TY - JOUR
T1 - Band Sharpening and Band Alignment Enable High Quality Factor to Enhance Thermoelectric Performance in n-Type PbS
AU - Xiao, Yu
AU - Wang, Dongyang
AU - Zhang, Yang
AU - Chen, Congrun
AU - Zhang, Shuxuan
AU - Wang, Kedong
AU - Wang, Guangtao
AU - Pennycook, Stephen J.
AU - Snyder, G. Jeffrey
AU - Wu, Haijun
AU - Zhao, Li Dong
N1 - Funding Information:
L.D.Z. acknowledges the support on this topic from the National Key Research and Development Program of China (2018YFA0702100 and 2018YFB0703600), National Natural Science Foundation of China (51772012 and 51671015), and Beijing Natural Science Foundation (JQ18004), Shenzhen Peacock Plan team (KQTD2016022619565991) and 111 Project (B17002). Y.X. is thankful for the financial support from National Postdoctoral Program for Innovative Talents (BX20190028) and Postdoctoral Science Foundation of China (2019M660399). G.W. is thankful for the support from the High Performance Computing Center of Henan Normal University. H.W. would like to acknowledge the financial support from Singapore Ministry of Education Tier 1 grant, R-284-000-212-114, for Lee Kuan Yew Postdoctoral Fellowship. S.J.P and H.W. would like to acknowledge the financial support by the Ministry of Education, Singapore under its Tier 2 Grant (MOE2017-T2-1-129). L.D.Z. is thankful for the support from the National Science Fund for Distinguished Young Scholars (51925101).
Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/2/26
Y1 - 2020/2/26
N2 - Low-cost and earth-abundant PbS-based thermoelectrics are expected to be an alternative for PbTe, and have attracted extensive attentions from thermoelectric community. Herein, a maximum ZT (ZTmax) ≈ 1.3 at 923 K in n-type PbS is obtained through synergistically optimizing quality factor with Sn alloying and PbTe phase incorporation. It is found that Sn alloying in PbS can sharpen the conduction band shape to balance the contradictory interrelationship between carrier mobility and effective mass, accordingly, a peak power factor of ∼19.8 μWcm-1K-2 is achieved. Besides band sharpening, Sn alloying can also narrow the band gap of PbS so as to make the conduction band position between Pb0.94Sn0.06S and PbTe well aligned, which can benefit high carrier mobility. Therefore, incorporating the PbTe phase into the Pb0.94Sn0.06S matrix can not only favorably maintain the carrier mobility at ∼150 cm2V-1s-1 but also suppress the lattice thermal conductivity to ∼0.61 Wm-1K-1 in Pb0.94Sn0.06S-8%PbTe, which contributes to a largely enhanced quality factor. Consequently, an average ZT (ZTave) ≈ 0.72 in 300-923 K is achieved in Pb0.94Sn0.06S-8%PbTe that outperforms other n-type PbS-based thermoelectric materials.
AB - Low-cost and earth-abundant PbS-based thermoelectrics are expected to be an alternative for PbTe, and have attracted extensive attentions from thermoelectric community. Herein, a maximum ZT (ZTmax) ≈ 1.3 at 923 K in n-type PbS is obtained through synergistically optimizing quality factor with Sn alloying and PbTe phase incorporation. It is found that Sn alloying in PbS can sharpen the conduction band shape to balance the contradictory interrelationship between carrier mobility and effective mass, accordingly, a peak power factor of ∼19.8 μWcm-1K-2 is achieved. Besides band sharpening, Sn alloying can also narrow the band gap of PbS so as to make the conduction band position between Pb0.94Sn0.06S and PbTe well aligned, which can benefit high carrier mobility. Therefore, incorporating the PbTe phase into the Pb0.94Sn0.06S matrix can not only favorably maintain the carrier mobility at ∼150 cm2V-1s-1 but also suppress the lattice thermal conductivity to ∼0.61 Wm-1K-1 in Pb0.94Sn0.06S-8%PbTe, which contributes to a largely enhanced quality factor. Consequently, an average ZT (ZTave) ≈ 0.72 in 300-923 K is achieved in Pb0.94Sn0.06S-8%PbTe that outperforms other n-type PbS-based thermoelectric materials.
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U2 - 10.1021/jacs.0c00306
DO - 10.1021/jacs.0c00306
M3 - Article
C2 - 32017566
AN - SCOPUS:85080993256
SN - 0002-7863
VL - 142
SP - 4051
EP - 4060
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 8
ER -