Graphitic C3N4 Decorated with CoP Co‐catalyst: Enhanced and Stable Photocatalytic H2 Evolution Activity from Water under Visible‐light Irradiation

Chemistry - An Asian Journal - Tập 12 Số 3 - Trang 361-365 - 2017
Hui Zhao1, Pingping Jiang2, Wen Cai3
1Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, Jiangsu Engineering and Technology Research Center of Environmental Cleaning Materials, Collaborative Innovation Center of Atmospheric Environment and Equipment Technology, School of Environmental Science and Engineering, Nanjing University of Information Science & Technology, 219 Ningliu Road, Nanjing, 210044 China
2Key Laboratory of Food Colloids and Biotechnology (Ministry of Education of China), School of Chemical and Material Engineering, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122 China
3Institute of Medical Engineering, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, 76 West Yanta Road, Xi'an, 710061 China

Tóm tắt

AbstractIn this work, graphitic C3N4 decorated with a CoP co‐catalyst (g‐C3N4/CoP) is reported for photocatalytic H2 evolution reaction based on two‐step hydrothermal and phosphidation method. The structure of g‐C3N4/CoP is well confirmed by XRD, FTIR, TEM, XPS, and UV/Vis diffuse reflection spectra techniques. When the weight percentage of CoP loading is 3.4 wt % (g‐C3N4/CoP‐3.4 %), the highest H2 evolution amount of 8.4×102 μmol g−1 is obtained, which is 1.1×103 times than that over pure g‐C3N4. This value also is comparable with that of g‐C3N4 loaded by the same amount of Pt. In cycling experiments, g‐C3N4/CoP‐3.4 % shows a stable photocatalytic activity. In addition, g‐C3N4/CoP‐3.4 % is an efficient photocatalyst for H2 evolution under irradiation with natural solar light. Based on comparative photoluminescence emission spectra, photoelectrochemical I–t curves, EIS Nyquist plots, and polarization curves between g‐C3N4/CoP‐3.4 % and pure g‐C3N4, it is concluded that the presence of the CoP co‐catalyst accelerates the separation and transfer of photogenerated electrons of g‐C3N4, thus resulting in improved photocatalytic activity in the H2 evolution reaction.

Từ khóa


Tài liệu tham khảo

10.1021/ja302846n

10.1039/C3GC42466A

10.1039/c3ee43750g

10.1021/cr0500535

10.1021/cr1001645

10.1039/c2nr11972b

10.1038/nmat2317

10.1002/anie.200903886

10.1002/ange.200903886

10.1002/anie.201101182

10.1002/ange.201101182

10.1021/cs300240x

10.1002/adma.201500033

10.1016/j.apcatb.2014.01.046

10.1016/j.apcatb.2014.01.047

10.1039/C4GC01517G

10.1021/jz500546b

10.1002/chem.201400060

10.1002/anie.201403375

10.1002/ange.201403375

10.1021/jp809119m

10.1002/cctc.201000057

10.1039/C5CC07936E

10.1002/cssc.201300647

10.1039/C5CP01657F

10.1016/j.ijhydene.2014.06.025

10.1002/anie.201210294

10.1002/ange.201210294

10.1039/c3ra46362a

10.1039/c3cy20878h

10.1021/jp200953k

10.1016/j.ijhydene.2012.03.123

10.1039/C4CP02613F

10.1002/anie.201404161

10.1002/ange.201404161

10.1021/acs.chemmater.6b02148

10.1021/ja503372r

10.1002/anie.201402646

10.1002/ange.201402646

10.1021/acs.jpclett.5b00495

10.1039/C5CC01799H

10.1039/C6RA04612F

10.1016/j.apcatb.2016.07.046

10.1039/C5EE02650D

10.1021/acsami.5b04947

10.1039/C4TA02368D

10.1021/acsami.5b09207

10.1039/C5CY02299A

10.1039/C4TA07149B

10.1021/jp5000232

10.1039/b904668b

10.1002/adfm.201200922

10.1021/ja305623m

10.1016/j.apcatb.2014.10.045