.1016/j.atmosres.2015.11.018
6. [6]
  J. Yu, X. Huang, J. Xu, M. Hu, Environ. Sci. Technol. 39 (2005) 128–33. doi: 10.1021/es049559f
7. [7]
  A.M. Carlton, B. Turpin, K. Altieri, et al., Atmos. Environ. 41 (2007) 7588–7602. doi: 10.1016/j.atmosenv.2007.05.035
8. [8]
  B. Laongsri, R.M. Harrison, Atmos. Environ. 71 (2013) 319–326. doi: 10.1016/j.atmosenv.2013.02.015
9. [9]
  T. Guo, K. Li, Y. Zhu, H. Gao, X. Yao, Atmos. Environ. 142 (2016) 19–31. doi: 10.1016/j.atmosenv.2016.07.026
10. [10]
  J. Meng, G. Wang, J. Li, et al., Sci. Total Environ. 493 (2014) 1088–1097. doi: 10.1016/j.scitotenv.2014.04.086
11. [11]
  H. Shen, X. Yan, M. Zhao, S. Zheng, X. Wang, Environ. Exp. Bot. 48 (2002) 1–9. doi: 10.1016/S0098-8472(02)00009-6
12. [12]
  T.A. Sokolova, Eurasian Soil Sci. 53 (2020) 580–594. doi: 10.1134/s1064229320050154
13. [13]
  B.W. Strobel, Geoderma. 99 (2001) 169–198. doi: 10.1016/S0016-7061(00)00102-6
14. [14]
  B. Faust, R. Zepp, Environ. Sci. Technol. 27 (1993) 2517–2522. doi: 10.1021/es00048a032
15. [15]
  A. Allmand, W. Webb, J. Chem. Soc. (Res. ) (1929) 1518–1531.
16. [16]
  A. Allmand, W. Webb, J. Chem. Soc. (Res. ) (1929) 1531–1537.
17. [17]
  A. Allmand, K. Young, J. Chem. Soc. (Res. ) (1931) 3079–3087.
18. [18]
  C.A. Parker, P. Roy. Soc. A Math. Phys. Sci. 220 (1953) 104–116.
19. [19]
  C.G. Hatchard, C.A. Parker, Phys. Eng. Sci. 235 (1956) 518–536.
20. [20]
  C. Parker, C. Hatchard, J. Phys. Chem. 63 (1959) 22–26. doi: 10.1021/j150571a009
21. [21]
  Z. Wang, W. Song, W. Ma, J. Zhao, Prog. Chem. 24 (2012) 423–432.
22. [22]
  H. Kuhn, S. Braslavsky, R. Schmidt, Pure Appl. Chem. 76 (2004) 2105–2146. doi: 10.1351/pac200476122105
23. [23]
  K. Aoki, Skin Res. 17 (1975) 29–33.
24. [24]
  J. Chen, H. Zhang, I. Tomov, X. Ding, P. Rentzepis, Chem. Phys. Lett. 437 (2007) 50–55. doi: 10.1016/j.cplett.2007.02.005
25. [25]
  S. Straub, P. Brünker, J. Lindner, P. Vöhringer, EPJ Web Conf. 205 (2019) 05016. doi: 10.1051/epjconf/201920505016
26. [26]
  E. Fernández, J. Figuera, A. Tobar, J. Photochem. 11 (1979) 69–71. doi: 10.1016/0047-2670(79)85008-X
27. [27]
  S. Steinberg, K. Kawamura, I. Kaplan, Int. J. Environ. Anal. Chem. 19 (1985) 251–260. doi: 10.1080/03067318508077036
28. [28]
  F. Joos, U. Baltensperger, Atmos. Environ. A Gen. Top. 25 (1991) 217–230. doi: 10.1016/0960-1686(91)90292-F
29. [29]
  Y. Zuo, Photochemistry of iron(Ⅲ)/iron(Ⅱ) complexes in atmospheric liquid phases and its environmental significance. Ph. D. Dissertation, ETH, Zurich, 1992.
30. [30]
  T. Kelly, P. Daum, S. Schwartz, J. Geophys. Res. Atmos. 90 (1985) 7861–7871. doi: 10.1029/JD090iD05p07861
31. [31]
  D. Gunz, M. Hoffmann, Atmos. Environ. Part A 24 (1990) 1601–1633. doi: 10.1016/0960-1686(90)90496-A
32. [32]
  C. Miles, P. Brezonik, Environ. Sci. Technol. 15 (1981) 1089–1095. doi: 10.1021/es00091a010
33. [33]
  R. Zepp, B. Faust, J. Hoigne, Environ. Sci. Technol. 26 (1992) 313–319. doi: 10.1021/es00026a011
34. [34]
  Z. Wang, C. Chen, W. Ma, J. Zhao, J. Phys. Chem. Lett. 3 (2012) 2044–2051. doi: 10.1021/jz3005333
35. [35]
  E. Harris, B. Sinha, P. Hoppe, et al., Atmos. Chem. Phys. 12 (2012) 407–423. doi: 10.5194/acp-12-407-2012
36. [36]
  B. Kocar, W. Inskeep, Environ. Sci. Technol. 37 (2003) 1581–1588. doi: 10.1021/es020939f
37. [37]
  S.J. Hug, H.U. Laubscher, B.R. James, Environ. Sci. Technol. 31 (1997) 160–170. doi: 10.1021/es960253l
38. [38]
  M. Lucas, J. Peres, Dyes Pigment. 74 (2007) 622–629. doi: 10.1016/j.dyepig.2006.04.005
39. [39]
  D. Prato-Garcia, R. Vasquez-Medrano, M. Hernandez-Esparza, Sol. Energy 83 (2009) 306–315. doi: 10.1016/j.solener.2008.08.005
40. [40]
  N. Klamerth, S. Malato, M.I. Maldonado, A. Agüera, A. Fernández-Alba, Catal. Today 161 (2011) 241–246. doi: 10.1016/j.cattod.2010.10.074
41. [41]
  D. Trigueros, A. Módenes, P. Souza, et al., J. Photochem. Photobiol. A 385 (2019) 112095. doi: 10.1016/j.jphotochem.2019.112095
42. [42]
  H. Bates, N. Uri, J. Am. Chem. Soc. 75 (1953) 2754–2759. doi: 10.1021/ja01107a062
43. [43]
  R. Larson, M. Schlauch, K.A. Marley, J. Agric. Food Chem. 39 (1991) 2057–2062. doi: 10.1021/jf00011a035
44. [44]
  P. Maruthamuthu, R.E. Huie, Chemosphere 30 (1995) 2199–2207. doi: 10.1016/0045-6535(95)00091-L
45. [45]
  E.G. Solozhenko, N.M. Soboleva, V.V. Goncharuk, Water Res. 29 (1995) 2206–2210. doi: 10.1016/0043-1354(95)00042-J
46. [46]
  Z.M. Li, P.J. Shea, S.D. Comfort, Chemosphere 36 (1998) 1849–1865. doi: 10.1016/S0045-6535(97)10073-X
47. [47]
  L.O. Conte, A.V. Schenone, O.M. Alfano, Environ. Sci. Pollut. Res. Int. 24 (2017) 6205–6212. doi: 10.1007/s11356-016-6400-3
48. [48]
  A.J. Exposito, J.M. Monteagudo, A. Duran, I. San Martin, L. Gonzalez, J. Hazard. Mater. 342 (2018) 597–605. doi: 10.1016/j.jhazmat.2017.08.069
49. [49]
  A. Durán, J.M. Monteagudo, A. Carnicer, I. San Martín, P. Serna, Sol. Energy Mat. Sol. C 107 (2012) 307–315. doi: 10.1016/j.solmat.2012.07.001
50. [50]
  Q. Zeng, S. Chang, M. Wang, et al., Chin. Chem. Lett. 32 (2021) 2212–2216. doi: 10.1016/j.cclet.2020.12.062
51. [51]
  Q. Zeng, S. Chang, A. Beyhaqi, et al., Nano Energy. 67 (2020) 104237. doi: 10.1016/j.nanoen.2019.104237
52. [52]
  C. Parker, Trans. Faraday Soc. 50 (1954) 1213–1221. doi: 10.1039/tf9545001213
53. [53]
  B. DeGraff, G. Cooper, J. Phys. Chem. 75 (1971) 2897–2902. doi: 10.1021/j100688a004
54. [54]
  J. Patterson, S. Perone, J. Phys. Chem. 77 (1973) 2437–2440. doi: 10.1021/j100639a015
55. [55]
  V. Nadtochenko, J. Kiwi, J. Photochem. Photobiol. A 99 (1996) 145–153. doi: 10.1016/S1010-6030(96)04377-8
56. [56]
  I. Pozdnyakov, O. Kel, V. Plyusnin, V. Grivin, N. Bazhin, J. Phys. Chem. A 112 (2008) 8316–8322. doi: 10.1021/jp8040583
57. [57]
  I.P. Pozdnyakov, A.A. Melnikov, N. Tkachenko, et al., Dalton Trans. 43 (2014) 17590–17595. doi: 10.1039/C4DT01419G
58. [58]
  J. Chen, A. Dvornikov, P. Rentzepis, J. Phy. Chem. A 113 (2009) 8818–8819. doi: 10.1021/jp809535q
59. [59]
  J. Chen, W.R. Browne, Coord. Chem. Rev. 374 (2018) 15–35. doi: 10.1016/j.ccr.2018.06.008
60. [60]
  L. Longetti, T.R. Barillot, M. Puppin, et al., Phys. Chem. Chem. Phys. 23 (2021) 25308–25316. doi: 10.1039/d1cp02872c
61. [61]
  H. Zipin, S. Speiser, Chem. Phy. Lett. 31 (1975) 102–103. doi: 10.1016/0009-2614(75)80067-4
62. [62]
  J. Šima, J. Makáňová, Coord. Chem. Rev. 160 (1997) 161–189. doi: 10.1016/S0010-8545(96)01321-5
63. [63]
  C. Weller, S. Horn, H. Herrmann, J. Photochem. Photobiol. A 268 (2013) 24–36. doi: 10.1016/j.jphotochem.2013.06.022
64. [64]
  I. Pozdnyakov, F. Wu, A. Melnikov, et al., Russ. Chem. B 62 (2013) 1579–1585. doi: 10.1007/s11172-013-0227-6
65. [65]
  P. Borer, S. Hug, J. Colloid Interfaces Sci. 416 (2014) 44–53. doi: 10.1016/j.jcis.2013.10.030
66. [66]
  R. Jamieson, S. Perone, J. Phys. Chem. 76 (1972) 830–839. doi: 10.1021/j100650a007
67. [67]
  P. Kennepohl, E. Solomon, Inorg. Chem. 42 (2003) 696–708. doi: 10.1021/ic0203320
68. [68]
  J. Chen, H. Zhang, I. Tomov, et al., J. Phys. Chem. A 111 (2007) 9326–9335. doi: 10.1021/jp0733466
69. [69]
  J. Chen, H. Zhang, I. Tomov, P. Rentzepis, Inorg. Chem. 47 (2008) 2024–2032. doi: 10.1021/ic7016566
70. [70]
  C. Brady, J. McGarvey, J. McCusker, et al., Time-resolved relaxation studies of spin crossover systems in solution. In: Spin crossover in transition metal compounds III, Top. Curr. Chem., 235, Springer, Berlin, Heidelberg, 2004, pp. 1–22.
71. [71]
  M. Khalil, M.A. Marcus, A.L. Smeigh, et al., J. Phys. Chem. A 110 (2006) 38–44. doi: 10.1021/jp055002q
72. [72]
  R.K. Pandey, S. Mukamel, J. Phys. Chem. A 111 (2007) 805–816. doi: 10.1021/jp0627022
73. [73]
  P. R G. Porter. Soc. A Math. Phys. Sci. 200 (1950) 284–300.
74. [74]
  R.G.W.N.G. Porter, Proc. R. Soc. A Math. Phys. Sci. 210 (1952) 439–460.
75. [75]
  P. Rentzepis, R.P. Jones, J. Jortner, Chem. Phys. Lett. 15 (1972) 480–482. doi: 10.1016/0009-2614(72)80353-1
76. [76]
  F. Duke, J. Am. Chem. Soc. 69 (1947) 2885–2888. doi: 10.1021/ja01203a073
77. [77]
  J.I.H. Patterson, S.P. Perone, J. Phys. Chem. 77 (1973) 2437–2440. doi: 10.1021/j100639a015
78. [78]
  C. Bressler, M. Chergui, Chem. Rev. 104 (2004) 1781–1812. doi: 10.1021/cr0206667
79. [79]
  L. Chen, Annu. Rev. Phys. Chem. 56 (2005) 221–254. doi: 10.1146/annurev.physchem.56.092503.141310
80. [80]
  G.D. Cooper, B.A. DeGraff, J. Phys. Chem. 76 (1972) 2618–2625. doi: 10.1021/j100662a027
81. [81]
  I. Pozdnyakov, O. Kel, V. Plyusnin, V. Grivin, N. Bazhin, J. Phys. Chem. A 113 (2009) 8820–8822. doi: 10.1021/jp810301g
82. [82]
  Y. Ogi, Y. Obara, T. Katayama, et al., Struct. Dyn. 2 (2015) 034901. doi: 10.1063/1.4918803
83. [83]
  S. Goldstein, J. Rabani, J. Photochem. Photobiol. A 193 (2008) 50–55. doi: 10.1016/j.jphotochem.2007.06.006
84. [84]
  C. Weller, S. Horn, H. Herrmann, J. Photochem. Photobiol. A 255 (2013) 41–49. doi: 10.1016/j.jphotochem.2013.01.014
85. [85]
  G.C. O'Neil, L. Miaja-Avila, Y.I. Joe, et al., J. Phys. Chem. Lett. 8 (2017) 1099–1104. doi: 10.1021/acs.jpclett.7b00078
86. [86]
  M. Kubin, M. Guo, T. Kroll, et al., Chem. Sci. 9 (2018) 6813–6829. doi: 10.1039/c8sc00550h
87. [87]
  C. Bressler, R. Abela, M. Chergui, Z. Krist. Cryst. Mater. 223 (2008) 307–321. doi: 10.1524/zkri.2008.0030
88. [88]
  P. Vohringer, Dalton Trans. 49 (2020) 256–266. doi: 10.1039/c9dt04165f
89. [89]
  H. Graener, A. Laubereau, Opt. Commun. 54 (1985) 141–146. doi: 10.1016/0030-4018(85)90279-2
90. [90]
  D.M. Mangiante, R.D. Schaller, P. Zarzycki, J.F. Banfield, B. Gilbert, ACS Earth Space Chem. 1 (2017) 270–276. doi: 10.1021/acsearthspacechem.7b00026
91. [91]
  S. Straub, P. Brunker, J. Lindner, P. Vohringer, Phys. Chem. Chem. Phys. 20 (2018) 21390–21403. doi: 10.1039/C8CP03824D
92. [92]
  S. Straub, P. Brunker, J. Lindner, P. Vohringer, Angew. Chem. 130 (2018) 5094–5099. doi: 10.1002/ange.201800672
93. [93]
  F.H. Pilz, J. Lindner, P. Vohringer, Phys. Chem. Chem. Phys. 21 (2019) 23803–23807. doi: 10.1039/c9cp05233j
94. [94]
  S. Straub, P. Brünker, J. Lindner, P. Vöhringer, EPJ Web of Conferences 205 (2009) 0516.
95. [95]
  O. Link, E. Lugovoy, K. Siefermann, et al., Appl. Phys. A 96 (2009) 117–135. doi: 10.1007/s00339-009-5179-1
96. [96]
  F. Buchner, A. Lübcke, N. Heine, T. Schultz, Rev. Sci. Instrum. 81 (2010) 113107. doi: 10.1063/1.3499240
97. [97]
  H. Okuyama, Y.I. Suzuki, S. Karashima, T. Suzuki, J. Chem. Phys. 145 (2016) 074502. doi: 10.1063/1.4960385
98. [98]
  A. Moguilevski, M. Wilke, G. Grell, et al., ChemPhysChem. 18 (2017) 465–469. doi: 10.1002/cphc.201601396
99. [99]
  M. Borgwardt, M. Wilke, I. Kiyan, E. Aziz, Phys. Chem. Chem. Phys. 18 (2016) 28893–28900. doi: 10.1039/C6CP05655E
100. [100]
  J. Ojeda, C. Arrell, L. Longetti, M. Chergui, J. Helbing, Phys. Chem. Chem. Phys. 19 (2017) 17052–17062. doi: 10.1039/C7CP03337K
101. [101]
  M. Chergui, J. Chem. Phys. 150 (2019) 070901. doi: 10.1063/1.5082644
1. [1]
  Yan Guo , Hongtao Bian , Le Yu , Jiani Ma , Yu Fang . Photochemical reaction mechanism of benzophenone protected guanosine at N7 position. Chinese Chemical Letters, 2025, 36(3): 109971-. doi: 10.1016/j.cclet.2024.109971
2. [2]
  Jiayin Zhou , Depeng Liu , Longqiang Li , Min Qi , Guangqiang Yin , Tao Chen . Responsive organic room-temperature phosphorescence materials for spatial-time-resolved anti-counterfeiting. Chinese Chemical Letters, 2024, 35(11): 109929-. doi: 10.1016/j.cclet.2024.109929
3. [3]
  Huizhong Wu , Ruiheng Liang , Ge Song , Zhongzheng Hu , Xuyang Zhang , Minghua Zhou . Enhanced interfacial charge transfer on Bi metal@defective Bi₂Sn₂O₇ quantum dots towards improved full-spectrum photocatalysis: A combined experimental and theoretical investigation. Chinese Chemical Letters, 2024, 35(6): 109131-. doi: 10.1016/j.cclet.2023.109131
4. [4]
  Yihu Ke , Shuai Wang , Fei Jin , Guangbo Liu , Zhiliang Jin , Noritatsu Tsubaki . Charge transfer optimization: Role of Cu-graphdiyne/NiCoMoO4 S-scheme heterojunction and Ohmic junction. Chinese Journal of Structural Chemistry, 2024, 43(12): 100458-100458. doi: 10.1016/j.cjsc.2024.100458
5. [5]
  Jieqiong Xu , Wenbin Chen , Shengkai Li , Qian Chen , Tao Wang , Yadong Shi , Shengyong Deng , Mingde Li , Peifa Wei , Zhuo Chen . Organic stoichiometric cocrystals with a subtle balance of charge-transfer degree and molecular stacking towards high-efficiency NIR photothermal conversion. Chinese Chemical Letters, 2024, 35(10): 109808-. doi: 10.1016/j.cclet.2024.109808
6. [6]
  Xiao Yu , Dongyue Cui , Mengmeng Wang , Zhaojin Wang , Mengzhu Wang , Deshuang Tu , Vladimir Bregadze , Changsheng Lu , Qiang Zhao , Runfeng Chen , Hong Yan . Boron cluster-based TADF emitter via through-space charge transfer enabling efficient orange-red electroluminescence. Chinese Chemical Letters, 2025, 36(3): 110520-. doi: 10.1016/j.cclet.2024.110520
7. [7]
  Ziyi Liu , Xunying Liu , Lubing Qin , Haozheng Chen , Ruikai Li , Zhenghua Tang . Alkynyl ligand for preparing atomically precise metal nanoclusters: Structure enrichment, property regulation, and functionality enhancement. Chinese Journal of Structural Chemistry, 2024, 43(11): 100405-100405. doi: 10.1016/j.cjsc.2024.100405
8. [8]
  Peipei CUI , Xin LI , Yilin CHEN , Zhilin CHENG , Feiyan GAO , Xu GUO , Wenning YAN , Yuchen DENG . Transition metal coordination polymers with flexible dicarboxylate ligand: Synthesis, characterization, and photoluminescence property. Chinese Journal of Inorganic Chemistry, 2024, 40(11): 2221-2231. doi: 10.11862/CJIC.20240234
9. [9]
  Zixi Zou , Jingyuan Wang , Yian Sun , Qian Wang , Da-Hui Qu . Controlling molecular assembly on time scale: Time-dependent multicolor fluorescence for information encryption. Chinese Chemical Letters, 2024, 35(7): 108972-. doi: 10.1016/j.cclet.2023.108972
10. [10]
  Ruowen Liang , Chao Zhang , Guiyang Yan . Enhancing CO2 cycloaddition through ligand functionalization: A case study of UiO-66 metal-organic frameworks. Chinese Journal of Structural Chemistry, 2024, 43(2): 100211-100211. doi: 10.1016/j.cjsc.2023.100211
11. [11]
  Ying Hou , Zhen Liu , Xiaoyan Liu , Zhiwei Sun , Zenan Wang , Hong Liu , Weijia Zhou . Laser constructed vacancy-rich TiO_2-x/Ti microfiber via enhanced interfacial charge transfer for operando extraction-SERS sensing. Chinese Chemical Letters, 2024, 35(9): 109634-. doi: 10.1016/j.cclet.2024.109634
12. [12]
  Hui Liu , Xiangyang Tang , Zhuang Cheng , Yin Hu , Yan Yan , Yangze Xu , Zihan Su , Futong Liu , Ping Lu . Constructing multifunctional deep-blue emitters with weak charge transfer excited state for high-performance non-doped blue OLEDs and single-emissive-layer hybrid white OLEDs. Chinese Chemical Letters, 2024, 35(10): 109809-. doi: 10.1016/j.cclet.2024.109809
13. [13]
  Xin Jiang , Han Jiang , Yimin Tang , Huizhu Zhang , Libin Yang , Xiuwen Wang , Bing Zhao . g-C₃N₄/TiO_2-X heterojunction with high-efficiency carrier separation and multiple charge transfer paths for ultrasensitive SERS sensing. Chinese Chemical Letters, 2024, 35(10): 109415-. doi: 10.1016/j.cclet.2023.109415
14. [14]
  Yuan Teng , Zichun Zhou , Jinghua Chen , Siying Huang , Hongyan Chen , Daibin Kuang . Dual atom-bridge effect promoting interfacial charge transfer in 2D/2D Cs₃Bi₂Br₉/BiOBr epitaxial heterojunction for efficient photocatalysis. Chinese Chemical Letters, 2025, 36(2): 110430-. doi: 10.1016/j.cclet.2024.110430
15. [15]
  Xing Xiao , Yunling Jia , Wanyu Hong , Yuqing He , Yanjun Wang , Lizhi Zhao , Huiqin An , Zhen Yin . Sulfur-defective ZnIn2S4 nanosheets decorated by TiO2 nanosheets with exposed {001} facets to accelerate charge transfer for efficient photocatalytic hydrogen evolution. Chinese Journal of Structural Chemistry, 2024, 43(12): 100474-100474. doi: 10.1016/j.cjsc.2024.100474
16. [16]
  Guixu Pan , Zhiling Xia , Ning Wang , Hejia Sun , Zhaoqi Guo , Yunfeng Li , Xin Li . Preparation of high-efficient donor-π-acceptor system with crystalline g-C3N4 as charge transfer module for enhanced photocatalytic hydrogen evolution. Chinese Journal of Structural Chemistry, 2024, 43(12): 100463-100463. doi: 10.1016/j.cjsc.2024.100463
17. [17]
  Haiyan Yin , Abdusalam Ablez , Zhuangzhuang Wang , Weian Li , Yanqi Wang , Qianqian Hu , Xiaoying Huang . Novel open-framework chalcogenide photocatalysts: Cobalt cocatalyst valence state modulating critical charge transfer pathways towards high-efficiency hydrogen evolution. Chinese Journal of Structural Chemistry, 2025, 44(4): 100560-100560. doi: 10.1016/j.cjsc.2025.100560
18. [18]
  Zili Ma , Zeyu Li , Jun Lv . Shortening the formation time of oxide thin film photoelectrodes from hours to seconds. Chinese Journal of Structural Chemistry, 2025, 44(4): 100450-100450. doi: 10.1016/j.cjsc.2024.100450
19. [19]
  Zhao-Xia Lian , Xue-Zhi Wang , Chuang-Wei Zhou , Jiayu Li , Ming-De Li , Xiao-Ping Zhou , Dan Li . Producing circularly polarized luminescence by radiative energy transfer from achiral metal-organic cage to chiral organic molecules. Chinese Chemical Letters, 2024, 35(8): 109063-. doi: 10.1016/j.cclet.2023.109063
20. [20]
  Chunxiu Yu , Zelin Wu , Hongle Shi , Lingyun Gu , Kexin Chen , Chuan-Shu He , Yang Liu , Heng Zhang , Peng Zhou , Zhaokun Xiong , Bo Lai . Insights into the electron transfer mechanisms of peroxydisulfate activation by modified metal-free acetylene black for degradation of sulfisoxazole. Chinese Chemical Letters, 2024, 35(8): 109334-. doi: 10.1016/j.cclet.2023.109334

Get Citation

PDF

XML

Metrics

PDF Downloads(9)
Abstract views(1026)
HTML views(85)

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142