光电催化二氧化碳还原研究进展

引用本文: 周威, 郭君康, 申升, 潘金波, 唐杰, 陈浪, 区泽堂, 尹双凤. 光电催化二氧化碳还原研究进展[J]. 物理化学学报, 2020, 36(3): 190604. doi: 10.3866/PKU.WHXB201906048 shu

Citation: Zhou Wei, Guo Jun-Kang, Shen Sheng, Pan Jinbo, Tang Jie, Chen Lang, Au Chak-Tong, Yin Shuang-Feng. Progress in Photoelectrocatalytic Reduction of Carbon Dioxide[J]. Acta Physico-Chimica Sinica, 2020, 36(3): 190604. doi: 10.3866/PKU.WHXB201906048 shu

光电催化二氧化碳还原研究进展

周威 ^1, ,
郭君康 ^1, ,
申升 ^1, ,
潘金波 ^1, ,
唐杰 ^1, ,
陈浪 ^1, ,
区泽堂 ^2, ,
尹双凤 ^{1,
,}

1.
湖南大学化学化工学院，化学/生物传感与化学计量学国家重点实验室，化石能源低碳化高效利用湖南省重点实验室，湖南长沙 410082
2.
湖南工程学院化学与化学工程学院，湖南湘潭 411104

作者简介:

尹双凤，1996年在北京化工大学获得学士学位，1999年在中石化石油化工科学研究院获得硕士学位，2003年在清华大学获得博士学位。2006年晋升为湖南大学教授。2008年至2009年在香港浸会大学和日本综合工业技术研究所任高级访问学者。现任湖南大学化学与化工学院教授、博导。研究方向：光催化、小分子烃催化转化及新材料研究;

通讯作者: 尹双凤, sf_yin@hnu.edu.cn

基金项目:

国家自然科学基金(21725602, 21476065, 21671062, 21776064), 湖南省创新研究群体(2019JJ10001), 湖南省研究生科研创新项目(CX2018B193)资助项目

摘要: CO₂是最常见的化合物，作为潜在的碳一资源，可用于制备多种高附加值的化学品，如一氧化碳、甲烷、甲醇、甲酸等。传统的热催化转化CO₂方法能耗高，反应条件苛刻。因此，如何在温和条件下高效地将CO₂转化成高附加值的化学品，一直以来是催化领域的研究热点和难点之一。光催化技术反应条件温和、绿色环保。然而，纯光催化反应普遍存在太阳能利用效率有限，光生载流子分离效率低等问题。针对上述问题，在光催化的基础上引入电催化，可以提高载流子的分离效率，在较低的过电位下，实现多电子、质子向CO₂转移，从而提高催化反应效率。总之，光电催化技术可以结合光催化和电催化的优势，提高CO₂催化还原反应效率，为清洁、绿色利用CO₂提供了一种新方法。本文依据光电催化CO₂还原反应基本过程，从光吸收、载流子分离和界面反应等三个角度综述了光电催化反应的基本强化策略，并对未来可能的研究方向进行了展望。

关键词:

English

Progress in Photoelectrocatalytic Reduction of Carbon Dioxide

1.
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Provincial Hunan Key Laboratory for Cost-Effective Utilization of Fossil Fuel Aimed at Reducing Carbon-Dioxide Emissions, Hunan University, Changsha 410082, P. R. China
2.
College of Chemistry and Chemical Engineering, Hunan Institute of Engineering, Xiangtan 411104, Hunan Province, P. R. China

Corresponding author: Shuang-Feng Yin, Email: sf_yin@hnu.edu.cn; Tel.: +86-13755068036

Received Date: 13 June 2019
Accepted Date: 13 August 2019
Revised Date: 30 July 2019
Available Online: 15 March 2020
Fund Project:

This project was financially supported by the National Natural Science Foundation of China (21725602, 21476065, 21671062, 21776064), Innovative Research Groups of Hunan Province, China (2019JJ10001), Hunan Provincial Innovation Foundation for Postgraduate, China (CX2018B193)

Abstract: Carbon dioxide is the most common compound. As a potential source of carbon, it can be used to prepare a variety of high value-added chemicals, such as carbon monoxide, methane, methanol, and formic acid. The traditional method of thermal catalytic conversion of CO₂ requires high energy consumption and harsh reaction conditions. Therefore, the efficient conversion of CO₂ to value-added chemicals under mild conditions has long been an area of great interest in the field of catalysis. Photocatalysis usually takes place under mild reaction conditions and is environmentally friendly. However, pure photocatalytic reactions generally have a limited solar energy utilization efficiency and low separation efficiency of photogenerated charge carriers. In view of the above problems, the introduction of electrocatalysis on the basis of photocatalysis can improve the charge separation efficiency. At a lower overpotential, multi-electrons and protons can be transferred to CO₂, thus improving the catalytic reaction efficiency. Photoelectrochemical catalysis combines the advantages of photocatalysis and electrocatalysis to improve the efficiency of the catalytic reduction of CO₂, offering a new method for the clean utilization of CO₂. According to the principle of photocatalysis, the absorption capacity of a semiconductor is governed by its band structure. Optimization of the band structure is a major strategy to enhance the absorptivity of photocatalysts. In addition, the loading of light-absorbent materials on photocatalysts is an effective way to enhance the photocatalytic absorption of a photocatalytic system. During photoelectrocatalytic CO₂ reduction, numerous photogenerated charge carriers recombine in bulk and on the surface of the catalyst, greatly reducing the efficiency of the catalytic reaction. Therefore, increasing the separation efficiency of charge carriers is an important means to improve the photoelectrocatalytic efficiency. In photoelectrocatalytic CO₂ reduction, heterojunction construction and electric field formation often lead to the efficient separation of charge carriers. The interfacial reaction is a crucial step in the photoelectrocatalytic process. After generation, the photogenerated charge carriers need to migrate to the surface of the catalyst to participate in the redox reaction. In photoelectrocatalytic CO₂ reduction, electrons participate in the reduction of CO₂, while holes participate in the oxidation of water. Studies show that acceleration of the interfacial reaction process is of paramount importance for improving the efficiency of the photoelectrocatalytic reduction of CO₂. This review summarizes the basic enhancement strategies of photoelectrocatalytic CO₂ reduction from three aspects: light absorption, charge separation, and surface reaction, based on the basic mechanism of the reduction. The future prospects and research areas are also proposed.

Key words:

1. [1]
  Wang, W.; Wang, S.; Ma, X.; Gong, J. L. Chem. Soc. Rev. 2011, 40, 3703. doi: 10.1039/C1CS15008A
2. [2]
  Halmann, M. Nature 1978, 275, 115. doi: 10.1038/275115a0
3. [3]
  Gonell, F.; Puga, A. V.; Julián-López, B.; García, H.; Corma, A. Appl. Catal. B-Environ. 2016, 180, 263. doi: 10.1016/j.apcatb.2015.06.019
4. [4]
  Zong, X.; Sun, C.; Yu, H.; Chen, Z. G.; Xing, Z.; Ye, D.; Lu, G. Q.; Li, X.; Wang, L. J. Phys. Chem. C 2013, 117, 4937. doi: 10.1021/jp311729b
5. [5]
  Handoko, A. D.; Tang, J. Int. J. Hydrog. Energy 2013, 38, 13017. doi: 10.1016/j.ijhydene.2013.03.128
6. [6]
  Chen, X. Y.; Zhou, Y.; Liu, Q.; Li, Z.; Liu, J.; Zou, Z. ACS Appl. Mater. Inter. 2012, 4, 3372. doi: 10.1021/am300661s
7. [7]
  Wang, S. B.; Wang, X. C. Appl. Catal. B-Environ. 2015, 162, 494. doi: 10.1016/j.apcatb.2014.07.026
8. [8]
  Barton, E. E.; Rampulla, D. M.; Bocarsly, A. B. J. Am. Chem. Soc. 2008, 130, 6342. doi: 10.1021/ja0776327
9. [9]
  Li, Q.; Zheng, M.; Zhong, M.; Ma, L.; Wang, F.; Ma, L.; Shen, W. Sci. Rep. 2016, 6, 29738. doi: 10.1038/srep29738
10. [10]
  Sun, Z.; Yang, Z.; Liu, H.; Wang, H.; Wu, Z. Appl. Surf. Sci. 2014, 315, 360. doi: 10.1016/j.apsusc.2014.07.153
11. [11]
  Chen, X. Y.; Yu, T.; Gao, F.; Zhang, H. T.; Liu, L. F.; Wang, Y. M.; Li, Z. S.; Zou, Z. G.; Liu, J. M. Appl. Phys. Lett. 2007, 91, 022114. doi: 10.1063/1.2757132
12. [12]
  Zhou, P.; Yan, S. C.; Zou, Z. G. CrystEngComm 2015, 17, 992. doi: 10.1039/c4ce02198c
13. [13]
  Thaweesak, S.; Lyu, M.; Peerakiatkhajohn, P.; Butburee, T.; Luo, B.; Chen, H.; Wang, L. Appl. Catal. B-Environ. 2017, 202, 184. doi: 10.1016/j.apcatb.2016.09.022
14. [14]
  Wang, S. B.; Ding, Z. X.; Wang, X. C. Chem. Commun. 2015, 51, 1517. doi: 10.1039/c4cc07225a
15. [15]
  Wang, S. B.; Hou, Y. D.; Wang, X. C. ACS Appl. Mater. Inter. 2015, 7, 4327. doi: 10.1021/am508766s
16. [16]
  Wang, S. B.; Wang, X. C. Angew. Chem. Int. Edit. 2016, 55, 2308. doi: 10.1002/anie.201507145
17. [17]
  Qin, J.; Wang, S.; Wang, X. C. Appl. Catal. B-Environ. 2017, 209, 476. doi: 10.1016/j.apcatb.2017.03.018
18. [18]
  Wang, S. B.; Yao, W. S.; Lin, J. L.; Ding, Z. X.; Wang, X. C. Angew. Chem. Int. Edit. 2014, 53, 1034. doi: 10.1002/ange.201310957
19. [19]
  Wang, X. C.; Maeda, K.; Thomas, A.; Takanabe, K.; Xin, G.; Carlsson, J. M.; Domen, K.; Antonietti, M. Nat. Mater. 2009, 8, 76. doi: 10.1142/9789814317665_0039
20. [20]
  Ou, H. H.; Lin, L. H.; Zheng, Y.; Yang, P. J.; Fang, Y. X.; Wang, X. C. Adv. Mater. 2017, 29, 1700008. doi: 10.1002/adma.201700008
21. [21]
  Qin, J. N.; Wang, S. B.; Ren, H.; Hou, Y. D.; Wang, X. C. Appl. Catal. B-Environ. 2015, 179, 1. doi: 10.1016/j.apcatb.2015.05.005
22. [22]
  García, A.; Fernandez-Blanco, C.; Herance, J. R.; Albero, J.; García, H. J. Mater. Chem. A 2017, 5, 16522. doi: 10.1039/c7ta04045h
23. [23]
  Wang, P. L.; Wang, S. C.; Wang, H. Q.; Wu, Z. B.; Wang, L. Z. Part. Part. Syst. Char. 2018, 35, 1700371. doi: 10.1002/ppsc.201700371
24. [24]
  Zhang, N.; Long, R.; Gao, C.; Xiong, Y. J. Sci. Chin. Mater. 2018, 61, 771. doi: 10.1007/s40843-017-9151-y
25. [25]
  Chang, X. X.; Wang, T.; Yang, P. P.; Zhang, G.; Gong, J. L. Adv. Mater. 2018, 31, 1804710. doi: 10.1002/adma.201804710
26. [26]
  Castro, S.; Albo, J.; Irabien, A. ACS Sustain. Chem. Eng. 2018, 6, 15877. doi: 10.1021/acssuschemeng.8b03706
27. [27]
  Pradhan, N.; Adhikari, S. D.; Nag, A.; Sarma, D. D. Angew. Chem. Int. Edit. 2016, 56, 7038. doi: 10.1002/anie.201611526
28. [28]
  Linic, S. J.; Christopher, P.; Ingram, D. B. Nat. Mater. 2011, 10, 911. doi: 10.1038/nmat3151
29. [29]
  Gu, J.; Wuttig, A.; Krizan, J. W.; Hu, Y.; Detweiler, Z. M.; Cava, R. J.; Bocarsly, A. B. J. Phys. Chem. C 2013, 117, 12415. doi: 10.1021/jp402007z
30. [30]
  Xie, K.; Umezawa, N.; Zhang, N.; Reunchan, P.; Zhang, Y.; Ye, J. H. Energ. Environ. Sci. 2011, 4, 4211. doi: 10.1039/c1ee01594j
31. [31]
  Cuong, D. D; Lee, B; Choi, K. M; Ahn, H-S; Han, S. W; Lee, J. C. Phys. Rev. Lett. 2007, 98, 115503. doi: 10.1103/physrevlett.98.115503
32. [32]
  Cordero, F. Phys. Rev. B 2007, 76, 172106. doi: 10.1103/physrevb.76.172106
33. [33]
  Cushing, S. K.; Li, J.; Meng, F.; Senty, T. R.; Suri, S.; Zhi, M. J.; Li, M.; Bristow, A. D.; Wu, N. Q. J. Am. Chem. Soc. 2012, 134, 15033. doi: 10.1021/ja305603t
34. [34]
  DuChene, J. S.; Tagliabue, G.; Welch, A. J.; Cheng, W. H.; Atwater, H. A. Nano Lett. 2018, 18, 2545. doi: 10.1021/acs.nanolett.8b00241
35. [35]
  Hou, J. G.; Cheng, H. J.; Takeda, O.; Zhu, H. M. Angew. Chem. Int. Edit. 2015, 127, 8480. doi: 10.1002/ange.201502319
36. [36]
  Kim, Y.; Creel, E. B.; Corson, E. R.; McCloskey, B. D.; Urban, J. J.; Kostecki, R. Adv. Energy Mater. 2018, 8, 1800363. doi: 10.1002/aenm.201800363
37. [37]
  Shen, Q.; Chen, Z. F.; Huang, X. F.; Liu, M. C.; Zhao, G. H. Environ. Sci. Technol. 2015, 49, 5828. doi: 10.1021/acs.est.5b00066
38. [38]
  Xu, Y. J.; Jia, Y. J.; Zhang, Y. Q.; Nie, R.; Zhu, Z. P.; Wang, J. G.; Jing, H. W. Appl. Catal. B-Environ. 2017, 205, 254. doi: 10.1016/j.apcatb.2016.12.039
39. [39]
  Song, Q. Q.; Li, J. Q.; Wang, L.; Qin, Y.; Pang, L. Y.; Liu, H. J. Catal. 2019, 370, 176. doi: 10.1016/j.jcat.2018.12.021
40. [40]
  Li, A.; Wang, T.; Li, C. C.; Huang, Z. Q.; Luo, Z. B.; Gong, J. L. Angew. Chem. Int. Edit. 2018, 58, 3804. doi: 10.1002/anie.201812773
41. [41]
  Xu, Q. L.; Zhang, L. Y.; Yu, J. G.; Wageh, S.; Al-Ghamdi, A. A.; Jaroniec, M. Mater. Today 2018, 21, 1042. doi: 10.1016/j.mattod.2018.04.008
42. [42]
  Zheng, J. G.; Li, X. J.; Qin, Y. H.; Zhang, S. Q.; Sun, M. S.; Duan, X. G.; Sun, H. Q.; Li, P. Q.; Wang, S. B. J. Catal. 2019, 371, 214. doi: 10.1016/j.jcat.2019.01.022
43. [43]
  Guzmán D. G.; Isaacs M.; Osorio-Román I; García, M.; Astudillo, J.; Ohlbaum, M. ACS Appl. Mater. Inter. 2015, 7, 19865. doi: 10.1021/acsami.5b05722
44. [44]
  Zheng, J. G.; Hu, F. Y.; Han, E.; Pan, Z. B.; Zhang, S.; Li, Y.; Qin, P. G.; Wang, H.; Li, P. Q.; Yin, H. Z. Colloids Surfaces A. 2019, 575, 329. doi: 10.1016/j.colsurfa.2019.05.016
45. [45]
  Cardoso, J. C.; Stulp, S.; de Brito, J. F.; Flor, J. B. S.; Frem, R. C. G.; Zanoni, M. V. B. Appl. Catal. B-Environ. 2018, 225, 563. doi: 10.1016/j.apcatb.2017.12.013
46. [46]
  Shen, Q.; Huang, X. F.; Liu, J. B.; Guo, C. Y.; Zhao, G. H. Appl. Catal. B-Environ. 2017, 201, 70. doi: 10.1016/j.apcatb.2016.08.008
47. [47]
  Huang, X. F.; Shen, Q.; Liu, J. B.; Yang, N. J.; Zhao, G. H. Energ. Environ. Sci. 2016, 9, 3161. doi: 10.1039/c6ee00968a
48. [48]
  Xiao, M.; Luo, B.; Wang, S. C.; Wang, L. Z. J. Energy Chem. 2018, 27, 1111. doi: 10.1016/j.jechem.2018.02.018
49. [49]
  Suhadolnik, L.; Pohar, A.; Likozar, B.; Čeh, M. Chem. Eng. J. 2016, 303, 292. doi: 10.1016/j.cej.2016.06.027
50. [50]
  Sun, T.; Wang, Y.; Al-Mamun, M.; Zhang, H.; Liu, P.; Zhao, H. J. RSC Adv. 2015, 5, 12860. doi: 10.1039/c4ra15336g
51. [51]
  Yang, X.; Fugate, E. A.; Mueanngern, Y.; Baker, L. R. ACS Catal. 2017, 7, 177. doi: 10.1021/acscatal.6b02984
52. [52]
  Mora-Hernandez, J M; Huerta-Flores, A M; Torres-Martínez, L. M. J. CO₂ Utiliz. 2018, 27, 179. doi: 10.1016/j.jcou.2018.07.014
53. [53]
  Meng, X. C.; Zhang, Z. S. Catal. Today 2018, 315, 2. doi: 10.1016/j.cattod.2018.03.015
54. [54]
  Hasan, M. R.; Hamid, S. B. A.; Basirun, W. J. Appl. Surf. Sci. 2015, 339, 22. doi: 10.1016/j.apsusc.2015.02.162
55. [55]
  Hasan, M. R.; Abd Hamid, S. B.; Basirun, W. J. RSC Adv. 2015, 5, 77803. doi: 10.1039/c5ra12525a

扫一扫看文章

计量

PDF下载量: 145
文章访问数: 4293
HTML全文浏览量: 2109

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

光电催化二氧化碳还原研究进展

通讯作者: 尹双凤, sf_yin@hnu.edu.cn

English

Progress in Photoelectrocatalytic Reduction of Carbon Dioxide

Corresponding author: Shuang-Feng Yin, Email: sf_yin@hnu.edu.cn; Tel.: +86-13755068036

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

光电催化二氧化碳还原研究进展

通讯作者: 尹双凤, sf_yin@hnu.edu.cn

English

Progress in Photoelectrocatalytic Reduction of Carbon Dioxide

Corresponding author: Shuang-Feng Yin, Email: sf_yin@hnu.edu.cn; Tel.: +86-13755068036

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

CCS Chemistry：颜徐州、鲍哲南：你的皮肤可能是一片SPMs