Xin He

Xin He


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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11 March 2019 in Nature Materials
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Journal Article
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YGYue Gao
Yue Gao
ZYZhifei Yan
Zhifei Yan
JGJennifer L. Gray
Jennifer L. Gray
XHXin He
Xin He
DWDaiwei Wang
Daiwei Wang
DWDonghai Wang
Donghai Wang

11 October 2017 in Nature Communications
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Journal Article
Open access
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GLGuoxing Li
Guoxing Li
YGYue Gao
Yue Gao
XHXin He
Xin He
QHQingquan Huang
Qingquan Huang
SCShuru Chen
Shuru Chen
DWDonghai Wang
Donghai Wang
Lithium metal is a promising anode candidate for the next-generation rechargeable battery due to its highest specific capacity (3860 mA h g−1) and lowest potential, but low Coulombic efficiency and formation of lithium dendrites hinder its practical application. Here, we report a self-formed flexible hybrid solid-electrolyte interphase layer through co-deposition of organosulfides/organopolysulfides and inorganic lithium salts using sulfur-containing polymers as an additive in the electrolyte. The organosulfides/organopolysulfides serve as “plasticizer” in the solid-electrolyte interphase layer to improve its mechanical flexibility and toughness. The as-formed robust solid-electrolyte interphase layers enable dendrite-free lithium deposition and significantly improve Coulombic efficiency (99% over 400 cycles at a current density of 2 mA cm−2). A lithium-sulfur battery based on this strategy exhibits long cycling life (1000 cycles) and good capacity retention. This study reveals an avenue to effectively fabricate stable solid-electrolyte interphase layer for solving the issues associated with lithium metal anodes.

4 May 2018 in The Journal of Physical Chemistry C
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Journal Article
Closed access
LCLei Chen
Lei Chen
XHXin He
Xin He
HLHongshen Liu
Hongshen Liu
LQLinmao Qian
Linmao Qian
Seong H. KimSeong H. Kim
Seong H. Kim

11 April 2014 in ACS Applied Materials & Interfaces
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Journal Article
Closed access
YLYafei Li
Yafei Li
YSYanlei Su
Yanlei Su
Xueting ZhaoXueting Zhao
Xueting Zhao
XHXin He
Xin He
RZRunnan Zhang
Runnan Zhang
Zhongyi JiangZhongyi Jiang
Zhongyi Jiang

1 September 2014 in Journal of Membrane Science
Verified
Journal Article
Closed access
JZJiaojiao Zhao
Jiaojiao Zhao
YSYanlei Su
Yanlei Su
XHXin He
Xin He
Xueting ZhaoXueting Zhao
Xueting Zhao
YLYafei Li
Yafei Li
ZJZhongyi Jiang
Zhongyi Jiang

22 August 2018 in Lubricants
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Journal Article
Open access
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ZCZhe Chen
Zhe Chen
XHXin He
Xin He
CXChen Xiao
Chen Xiao
Seong H. KimSeong H. Kim
Seong H. Kim
The friction and wear behavior of materials are not intrinsic properties, but extrinsic properties; in other words, they can drastically vary depending on test and environmental conditions. In ambient air, humidity is one such extrinsic parameter. This paper reviews the effects of humidity on macro- and nano-scale friction and wear of various types of materials. The materials included in this review are graphite and graphene, diamond-like carbon (DLC) films, ultrananocrystalline diamond (UNCD), transition metal dichalcogenides (TMDs), hexagonal boron nitride (h-BN), boric acid, silicon, silicon oxide, silicates, advanced ceramics, and metals. Details of underlying mechanisms governing friction and wear behaviors vary depending on materials and humidity; nonetheless, a comparison of various material cases revealed an overarching trend. Tribochemical reactions between the tribo-materials and the adsorbed water molecules play significant roles; such reactions can occur at defect sites in the case of two-dimensionally layered materials and carbon-based materials, or even on low energy surfaces in the case of metals and oxide materials. It is extremely important to consider the effects of adsorbed water layer thickness and structure for a full understanding of tribological properties of materials in ambient air.