Ni, Co-Based Selenide Anchored g-C<sub>3</sub>N<sub>4</sub> for Boosting Photocatalytic Hydrogen Evolution

Citation: Zhiliang Jin, Yanbing Li, Xuqiang Hao. Ni, Co-Based Selenide Anchored g-C₃N₄ for Boosting Photocatalytic Hydrogen Evolution[J]. Acta Physico-Chimica Sinica, 2021, 37(10): 191203. doi: 10.3866/PKU.WHXB201912033 shu

Ni, Co基硒化物修饰g-C₃N₄光催化产氢研究

.
北方民族大学化学与化学工程学院，宁夏太阳能化学转化技术重点实验室，国家民委化工技术基础重点实验室，银川 750021

通讯作者: 李彦兵, 1757039358@qq.com
郝旭强, haoxuqiang@126.com

基金项目:
国家自然科学基金 21862002

国家自然科学基金 41663012

北方民族大学重大科研项目“清洁能源催化生产中的新技术、新体系” ZDZX201803

摘要: 新型高效的催化剂是突破单体光催化材料载流子低分离和转移效率的重要途径。本文将Ni₃Se₄和CoSe₂纳米粒子锚定在具有良好分散性的g-C₃N₄纳米片表面，合成了两种新的g-C₃N₄@Ni₃Se₄和g-C₃N₄@CoSe₂光催化剂并实现了原位光催化析氢。相当严重的载流子的重组导致g-C₃N₄单体展现了大约只有1.9 μmol·h^-1的极差的光催化析氢活性。Ni₃Se₄和CoSe₂纳米颗粒对于加速载流子快速分离和转移的独特作用使得在g-C₃N₄表面负载Ni₃Se₄和CoSe₂纳米粒子极大地提高了其产氢活性。G-C₃N₄@Ni₃Se₄展示了一个大约16.4 μmol·h^-1的光催化产氢活性并且g-C₃N₄@CoSe₂展现了一个大约25.6 μmol·h^-1的光催化产氢活性，这分别是g-C₃N₄单体的8倍和13倍。其中，将Ni₃Se₄和CoSe₂与g-C₃N₄耦合可以显著提高光吸收密度以及扩展光响应范围。激发态EY在g-C₃N₄@Ni₃Se₄和g-C₃N₄@CoSe₂存在时比在g-C₃N₄存在时展现了更低的荧光强度，并且在g-C₃N₄@Ni₃Se₄和g-C₃N₄@CoSe₂体系中可观察到最大的电子转移速率。相比g-C₃N₄@Ni₃Se₄@FTO和g-C₃N₄@CoSe₂@FTO电极，g-C₃N₄@@FTO显现了最小的光电流响应密度和最大的电化学，这表明在g-C₃N₄纳米片表面引入Ni₃Se₄和CoSe₂纳米颗粒增强了光生载流子的分离和转移效率，即基于g-C₃N₄的金属硒化的合成有效地抑制了光生载流子的复合以及促进了光催化水裂解制氢反应。同时，吸收带边的红移有效地降低了光激电子从价带到导带跃迁的阈值。此外，g-C₃N₄@Ni₃Se₄和g-C₃N₄@CoSe₂复合催化剂的zeta电位比g-C₃N₄的更负，说明样品表面对质子增强的吸附。并且密度泛函理论结果表明：g-C₃N₄中N位点对H的吸附能为-0.22 eV，还发现氢原子更倾向于吸附在两个硒原子的桥位点上形成Se―H―Se键，并且吸附能为1.53 eV。所有对样品进行的透射电子显微镜(TEM)、扫描电子显微镜(SEM)、X射线光电子能谱(XPS)、X射线衍射(XRD)、紫外可见漫反射光谱(UV-Vis-DRS)、瞬态光电流、傅立叶变换红外光谱(FT-IR)等相关表征都展示了彼此匹配的结果。

关键词:

Ni₃Se₄
/ CoSe₂
/ g-C₃N₄
/ 析氢

English

Ni, Co-Based Selenide Anchored g-C₃N₄ for Boosting Photocatalytic Hydrogen Evolution

School of Chemistry and Chemical Engineering, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, Ningxia Key Laboratory of Solar Chemical Conversion Technology, North Minzu University, Yinchuan 750021, China

Corresponding author: Yanbing Li, 1757039358@qq.com Xuqiang Hao, haoxuqiang@126.com

Received Date: 11 December 2019
Revised Date: 05 January 2020
Available Online: 15 October 2021
Fund Project:

Abstract: Developing novel and efficient catalysts is a significant way to break the bottleneck of low separation and transfer efficiency of charge carriers in pristine photocatalysts. Here, two fresh photocatalysts, g-C₃N₄@Ni₃Se₄ and g-C₃N₄@CoSe₂ hybrids, are first synthesized by anchoring Ni₃Se₄ and CoSe₂ nanoparticles on the surface of well-dispersed g-C₃N₄ nanosheets. The resulting materials show excellent performance for photocatalytic in situ hydrogen generation. Pristine g-C₃N₄ has poor photocatalytic hydrogen evolution activity (about 1.9 μmol·h^-1) because of the rapid recombination of electron-hole pairs. However, the hydrogen generation activity is well improved after growing Ni₃Se₄ and CoSe₂ on the surface of g-C₃N₄, owing to the unique effect of these selenides in accelerating the separation and migration of charge carriers. The hydrogen production activities of G-C₃N₄@Ni₃Se₄ and g-C₃N₄@CoSe₂ are about 16.4 μmol·h^-1 and 25.6 μmol·h^-1, which are 8-fold and 13-fold that of pristine g-C₃N₄, respectively. In detail, coupling Ni₃Se₄ and CoSe₂ with g-C₃N₄ greatly improves the light absorbance density and extends the light response region. The photoluminescence intensity of the photoexcited Eosin Y dye in the presence of g-C₃N₄@Ni₃Se₄ and g-C₃N₄@CoSe₂ is weaker than that in the presence of pure g-C₃N₄. On the other hand, the upper limit of the electron-transfer rate constants in the presence of g-C₃N₄@Ni₃Se₄ and g-C₃N₄@CoSe₂ is greater than that in the presence of pure g-C₃N₄. Among the g-C₃N₄@Ni₃Se₄@FTO, g-C₃N₄@CoSe₂@FTO, and g-C₃N₄@FTO electrodes, the g-C₃N₄@FTO electrode has the lowest photocurrent density and the highest electrochemical impedance, implying that the introduction of CoSe₂ and Ni₃Se₄ onto the surface of g-C₃N₄ enhances the separation and transfer efficiency of photogenerated charge carriers. In other words, the formation of two star metals selenide based on g-C₃N₄ can efficiently inhibit the recombination of photogenerated charge carriers and accelerate photocatalytic water splitting to generate H₂. Meanwhile, the right shift of the absorption band edge effectively reduces the transition threshold of the photoexcited electrons from the valence band to the conduction band. In addition, the more negative zeta potential for the g-C₃N₄@Ni₃Se₄ and g-C₃N₄@CoSe₂ catalysts as compared with that for pure g-C₃N₄ leads to a notable enhancement in the adsorption of protons by the sample surface. Moreover, the results of density functional theory calculations indicate that the hydrogen adsorption energy of the N sites in g-C₃N₄ is -0.22 eV; further, the hydrogen atoms are preferentially adsorbed at the bridge site of two selenium atoms to form a Se―H―Se bond, and the adsorption energy is 1.53 eV. In-depth characterization has been carried out by transmission electron microscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, X-ray diffraction, ultraviolet-visible diffuse reflectance spectroscopy, transient photocurrent measurements, and Fourier transform infrared spectroscopy; the results of these experiments are in good agreement with one another.

Key words:

1. [1]
  Fang, Y. X.; Xu, Y. T.; Li, X. C.; Ma, Y. W.; Wang, X. C. Angew. Chem. Int. Edit. 2018, 57, 9749. doi: 10.1002/anie.201804530
2. [2]
  Cui, Y.; Pan, Y. X.; Qin, H. L.; Cong, H. P.; Yu, S. H. Small Methods 2018, 2, 1800029. doi: 10.1002/smtd.201800029
3. [3]
  Batmunkh, M.; Shrestha, A.; Bat-Erdene, M.; Nine, M. J.; Shearer, C. J.; Gibson, C. T.; Slattery, A. D.; Tawfik, S. A.; Ford, M. J.; Dai, S.; et al. Angew. Chem. Int. Edit. 2018, 57, 2644. doi: 10.1002/anie.201712280
4. [4]
  Zhang, F.; Zhuang, H. Q.; Song, J.; Men, Y. L.; Pan, Y. X.; Yu, S. H. Appl. Catal. B: Environ. 2018, 226, 103. doi: 10.1016/j.apcatb.2017.12.046
5. [5]
  Fu, J. W.; Xu, Q. L.; Low, J. X.; Jiang, C. J.; Yu, J. G. Appl. Catal. B: Environ. 2019, 243, 556. doi: 10.1016/j.apcatb.2018.11.011
6. [6]
  Zheng, M.; Cao, X. H.; Ding, Y.; Tian, T.; Lin, J. Q. J. Catal. 2018, 363, 109. doi: 10.1016/j.jcat.2018.04.022
7. [7]
  Nocera, D. G. Acc. Chem. Res. 2017, 50, 616. doi: 10.1021/acs.accounts.6b00615
8. [8]
  Zheng, M.; Ding, Y.; Yu, L.; Du, X. Q.; Zhao, Y. K. Adv. Funct. Mater. 2017, 27, 1605846. doi: 10.1002/adfm.201605846
9. [9]
  Zhao, Y. F.; Zhao, Y. X.; Waterhouse, G. I. N.; Zheng, L. R.; Cao, X. Z.; Teng, F.; Wu, L. Z.; Tung, C. H.; Hare, D. O.; Zhang, T. R. Adv. Mater. 2017, 29, 1703828. doi: 10.1002/adma.201703828
10. [10]
  Li, H.; Sun, Y.; Yuan, Z. G.; Zhu, Y. P.; Ma, T. Y. Angew. Chem. Int. Edit. 2018, 57, 3222. doi: 10.1002/anie.201712925
11. [11]
  Zhu, M. S.; Kim, S. Y.; Mao, L.; Fujitsuka, M.; Zhang, J. Y.; Wang, X. C.; Majima, T. J. Am. Chem. Soc. 2017, 139, 13234. doi: 10.1021/jacs.7b08416
12. [12]
  Li, Y. X.; Li, H.; Li, Y. F.; Peng, S. Q.; Hu, Y. H. Chem. Eng. J. 2018, 344, 506. doi: 10.1016/j.cej.2018.03.117
13. [13]
  Ye, P.; Liu, X. L.; Iocozzia, J.; Yuan, Y. P.; Gu, L.; Xu, G. S.; Lin, Z. Q. J. Mater. Chem. A 2017, 5, 8493. doi: 10.1039/C7TA01031A
14. [14]
  She, X. J.; Wu, J. J.; Zhong, J.; Xu, H.; Yang, Y. C.; Vajtai, R.; Lou, J.; Liu, Y.; Du, D. L.; Li, H. M.; Ajayan, P. M. Nano Energy 2016, 27, 138. doi: 10.1016/j.nanoen.2016.06.042
15. [15]
  Cao, S, W.; Low, J. X.; Yu, J. G.; Jaroniec, M. Adv. Mater. 2015, 27, 2150. doi: 10.1002/adma.201500033
16. [16]
  Hao, X. Q.; Wang, Y. C.; Zhou, J.; Cui, Z. W.; Wang, Y.; Zou, Z. G. Appl. Catal. B: Environ. 2018, 221, 302. doi: 10.1016/j.apcatb.2017.09.006
17. [17]
  Chen, J.; Shen, S. H.; Guo, P. H.; Wang, M.; Wu, P.; Wang, X. X.; Guo, L. J. Appl. Catal. B: Environ. 2014, 152–153, 335. doi: 10.1016/j.apcatb.2014.01.047
18. [18]
  Feng, C. C.; Wang, Z. H.; Ma, Y.; Zhang, Y. J.; Wang, L.; Bi, Y. P. Appl. Catal. B: Environ. 2017, 205, 19. doi: 10.1016/j.apcatb.2016.12.014
19. [19]
  Chen, J.; Shen, S. H.; Wu, P.; Guo, L. J. Green Chem. 2015, 17, 509. doi: 10.1039/C4GC01683A
20. [20]
  Wang, Q. Z.; Shi, Y. B.; Du, Z. Y.; He, J. J.; Zhong, J. B.; Zhao, L. C.; She, H. D.; Liu, G.; Su, B. T. Eur. J. Inorg. Chem. 2015, 24, 4108. doi: 10.1002/ejic.201500552
21. [21]
  Zhai, C. Y.; Sun, M. J.; Zeng, L. X.; Xue, M. Q.; Pan, J. G.; Du, Y. K.; Zhu, M. S. Appl. Catal. B: Environ. 2019, 243, 283. doi: 10.1016/j.apcatb.2018.10.047
22. [22]
  Yang, H.; Jin, Z. L.; Hu, H. Y.; Bi, Y. P.; Lu, G. X. Appl. Surf. Sci. 2018, 427, 587. doi: 10.1016/j.apsusc.2017.09.021
23. [23]
  Ding, C. M.; Shi, J. Y.; Wang, Z. L.; Li, C. ACS Catal. 2017, 7, 675. doi: 10.1021/acscatal.6b03107
24. [24]
  Wang, G. R.; Jin, Z. L. Appl. Surf. Sci. 2019, 467–468, 1239. doi: 10.1016/j.apsusc.2018.10.239
25. [25]
  Wang, H. Y.; Wang, G. R.; Liu, Z. W.; Jin, Z. L. Mol. Catal. 2018, 453, 1. doi: 10.1016/j.mcat.2018.04.028
26. [26]
  Chao, Y. G.; Zhou, P.; Li, N.; Lai, J. P.; Yang, Y.; Zhang, Y. L.; Tang, Y. H.; Yang, W. X.; Du, Y. P.; Su, D.; et al. J. Adv. Mater. 2018, 31, 1807226. doi: 10.1002/adma.201807226
27. [27]
  Yang, Y.; Kang, Y. K.; Zhao, H. H.; Dai, X. P.; Cui, M. L.; Luan, X. B.; Zhang, X.; Nie, F.; Ren, Z. T.; Song, W. Y. Small 2019, 16, 1905083. doi: 10.1002/smll.201905083
28. [28]
  Wang, P. W.; Pu, Z. H.; Li, W. Q.; Zhu, J. W.; Zhang, C. T.; Zhao, Y. F.; Mu, S. C. J. Catal. 2019, 377, 600. doi: 10.1016/j.jcat.2019.08.005
29. [29]
  Sun, Y. Q.; Xu, K.; Wei, Z. X.; Li, H. L.; Zhang, T.; Li, X. Y.; Cai, W. P.; Ma, J. M.; Fan, H. J.; Li, Y. Adv. Mater. 2018, 30, 1802121. doi: 10.1002/adma.201802121
30. [30]
  Tang, C.; Cheng, N. Y.; Pu, Z. H.; Xing, W.; Sun, X. P. Angew. Chem. Int. Edit. 2015, 54, 9351. doi: 10.1002/anie.201503407
31. [31]
  Che, Y. P.; Lu, B. X.; Qi, Q.; Chang, H. Q.; Zhai, J.; Wang, K. F.; Liu, Z. Y. Sci. Rep. 2018, 8, 16504. doi: 10.1038/s41598-018-34287-w
32. [32]
  Liu, Y. N.; Shen, C. C.; Jiang, N.; Zhao, Z. W.; Zhou, X.; Zhao, S. J.; Xu, A. W. ACS Catal. 2017, 7, 8228. doi: 10.1021/acscatal.7b03266
33. [33]
  Wu, X. H.; Chen, F. Y.; Wang, X. F.; Yu, H. G. Appl. Surf. Sci. 2018, 427, 645. doi: 10.1016/j.apsusc.2017.08.050
34. [34]
  Akple, M. S.; Low, J. X.; Wageh, S.; Ghamdi, A. A. A.; Yu, J. G.; Zhang, J. Appl. Surf. Sci. 2015, 358, 196. doi: 10.1016/j.apsusc.2015.08.250
35. [35]
  Li, Y. B.; Jin, Z. L.; Zhang, L. J.; Fan, K. Chin. J. Catal. 2019, 40, 390. doi: 10.1016/S1872-2067(18)63173-0
36. [36]
  Xu, M.; Han, L.; Dong, S. J. ACS Appl. Mater. Inter. 2013, 5, 12533. doi: 10.1021/am4038307
37. [37]
  Meng, J.; Lan, Z. Y.; Chen, T.; Lin, Q. Y.; Liu, H.; Wei, X.; Lu, Y. H.; Li, J. X.; Zhang, Z. J. Phys. Chem. 2018, 122, 24725. doi: 10.1021/acs.jpcc.8b07014
38. [38]
  Kang, Y. Y.; Yang, Y. Q.; Yin, L. C.; Kang, X. D.; Liu, G.; Cheng, H, M. Adv. Mater. 2015, 27, 4572. doi: 10.1002/adma.201501939
39. [39]
  Han, Q.; Zhao, F.; Hu, C. G.; Lv, L. X.; Zhang, Z. P.; Chen, N.; Qu, L. T. Nano Res. 2015, 8, 1718. doi: 10.1007/s12274-014-0675-9
40. [40]
  Liang, Q. H.; Li, Z.; Huang, Z. H.; Kang, F. Y.; Yang, Q. H. Adv. Funct. Mater. 2015, 25, 6885. doi: 10.1002/adfm.201503221
41. [41]
  Zhang, G.G.; Zhang, M. W.; Ye, X. X.; Qiu, X. Q.; Lin, S.; Wang, X. C. Adv. Mater. 2014, 26, 805. doi: 10.1002/adma.201303611
42. [42]
  Wang, H. Y.; Jin, Z. L.; Hao, X. Q. Dalton Trans. 2019, 48, 4015. doi: 10.1039/C9DT00586B
43. [43]
  Xing, Z. C.; Liu, Q.; Asiri, A. M.; Sun, X. P. Adv. Mater. 2014, 26, 5702. doi: 10.1002/adma.201401692
44. [44]
  Li, H. Y.; Gao, D.; Cheng, X. Electrochim. Acta 2014, 138, 232. doi: 10.1016/j.electacta.2014.06.065
45. [45]
  Zhang, H. X.; Yang, B.; Wu, X. L.; Li, Z. J.; Lei, L. C.; Zhang, X. W. ACS Appl. Mater. Inter. 2015, 7, 1772. doi: 10.1021/am507373g
46. [46]
  Elbanna, O.; Fujitsuka, M.; Majima, T. ACS Appl. Mater. Inter. 2017, 9, 34844. doi: 10.1021/acsami.7b08548
47. [47]
  Lin, Z. Y.; Du, C.; Yan, B.; Wang, C. X.; Yang, G. W. Nat. Commun. 2018, 9, 4036. doi: 10.1038/s41467-018-06456-y
48. [48]
  Liang, Q. H.; Li, Z.; Huang, Z. H.; Kang, F. Y.; Yang, Q. H. Adv. Funct. Mater. 2015, 25, 6885. doi: 10.1002/adfm.201503221
49. [49]
  Tong, Z. W.; Yang, D.; Li, Z.; Nan, Y. H.; Ding, F.; Shen, Y. C.; Jiang, Z. Y. ACS Nano 2017, 11, 1103. doi: 10.1021/acsnano.6b08251
50. [50]
  Yan, J. M.; Yi, S. S.; Wulan, B. R.; Li, S. J.; Liu, K. H.; Jiang, Q. Appl. Catal. B: Environ. 2017, 200, 477. doi: 10.1016/j.apcatb.2016.07.046.

扫一扫看文章

计量

PDF下载量: 72
文章访问数: 996
HTML全文浏览量: 52

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

Ni, Co基硒化物修饰g-C₃N₄光催化产氢研究

通讯作者: 李彦兵, 1757039358@qq.com
郝旭强, haoxuqiang@126.com

English

Ni, Co-Based Selenide Anchored g-C₃N₄ for Boosting Photocatalytic Hydrogen Evolution

Corresponding author: Yanbing Li, 1757039358@qq.com Xuqiang Hao, haoxuqiang@126.com

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

CCS Chemistry：颜徐州、鲍哲南：你的皮肤可能是一片SPMs

CCS Chemistry：工作高效不疲劳，只须让催化剂动起来

CCS Chemistry：静电组装导向聚合- 聚电解质纳米凝胶量化制备新策略

CCS Chemistry：金黄色葡萄球菌醛基脱氢酶是如何识别特异性底物的？

计量

通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处

Ni, Co基硒化物修饰g-C3N4光催化产氢研究

通讯作者: 李彦兵, 1757039358@qq.com 郝旭强, haoxuqiang@126.com

English

Ni, Co-Based Selenide Anchored g-C3N4 for Boosting Photocatalytic Hydrogen Evolution

Corresponding author: Yanbing Li, 1757039358@qq.com Xuqiang Hao, haoxuqiang@126.com

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

CCS Chemistry：颜徐州、鲍哲南： 你的皮肤可能是一片SPMs

CCS Chemistry：工作高效不疲劳，只须让催化剂动起来

CCS Chemistry：静电组装导向聚合- 聚电解质纳米凝胶量化制备新策略

CCS Chemistry：金黄色葡萄球菌醛基脱氢酶是如何识别特异性底物的？

计量

文章相关

通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处

Ni, Co基硒化物修饰g-C₃N₄光催化产氢研究

通讯作者: 李彦兵, 1757039358@qq.com
郝旭强, haoxuqiang@126.com

Ni, Co-Based Selenide Anchored g-C₃N₄ for Boosting Photocatalytic Hydrogen Evolution

CCS Chemistry：颜徐州、鲍哲南：你的皮肤可能是一片SPMs